Patent Application
20240025939
The present disclosure generally relates to compositions and methods for the synthesis of nucleic acid molecules with low error rates. Provided, as examples, are compositions and methods for high throughput synthesis and assembly of nucleic acid molecules, in many instances, with high sequence fidelity. In many instances, thermostable mismatch recognition proteins (e.g., thermostable mismatch binding protein, thermostable mismatch endonucleases) will be present in compositions and use methods provided.
Over the years, gene synthesis has become more cost effective and efforts to develop high throughput synthesis platforms in which the nucleic acid molecules produced have high sequence fidelity.
Biological materials that can be used in processes for generating nucleic acid molecules produced have high sequence fidelity have evolved along with the organisms that produce these materials. Such biological materials include DNA polymerases with proof reading abilities and materials involved in various pathways for correction of nucleic acid sequence errors (e.g., mismatch endonucleases, mismatch binding proteins, etc.).
With progress in genetic engineering, a need for the generation of larger nucleic acid molecules has developed. In many instances, nucleic acid assembly methods start with the synthesis of relatively short nucleic acid molecules (e.g., chemically synthesized oligonucleotides), followed by the generation of double-stranded fragments or sub-assemblies (e.g., by annealing and elongating multiple overlapping oligonucleotides), and often proceeds to build larger assemblies such as genes, operons or even functional biological pathways (e.g., by ligation, enzymatic elongation, recombination or a combination thereof). The present disclosure generally relates to compositions and methods for the assembly of nucleic acid molecules having high sequence fidelity.
The present disclosure relates, in part, to compositions and methods for the assembly (e.g., by assembly PCR) and amplification of nucleic acid molecules having high nucleotide sequence fidelity. Compositions and methods set out herein may contain or employ proteins that can detect and/or eliminate nucleic acid molecules that contain errors (e.g., DNA polymerases, mismatch endonucleases, mismatch binding proteins, etc.).
In some aspects, provided herein are methods for generating error corrected populations of nucleic acid molecules. Such methods may include: (a) assembling oligonucleotides with regions of terminal sequence complementarity (single-stranded regions that, upon hybridization, form double-stranded regions of from about 10 to about 30, from about 12 to about 30, from about 15 to about 30, from about 20 to about 30, from about 15 to about 40, from about 6 to about 20, from about 8 to about 25, etc., base pairs in length) by primary assembly PCR to form a population of assembled nucleic acid molecules, and (b) amplifying the population of assembled nucleic acid molecules formed in step (a) by primary amplification to form a population of amplified assembled nucleic acid molecules. In some instances, the population of amplified assembled nucleic acid molecules may contain fewer than two errors per 1,000 base pairs (e.g., from about two to about 0.01, from about two to about 0.05, from about two to about 0.08, from about two to about 0.1, from about two to about 0.5, from about two to about 0.75, from about one to about 0.01, from about one to about 0.05, from about one to about 0.1, from about two to about 0.001, from about one to about 0.001, from about 0.5 to about 0.001, from about 0.1 to about 0.001, etc., errors per 1,000 base pairs). In some instances, steps (a) and/or (b) above may be performed in the presence of one or more (e.g., from one to ten, one to eight, one to five, one to three, one to two, etc.) thermostable mismatch recognition proteins. In some aspects, at least one of the one or more thermostable mismatch recognition proteins is a thermostable mismatch binding protein, such as, for example, a thermostable mismatch binding protein selected from a mismatch binding protein having an amino acid sequence set out in Table 13 or Table 15. In some aspects, at least one of the one or more thermostable mismatch recognition proteins is a thermostable mismatch endonuclease, such as a mismatch endonuclease selected from a mismatch endonuclease having an amino acid sequence set out in Table 12 or Table 15 (e.g., TkoEndoMS, PfuEndoMS, etc.).
In some instances, a high-fidelity DNA polymerase may be used in methods set out herein. Further in more specific instances, a high-fidelity DNA polymerase may be used in steps (a) and/or (b) set out in the above methods for generating error corrected populations of nucleic acid molecules. Further, the high-fidelity DNA polymerase may be a component of an error reducing polymerase reagent. Error reducing polymerase reagents may comprise one or more (e.g., from one to ten, one to eight, one to five, one to three, one to two, etc.) amine compounds, such as one or more amine compounds are selected from the group consisting of (a) dimethylamine hydrochloride, (b) diisopropylamine hydrochloride, (c) ethyl(methyl)amine hydrochloride, and (d) trimethylamine hydrochloride.
In specific variations of methods set out herein and in the above methods for generating error corrected populations of nucleic acid molecules, at least one of the one or more thermostable mismatch recognition proteins may be present in step (a). Further, in some instances, at least one of the one or more thermostable mismatch recognition proteins may be present in step (b). Additionally, one or more (e.g., from one to ten, one to eight, one to five, one to three, one to two, etc.) error correction step may be performed after primary amplification. Also, post-primary amplification of the population of amplified assembled nucleic acid molecules may performed after step (b). In some instances, the population of amplified assembled nucleic acid molecules may be contacted with one or more mismatch recognition proteins prior to the post-primary amplification. Additionally, the at least one of the one or more mismatch recognition proteins may a mismatch endonuclease, such as one or more (e.g., from one to ten, one to eight, one to five, one to three, one to two, etc.) non-thermostable mismatch endonuclease (e.g., T7 endonuclease I, CEL II nuclease, CEL I nuclease, and/or T4 endonuclease VII).
Methods set out herein are also directed to the generation of populations of amplified assembled nucleic acid molecules that comprise subfragments of larger nucleic acid molecules. Further, in some instances, such populations of amplified assembled nucleic acid molecules may be combined with one or more (e.g., from one to ten, one to eight, one to five, one to three, one to two, etc.) additional nucleic acid molecules that are also subfragments of larger nucleic acid molecule, to form nucleic acid molecule pools. In some instances, the nucleic acid molecules of such nucleic acid molecule pools may be assembled by secondary assembly PCR to form the larger nucleic acid molecules. In some instances, the subfragments may be contacted with the one or more mismatch recognition proteins prior to or during assembly by secondary assembly PCR. Further, the larger nucleic acid molecule may be heat denatured, then renatured, followed by contacting with the one or more (e.g., from one to ten, one to eight, one to five, one to three, one to two, etc.) mismatch recognition proteins. Additionally, at least one (e.g., from one to ten, one to eight, one to five, one to three, one to two, etc.) of the one or more mismatch recognition proteins may be a mismatch binding protein, such as a mismatch binding protein that is bound to a solid support. Thus, methods set out herein include methods for the separation of nucleic acid molecule which contain errors from those that do not contain errors. In some instances, the population of amplified assembled nucleic acid molecules may be sequenced. Such sequencing may be performed to determine whether errors are present and, if so, how many errors and what types(s) of errors there are.
Also provided herein are compositions, such as compositions that may be used in methods et out herein. In some instances, compositions set out herein may comprise one or more (e.g., from one to ten, one to eight, one to five, one to three, one to two, etc.) thermostable mismatch recognition protein, one or more (e.g., from one to ten, one to eight, one to five, one to three, one to two, etc.) DNA polymerase, and one or more (e.g., from one to ten, one to eight, one to five, one to three, one to two, etc.) amine compound. Further, at least one of the one or more amine compound may be selected from the group consisting of (a) dimethylamine hydrochloride, (b) diisopropylamine hydrochloride, (c) ethyl(methyl)amine hydrochloride, and/or (d) trimethylamine hydrochloride.
Compositions set out herein may further comprise two or more nucleic acid molecules (e.g., two or more nucleic acid molecules are subfragments of a larger nucleic acid molecule). Further, the two or more nucleic acid molecules may be single-stranded. Such single-stranded nucleic acid molecules may vary greatly in length but, in many instances, will be between less than 100 (e.g., from about 35 to about 90, from about 35 to about 80, from about 35 to about 70, from about 35 to about 65, from about 40 to about 90, from about 30 to about 60, from about 30 to about 65, etc.) nucleotides in length.
Compositions set out herein may further comprise two or more nucleic acid molecules wherein at least one of the two or more nucleic acid molecules is single-stranded and wherein at least one of the two or more nucleic acid molecules is double-stranded.
In some compositions set out herein, at least one of the thermostable mismatch recognition protein may be a thermostable mismatch endonuclease, such as a thermostable mismatch endonuclease having an amino acid sequence set out in Table 12 or Table 15 (e.g., TkoEndoMS, PfuEndoMS, etc.), as well as variants thereof having at least 80% (e.g., at least from about 80% to about 99%, from about 80% to about 95%, from about 80% to about 90%, from about 85% to about 95%, from about 90% to about 99%, from about 92% to about 99%, from about 95% to about 99%, from about 97% to about 99%, etc.) sequence identity thereto.
In some specific instances, compositions and methods provided herein may contain or use mismatch specific endonucleases that share at least 30%, 40%, 50%, or 60% (e.g., from about 30% to about 70%, from about 30% to about 60%, from about 30% to about 50%, from about 30% to about 45%, from about 30% to about 40%, etc.) amino acid sequence identity with TkoEndoMS (SEQ ID NO: 3). Examples of such mismatch specific endonucleases are PisEndoMS (SEQ ID: 11) or SacEndoMS (SEQ ID: 12).
In some compositions set out herein at least one of the thermostable mismatch recognition protein may be a thermostable mismatch binding protein, such as a thermostable mismatch binding protein having an amino acid sequence set out in Table 13 or Table 15, as well as variants thereof having at least 80% (e.g., at least from about 80% to about 99%, from about 80% to about 95%, from about 80% to about 90%, from about 85% to about 95%, from about 90% to about 99%, from about 92% to about 99%, from about 95% to about 99%, from about 97% to about 99%, etc.) sequence identity thereto.
Also set out herein are methods of generating nucleic acid molecules with a predetermined sequence. In some instances, such methods may comprise: (a) providing a plurality of single-stranded oligonucleotides with complementary overlapping regions, each of the single-stranded oligonucleotides comprising a sequence region of the target nucleic acid molecule, wherein the plurality of single-stranded oligonucleotides comprises: (i) a plurality of internal oligonucleotides having overlapping sequence regions with two other oligonucleotides in the plurality, and (ii) two terminal oligonucleotides designed to be positioned at the 5′ and 3′ terminal ends of the full-length nucleic acid molecule and having an overlapping sequence region with one of the internal oligonucleotides in the plurality, (b) assembling the plurality of oligonucleotides by primary assembly PCR to obtain assembled double-stranded nucleic acid assembly products, (c) combining at least a portion of the assembly products obtained in step (b) with a pair of primers. In some instances, the primers of the pair may be designed to bind to the 5′ and 3′ terminal ends of the assembly products and performing a PCR amplification reaction to produce amplified assembly products. Further, in some instances, step (b) and/or step (c) may be conducted in the presence of one or more thermostable mismatch recognition protein.
Further set out herein are methods of generating nucleic acid molecules with a predetermined sequence further comprising (d) conducting one or more error correction steps. In some instances, such error correction steps may comprise: (i) denaturing and reannealing the amplified assembly products of step (c) to generate one or more mismatch containing double-stranded nucleic acids, (ii) treating the mismatch containing double-stranded nucleic acids with one or more mismatch recognition protein, and (iii) optionally, conducting an amplification reaction. In some instances, the mismatch recognition protein(s) used in step (d) is a mismatch endonuclease (e.g., T7 endonuclease I) or a mismatch binding protein (e.g., MutS). Further, the thermostable mismatch endonuclease(s) employed may be derived from hyperthermophilic Archaea, optionally, wherein the hyperthermophilic archaeon is Pyrococcus furiosus or Pyrococcus abyssi. Additionally, the thermostable mismatch recognition protein(s) may be selected from the group of proteins having an amino acid sequence set out in Table 12, 13, or 15, and variants thereof having at least 80% (e.g., at least from about 80% to about 99%, from about 80% to about 95%, from about 80% to about 90%, from about 85% to about 95%, from about 90% to about 99%, from about 92% to about 99%, from about 95% to about 99%, from about 97% to about 99%, etc.) sequence identity thereto.
In some instances, one or more of the thermostable mismatch recognition protein employed may be produced and/or obtained by in vitro transcription/translation. In other instances, one or more of the thermostable mismatch recognition protein employed may be produced and/or obtained by cellular expression.
When polymerases are present in compositions and used in methods set out herein, these polymerases may be high fidelity DNA polymerases. Thus, provided herein are methods such as methods of generating nucleic acid molecules with a predetermined sequence set out above, wherein one or more of steps (b), (c) and (d) (iii) may be conducted in the presence of a high fidelity DNA polymerase, optionally, wherein the polymerase may be selected from the group consisting of P
In some variations of, for example, the above methods of generating nucleic acid molecules with a predetermined sequence, two or more amplified assembly products may be pooled prior to conducting the one or more error correction steps. Additional variations may further comprise treating the amplified assembly products with an exonuclease prior to the one or more error correction steps, optionally, wherein the exonuclease is Exonuclease I.
A better understanding of the features and advantages of subject matter set out herein may be obtained by reference to the following detailed description that sets forth illustrative aspects, in which the principles of subject matter set out herein are utilized, and the accompanying drawings of which:
The term “nucleic acid molecule”, as used herein, refers to a covalently linked sequence of nucleotides or bases (e.g., ribonucleotides for RNA and deoxyribonucleotides for DNA but also include DNA/RNA hybrids where the DNA is in separate strands or in the same strands) in which the 3′ position of the pentose of one nucleotide is joined by a phosphodiester linkage to the 5′ position of the pentose of the next nucleotide. Nucleic acid molecules may be single- or double-stranded or partially double-stranded. Nucleic acid molecule may appear in linear or circularized form in a supercoiled or relaxed formation with blunt or sticky ends and may contain “nicks”. Nucleic acid molecules may be composed of completely complementary single strands or of partially complementary single strands forming at least one mismatch of bases. Nucleic acid molecules may further comprise two self-complementary sequences that may form a double-stranded stem region, optionally separated at one end by a loop sequence. The two regions of nucleic acid molecules which comprise the double-stranded stem region are substantially complementary to each other, resulting in self-hybridization. However, the stem can include one or more mismatches, insertions or deletions.
