Patent Application
20110262902
The present invention relates to a method for selective diversification of a target nucleic acid sequence in a recombinant recipient cell by employing a regulatory sequence from the immunoglobulin locus that activates genetic diversification in linked transcription units.
Mutated and sequence optimized genes and gene products have extended application in medical, chemical and technical areas. Present strategies for diversification of genes and gene products rely mainly on the generation of a vast number of mutant sequences in vitro, artificial expression and subsequent selection for a desired property. These methods have the drawback that the mutated genes are difficult to express in the physiological context and their mutant repertoire is fixed in time when they are expressed. On the other hand, if genome wide mutagenesis is induced in living cells, this is accompanied by high toxicity due to accidentally lethal mutations and the mutation rates in individual genes are low, i.e., the mutagenesis lacks selectivity.
Accordingly, attempts were made to provide a genetic system that allows for locus specific nucleic acid diversification within living cells. In nature, directed and selective diversification is primarily employed to create diversity within the immunoglobulin genes. Thus, vertebrate B cells are able to diversify their rearranged immunoglobulin (Ig) genes by hypermutation, gene conversion and class switch recombination. All three phenomena require expression of Activation Induced cytidine Deaminase (AID, NC—006088) [Miramatsu et al., 2000; Arakawa et al., 2002; Harris et al., 2002), which most likely initiates Ig gene diversification by deaminating cytidines within the mutating and recombining sequences [Di Noia and Neuberger, 2002; Rada et al., 2004]. A further requirement for hypermutation and switch recombination is the transcription of the Ig genes and the switch regions respectively [Peters and Storb, 1996; Shinkura et al., 2003].
Thus, it was also observed that the inactivation of the E2A transcription factor gene reduces the rate of IgL chain mutations without affecting the levels of surface Ig or AID expression, suggesting that E2A-encoded proteins enhance Ig hypermutation by recruitment of AID to the Ig loci [Schoetz et al., 2006].
Sequence analysis of transcribed non-Ig genes from AID expressing B cells revealed either none or very few mutations compared to Ig genes [Shen et al., 1998]. A recent study of numerous expressed genes in B cells indicated that the number of mutations in wild-type mice is significantly higher than in AID knock-out mice [Liu et al., 2008]. However, the mutation rates for the non-Ig genes in AID expressing B cells were still orders of magnitude lower than for the Ig genes. To explain this difference between Ig and non-Ig genes it was suggested that cis-acting sequences in the Ig loci activate hypermutation possibly by recruiting AID. However, efforts to unambiguously define these sequences for the murine and human Ig loci were unsuccessful [Odegard and Schatz, 2006]. Studies using chimeric reporter genes in transgenic mice indicated that certain Ig enhancers and their surrounding sequences conferred hypermutation activity [Betz et al., 1994; Klotz and Storb, 1996; Klix et al., 1998]. However, deletion of Igk enhancers in knock-out mice did not prevent hypermutation of the Igk gene (CAA36032) [van der Stoep et al., 1998; Inlay, 2006]. At least one murine B cell line [Wang et al., 2004] and AID expressing fibroblasts [Yoshikawa et al., 2002] mutated transcribed transgenes in the absence of nearby Ig locus sequences, further confounding the issue of whether cis-acting regulatory sequences are needed for hypermutation.
Previously the inventors demonstrated that the chicken B cell line DT40 diversifies its rearranged Ig light chain (IgL) gene by gene conversion in the presence of nearby pseudo V (ψV) genes [Arakawa et al., 2002] or by hypermutation, if the ψV genes are deleted [Arakawa et al., 2004; WO 2005/080552]. Both activities strictly depend on the expression of AID. Subsequently, the inventors showed that a Green Fluorescent Protein (GFP, AAB08058) transgene is rapidly diversified by mutations when inserted into the rearranged IgL locus [Arakawa et al., 2008], consistent with the initial finding that the deletion of homologous gene conversion donors leads to hypermutation of the IgL gene [Arakawa et al., 2004]. At the same time, no mutations were found in the highly transcribed Elongation Factor alpha gene (NP—989488) [Arakawa et al., 2004], indicating that hypermutation occurs only within the IgL locus. Also the VpreB3 (NC—006102) or the Carbonic Anhydrase (XP—415218) gene, upstream and downstream neighbors of the IgL locus, respectively showed no sequence heterogeneity in DT40 [Gopal and Fugmann, 2008]. It was observed that a 4.1 kb deletion of the rearranged IgL locus downstream of the enhancer region stopped IgL gene conversion in ψV positive DT40 [Kothapalli et al., 2008], indicating that parts of the IgL locus are necessary for gene conversion. However, the technique used in this study could not be used for a precise identification of small specific diversification active sequences. Moreover, the question whether a putative diversification sequence is sufficient for activation of diversification could also not be resolved.