Nucleic acid molecules may comprise chemically, enzymatically, or metabolically modified forms of nucleotides or combinations thereof. Chemically synthesized nucleic acid molecules may refer to nucleic acids typically less than or equal to 200 nucleotides long (e.g., between 5 and 200, between 10 and 150, between 15 and 100, or between 20 and 50 nucleotides in length), whereas enzymatically synthesized nucleic acid molecules may encompass smaller as well as larger nucleic acid molecules as described elsewhere herein. Enzymatic synthesis of nucleic acid molecules may include stepwise processes using enzymes such as polymerases, ligases, exonucleases, endonucleases, recombinases or the like or a combination thereof. Thus, provided herein, in part, are compositions and combined methods relating to the enzymatic assembly of chemically synthesized nucleic acid molecules.
A nucleic acid molecule has a “5′-terminus” and a “3′-terminus” because nucleic acid molecule phosphodiester linkages occur between the 5′ carbon and 3′ carbon of the pentose ring of the substituent mononucleotides. The end of a nucleic acid molecule at which a new linkage would be to a 5′ carbon is its 5′ terminal nucleotide. The end of a nucleic acid molecule at which a new linkage would be to a 3′ carbon is its 3′ terminal nucleotide. A terminal nucleotide or base, as used herein, is the nucleotide at the end position of the 3′- or 5′-terminus. A nucleic acid molecule region, even if internal to a larger nucleic acid molecule (e.g., a sequence region within a nucleic acid molecule), also can be said to have 5′- and 3′-ends. Nucleic acid molecule also refers to short nucleic acid molecules, often referred to as, for example, primers or probes. Also, the terms “5′-” and “3′-” refer to strands of nucleic acid molecules. Thus, a linear, single-stranded nucleic acid molecule will have a 5′-terminus and a 3′-terminus. However, a linear, double-stranded nucleic acid molecule will have a 5′-terminus and a 3′-terminus for each strand. Thus, for nucleic acid molecules that encode proteins, for example, the 3′-terminus of the sense strand may be referred to.
The term “oligonucleotide”, as used herein, refers to DNA and RNA, and to any other type of nucleic acid molecule that is an N-glycoside of a purine or pyrimidine base but will typically be DNA. Oligonucleotides are thus a subset of nucleic acid molecules and may be single-stranded or double-stranded. Oligonucleotides (including primers as described below) may be referred to as “forward” or “reverse” to indicate the direction in relation to a given nucleic acid sequence. For example, a forward oligonucleotide may represent a portion of a sequence of the first strand of a nucleic acid molecule (e.g., the “sense” strand), whereas a reverse oligonucleotide may represent a portion of a sequence of the second strand (e.g., “antisense” strand) of said nucleic acid molecule or vice versa. In many instances, a set of oligonucleotides used to assemble longer nucleic acid molecules will comprise both forward and reverse oligonucleotides capable of hybridizing to each other via complementary regions. Oligonucleotides are typically less than 200 nucleotides, more typically less than 100 nucleotides in length. Thus, “primers” will generally fall into the category of oligonucleotide. Oligonucleotides can be prepared by any suitable method, including direct chemical synthesis by a method such as the phosphotriester method of Narang et al., Meth. Enzymol. 68:90-99 (1979); the phosphodiester method of Brown et al., Meth. Enzymol. 68:109-151 (1979); the diethylphosphoramidite method of Beaucage et al., Tetrahedron Letters 22:1859-1862 (1981); and the solid support method of U.S. Pat. No. 4,458,066. A review of synthesis methods of conjugates of oligonucleotides and modified nucleotides is provided in Goodchild, Bioconjugate Chemistry 1:165-187 (1990). Where appropriate, the term oligonucleotide may refer to a primer or probe and these terms may be exchangeably used herein.
Term “primer”, as used herein, refers to a short nucleic acid molecule capable of acting as a point of initiation of nucleic acid synthesis under suitable conditions. Such conditions include those in which synthesis of a primer extension product complementary to a nucleic acid strand is induced in the presence of different nucleoside triphosphates (e.g., A, C, G, T and/or U) and an agent for extension (for example, a DNA polymerase or reverse transcriptase) in an appropriate buffer and at a suitable temperature. A primer is generally composed of single-stranded DNA but can be provided as a double-stranded molecule for specific applications (e.g., blunt end ligation). Optionally, a primer can be naturally occurring or synthesized using chemical synthesis of recombinant procedures. The appropriate length of a primer depends on the intended use of the primer but typically ranges from about 6 to about 200 nucleotides, including intermediate ranges, such as from about 10 to about 50 nucleotides, from about 15 to about 35 nucleotides, from about 18 to about 75 nucleotides and from about 25 to about 150 nucleotides. The design of suitable primers for the amplification of a given target sequence is well known in the art and described in the literature (see for example O
A set of primers used in the same amplification reaction may have melting temperatures that are substantially the same, where the melting temperatures are within about 10-5° C. of each other, or within about 5-2° C. of each other, or within about 2-0.5° C. of each other, or less than about 0.5° C. of each other.
The terms “complementary” or “complementarity”, as used herein, refer to the natural binding of nucleic acid molecules (primers, oligonucleotides or polynucleotides etc.) under permissive salt and temperature conditions by base pairing. For example, the sequence “A-G-T” binds to the complementary sequence “T-C-A.” Complementarity between two single-stranded molecules may be “partial,” such that only some of the nucleic acids bind, or it may be “complete,” such that total complementarity exists between the single-stranded molecules. The degree of complementarity between nucleic acid strands has significant effects on the efficiency and strength of the hybridization between the nucleic acid strands. This is of particular importance in amplification reactions, which depend upon binding between nucleic acids strands. Complementary regions between nucleic acid molecules such as oligonucleotides may also be referred to as “overlaps” or “overlapping” regions as defined below.
The term “hybridization”, as used herein, refers to any process by which a strand of nucleic acid binds with a complementary strand through base pairing. Hybridization and the strength of hybridization (for example, the strength of the association between the nucleic acids) is impacted by such factors as the degree of complementary between the nucleic acids, stringency of the conditions involved, the Tm of the formed hybrid, and the G:C ratio within the nucleic acids.
The term “homologous”, as used herein, refers to a degree of complementarity. Nucleic acid sequences may be partially or completely homologous (identical). A partially complementary sequence is one that at least partially inhibits a completely complementary sequence from hybridizing to a target nucleic acid and is referred to using the functional term “substantially homologous”.
The term “overlap” or “overlapping”, as used herein, refers to a sequence homology or sequence identity shared by a portion of two or more oligonucleotides.
The term “gene” or “gene sequence”, as used herein, generally refers to a nucleic acid sequence that encodes a discrete cellular product. In many instances, a gene or gene sequence includes a DNA sequence that comprises an open reading frame (ORF) and can be transcribed into mRNA which can be translated into polypeptide chains, transcribed into rRNA or tRNA or serve as recognition sites for enzymes and other proteins involved in DNA replication, transcription and regulation. These genes include, but are not limited to, structural genes, immunity genes, regulatory genes and secretory (transport) genes etc. However, as used herein, “gene” refers not only to the nucleotide sequence encoding a specific protein, but also to any adjacent 5′ and 3′ non-coding nucleotide sequence involved in the regulation of expression of the protein encoded by the gene of interest. These non-coding sequences include terminator sequences, promoter sequences, upstream activator sequences, regulatory protein binding sequences, and the like. In many instances, a gene is assembled from shorter oligonucleotides or nucleic acid fragments.
The terms “fragment”, “subfragment”, “segment”, or “component” or similar terms, as used herein, in connection with a nucleic acid molecule or sequence either refer to a product or intermediate product obtained from one or more process steps (e.g., synthesis, assembly PCR, amplification etc.), or refer to a portion, part or template of a longer or modified nucleic acid product to be obtained by one or more process steps (e.g., assembly PCR, amplification, ligation, cloning etc.). In some instances, a nucleic acid fragment or subfragment may represent both, an assembly product (e.g., assembled from multiple oligonucleotides) and a starting compound for higher order assembly (e.g., a gene assembled from multiple fragments or a fragment assembled from multiple subfragments etc.).
As used herein, “amines” or “amine compound”, as used herein, includes chemicals of Formula I, immediately below, or salts thereof:
wherein R1 is H; R2 is chosen from alkyl, alkenyl, alkynyl, or (CH2)n-R5, wherein n=1 to 3, and R5 is aryl, amino, thiol, mercaptan, phosphate, hydroxy, alkoxy; and R3 and R4 may be the same or different and are independently chosen from H or alkyl, with the proviso that if R2 is (CH2)n-R5, then at least one of R3 and/or R4 is alkyl. As such, amines include diethylamine hydrochloride, diisopropylamine hydrochloride, ethyl(methyl)amine hydrochloride, trimethylamine hydrochloride, and dimethylamine hydrochloride.
The term “vector”, as used herein, refers to any nucleic acid molecule capable of transferring genetic material into a host organism. The vector may be linear or circular in topology and includes but is not limited to plasmids, viruses, bacteriophages. The vector may include amplification genes, enhancers or selection markers and may or may not be integrated into the genome of the host organism.
The term “plasmid”, as used herein, refers to a vector that can be genetically modified to insert one or more nucleic acid molecules (e.g., assembly products). Plasmids will typically contain one or more region that renders it capable of replication in at least one cell type.
The term “amplification”, as used herein, relates to the production of additional copies of a nucleic acid molecule. Amplification is often carried out using polymerase chain reaction (PCR) technologies well known in the art (see, e.g., Dieffenbach, C. W. and G. S. Dveksler (1995) PCR Primer, a Laboratory Manual, Cold Spring Harbor Press, Plainview, N.Y.) but may also be carried out by other means including isothermal amplification methods such as, e.g., transcription mediated amplification, strand displacement amplification, rolling circle amplification, loop-mediated isothermal amplification, helicase-dependent amplification, single primer isothermal amplification or recombinase polymerase amplification (see, e.g., Fakruddin et al., “Nucleic acid amplification: Alternative methods of polymerase chain reaction”, J. Pharm Bioallied Sci, 2013, v.5(4), 245-252; or Gill and Ghaemi, “Nucleic acid isothermal amplification technologies: a review”, Nucleosides Nucleotides Nucleic Acids. 2008 27(3), 224-43). Amplification reactions may be carried out using terminal primers to reconstruct each strand of a denatured double-stranded nucleic acid molecules.
The term “assembly chain reaction”, also referred to herein as “assembly PCR”, when used herein, refers to the assembly of larger nucleic acid molecules from smaller nucleic acid molecules by polymerase mediated extensions of overlapping, partially complementary nucleic acid molecules. The overlapping, partially complementary nucleic acid molecules may be single-stranded or double-stranded. Further, double-stranded nucleic acid molecules will typically be denatured before or as port of use in an assembly chain reaction. An example of an assembly chain reaction is set out at the top of
The term “post-primary amplification error correction”, as used herein, refers to the amplification-based error correction steps that occur after the end of the workflow shown in
Error correction will often involve the use of a mismatch endonuclease. An exemplary error correction process is set out in
The term “non-amplification error correction”, as used herein, refers to error correction processes that do not involve nucleic acid amplification. An example of such a method is one where nucleic acid strands are hybridized to each other, followed by removal of double-stranded nucleic acid molecule containing mismatches using mismatch binding proteins (see, e.g.,
The term “adjacent”, as used herein, refers to a position in a nucleic acid molecule immediately 5′ or 3′ to a reference region.
The term “sequence fidelity”, as used herein, refers to the level of sequence identity of a nucleic acid molecule as compared to a reference sequence. Full identity being 100% identical over the full-length of the nucleic acid molecules being scored for sequence identity. Sequence fidelity can be measure in a number of ways, for example, by the comparison of the actual nucleotide sequence of a nucleic acid molecule to a desired nucleotide sequence (e.g., a nucleotide sequence that one wishes to be used to generate a nucleic acid molecule). Another way sequence fidelity can be measured is by comparison of sequences of two nucleic acid molecules in a reaction mixture. In many instances, the difference on a per base basis will be, on average, the same.
The error rates for DNA polymerases can be measured by the quantification of total errors or different types of errors. With respect to high fidelity DNA polymerases as set out herein, the error rate “benchmark” is set based upon the substitution rate. In particular, a high fidelity DNA polymerase will exhibit a substitution error rate that is lower of 1.0×10−5 substitution per base. Examples of high fidelity polymerase include P
The term “transition”, when used in reference to the nucleotide sequence of a nucleic acid molecule, refers to a point mutation that changes a purine nucleotide to another purine (A ↔G) or a pyrimidine nucleotide to another pyrimidine (C↔T).
The term “transversion”, when used in reference to the nucleotide sequence of a nucleic acid molecule, refers to a point mutation involving the substitution of a (two ring) purine for a (one ring) pyrimidine or a (one ring) pyrimidine for a (two ring) purine.
The term “indel”, as used herein, refers to the insertion or deletion of one or more bases in a nucleic acid molecule.
The term “mismatch”, as used herein, refers to two bases in different strands of a double-stranded nucleic acid molecule that do not form Watson-Crick base pairing, while surrounding bases in of different nucleic acid strands have sequence complementarity and do form Watson-Crick base pairing bases. The length of the complementary regions may vary but with often be of at least twenty base pairs. With respect to each strand of a nucleic acid molecule which contains only the four standard DNA bases, there are four correct (Watson-Crick base pairing) complementary matches (i.e., A/T, T/A/G/C, and C/G) and twelve “mismatches” (i.e., A/A, A/C, A/G, T/T, T/C, T/G, G/G, G/A, G/T, C/C, C/T, and C/A). With respect to base pairing, in the absence of strand reference, there are two correct complementary matches (i.e., A/T and G/C) and eight “mismatches” (i.e., A/A, A/C, A/G, T/T, T/C, T/G, G/G, and C/C). In terms of substitutions, these mismatches can be expressed as (1) A to G and T to C, (2) G to A and C to T, (3) A to C and T to G, (4) A to T and T to A, (5) G to C and C to G, and (6) G to T and C to A.
The term “thermostable”, as used herein in reference to protein refers to a protein that retains at least 85% the protein biological activity after heating to 95° C. for 5 minutes. Thermostable proteins may or may not have biological activity at 95° C. Thus, depending on the protein, an assay of retained biological activity may be performed after incubation at 95° C. for 5 minutes or at another (e.g., lower) temperature, using as a “benchmark” of the same protein not heated to 95° C. for 5 minutes.
The term “mismatch recognition protein”, as used herein, refers to a protein with specific biological activity for mismatched bases in double-stranded DNA. These activities may include nuclease activity and/or binding activity. Such proteins include resolvases, MutS and MutS homologs, MutM and MutM homologs, MutY and MutY homologs, and members of the RecB nuclease family of proteins. Mismatch binding proteins and mismatch endonucleases are both mismatch recognition proteins. Mismatch recognition proteins may be thermostable or non-thermostable. Some exemplary mismatch recognition proteins are set out in Table 15, as well as other tables provided herein.
The term “mismatch endonuclease” or “MME” (also referred to as a “mismatch repair endonuclease”), as used herein refers to a nuclease having the activity of cleaving (one or both strands) of double-stranded nucleic acid molecules at or near (e.g., within from about one to about five base pairs) mismatch sites. Mismatch endonuclease activity includes the ability to cleave phosphodiester bonds at or near nucleotides forming mismatched base pairs, and an activity of cleaving phosphodiester bonds adjacent to nucleotides located 1 to 5, often 1 to 3 base pairs away from mismatched base pairs. Examples of proteins with mismatch endonuclease activity are set out below in Tables 13 and 15. Specific examples of mismatch endonucleases include as CEL I (Till et al., Nucl. Acid Res. 32:2632-2641 (2004)) and CEL II (U.S. Pat. No. 7,129,075), bacteriophage resolvases, such as T7NI and T4 endonucleases VII (Mashal, et al., Nature Genetics 9:177-183 (1995)), E. coli Endonuclease V (Yao and Kow, J. Biol. Chem. 272:30774-30779 (1997)), TkoEndoMS (Ishino et al., Nucl. Acids Res. 44:2977-2986 (2016)), and Pyrococcus furiosus EndoMS (referred to herein as “PfuEndoMS”). Mismatch endonucleases may be thermostable (TsMME) or non-thermostable.
The term “EndoMS”, as used herein, refers to mismatch specific endonucleases that share at least 50% amino acid sequence identity with one or more of the EndoMS proteins set out in Table 15 and have mismatch specific endonuclease activity. “Nucs” has been used in the art as an alternative term for EndoMS. Thus, the terms “EndoMS” and “Nucs” may be used interchangeably.
The term “mismatch binding protein” (also referred to as a “mismatch repair binding protein”), as used herein refers to a protein with specific binding activity for mismatched bases in double-stranded DNA. Examples of such proteins are set out below in Tables 12 and 15. Many of these proteins are MutS homologs. Mismatch binding proteins may be thermostable or non-thermostable.
The term “error correction”, as used herein refers to processes designed to a decrease the total number nucleotide sequence defects in nucleic acid molecules of a population. These defects can be mismatches, insertions, deletions and/or substitutions. Defects can occur when nucleic acid molecules generated (e.g., by chemical or enzymatic synthesis) are each intended to contain a particular base at a location, but a different base is present at that location in one or more nucleic acid molecules.
An exemplification of error correction is as follows. Assume that there is a population of double-stranded nucleic acid molecules have a desired length of 100 base pairs. Also, assume that the two strands of the double-stranded nucleic acid molecules were each synthesized separately and the hybridized to each other to form double-stranded nucleic acid molecules of the population. Further assume that nucleic acid synthesis results in an average of 1 error per 200 nucleotides. In such an instance, there would be 1 “error” per 100 base pairs. Thus, on average, each double-stranded nucleic acid molecule of the population would contain one error. Of course, some of the double-stranded nucleic acid molecules in the population would have no errors and other double-stranded nucleic acid molecules would have more than one error. If an error correction process removed half of the nucleic acid molecules from the population and none of the nucleic acid molecules without errors were removed, then the error rate in the remaining double-stranded nucleic acid molecules in the population would be less than 1 in 200 base pairs. This is so because, as suggested above, some of the removed nucleic acid molecules would have more than one error and none of the “correct” nucleic acid molecules were removed.
As used herein, the phases “error correction round” and “round of error correction” refers to a series of steps that result in the cleavage or removal of nucleic acid molecules with errors from a population of nucleic acid molecules. Using
As used herein, an “error reducing polymerase reagent” is a composition which comprises a polymerase (e.g., a DNA polymerase) and an additional component that reduces the number of errors in amplified nucleic acid molecules (e.g., by from about 5% to about 30%, from about 5% to about 30%, from about 5% to about 30%, from about 10% to about 40%, from about 10% to about 70%, etc.), wherein the additional component is not a mismatch recognition protein. One category of such compounds are amines, such as amines set out herein.
The term “transformation”, as used herein, describes a process by which an exogenous nucleic acid molecule enters and changes a recipient cell. It may occur under natural or artificial conditions using various methods well known in the art. Transformation may rely on any known method for the insertion of foreign nucleic acid sequences into a prokaryotic or eukaryotic host cell. The method is selected based on the host cell being transformed and may include, but is not limited to, viral infection, electroporation, lipofection, and particle bombardment. Such “transformed” cells include stably transformed cells in which the inserted nucleic acid is capable of replication either as an autonomously replicating plasmid or as part of the host chromosome. They also include cells that transiently express the inserted DNA or RNA for limited periods of time.
The term “solid support”, as used herein refers to a porous or non-porous material on which polymers such as oligonucleotides or nucleic acid molecules can be synthesized and/or immobilized. As used herein “porous” means that the material contains pores which may be of non-uniform or uniform diameters (for example in the nm range). Porous materials include paper, synthetic filters etc. In such porous materials, the reaction may take place within the pores. The solid support can have any one of a number of shapes, such as pin, strip, plate, disk, rod, fiber, bends, cylindrical structure, planar surface, concave or convex surface or a capillary or column. The solid support can be a particle, including bead, microparticles, nanoparticles and the like. The solid support can be a non-bead type particle (e.g., a filament) of similar size. The support can have variable widths and sizes. For example, sizes of a bead (e.g., a magnetic bead) which may be used in the practice of aspects of methods set out herein may vary widely but include beads with diameters between 0.01 μm and 100 μm, 0.005 μm and 100 μm, 0.005 μm and 10 μm, 0.01 μm and 100 μm, 0.01 μm and 1,000 μm, between 1.0 μm and 2.0 m, between 1.0 μm and 100 μm, 15 between 2.0 μm and 100 μm, between 3.0 μm and 100 μm, between 0.5 μm and 50 μm, between 0.5 μm and 20 μm, between 1.0 μm and 10 μm, between 1.0 μm and 20 μm, between 1.0 μm and 30 μm, between 10 μm and 40 μm, between 10 m and 60 μm, between 10 μm and 80 μm, or between 0.5 μm and 10 μm.
The support can be hydrophobic or capable of binding a molecule via hydrophobic interaction. The support can be hydrophilic or capable of being rendered hydrophilic and includes inorganic powders such as silica, magnesium sulfate, and alumina; natural polymeric materials, particularly cellulosic materials and materials derived from cellulose, such as fiber containing papers such as filter paper, chromatographic paper or the like. The support can be immobilized at an addressable position of a carrier such as, e.g., a multiwell plate or a microchip. The support can be loose or particulate (such as, e.g., a resin material or a bead in a well) or can be reversibly immobilized or linked to the carrier (e.g., by cleavable chemical bonds or magnetic forces etc.). In some aspects, solid support may be fragmentable. Solid supports may be synthetic or modified naturally occurring polymers, such as nitrocellulose, carbon, cellulose acetate, polyvinyl chloride, polyacrylamide, cross linked dextran, agarose, polyacrylate, polyethylene, polypropylene, poly (4-methylbutene), polystyrene, polymethacrylate, poly(ethylene terephthalate), nylon, poly(vinyl butyrate), polyvinylidene difluoride (PVDF) membrane, glass, controlled pore glass, magnetic controlled pore glass, magnetic or non-magnetic beads, ceramics, metals, and the like; either used by themselves or in conjunction with other materials. In some aspects, the support can be in a chip, array, microarray or microwell plate format. In many instances, a support used in methods or compositions of set out herein will be one where individual nucleic acid molecules are synthesized on separate or discrete areas to generate features (i.e., locations containing individual nucleic acid molecules) on the support. In some aspects, the size of the defined feature is chosen to allow formation of a microvolume droplet or reaction volume on the feature, each droplet or reaction volume being kept separate from each other. As described herein, features are typically, but need not be, separated by interfeature spaces to ensure that droplets or reaction volumes or between two adjacent features do not merge. Interfeatures will typically not carry any nucleic acid molecules on their surface and will correspond to inert space. In some aspects, features and interfeatures may differ in their hydrophilicity or hydrophobicity properties. In some aspects, features and interfeatures may comprise a modifier. In some instances set out herein, the feature is a well or microwell or a notch. Nucleic acid molecules may be covalently or non-covalently attached to the surface or deposited or synthesized or assembled on the surface.
“a”, “an”, and “the” include plural reference unless the context clearly dictates otherwise.
Compositions and methods set out herein are directed, in part, to the preparation of nucleic acid molecules having high sequence fidelity. While numerous aspects and variations may be employed, in many instances, nucleic acid molecules will be synthesized (e.g., chemically, enzymatically, etc.). These synthesized nucleic acid molecules may, optionally, then be assembled to form one or more larger nucleic acid molecules by, for example, assembly PCR (e.g., primary assembly PCR).
There is generally relatively low abundance and the semi-random distribution of sequence errors in synthesized oligonucleotides. In many instances, when nucleic acid molecules with erroneous bases (e.g., deletions, insertion, substitutions) hybridize with nucleic acid molecules with correct bases, a region is formed that does not exhibit standard Watson-Crick base pairing. These “non-standard” regions may be used for recognition of nucleic acid molecules that contain errors. Further, once these “non-standard” regions are detected in a population of nucleic acid molecules, nucleic acid molecules containing these regions may be removed from the population or they may be modified in such a way as to prevent their amplification or low their ability to be amplified.
A number of methods may be used to reduce the percentage of nucleic acid molecules containing errors (e.g., deletions, insertion, substitutions) in a population. These methods include:
Further, two or more of the above methods may be used to reduce the number of errors present in nucleic acid molecules.
Much of the disclosure set out herein is directed to compositions and methods for the synthesis, assembly (e.g., assembly PCR) and amplification of nucleic acid molecules. Provided herein are compositions and methods for the generation of nucleic acid molecules with high sequence fidelity.
For some applications, it is important to use of nucleic acid molecules with low error rates. For purposes of illustration, consider the situation where one hundred nucleic acid molecules are to be assembled, each molecule is one hundred base pairs in length and there is one error per 200 base pairs. The net result is that there will be, on average, 50 sequence errors in each 10,000 base pair assembled nucleic acid molecule. If one intends, for example, to express one or more proteins from the assembled nucleic acid molecule, then the number of amino acid sequence errors would likely be considered to be too high. Further, a number of the protein coding region nucleotide sequence errors will result in “frame shifts” mutations yielding proteins that will generally not be desired. Also, non-frame shift coding regions may result in the formation of proteins with point mutations. All of these will “dilute the purity” of the desired protein expression product and many of the produced “contaminant” proteins will be carried over into the final expression product mixture even if affinity purification is employed.
High sequence fidelity can be achieved by several means, including sequencing of nucleic acid fragments prior to assembly or partially assembled nucleic acid molecules, sequencing of fully assembled nucleic acid molecules to identify ones with correct sequences, and/or error correction.
Errors may find their way into nucleic acid molecules in a number of ways. Examples of such ways include chemical synthesis errors, amplification/polymerase mediated errors (especially when non-proofreading polymerases are used), and assembly PCR mediated errors (usually occurring at nucleic acid fragment junctions).
Sequence errors in nucleic acid molecules may be referenced in a number of ways. As examples, there is the error rate associated with the synthesis nucleic acid molecules, the error rate associated with nucleic acid molecules after error correct and/or the selection, and the error rate associated with end product nucleic acid molecules (e.g., error rates of (1) a synthetic nucleic acid molecules that have either been selected for the correct sequence or (2) assembled chemically synthesized nucleic acid molecules). These errors may come from the chemical synthesis process, assembly processes, and/or amplification processes. Errors may be removed or prevented by methods, such as, the selection of nucleic acid molecules having correct sequences, error correction, and/or improved chemical synthesis methods.
In some instances, methods set out herein may combine error removal and prevention methods to produce nucleic acid molecules with relative low numbers of errors. Thus, assembled nucleic acid molecules produced by methods of set out herein may have error rates from about 1 base in 1,500 to about 1 base in 30,000, from about 1 base in 2,000 to about 1 base in 30,000, from about 1 base in 4,000 to about 1 base in 30,000, from about 1 base in 8,000 to about 1 base in 30,000, from about 1 base in 10,000 to about 1 base in 30,000, from about 1 base in 15,000 to about 1 base in 30,000, from about 1 base in 10,000 to about 1 base in 20,000, etc.
Two ways to lower the number of errors in assembled nucleic acid molecules is by (1) selection of nucleic acid molecules (e.g., oligonucleotides, subfragments, etc.) for assembly with corrects sequences and (2) correction of errors in nucleic acid molecules, partially assembled sub-assemblies, or fully assembled nucleic acid molecules.