Thus, none of the known studies either in human, murine or DT40 cells revealed a cis-acting regulatory sequence that is both necessary and sufficient for the Ig locus specificity of AID-dependent genetic diversification. Such a sequence would allow generating diversity of nucleic acid target sequences outside the Ig loci in AID expressing cells.
Therefore, there exists a need for a regulatory sequence that activates diversification in the nucleic acids linked thereto and a method to achieve specific diversification of a target nucleic acid. The present invention satisfies the need and provides further advantages as well.
The invention makes available a regulatory nucleic acid molecule, a cis-acting diversification activator (DIVAC), that has the function of activating diversification in transcription units linked thereto. A diversification activator of the invention is derived from the immunoglobulin (Ig) locus of a chicken B cell and comprises a nucleic acid having the sequence SEQ ID NO:1, a fragment of said nucleic acid or a nucleic acid homologous to SEQ ID NO:1 or a fragment thereof, whereby said fragment and said homologue retain the DIVAC function.
Accordingly, the invention provides a method for diversification of a target nucleic acid comprising introducing a genetic construct comprising a diversification activator of the invention into a recipient cell to produce a recombinant recipient cell, wherein said diversification activator is linked to the target nucleic acid.
A target nucleic acid can be supplied to the recipient cell from outside as a transgene, or be part of the recipient cell genome. In each case, it is secured that the target nucleic acid is linked to DIVAC, i.e., DIVAC activates and directs the diversification of the target nucleic acid.
The invention further provides a method for producing a target nucleic acid having a desired activity, comprising the steps of (a) transfecting or infecting a recipient cell one or more times with one or more genetic construct(s) comprising a diversification activator and, optionally, the target nucleic acid to obtain a recombinant recipient cell, (b) identifying a recombinant recipient cell, wherein said diversification activator is linked to said target nucleic acid, (c) propagating and expanding the cell from (b) under conditions appropriate for the expression and diversification of the target nucleic acid, and (d) selecting within the population of cells from (c) individual cells or cell populations containing a mutated target nucleic acid having a desired activity.
The invention further provides a recombinant nucleic acid construct comprising one or more diversification activator(s) of the invention either alone or linked to a target gene.
Further provided is a recombinant cell comprising a diversification activator of the invention integrated into the cell chromosome at a position different from the immunoglobulin (Ig) locus.
The present invention makes available an improved method for genetic diversification of a target nucleic acid within a living cell. The method is based on the discovery of a regulatory nucleic acid molecule, a cis-acting diversification activator (DIVAC), that is essential and sufficient for the activation of genetic diversification of a nucleic acid that is linked thereto.
For the purpose of the invention the following definitions apply.
“Genetic diversification” is alteration of individual nucleotides or stretches of nucleotides in a target nucleic acid. Genetic diversification according to the invention preferably occurs by hypermutation. In the event that in the method of the invention homologous donors for the target nucleic acid are provided, genetic diversification may occur by gene conversion or a combination of hypermutation and gene conversion.
“Hypermutation” diversifies a target nucleic acid primarily by single nucleotide substitutions. Preferably, hypermutation refers to a rate of mutation of between 10−5 and 10−3 bp−1 generation−1 which at least 100 fold higher than the background mutation rate in non-hypermutating genes within the same cell.
“Gene conversion” is a phenomenon in which sequence information is transferred in unidirectional manner from a homologous gene conversion donor to a gene conversion target sequence. Gene conversion may be the result of a DNA polymerase switching templates and copying from a homologous sequence, or the result of mismatch repair (nucleotides being removed from one strand and replaced by repair synthesis using the other strand) after the formation of a heteroduplex. An example of natural gene conversion is the diversification of the rearranged VJ IgL segments by nearby pseudo-V gene conversion donors in certain species.