Errors may be incorporated into nucleic acid molecules regardless of the method by which the nucleic acid molecules are generated. Even when nucleic acid molecules known to have correct sequences are used for assembly PCR, errors can find their way into the final assembly products. Thus, in many instances, error reduction will be desirable.
In many instances, regardless of the method by which a larger nucleic acid molecule is generated from chemically synthesized oligonucleotides, errors from the chemical synthesis process will be present. While sequencing of individual nucleic acid molecules may be performed to identify and select error-free nucleic acid molecules, alternative approaches may comprise one or more error correction or removal steps. Thus, in many instances, error correction will be desirable. Error correction can be achieved by any number of means. Typically, such error removal steps will be performed after a first round of assembly PCR. Thus, in some aspects, methods set out herein may involve the following (in this order or different orders): (i) fragment amplification and/or assembly PCR (e.g., according to the methods described herein), (ii) error correction, (iii) final assembly (e.g., according to the in vitro or in vivo methods described herein, e.g., using a protocol as illustrated in
Errors may be removed from nucleic acid molecules or otherwise avoided at one or more locations in workflows used to generate these molecules. Using the workflow set out in
Further, the introduction of errors into nucleic acid molecules can be avoided or lessened in a number of ways. Some of these ways include the use of nucleic acid starting materials that contain few errors. Set out in Example 2 and Tables 10 and 11, the use of nucleic acid starting materials that contain few errors results in fewer errors being present in assembled, error corrected molecules. This is believed to be due to error correction methods not always being able to correct 100% of errors present. Thus, in general, the fewer errors that are present for correction results in fewer errors after error correction.
In many instances, nucleic acid molecule starting material will have an initial average number of sequence errors that is from about 1 in 250 to about 1 in 2,000 (e.g., from about 1 in 250 to about 1 in 1,900, from about 1 in 250 to about 1 in 1,500, from about 1 in 250 to about 1 in 1,200, from about 1 in 250 to about 1 in 1,000, from about 1 in 250 to about 1 in 800, from about 1 in 400 to about 1 in 1,900, from about 1 in 400 to about 1 in 1,500, from about 1 in 400 to about 1 in 1,100, from about 1 in 650 to about 1 in 2,000, from about 1 in 650 to about 1 in 1,700, from about 1 in 650 to about 1 in 1,500, etc.).
As also set out in Example 2, to some extent, error correction efficiency various with thermocycling conditions used. Thus, one factor that may be changed to yield product nucleic acid molecules with low numbers of error is thermocycling conditions.
Another way to avoid the introduction of errors into nucleic acid molecules, for example, is by the use of synthesis methods to generate nucleic acid sub-units with few errors. Another way is to use high fidelity polymerases and high-fidelity amplification methods for low error replication assembly and amplification of nucleic acid molecules.
Using the workflow in
Again using the workflow of
Reagents that may be used to perform error correcting include mismatch endonucleases, mismatch binding proteins, and high-fidelity polymerases and reagents that contain high fidelity polymerases. Further, proteins used in methods set out herein may be thermostable or non-thermostable. One example of a reagent that contains a high-fidelity polymerase is P
One general workflow for error correction of nucleic acid molecules is where either single-stranded nucleic acid molecules with regions of sequence complementarity are hybridized to each other or double-stranded nucleic acid molecules are denatured and then hybridized to each other. In such instances, when two nucleic acid strands that differ in nucleotide sequence by one or more nucleotides hybridize to each other and the resulting double-stranded nucleic acid molecule will generally form a region where Watson-Crick base pairing is not exhibited. In some instances, error correction processes may be based upon recognition of regions where Watson-Crick base pairing is not exhibited. Thus, in many instances, error correction processes will involve the hybridization of single-stranded nucleic acid molecules to form double-stranded nucleic acid molecules. While error correction may be performed in the absence of a DNA polymerase, assembly PCR and amplification processes that may include error correction are shown in
Methods set out herein include various combinations of error reduction, error correction related to assembly PCR and/or amplification steps. Further, error correction processes may be integrated into such steps or occur before or after such steps.
Methods set out herein may involve any number of steps and combinations of workflows set out herein. Using the workflow of
Using the data set out in
In summary, in some aspect, provided herein are methods comprising a combination of assembly PCR and/or amplification steps, where error correction may occur during or between any of such steps. In many instances, one or more thermostable mismatch recognition protein may be present during assembly PCR and/or amplification steps.
The term “primary assembly PCR” refers to an assembly PCR reaction where single-stranded nucleic acid molecules are assembled to form double-stranded nucleic acid molecules that are longer in length than the individual single-stranded nucleic acid molecules. Even though the workflow in
The term “secondary assembly PCR” refers to an assembly PCR reaction where initial double-stranded nucleic acid molecules are assembled to form product double-stranded nucleic acid molecules that are longer in length than the initial double-stranded nucleic acid molecules.
The term “primary amplification” refers to the first set of amplification reactions performed on the products of an assembly PCR reaction where single-stranded nucleic acid molecules are assembled to form double-stranded nucleic acid molecules. Later amplification cycles are termed “secondary”, “tertiary”, “quaternary”, etc. By way of illustration step 3 in
One of the first steps in producing a nucleic acid molecule or protein of interest, after the molecule(s) has been identified, is nucleic acid molecule design. A number of factors go into design of the nucleic acid sequence to be synthesized and the oligonucleotides used to generate the nucleic acid molecule. These factors include one or more of the following: (1) the AT/GC content of all or part of the nucleic acid molecule (e.g., the coding region), (2) the presence or absence of restriction endonuclease cleavage sites (including the addition and/or removal of restriction sites), (3) preferred codon usage for the particular protein production or host expression system that is to be employed, (4) junctions of the oligonucleotides being assembled, (5) the number and lengths of the oligonucleotides used to produce the desired nucleic acid molecule, (6) minimization of undesirable regions (e.g., “hairpin” sequences, regions of sequence homology to cellular nucleic acids, repetitive sequences, inhibitory cis-acting elements, restriction enzyme cleavage sites, internal splice sites etc.) and (7) coding region flanking segments that may be used for attachment of 5′ and 3′ components (e.g., restriction endonuclease sites, primer binding sites, sequencing adaptors or barcodes, recombination sites, etc.).
In many instances, parameters will be input into a computer and software will generate an in silico nucleotide sequence that balances the input parameters. The software may place “weights” on the input parameters in that, for example, what is considered to be a nucleic acid molecule that closely matches some of the input criteria may be difficult or impossible to assemble. Exemplary nucleic acid design methods are set out in U.S. Pat. No. 8,224,578. As further described below, the sequence design may also take into account requirements for multiplexing of oligonucleotides belonging to different subfragments of a product nucleic acid molecule.
Further, nucleic acid molecules design factors may be considered across the length of the nucleic acid molecule or in specific regions of the molecule. For example, GC content may be limited across the length of the nucleic acid molecule to prevent synthesis “failures” resulting from specific locations within the molecule. Thus, synthesizability of the nucleic acid molecule is a characteristic of the entire nucleic acid molecule in that a regional “failure to assemble” results in the designed nucleic acid molecule not being assembled. From a regional perspective, codon may be selected for optimal translation, but this may conflict with, for example, region limitation of GC content.
Assembly success often involves multiple parameters and regional characteristics of the desired nucleic acid molecule. Total and regional GC content is only one example of a parameter. For example, the total GC content of a nucleic acid molecule may be 50% but the GC content in a particular region of the same nucleic acid molecule may be 75%. Thus, in many instances, GC content will be “balanced” across the entire nucleic acid molecule and may vary regionally by less than 15%, 10%, 8%, 7%, or 5% from the total GC content.
The aim therefore is to reach a compromise which is as optimal as possible between satisfying the various requirements. In instances where the product nucleic acid molecule encodes a protein, the large number of amino acids in the protein leads to a combinatorial explosion of the number of possible DNA sequences which—in principle—are able to express the desired protein based on the degeneracy of the genetic code. For this reason, various computer-assisted methods have been proposed for ascertaining an optimal codon sequence.
Oligonucleotides or nucleic acid subfragments used for assembly PCR of a desired nucleic acid molecule may be derived from a number of sources, for example, they may be cloned, derived from polymerase chain reactions, chemically synthesized or purchased. In many instances, chemically synthesized nucleic acids tend to be of less than 100 nucleotides in length. PCR and cloning can be used to generate much longer nucleic acids. Further, the percentage of erroneous bases present in nucleic acids (e.g., nucleic acid fragments) is, to some extent, tied to the method by which it is made. Typically, chemically synthesized nucleic acids have the highest error rate.
A number of methods for chemical synthesis of oligonucleotides are known. In many instances, oligonucleotide synthesis is performed by a stepwise addition of nucleotides to the 5′-end of the growing chain until oligonucleotides of desired length and sequence are obtained. Further, each nucleotide addition can be referred to as a synthesis cycle and often consists of four chemical reactions: (1) De-Blocking/De-Protection, (2) Coupling, (3) Capping, and (4) Oxidation.
EGA and PGA deprotection reagents and methods for generating such acids, as well as their use in oligonucleotide synthesis are set out for example in Maurer et al., “Electrochemically Generated Acid and Its Containment to 100 Micron Reaction Areas for the Production of DNA Microarrays”, PLoS, Issue 1, e34 (2006), or in PCT Publications WO 2013/049227 and WO 2016/094512. Thus, in some instances, EGA is generated as part of the deprotection process. Further, in certain instances, all or part of the oligonucleotide synthesis reaction may be performed in aqueous solutions. In other instances, organic solvents will be used.
In many instances, a typical nucleic acid assembly PCR protocol may comprise a combination of methods set out herein, such as, for example, a combination of exonuclease-mediated generation of single-stranded overhangs followed by PCR-based assembly (referred to as a “standard workflow”). In some aspects, such standard workflow may comprise at least the following steps: (i) synthesizing single-stranded oligonucleotides together comprising a sequence of a desired assembly product, wherein each oligonucleotide has a sequence region that is complementary to a sequence region in another oligonucleotide, (ii) hybridizing the oligonucleotides via their complementary sequence regions and elongating the oligonucleotides in an overlap extension PCR reaction (primary assembly PCR) to assemble one or more double-stranded nucleic acid molecules, (iii) amplifying the assembled nucleic acid molecules in the presence of terminal primers (primary amplification), (iv) purifying the amplified nucleic acid molecules, (v) generating single-stranded overhangs at the terminal ends of the amplified one or more nucleic acid molecules and optionally, generating single-stranded overhangs at the terminal ends of a linearized target vector for subsequent cloning (e.g., by treatment of the fragments with one or more restriction endonucleases and/or an exonuclease), (vi) inserting the one or more nucleic acid molecules into the target vector via the complementary single-stranded overhangs, optionally followed by a ligation step, and (vii) transforming host cells (such as, e.g., E. coli) with the resulting vector construct. In some aspects, assembled nucleic acid molecules may be ligated “in vivo” by endogenous enzymatic activities of the transformed cell. For example, a gapped or nicked assembly product may be directly transformed into E. coli and gaps or nicks may be repaired by the E. coli endogenous repair machinery.
Two methods for assembling nucleic acid molecules are depicted in
Further, multiple cycles of polymerase chain reactions may be used to generate successively larger nucleic acid molecules. In many instances, stitched oligonucleotides will be chemically synthesized and will be less than 100 nucleotides in length (e.g., from about 40 to 100, from about 50 to 100, from about 60 to 100, from about 40 to 90, from about 40 to 80, from about 40 to 75, from about 50 to 85, etc. nucleotides). Primers may also be used which contain restriction sites for instances where insertion into a cloning vector is desired. Where desirable, assembled nucleic acid molecules may be directly inserted into vectors and host cells. PCR-based insertion into a target vector may be appropriate when the desired construct is fairly small (e.g., less than 5 kilobases).
A standard workflow is represented in
Another assembly PCR method comprises a combined sequence elongation and ligation reaction (
In assembly chain reactions, overlapping oligonucleotides are assembled into linear double-stranded DNA fragments by successive cycles of denaturation, annealing and reciprocal extension of the oligonucleotides (primary assembly PCR) (see
In some aspects set out herein, one or more thermostable mismatch recognition proteins are present in assembly PCR and/or amplification reactions (see, e.g.,
A schematic of one process for the correction of error in nucleic acid molecules during amplification (primers not shown) is set out in
In more detail,
In many instances, a ligase may be present in reaction mixtures during error correction. It is believed that some endonucleases used in error correction processes have nickase activity. The inclusion of one or more ligase is believed to seal nicks caused by such enzymes and increase the yield of error corrected nucleic acid molecules after amplification. Exemplary ligases that may be used are T4 DNA ligase, Taq ligase, and PBCV-1 DNA ligase. Ligases used in the practice of methods et out herein may be thermolabile or thermostable (e.g., Taq ligase). If a thermolabile ligase is employed, it will typically need to be readied to a reaction mixture for each error correction round. Thermostable ligases will typically not need to be readded during each round, so long as the temperature is kept below their denaturation point.
In many instances, error correction of nucleic acid molecules may be mediated by one or more different mismatch recognition proteins. Examples of categories of such proteins are mismatch binding proteins and mismatch endonucleases. Further, mismatch binding proteins and mismatch endonucleases may be thermostable or non-thermostable, which will often depend on factors the conditions under which the proteins are used and biological activities of the specific protein (e.g., the type of errors recognized).
One exemplary method of error correction that may be used in methods described herein is set out in
In the optional second step (
In the third step (line 3 of
In the fourth step (line 4 of
In the fifth step (line 5 of
In the sixth step (line 6 of
In the seventh step (line 7 of
The process set out above and in
One representative workflow that may be used in methods set out in
Another process for effectuating error correction in chemically synthesized nucleic acid molecules that may be used in methods set out herein is by a commercial process referred to as ERRASE™ (Novici Biotech).
A variation of the workflow of
Using the workflow set out in
Variations of this process are as follows. First, two or more (e.g., two, three, four, five, six, etc.) rounds of error correction may be performed, and in each round a thermostable mismatch recognition protein may be used. Second, more than one endonuclease may be used in one or more rounds of error correction. For example, T7NI and Cel II may be used in each round of error correction. Third, different endonucleases may be used in different error correction rounds or may be combined with steps of error filtration using mismatch binding proteins. For example, a pool of re-annealed oligonucleotides may be subject to an error filtration step using a mismatch binding protein (such as MutS) to remove a first plurality of oligonucleotides having errors from the pool (see
In some instances, T7NI and Cel II, for example, may be used in a first round of error correction and Cel II may be used alone in a second round of error correction. Of course, other mismatch endonucleases may also be used. In another exemplary embodiment, the molecules are cleaved only with one endonuclease (which may be a single-strand nuclease, such as Mung Bean endonuclease or a resolvase, such as T7NI or another endonuclease of similar functionality). In yet another embodiment the same endonuclease (e.g., T7NI) may be used in two subsequent error correction rounds (line 4 of
In many instances, one or more ligase may be present in reaction during error correction. It is believed that some endonucleases used in error correction processes have nickase activity. The inclusion of one or more ligase is believed to seal nicks caused by such enzymes and increase the yield of error corrected nucleic acid molecules after amplification. Exemplary ligases that may be used are T4 DNA ligase, Taq ligase, and PBCV-1 DNA ligase. Ligases used in the practice of methods set out herein may be thermolabile or thermostable (e.g., Taq ligase). If a thermolabile ligase is employed, it will typically need to be added to a reaction mixture for each error correction round. Thermostable ligases will typically not need to be re-added during each round, so long as the temperature is kept below their denaturation point.
In instances where the second set of molecules represents a subfragment of a larger nucleic acid molecule, two or more subfragments (e.g., two or three or more subfragments) together representing the larger nucleic acid molecule may be combined and reacted with the one or more mismatch cleaving endonucleases in a single reaction mix. For example, where the open reading frame that is to be assembled is longer than 1 kb, it may be broken up into two or more subfragments separately assembled in parallel reactions in step three and the resulting two or more subfragments may be combined and error-corrected in a single reaction as indicated in
Nucleic acid molecules with mismatches may be separated from those without mismatches by binding with a mismatch binding agent in a number of ways. For example, mixtures of nucleic acid molecules, some having mismatches, may be (1) passed through a column containing a bound mismatch binding protein or (2) contacted with a surface (e.g., a bead (such as a magnetic bead), plate surface, etc.) to which a mismatch binding protein is bound.
Exemplary formats and associated methods involve those using beads, or other supports, to which a mismatch binding protein is bound. For example, a solution of nucleic acid molecules may be contacted with beads to which is bound a mismatch binding protein. Nucleic acid molecules that are bound to the mismatch binding protein are then linked to the surface and not easily removed or transferred from the solution.
In a specific format set out in
As an example, a protein that has been shown to bind double-stranded nucleic acid molecules containing mismatches is E. coli MutS (Wagner et al., Nucleic Acids Res., 23:3944-3948 (1995)). Wan et al., Nucleic Acids Res., 42:e102 (2014) demonstrated that chemically synthesized nucleic acid molecules containing errors can be retained on a MutS-immobilized cellulose column with nucleic acid molecules not containing errors not being so retained.
Subject matter set out herein thus includes methods, as well as associated compositions, in which nucleic acid molecules are denatured, followed by reannealing, followed by the separation of reannealed nucleic acid molecules containing mismatches. In some aspects, the mismatch binding protein used is MutS (e.g., E. coli MutS). Of course, other mismatch binding proteins, such as those set out in Tables 12 and 15, may also be used.
Further, mixtures of mismatch binding proteins may be used in the practice of methods set out herein. It has been found that different mismatch binding proteins have different activities with respect to the types of mismatches they bind to. For example, Thermus aquaticus MutS has been shown to effectively remove insertion/deletion errors but is less effective in removing substitution errors than E. coli MutS. Further, a combination the two MutS homologs was shown to further improve the efficiency of the error correction with respect to the removal of both substitution and insertion/deletion errors, and also reduced the influence of biased binding. Subject matter set out herein thus includes mixtures of two or more (e.g., from about two to about ten, from about three to about ten, from about four to about ten, from about two to about five, from about three to about five, from about four to about six, from about three to about seven, etc.) mismatch binding proteins.
Subject matter set out herein further includes the use of multiple rounds (e.g., from about two to about ten, from about three to about ten, from about four to about ten, from about two to about five, from about three to about five, from about four to about six, from about three to about seven, etc.) of error correction using mismatch binding proteins. One or more of these rounds of error correction may employ the use of two or more mismatch binding proteins. Alternatively, a single mismatch binding protein may be used in a first round of error correction whereas the same or another mismatch binding protein may be used in a second round of error correction.
Once the oligonucleotide synthesis has been completed, the resulting oligonucleotides are typically subjected to a series of post processing steps that may include one or more of the following: (a) cleavage of the oligonucleotides or elution from the support upon which they were synthesized, (b) concentration measurement, (c) concentration adjustment or dilution of oligonucleotide solutions, often referred to as “normalization”, to obtain equally concentrated dilutions of each oligonucleotide species, and/or (d) pooling or mixing aliquots of two or more normalized oligonucleotide samples to obtain equimolar mixtures of all oligonucleotides required to assemble one or more specific nucleic acid molecules, wherein the aforementioned steps may be combined in different orders.
Yet another process for reducing errors during nucleic acid synthesis that may be used in aspects of subject matter set out herein is referred to as Circular Assembly Amplification and described in PCT Publication WO 2008/112683 A2.
Synthetically generated nucleic acid molecules typically have error rate of about 1 base in 300-500 bases. Conditions can be adjusted so that synthesis errors are substantially lower than 1 base in 300-500 bases. Further, in many instances, greater than 80% of errors are single base frame shift deletions and insertions. Also, less than 2% of errors result from the action of polymerases when high fidelity PCR amplification is employed. Therefore, error-correction processes using PCR-based assembly steps as described above may be combined with one or more error-correction methods not involving polymerase activity. In many instances, mismatch endonuclease (MME) correction will be performed using fixed protein:DNA ratio. Non-PCR-based error correction may, e.g., be achieved by separating nucleic acid molecules with mismatches from those without mismatches by binding with a mismatch binding agent in a number of ways. For example, mixtures of nucleic acid molecules, some having mismatches, may be (1) passed through a column containing a bound mismatch binding protein or (2) contacted with a surface (e.g., a bead (such as a magnetic bead), plate surface, etc.) to which a mismatch binding protein is bound.
Exemplary formats and associated methods involve those using surfaces or supports (e.g., beads) to which a mismatch binding protein is bound. For example, a solution of nucleic acid molecules may be contacted with beads to which is bound a mismatch binding protein. One mismatch binding protein that may be used in various aspects of methods set out herein is MutS from Thermus aquaticus the gene sequence of which is published in Biswas and Hsieh, J. Biol. Chem. 271:5040-5048 (1996) and is available in GenBank, accession number U33117. Furthermore, mismatch cleavage endonucleases such as an EndoMS (e.g., PfuEndoMS, TkoEndoMS, etc.), T7NI or Cel I from, for example, celery may be genetically engineered to inactivate the cleavage function for use in error filtration processes based on mismatch binding. Nucleic acid molecules that are bound to a mismatch binding protein may either be actively removed from a pool of nucleic acid molecules (e.g., via magnetic force where magnetic beads coated with mismatch binding proteins are used) or may be immobilized or linked to a surface such that they remain in the sample whereas unbound nucleic acids are removed or transferred (e.g., by pipetting, acoustic liquid handling etc.) from the sample. Such methods are set out, for example, in PCT Publication WO 2016/094512.
As indicated above, mismatch recognition proteins may be used in conjunction with the hybridization of nucleic acid molecules. Mismatch recognition proteins included in compositions and used in methods set out herein may be thermostable or non-thermostable. Further, methods set out herein include those where more than one mismatch recognition protein is used at more than one location in nucleic acid related workflows (e.g., assembly PCR, amplification, error correction alone, or one or more combinations of these processes).
Thermostable mismatch recognition proteins (e.g., one or more thermostable mismatch endonuclease) allow for the elimination of sequence errors during processes such as assembly PCR, amplification and error correction without the need for re-addition of mismatch recognition protein after each thermal denaturation step. Thus, compositions and methods set out herein allow for the multiple rounds of error correction where mismatch recognition protein is not added after each nucleic acid denaturation step. Of course, non-thermostable mismatch recognition proteins may also be used in such workflows but mismatch recognition activity of such proteins would generally be eliminated or substantially decreased by each thermal denaturation cycle. In many instances, it would be necessary or desirable to add more non-thermostable mismatch recognition proteins after each thermal denaturation cycle.
The type or types of mismatch recognition proteins used in workflows may vary. In some instances, error correction may be performed at one or more location in a workflow. In some instances, a thermostable mismatch recognition protein will be used and, often, in conjunction with a non-thermostable mismatch recognition protein.
One method for removing nucleic acid molecules with errors is by the separation of such nucleic acid molecules from nucleic acid molecules that do not contain errors. Thus, provided herein are workflows, and composition used in such workflows, that use agents that bind to nucleic acid molecules containing errors and the separation of them from nucleic acid molecules that do not contain errors. Examples of such agents are mismatch binding proteins.
Mismatch binding proteins may be bound to a support, for example, may be contacted with a sample containing nucleic acid molecules with mismatches and nucleic acid molecules without mismatches under conditions where the nucleic acid molecule with mismatches will be bound to the support. The support to which nucleic acid molecule with mismatches are bound may then be removed from contact with nucleic acid molecules without mismatches, thereby separating nucleic acid molecules with mismatches from nucleic acid molecules without mismatches.
Another method for increasing the percentage of correct nucleic acid molecules in a composition is by suppressing amplification of nucleic acid molecules containing errors (e.g., deletions, insertion, mismatches, etc.). In some instances, one or more protein (e.g., one or more mismatch binding proteins) may be used which reduces the number of errors in a population of nucleic acids molecules by inhibiting assembly PCR and/or amplification of nucleic acid molecules that contain one or more error. In some instances, a polymerase reagent may be used which reduces the number of errors in a population of nucleic acids molecules by disfavoring assembly PCR and/or amplification of nucleic acid molecules that contain one or more error.
Some examples of workflows that may be performed are set out in Table 1.
As shown by, for example, the workflow variations set out in Table 1, provided herein are compositions and methods for generating populations of nucleic acid molecules. In some such methods, these workflows comprise two or more different types of processes (e.g., nucleic acid assembly, nucleic acid amplification, nucleic acid denaturation/renaturation, etc.) in which single-stranded nucleic acid molecules hybridize to each other to form double-stranded nucleic acid molecules. In all or part of such workflows, either error correction or error reduction may occur. In some instances, error correct may occur between steps referenced in Table 1. For example, when one or more non-thermostable mismatch endonuclease (e.g., T7NI) is used after primary amplification, it will typically be contacted with amplification products before secondary amplification. This is so because thermal cycling will normally denature non-thermostable mismatch endonucleases. Mismatch binding proteins may also be used between amplifications steps where the mismatch binding proteins are used to separate mismatched nucleic acid molecule from non-mismatched nucleic acid molecules.
In some instances, the collective effect of processes set out herein may result in populations of nucleic acid molecules which contain fewer errors than 1 per 500 base pairs (e.g., from about 1 per 500 to about 1 per 2,000, from about 1 per 600 to about 1 per 2,000, from about 1 per 700 to about 1 per 2,000, from about 1 per 800 to about 1 per 2,000, from about 1 per 900 to about 1 per 2,000, from about 1 per 1,000 to about 1 per 2,000, from about 1 per 700 to about 1 per 1,500, from about 1 per 700 to about 1 per 1,200, from about 1 per 700 to about 1 per 1,000, from about 1 per 800 to about 1 per 1,200, etc. base pairs).
Addition of one or more mismatch binding protein (e.g., thermostable mismatch binding proteins) to assembly PCR mixtures may be used for functional removal of oligonucleotides containing sequence errors by blocking the extension by a polymerase when a mismatch binding protein is bound to the mismatch formed during annealing (see Fukui et al., “Simultaneous Use of MutS and RecA for Suppression of Nonspecific Amplification during PCR” J. Nucleic Acids, Volume 2013, Article ID 823730).
Mismatch-binding proteins and mismatch endonucleases often show specificity for certain types of mismatches. Thus, in some instances more than one mismatch recognition protein may be used in workflows set out herein. Further, in many instances, when more than one mismatch recognition protein is present, the error recognition activities of the proteins will differ. For example, the mismatch endonucleases TkoEndoMS and T7NI differ in that T7NI is believed to have higher activities with respect to deletions and insertions than TkoEndoMS (see
Sample Number 1 (Std-noEC) was a control run where 66 fragments were assembled with no error correction. As can be seen from this figure, the median error rate for Sample Number 1 is 1 in 308. This increases to 1 in 456 when post-primary amplification T7NI mediated error correction was used (Sample Number 2). Sample Numbers 1 and 2 represents an error correction baseline of conditions in which there was no error correction and error correction using T7NI post-primary amplification of the assembled fragments.
The data for Sample Numbers 3 and 4 in
The data for Sample Numbers 5 and 6 in
The data for Sample Numbers 7 and 8 in
The data set out in
Table 1 below shows data derived from
The data in
Provided herein are compositions and methods in which the error rates of assembled and amplified nucleic acid molecules is from about 1 in 500 to about 1 in 5,000 base pairs (e.g., from about 1 in 550 to about 1 in 1,500, from about 1 in 600 to about 1 in 1,500, from about 1 in 650 to about 1 in 1,500, from about 1 in 700 to about 1 in 1,500, from about 1 in 800 to about 1 in 1,500, from about 1 in 500 to about 1 in 1,400, from about 1 in 500 to about 1 in 1,350, from about 1 in 500 to about 1 in 1,300, from about 1 in 500 to about 1 in 1,250, from about 1 in 500 to about 1 in 1,200, from about 1 in 500 to about 1 in 1,150, from about 1 in 500 to about 1 in 1,000, from about 1 in 600 to about 1 in 1,000, from about 1 in 650 to about 1 in 1,000, from about 1 in 600 to about 1 in 900, from about 1 in 650 to about 1 in 900, from about 1 in 700 to about 1 in 850, from about 1 in 550 to about 1 in 2,000, from about 1 in 550 to about 1 in 2,500, from about 1 in 550 to about 1 in 3,500, from about 1 in 550 to about 1 in 4,500, from about 1 in 900 to about 1 in 3,500, from about 1 in 1,500 to about 1 in 5,000, from about 1 in 2,000 to about 1 in 5,000, from about 1 in 2,500 to about 1 in 5,000, etc. base pairs). Such nucleic acid molecule may be generated by primary assembly PCR and primary assembly, optionally followed by secondary amplification.
Provided herein are compositions and methods in which the fold decrease (“X”) in the error rate of assembled and amplified nucleic acid molecules is greater than 1.75 (e.g., from about 1.75 to about 8, from about 1.75 to about 7, from about 1.75 to about 8, from about 1.75 to about 5, from about 1.75 to about 4, from about 1.75 to about 3, from about 2.0 to about 8, from about 2.1 to about 8, from about 2.2 to about 8, from about 2.3 to about 8, from about 2.5 to about 8, from about 2.75 to about 8, from about 2.0 to about 7, from about 2.0 to about 6, from about 2.0 to about 5, from about 2.0 to about 4.5, from about 2.2 to about 8, from about 2.2 to about 7, from about 2.2 to about 6, from about 2.2 to about 5, from about 2.2 to about 3, from about 2.2 to about 2.8, from about 2.1 to about 2.8, etc.) when compared to the error rate of assembled and amplified nucleic acid molecules without error correction using either a single control/“benchmark” sample run or an average of control/“benchmark” sample runs (see data in
where X is the fold decrease in errors, Y is the number of error rate after the error correction step, and Z is the number of error rate before the error correction step.
Sample Numbers 8, 6, 4, and 2 (T7NI treated) all show similarly low levels of deletions and insertions in
A number of different types of substitutions can be found in double-stranded nucleic acid molecules. Further, mismatch recognition proteins often vary in specificity of the types of substitutions they demonstrate activity towards. This specificity can vary with specific conditions, such as the presence or absence of divalent metal ions and the surrounding nucleic acid region. Some of these variations of EndoMS are set out in Ishino et al., Nucl. Acids Res. 44:2977-2989 (2016). Additional EndoMS proteins are set out in Table 15. Also, altered forms of wild-type thermostable mismatch endonuclease from Pyrococcus furiosus have been generated (see U.S. Pat. No. 10,196,618 and U.S. Patent Publication No. 2017/253909). Further, altered forms of wild-type mismatch recognition proteins (e.g., mismatch endonucleases) may be generated that vary in mismatch recognition activities. Such altered forms of wild-type mismatch recognition proteins may be included in and/or used in methods set out herein.
S
A number of mismatch recognition proteins (e.g., mismatch recognition proteins set out in Table 15) are known to have recognition activity for different types of mismatches. Error correction specificities of some mismatch recognition proteins are set out in Table 3.
Pyrococcus
furiosus
Thermococcus
kodakarensis
Thermus
aquaticus
Thermus
thermophilus
Methods set out herein include those where more than one mismatch recognition protein are used in conjunction. Using the workflow shown in
Provided herein are methods for the correction of error in nucleic acid molecules involving the sequence or simultaneous use of mismatch recognition proteins that differ in the types of errors they recognize,
Error correction methods and reagents suitable for use in methods provided herein are set out in U.S. Pat. Nos. 7,838,210 and 7,833,759, U.S. Patent Publication No. 2008/0145913 A1 (mismatch endonucleases), PCT Publication WO 2011/102802 A1, and in Ma et al., Trends in Biotechnology, 30(3):147-154 (2012). Furthermore, the skilled person will recognize that other methods of error correction and/or error filtration (i.e., specifically removing error-containing molecules) may be practiced in certain aspects of subject matter set out herein such as those described, for example, in U.S. Patent Publication Nos. 2006/0127920 AA, 2007/0231805 AA, 2010/0216648 A1, or 2011/0124049 A1.
Provided herein are compositions and methods which contain and use a number of different error correcting agents. Such error correcting agents will have activity related to the correction of one or more of the following error types, deletions, insertion and substitution, also referred to as mismatches. Further, with respect to substitutions, activity will generally be directed to different types of substitutions.
A number of different polymerases and types of polymerases may be contained and used in compositions and methods set out herein. It is believed that the type of polymerase used in one or more steps of assembly PCR and amplification workflows affect the number of errors present in assembled nucleic acid molecules.
A representative workflow of methods provided herein is set out in
Following synthesis oligonucleotides may be assembled (primary assembly PCR) into larger nucleic acid molecules in a stepwise manner and optionally, amplified. Methods used to assemble nucleic acid molecules may vary (see, e.g.,
In some aspects, assembled nucleic acid molecule length may vary from about 20 base pairs to about 10,000 base pairs, from about 100 base pairs to about 5,000 base pairs, from about 150 base pairs to about 5,000 base pairs, from about 200 base pairs to about 5,000 base pairs, from about 250 base pairs to about 5,000 base pairs, from about 300 base pairs to about 5,000 base pairs, from about 350 base pairs to about 5,000 base pairs, from about 400 base pairs to about 5,000 base pairs, from about 500 base pairs to about 5,000 base pairs, from about 700 base pairs to about 5,000 base pairs, from about 800 base pairs to about 5,000 base pairs, from about 1,000 base pairs to about 5,000 base pairs, from about 100 base pairs to about 4,000 base pairs, from about 150 base pairs to about 4,000 base pairs, from about 200 base pairs to about 4,000 base pairs, from about 300 base pairs to about 4,000 base pairs, from about 500 base pairs to about 4,000 base pairs, from about 50 base pairs to about 3,000 base pairs, from about 100 base pairs to about 3,000 base pairs, from about 200 base pairs to about 3,000 base pairs, from about 250 base pairs to about 3,000 base pairs, from about 300 base pairs to about 3,000 base pairs, from about 400 base pairs to about 3,000 base pairs, from about 600 base pairs to about 3,000 base pairs, from about 800 base pairs to about 3,000 base pairs, from about 100 base pairs to about 2,000 base pairs, from about 200 base pairs to about 2,000 base pairs, from about 300 base pairs to about 1,500 base pairs, etc.
Any number of methods may be used for nucleic acid amplification and assembly. One exemplary method is described in Yang et al., Nucleic Acids Research 21:1889-1893 (1993) and U.S. Pat. No. 5,580,759. In the process described in Yang et al., a linear vector is mixed with double-stranded nucleic acid molecules which share sequence homology at the termini. An enzyme with exonuclease activity (i.e., T4 DNA polymerase, T5 exonuclease, T7 exonuclease, etc.) is added which generates single-stranded overhangs of all termini present in the mixture. The nucleic acid molecules having single stranded overhangs are then annealed and incubated with a DNA polymerase and deoxynucleotide triphosphates under condition which allow for the filling in of single-stranded gaps. Nicks in the resulting nucleic acid molecules may be repaired by introduction of the molecule into a cell or by the addition of ligase. Of course, depending on the application and workflow, the vector may be omitted. Further, the resulting nucleic acid molecules, or sub-portions thereof, may be amplified by polymerase chain reaction.
Other methods of nucleic acid assembly include those described in U.S. Patent Publication Nos. 2010/0062495 A1; 2007/0292954 A1; 2003/0152984 AA; and 2006/0115850 AA, in U.S. Pat. Nos. 6,083,726; 6,110,668; 5,624,827; 6,521,427; 5,869,644; and 6,495,318 and WO 2020/001783 A1.
A method for the isothermal assembly of nucleic acid molecules is set out in U.S. Patent Publication No. 2012/0053087. In one aspect of this method, nucleic acid molecules for assembly are contacted with a thermolabile protein with exonuclease activity (e.g., T5 polymerase) and optionally, a thermostable polymerase, and/or a thermostable ligase under conditions where the exonuclease activity decreases with time (e.g., 50° C.). The exonuclease “chews back” one strand of the nucleic acid molecules and, if there is sequence complementarity, nucleic acid molecules will anneal with each other. In one embodiment, a thermostable polymerase may be used to fill in gaps and a thermostable ligase may be provided to seal nicks. In another embodiment, the annealed nucleic acid product may be directly used to transform a host cell and gaps and nicks will be repaired “in vivo” by endogenous enzymatic activities of the transformed cell.
Single-stranded binding proteins, such as T4 gene 32 protein and RecA, as well as other nucleic acid binding or recombination proteins known in the art, may be included, for example, to facilitate the annealing of nucleic acid molecules.
In some instances, standard ligase-based joining of partially and fully assembled nucleic acid molecules may be employed. For example, assembled nucleic acid molecule may be generated with restriction enzyme sites near their termini. These nucleic acid molecules may then be treated with one of more suitably restrictions enzymes to generate, for example, either one or two “sticky ends”. These sticky end molecules may then be introduced into a vector by standard restriction enzyme-ligase methods. In instances where the inert nucleic acid molecules have only one sticky end, ligases may be used for blunt end ligation of the “non-sticky” terminus.
The complexity of a population of oligonucleotides is, in part, determined by the number of different oligonucleotides present. In some instances, the number of oligonucleotides present that are designed to have different nucleotide sequences, may be from about 2,000 to about 20,000 (e.g., from about 2,000 to about 20,000, from about 2,000 to about 20,000, from about 2,000 to about 20,000, from about 2,000 to about 20,000, from about 2,000 to about 20,000, from about 2,000 to about 20,000, from about 2,000 to about 20,000, from about 2,000 to about 20,000, from about 2,000 to about 20,000, from about 2,000 to about 20,000, from about 2,000 to about 20,000, from about 2,000 to about 20,000, from about 2,000 to about 20,000, from about 2,000 to about 20,000, from about 2,000 to about 20,000, from about 2,000 to about 20,000, etc.).
Further, oligonucleotides in a reaction mixture may represent subfragments of more than one larger nucleic acid molecule. By way of example, if it is desired to assemble three assembled nucleic acid molecules in one reaction mixture and ten oligonucleotides are required to assemble each of the assembled nucleic acid molecules, then the reaction mixture would initially contain at least thirty oligonucleotides.
Provided herein are compositions useful for and methods of assembling more than one assembled, error corrected nucleic acid. In some instances, the number assembled error corrected nucleic acid molecule generated by these methods will be from about two to about one hundred (e.g., from about two to about ninety, from about two to about eighty, from about two to about seventy, from about two to about fifty, from about five to about ninety, from about five to about sixty, from about eight to about ninety, from about eight to about fifty, from about eight to about thirty-five, from about ten to about ninety, from about two to about sixty, from about fifteen to about ninety, from about fifteen to about fifty-five, etc.).
There are a number of different types of DNA polymerase. By way of example, many prokaryotic cells contain DNA polymerase Type I, II and III. DNA polymerases may or may not have proofreading activity. Proofreading DNA polymerases typically also have 3′ to 5′ exonuclease activity. Further DNA polymerases may be thermostable or non-thermostable.
While any type of DNA polymerase may be contained and used in compositions and methods set out herein, in many instances, proofreading polymerases will be employed herein. In some instances, DNA polymerases will be formulated for “hot start”, where the DNA polymerase is bound to antibodies that release the DNA polymerase upon heating.
DNA polymerases that may be contained and used in compositions and methods set out herein. Exemplary DNA polymerases and DNA polymerase reagents include Phi29 DNA polymerase or its derivatives, Bsm, Bst, T4, T7, DNA Pol I, or Klenow Fragment; or mutants, variants and derivatives thereof. Additional exemplary DNA polymerases and DNA polymerase reagents include Taq, Tbr, Tfl, Tth, Tli, Tfi, Tne, Tma, Pfu, Pwo, and Kod DNA polymerase, as well as V
In some instances, the DNA polymerase may comprise a chimeric DNA polymerase. Further, the chimeric DNA polymerase may comprise a sequence nonspecific double-stranded DNA (dsDNA) binding domain. In some instances, the dsDNA binding domain may comprise Sso7d from Sulfolobus solfataricus; Sac7d, Sac7a, Sac7b, and Sac7e from S. acidocaldarius; and Ssh7a and Ssh7b from Sulfolobus shibatae; Pae3192; Pae0384; Ape3192; HMf family archaeal histone domains; or an archaeal proliferating-cell nuclear antigen (PCNA) homolog. Additionally, DNA polymerases present in compositions and used in methods set out herein may also comprise exonuclease activity and/or an exonuclease domain.
Further, DNA polymerases that may be contained and used in compositions and methods set out herein include all or part of a DNA polymerase set out in Table 14, as well as modified forms of such polymerases (e.g., DNA polymerases that are at least 90%, at least 95%, or at least 97.5% identical to a DNA polymerase set out in Table 14).
P
DNA polymerases that may be present in compositions and used in methods set out herein include those that have been modified to reduce the effect of inhibiting substances and/or are formulated with one or more compound that reduces the effect of inhibiting substances. As an example, P
DNA polymerase reagents may also be formulated to lessen the effect of interfering compounds. One category of compounds that may be used in such formulations are “amines”. Amines have been found to improve (1) nucleic acid synthesis product yields and/or (2) tolerance to inhibitors of nucleic acid synthesis. Amine contain compounds that may be contained and used in compositions and methods set out herein including compounds comprising one or more amines of formula I:
or salts thereof wherein R1 is H; R2 is chosen from alkyl, alkenyl, alkynyl, or (CH2)n-R5, wherein n=1 to 3, and R5 is aryl, amino, thiol, mercaptan, phosphate, hydroxy, or alkoxy; and R3 and R4 may be the same or different and are independently chosen from H or alkyl, with the proviso that if R2 is (CH2)n-R5, then at least one of R3 and/or R4 is alkyl.
Specific amine containing compounds that may be contained and used in compositions and methods set out herein include dimethylamine hydrochloride, diethylamine hydrochloride, diisopropylamine hydrochloride, ethyl(methyl)amine hydrochloride, and/or trimethylamine hydrochloride.
When one or more amine compounds are present in a formulation, the concentration of this or these compounds will generally be in the range of 5 mM to 500 mM (e.g., from about 5 mM to about 500 mM, from about 10 mM to about 500 mM, from about 20 mM to about 500 mM, from about 30 mM to about 500 mM, from about 40 mM to about 500 mM, from about 5 mM to about 300 mM, from about 5 mM to about 250 mM, from about 5 mM to about 200 mM, from about 5 mM to about 100 mM, from about 10 mM to about 250 mM, from about 20 mM to about 200 mM, from about 25 mM to about 180 mM, from about 50 mM to about 110 mM, etc.).
One specific example of a DNA polymerase reagent that may be used in methods set out herein is P
Vectors that may be used in methods set out herein may be any vector suitable for cloning and transforming a host cell. In many instances, high-copy number vectors may be used to obtain high yields of the desired polynucleotide. Common high-copy number vectors include pUC (˜500-˜700 copies),
An exemplary list of vectors that can be used in any of the assembly or cloning methods disclosed herein, includes the following: B
In some aspects, the vector may have a limited size to allow for PCR-mediated elongation of the full-length fusion construct. Under certain conditions, full-length elongation and/or amplification of the fusion construct may not be required. In such circumstances, the size of the target vector may not be limiting. Thus, in some aspects the target vector may have a size of between about 0.5 and about 5 kb, or between about 1 kb and about 3 kb, whereas in other aspects the target vector may have a size of between about 2 kb and about 10 kb or between about 5 kb and about 20 kb.
Assembled nucleic acid molecules may also include functional elements which confer desirable properties. These elements may either be provided by the plurality of oligonucleotides or by the target vector. Examples of such elements include origins of replication, long terminal repeats, resistance markers (such as antibiotic resistance genes), selectable markers and antidote coding sequences (e.g., ccdA coding sequences for counter-acting toxic effects of ccdB), promoters, enhancers, polyadenylation signal coding sequences, 5′ and 3′ UTRs and other components suitable for the particular use(s) of the nucleic acid molecules (e.g., enhancing mRNA or protein production efficiency). In aspects where nucleic acid molecules are assembled to form an operon, the assembled nucleic acid products will often contain promoter and terminator sequences. Furthermore, assembled nucleic acid molecules may contain multiple cloning sites, such as, e.g., type II or type IIs cleavage sites and/or G
The vector may be linearized by any means including PCR amplification of a closed circular template vector molecule. Alternatively, the vector may be linearized by restriction enzyme cleavage with one or more enzymes producing either blunt or sticky ends. Such enzymes include restriction endonucleases of type II which cleave nucleic acid at fixed positions with respect to their recognition sequence. Restriction enzymes that can be selected to produce either “blunt” or “sticky” ends upon cleavage of a double-stranded nucleic acid are known to those skilled in the art and can be selected by the skilled person depending on the vector sequence and assembly requirements. In some instances, a vector may be linearized using a restriction endonuclease that generates blunt ends.
Following cleavage, the vector may either be used directly in, for example, an assembly PCR reaction (e.g., a sequence elongation and ligation reaction), or purified using gel extraction, or amplified in a PCR reaction prior to use in an assembly PCR reaction. Purification of a linearized vector generated by PCR amplification is often not required and the PCR product can be directly used in an assembly PCR reaction. Alternatively, a circular vector may be used comprising type IIS restriction enzyme cleavage sites and be subject to a one-step cleavage and ligation process to seamlessly clone one or more assembled nucleic acid molecules into the vector which is commonly known as Golden Gate cloning system as described below.
Following assembly PCR, the reaction mix comprising the assembled circularized construct or an aliquot thereof may be directly used to transform suitable competent host cells such as, e.g., a common E. coli strain according to standard protocols. The skilled person can select suitable host cells depending on construct size and nucleotide composition, plasmid copy number, selection criteria etc. Useful strains are available through the American Type Culture Collection and the E. coli Genetic Stock Center at Yale, as well as from commercial suppliers such as Agilent, Promega, Merck, Thermo Fisher Scientific, and New England Biolabs, respectively.
In many instances, nucleic acid molecules prepared by methods of provided herein will be replicable. Further, many of these replicable nucleic acid molecules will be circular (e.g., plasmids). Replicable nucleic acid molecules, regardless of whether they are circular, will generally be formed from the assembly of two or more (e.g., three, four, five, eight, ten, twelve, etc.) nucleic acid fragments. In some instances, methods provided herein employ selection based upon the reconstitution of one or more (e.g., two, three, four, etc.) selection marker or one or more (e.g., two, three, four, etc.) origin of replication resulting from the linking of different nucleic acid fragments. Further selection may result from the formation of a circular nucleic acid molecule, in instances where circularity is required for replication.
In an alternative embodiment, the single-stranded oligonucleotides used in a sequence elongation and ligation reaction (
Assembled constructs obtained by an assembly workflow may be further combined with other assembly workflow products or nucleic acid molecules obtained from other sources to assemble larger nucleic acid molecules (e.g., genes). Constructs of larger sizes may be assembled by any means known to the person skilled in the art. For example, Type IIs restriction site mediated assembly methods may be used to assemble multiple fragments (e.g., two, three, five, eight, ten, etc.) when larger constructs are desired (e.g., 5 to 100 kilobases). One suitable cloning system is referred to as Golden Gate which is set out in various forms in U.S Patent Publication No. 2010/0291633 A1 and PCT Publication WO 2010/040531.
It may be desirable at a number of points during workflows of provided herein to separate nucleic acid molecules or assembly products from reaction mixture components (e.g., dNTPs, primers, truncated oligonucleotides, tRNA molecules, buffers, salts, proteins, etc.). This may be done in a number of ways, such as, e.g., by enzymatically removing undesired nucleic acid side-products with an exonuclease, restriction enzyme or UNG glycosylase as described above. In some instances, the nucleic acid molecules may be precipitated or bound to a solid support (e.g., magnetic beads). Once separated from reaction components for facilitating a process (e.g., pooling or multiplexing of selected oligonucleotides, nucleic acid synthesis, error correction, etc.), nucleic acid molecules may then be used in additional reactions (e.g., assembly PCR reactions, amplification, cloning etc.).
Larger nucleic acid molecules may also be assembled in vivo. In in vivo assembly methods, a mixture of all of the subfragments to be assembled is often used to transfect the host cell using standard transfection techniques. The ratio of the number of molecules of subfragments in the mixture to the number of cells in the culture to be transfected should be high enough to permit at least some of the cells to take up more molecules of subfragments than there are different subfragments in the mixture. Thus, in most instances, the higher the efficiency of transfection, the larger number of cells will be present which contain all of the nucleic acid subfragments required to form the final desired assembly product. Technical parameters along these lines are set out in U.S. Patent Publication No. 2009/0275086 A1.
Large nucleic acid molecules are relatively fragile and, thus, shear readily. One method for stabilizing such molecules is by maintaining them intracellularly. Thus, in some aspects, subject matter set out herein involves the assembly and/or maintenance of large nucleic acid molecules in host cells. Large nucleic acid molecules will typically be 20 kb or larger (e.g., larger than 25 kb, larger than 35 kb, larger than 50 kb, larger than 70 kb, larger than 85 kb, larger than 100 kb, larger than 200 kb, larger than 500 kb, larger than 700 kb, larger than 900 kb, etc.).
Methods for producing and even analyzing large nucleic acid molecules are known in the art. For example, Karas et al., “Assembly of eukaryotic algal chromosomes in yeast, Journal of Biological Engineering 7:30 (2013) shows the assembly of an algal chromosome in yeast and pulse-field gel analysis of such large nucleic acid molecules.
As suggested above, one group of organisms known to perform homologous recombination fairly efficient is yeasts. Thus, host cells used in the practice of methods set out herein may be yeast cells (e.g., Saccharomyces cerevisiae, Schizosaccharomyces pombe, Pichia, pastoris, etc.).
Yeast hosts are particularly suitable for manipulation of donor genomic material because of their unique set of genetic manipulation tools. The natural capacities of yeast cells, and decades of research have created a rich set of tools for manipulating DNA in yeast. These advantages are well known in the art. For example, yeast, with their rich genetic systems, can assemble and re-assemble nucleotide sequences by homologous recombination, a capability not shared by many readily available organisms. Yeast cells can be used to clone larger pieces of DNA, for example, entire cellular, organelle, and viral genomes that are not able to be cloned in other organisms. Thus, in some aspects, the enormous capacity of yeast genetics to generate large nucleic acid molecules (e.g., synthetic genomics) may be harnessed by using yeast as host cells for assembly and maintenance.
A codon optimized coding sequence for TkoEndoMS containing an amino terminal signal peptide (METDTLLLWV LLLWVPGSTG SKDKVTVIT (SEQ ID NO: 5)) and a carboxy terminal six histidine purification tag (
During the optimization process the following cis-acting sequence motifs were avoided where applicable: (1) internal TATA-boxes, chi-sites and ribosomal entry sites, (2) AT-rich or GC-rich sequence stretches, (3) RNA instability motifs, (4) repeat sequences and RNA secondary structures, and (5) (cryptic) splice donor and acceptor sites in higher eukaryotes. The result was the nucleotide sequence shown in
The nucleotide sequence set out in
Benchmark Oligonucleotide Assembly Protocol
Assembly PCR
A master mix for all the reaction components was made except the mixture of oligonucleotides for assembly. 730 nl of the master mix was transferred to wells of a 384 well-plate using an E
Amplification
A master mix of all the components except the assembly PCR products was prepared. 8.8 μl of the master mix was then transferred to wells of a 384 well-plate containing assembly PCR products with a multistep pipettor. Thermocycling was then performed using the cycler protocol set out below.
EndoMS Oligonucleotide Assembly Protocol Using P
A. Assembly PCR
Identical to benchmark protocol, but reaction contains 0.020 μl TkoEndoMS (130 ng/μl). H2O is 0.420 μl accordingly.
B. Amplification
Identical to benchmark protocol, but reaction contains 0.140 μl TkoEndoMS (130 ng/μl). H2O is 6.386 μl accordingly.
Oligonucleotide Assembly Protocol Using S
A. Assembly PCR
A master mix for all the reaction components was made except the mixture of oligonucleotides for assembly. 730 nl of the master mix was transferred to wells of a 384 well-plate using an E
B. Amplification
A master mix of all the components except the assembly PCR products was prepared. 8.8 μl of the master mix was then transferred to wells of a 384 well-plate containing assembly PCR products with a multistep pipettor. Thermocycling was then performed using the cycler protocol set out below.
Error Correction Protocol Using T7 Endonuclease I (T7NI)
A. Error Correction I (Denature and Re-Anneal)
Error Correction II (Mismatch cleavage)
Cyler Protocol: 45° C., 20 min. in Cycler
B. Error Correction III (Amplification)
Thermostable Mismatch Endonucleases (TsMMEs)
After having shown in Example 1 that the use of TkoEndoMS during assembly and/or amplification results in the generation of nucleic acid molecules with reduced error rates, conditions were tested for additional reduction of error rates. These conditions included the use of different thermostable mismatch endonucleases (abbreviated herein as “TsMMEs”), such as homologs of TkoEndoMS, different DNA polymerases, and different cycler protocols.
Materials and Methods:
“TsMMEs”, set out in Table 4, with the amino acid sequence of these enzymes shown in Table 15, and used in the experiments set out in this example were produced in Expi293 for thermostable error correction (abbreviated herein as “TsEC”). These enzymes produced by Thermo Fisher Scientific GeneArt GmbH (Regensburg, DE), were greater than 95% pure, and were each stored in the following buffer solution: 50 mM Tris-HCl pH 8.0, 0.5 mM DTT, 0.1 mM EDTA, 0.5 M NaCl, 50% glycerol.
No error correction using T7 endonuclease I was performed in experiments set out in this example.
Benchmark Oligonucleotide Assembly Protocol
Benchmark data set out in this example was generated using P
Assembly PCR
A master mix was produced containing all the components except the Oligonucleotide-Mix. 730 nl of the master mix was transferred to individual wells of a 384 well-plate using a Labcyte E
Amplification
A master mix was prepared containing all the components except the assembly reaction product. 8.8 μl of this master mix was then transferred with a multistep pipettor to individual wells of a 384 well-plate containing the assembly reaction product.
TsEC Oligonucleotide Assembly Protocol using P
Assembly
The methods used were identical to Benchmark Protocol set out earlier in this example but the reaction mixture contained 0.020 μl TkoEndoMS (130 ng/μl) and 0.420 μl of H2O.
Amplification
The methods used were identical to the benchmark protocol set out above but the reaction mixture contained 0.140 μl TkoEndoMS (130 ng/μl) and 6.386 μl of H2O.
Oligonucleotide Assembly Protocol using P
A master mix was produced containing all the components except the Oligonucleotide-Mix. 730 nl of the master mix was transferred to individual wells of a 384 well-plate using a Labcyte E
Amplification
A master mix was prepared containing all the components except the assembly reaction product. 8.8 μl of this master mix was then transferred with a multistep pipettor to a well of a 384 well-plate containing the assembly reaction product.
Results:
Assembly of 20 individual fragments using the “Benchmark Oligonucleotides Assembly Protocol” and P
The data set out in Table 5 indicates that processing with S
Data set out in Table 6 shows that nucleic acid molecules assembled and amplified using P
Data set out in Table 6 also suggest that the PhoNucS and the SacEndoMS enzymes do not exhibit high levels of cleavage activity for (1) A>C and T>G and (2) G>T and C>A transversions. Upon hybridization with a wild-type molecule, these transversions form mismatches for which their homolog TkoEndoMS has low cleavage activity (Ishino et al., Nucl. Acids Res. 44:2977-2989 (2016)).
Table 7 shows a comparison of error rate data of nucleic acid fragments assembly and amplification by S
As seen in Table 8, use of the Benchmark Oligonucleotide Assembly Protoco with P
Data set out in Table 9 shows that nucleic acid molecules assembled and amplified using P
Data set out in Table 9 also suggest that the TkoEndoMS enzyme does not exhibit high levels of cleavage activity for (1) A>C and T>G and (2) G>T and C>A transversions. Upon hybridization with a wild-type molecule, these transversions form mismatches for which TkoEndoMS has low cleavage activity (Ishino et al., Nucl. Acids Res. 44:2977-2989 (2016)).
A number of effects are seen in Table 10, one is that the use of different thermostable error correction enzymes results in different error rates in product nucleic acid molecules after assembly and amplification. Also, the number of errors present in nucleic acid molecules after assembly and amplification varies to some extent with the cycler protocol used. Thus, two factors that may be varied to yield assembled and amplified nucleic acid molecules with low error rates are (1) the error correction enzyme (or error correction enzymes) used and (2) the manner by which nucleic acid molecule sub-components are assembled and amplified (e.g., thermocycler protocol, buffer and buffer components used/present, etc.).
Data in Table 11 also show that efficient reduction of error rates can be achieved independently of the initial error rate. For assembly and amplification using S
While specific aspects of subject matter set out herein have been shown and described herein, it will be obvious to those skilled in the art that such aspects are provided by way of example only. Numerous variations, changes, and substitutions will now occur to those skilled in the art without departing subject matter set out herein. It should be understood that various alternatives to the aspects of subject matter set out herein described herein may be employed in practicing subject matter set out herein. It is intended that the following claims define the scope of subject matter set out herein and that methods and structures within the scope of these claims and their equivalents be covered thereby.
Thermococcus kodakarensis (TkoEndoMS)
Pyrococcus furiosus (PfuEndoMS)
Thermococcus kodakarensis (TkoEndoMS with N-Terminal Signal
Thermus aquaticus
Meiothermus taiwanensis WR-220
Meiothermus silvanus
Methanothrix thermoacetophila
Thermus aquaticus
Thermus thermophilus
Aquifex aeolicus
Archaeoglobus profundus
Caldicellulosiruptor
saccharolyticus
Caldicellulosiruptor
saccharolyticus
Dictyoglomus
thermophilum
Dictyoglomus
thermophilum
Methanothermobacter
thermautotrophicus
Pyrococcus furiosus
Pyrolobus fumarii
Pyrolobus fumarii
Thermococcus barophilus
Thermotoga maritima
Thermotoga maritima
Thermus thermophilus
Pyrococcus furiosus
Thermococcus
kodakarensis
Aeropyrum pernix
Aeropyrum pernix
Aeropyrum pernix
Aeropyrum pernix
Archaeoglobus
profundus
Caldivirga
maquilingensis
Caldicellulosiruptor
saccharolyticus
Desulfurococcus
kamchatkensis
Desulfurococcus
kamchatkensis
Desulfurococcus
mucosus
Dictyoglomus turgidum
Dictyoglomus turgidum
Hyperthermus butylicus
Ignisphaera aggregans
Ignisphaera aggregans
Ignisphaera aggregans
Ignicoccus hospitalis
Methanocaldococcus
jannaschii
Methanopyrus kandleri
Methanopyrus kandleri
Methanopyrus kandleri
Methanothermobacter
thermautotrophicus
Nanoarchaeum equitans
Pyrococcus abyssi
Pyrococcus abyssi
Pyrobaculum aerophilum
Pyrobaculum aerophilum
Pyrobaculum aerophilum
Pyrobaculum aerophilum
Pyrococcus horikoshii
Pyrococcus horikoshii
Pyrolobus fumarii
Pyrolobus fumarii
Sulfolobus
acidocaldarius
Sulfolobus
acidocaldarius
Sulfolobus
acidocaldarius
Staphylothermus
hellenicus
Staphylothermus
hellenicus
Staphylothermus
marinus
Sulfolobus solfataricus
Sulfolobus solfataricus
Sulfolobus solfataricus
Thermoplasma
acidophilum
Thermosphaera
aggregans
Thermosphaera
aggregans
Thermococcus
barophilis
Thermotoga maritima
Thermotoga maritima
Thermofilum pendens
Thermofilum pendens
Thermoproteus tenax
Thermus thermophilus
Thermus thermophilus
Thermus thermophilus
Thermoproteus
uzoniensis
Thermoplasma
volcanium
All publications, patents, and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication, patent, or patent application was specifically and individually indicated to be incorporated by reference. This includes following patent documents U.S. Patent Publication Nos. 2003/0152984; 2006/0115850; 2006/0127920; 2007/0231805; 2007/0292954; 2009/0275086; 2010/0062495; 2010/0216648; 2010/0291633; 2011/0124049; 2012/0053087; and 2017/253909. U.S. Pat. Nos. 5,580,759; 5,624,827; 5,869,644; 6,110,668; 6,495,318; 6,521,427; 7,704,690; 7,833,759; 7,838,210; 8,224,578; 10,626,383; and 10,196,618. PCT Publications WO 2005/095605; WO 2010/040531; WO 2011/102802; WO 2013/049227; WO 2016/094512; and WO 2020/001783.
Exemplary Subject Matter of the Invention is represented by the following clauses:
Clause 1. A method for generating an error corrected population of nucleic acid molecules, the method comprising:
Clause 2. The method of clause 1, wherein at least one of the one or more thermostable mismatch recognition proteins is a thermostable mismatch binding protein.
Clause 3. The method of clause 2, wherein the thermostable mismatch binding protein is selected from a mismatch binding protein having an amino acid sequence set out in Table 13 or Table 15.
Clause 4. The method of clause 1, wherein at least one of the one or more thermostable mismatch recognition proteins is a thermostable mismatch endonuclease.
Clause 5. The method of clauses 1 or 4, wherein the thermostable mismatch endonuclease is selected from an endonuclease having an amino acid sequence set out in Table 12 or Table 15.
Clause 6. The method of clauses 4 or 5, wherein the thermostable mismatch endonuclease is TkoEndoMS.
Clause 7. The method of any of clauses 1 to 6, wherein a high-fidelity DNA polymerase is used in steps (a) and/or (b).
Clause 8. The method of clause 7, wherein the high-fidelity DNA polymerase is a component of an error reducing polymerase reagent.
Clause 9. The method of clauses 7 or 8, wherein the high-fidelity DNA polymerase is a polymerase have an amino acid sequence selected from the group consisting of: (1) DNA Polymerase 1, (2) DNA Polymerase 2, (3) DNA Polymerase 3, (4) DNA Polymerase 4, (5) DNA Polymerase 5, (6) DNA Polymerase 6, (7) DNA Polymerase 7 set out in Table 14.
Clause 10. The method of clauses 8 or 9, wherein the error reducing polymerase reagent comprises one or more amine compounds.
Clause 11. The method of clause 10, wherein the one or more amine compounds are selected from the group consisting of:
Clause 12. The method of any of clauses 1 to 11, wherein at least one of the one or more thermostable mismatch recognition proteins is present in step (a).
Clause 13. The method of any of clauses 1 to 12, wherein at least one of the one or more thermostable mismatch recognition proteins is present in step (b).
Clause 14. The method of any of clauses 1 to 13, wherein one or more error correction steps are performed after primary amplification.
Clause 15. The method of any of clauses 1 to 14, wherein post-primary amplification of the population of amplified assembled nucleic acid molecules is performed after step (b).
Clause 16. The method of any of clauses 1 to 15, wherein the population of amplified assembled nucleic acid molecules are contacted with one or more mismatch recognition proteins prior to the post-primary amplification.
Clause 17. The method of clause 16, wherein at least one of the one or more mismatch recognition proteins is a mismatch endonuclease.
Clause 18. The method of clause 17, wherein the mismatch endonuclease is a non-thermostable mismatch endonuclease.
Clause 19. The method of clause 18, wherein the non-thermostable mismatch endonuclease is selected from the group consisting of:
Clause 20. The method of any of clauses 1 to 19, wherein the population of amplified assembled nucleic acid molecules comprises a subfragment of a larger nucleic acid molecule and are combined with another nucleic acid molecule that is also a subfragment of the larger nucleic acid molecule, to form a nucleic acid molecule pool.
Clause 21. The method of clause 20, wherein the nucleic acid molecules of the nucleic acid molecule pool are assembled by secondary assembly PCR to form the larger nucleic acid molecule.
Clause 22. The method of clause 21, wherein the subfragments are contacted with the one or more mismatch recognition proteins prior to or during assembly by secondary assembly PCR.
Clause 23. The method of any of clauses 20 to 22, wherein the larger nucleic acid molecule is heat denatured, then renatured, followed by contacting with the one or more mismatch recognition proteins.
Clause 24. The method of clause 23, wherein the at least one of the one or more mismatch recognition proteins is a mismatch binding protein.
Clause 25. The method of clause 24, wherein the mismatch binding protein is bound to a solid support.
Clause 26. The method of any of clauses 1 to 25, wherein the population of amplified assembled nucleic acid molecules are sequenced.
Clause 27. The method of any of clauses 1 to 26, wherein the population of amplified assembled nucleic acid molecules contains fewer than two errors per 1,000 base pairs.
Clause 28. A composition comprising a thermostable mismatch recognition protein, a DNA polymerase, and one or more amine compound.
Clause 29. The composition of clause 28, wherein the DNA polymerase is a high-fidelity DNA polymerase.
Clause 30. The composition of clause 29, wherein the high-fidelity DNA polymerase is a component of an error reducing polymerase reagent.
Clause 31. The composition of clauses 29 or 30, wherein the high-fidelity DNA polymerase comprises an amino acid sequence set out in Table 14.
Clause 32. The composition of clause 28, wherein the one or more amine compound is selected from the group consisting of:
Clause 33. The composition of any of clauses 28 to 32, further comprising two or more nucleic acid molecules.
Clause 34. The composition of clause 33, wherein the two or more nucleic acid molecules are subfragments of a larger nucleic acid molecule.
Clause 35. The composition of any of clauses 33 to 34, wherein the two or more nucleic acid molecules are single-stranded.
Clause 36. The composition of clause 35, wherein the two or more single-stranded nucleic acid molecules are less than 100 nucleotides in length.
Clause 37. The composition of clause 35, wherein the two or more single-stranded nucleic acid molecules are from about 35 to about 90 nucleotides in length.
Clause 38. The composition of clause 35, wherein the two or more single-stranded nucleic acid molecules are from about 30 to about 65 nucleotides in length.
Clause 39. The composition of any of clauses 28 to 38, wherein the thermostable mismatch recognition protein is a mismatch endonuclease.
Clause 40. The composition of clause 39, wherein the thermostable mismatch endonuclease is selected from an endonuclease having an amino acid sequence set out in Table 12 or Table 15.
Clause 41. The composition of clause 40, wherein the thermostable mismatch endonuclease is TkoEndoMS.
Clause 42. The composition of any of clauses 28 to 38, wherein the thermostable mismatch recognition protein is a mismatch binding protein.
Clause 43. The composition of clause 42, wherein the thermostable mismatch binding protein is selected from a mismatch binding protein having an amino acid sequence set out in Table 13 or Table 15.
Clause 44. The composition of any of clauses 33 to 34, wherein at least one of the two or more nucleic acid molecules are single-stranded and at least one of the two or more nucleic acid molecules are double-stranded.
Clause 45. A method of generating a nucleic acid molecule with a predetermined sequence, the method comprising:
wherein step (b) and/or step (c) is conducted in the presence of one or more thermostable mismatch recognition protein.
Clause 46. The method of clause 45, further comprising (d) conducting one or more error correction steps, wherein an error correction step comprises:
Clause 47. The method of clause 46, wherein the mismatch recognition protein used in step (d) is a mismatch endonuclease or a mismatch binding protein.
Clause 48. The method of clause 47, wherein the mismatch endonuclease is T7 endonuclease I.
Clause 49. The method of clause 47, wherein the mismatch binding protein is MutS.
Clause 50. The method of clauses 45 or 46, wherein the thermostable mismatch recognition protein is as thermostable mismatch endonuclease.
Clause 51. The method of clause 50, wherein the thermostable mismatch endonuclease is derived from hyperthermophilic Archaea, optionally wherein the hyperthermophilic archaeon is Pyrococcus furiosus or Pyrococcus abyssi.
Clause 52. The method of any of clauses 45 or 46, wherein the thermostable mismatch recognition protein is selected from the group of proteins having an amino acid sequence set out in Table 12, 13, or 15, and variants thereof having at least 95% sequence identity thereto.
Clause 53. The method of any of clauses 49 to 52, wherein the thermostable mismatch recognition protein is obtained by in vitro transcription/translation.
Clause 54. The method of any one of clauses 45 to 53 wherein one or more of steps (b), (c) and (d) (iii) is conducted in the presence of a high fidelity DNA polymerase, optionally wherein the polymerase is selected from the group consisting of P
Clause 55. The method of any one of clauses 45 to 53 wherein one or more of steps (b), (c) and (d) (iii) is conducted in the presence of a high fidelity DNA polymerase, optionally wherein the polymerase is a polymerase having an amino acid sequence selected from the group consisting of: (1) DNA Polymerase 1, (2) DNA Polymerase 2, (3) DNA Polymerase 3, (4) DNA Polymerase 4, (5) DNA Polymerase 5, (6) DNA Polymerase 6, (7) DNA Polymerase 7 set out in Table 14.
Clause 56. The method of any one of clauses 45 to 53, wherein two or more amplified assembly products are pooled prior to conducting the one or more error correction steps.
Clause 57. The method of any one of clauses 46 to 53, further comprising treating the amplified assembly products with an exonuclease prior to the one or more error correction steps, optionally wherein the exonuclease is Exonuclease I.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2021/021104 | 3/5/2021 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 62986209 | Mar 2020 | US |