In many vertebrates, hypermutation and gene conversion generate diversity within the immunoglobulin V(D)J segment of B cells. Hypermutation takes place in the germinal centers of such species as mouse and human following antigen stimulation. Gene conversion takes place in primary lymphoid organs like the Bursa of Fabricius or the gut-associated lymphoid tissue in such species as chicken, cow, rabbit, sheep and pig independent of antigen stimulation.
“Diversification activator” is a cis-acting regulatory sequence that activates the genetic diversification of neighboring transcription units which behave as target nucleic acids.
“Target nucleic acid” is a nucleic acid molecule subjected to genetic diversification. The target nucleic acid is preferably a transgene and may comprise one or more transcription units encoding gene products. The target nucleic acid may also be a non-coding transcription unit or an endogenous gene whose diversification is activated by the nearby insertion of a diversification activator. The target nucleic acid altered as a result of DIVAC-related diversification is also called mutant nucleic acid.
“Transgene” is an exogenous nucleic acid molecule that is inserted into the recipient cell, such as by transfection, transduction, or infection. For example, a transgene may comprise a heterologous transcription unit which may be inserted into the genome randomly or at a defined location by targeted integration. For the purpose of the invention the transgene is preferably located next to a diversification activator thereby becoming a target nucleic acid.
“Targeted integration” is integration of a transfected nucleic acid construct comprising a nucleic acid sequence homologous to an endogenous nucleic acid sequence by homologous recombination into the endogenous locus. Targeted integration allows to directly insert any nucleic acid into a defined chromosomal position.
“Recombinant recipient cell” refers to a cell that is engineered for genetic diversification of a target nucleic acid. Preferably, the recipient cell expresses AID and is the recipient of the transgene linked to the diversification activator.
“Selection” refers to the determination of the presence of sequence alterations in the target nucleic acid that result in a desired activity of the gene product encoded by the target nucleic acid or in a desired activity of the regulatory function of the target nucleic acid.
Method for Diversification of a Target Nucleic Acid
In one aspect, there is provided a method for diversification of a target nucleic acid comprising introducing a genetic construct comprising a diversification activator into a recipient cell to produce a recombinant recipient cell,
In one embodiment, the diversification takes place by the process of somatic hypermutation. A preferred rate of somatic hypermutation is between 10−5 and 10−3 bp−1 generation−1.
In another embodiment, the target nucleic acid is in addition linked to at least one nucleic acid capable of serving as a gene conversion donor for the target nucleic acid, and the diversification takes place by a process involving both somatic hypermutation and gene conversion.
Diversification Activator
A diversification activator (DIVAC) of the invention is derived from the immunoglobulin (Ig) locus of a chicken B cell. In one embodiment, DIVAC is a 9.8 kb fragment (also called “W” fragment) of the rearranged IgL locus extending from the IgL transcription start site to the 3′ end of the carbonic anhydrase gene. The 9.8 kb fragment maps to Gallus gallus chromosome some chr15:8165070-8176699.
The 9.8 kb fragment isolated from the chicken B cell line DT40 has the nucleotide sequence SEQ ID NO:1. In another embodiment, DIVAC of the invention is a fragment of the 9.8 kb fragment that retains the DIVAC function of activating diversification of a nucleic acid linked thereto. The DIVAC fragment may be as short as 50 nucleotides and as long as 5000 nucleotides. For example, the length of DIVAC may be at least 50 nucleotides, at least 100 nucleotides, at least 200 nucleotides, at least 300 nucleotides, at least 400 nucleotides, at least 500 nucleotides, at least 600 nucleotides, at least 700 nucleotides, al least 800 nucleotides, at least 900 nucleotides, at least 1000 nucleotides, at least 1250 nucleotides, at least 1500 nucleotides, at least 1750 nucleotides, at least 2000 nucleotides, at least 2250 nucleotides, at least 2500 nucleotides, at least 2750 nucleotides, at least 3000 nucleotides, at least 3250 nucleotides, at least 3500 nucleotides, at least 3750 nucleotides, at least 4000 nucleotides, at least 4250 nucleotides, at least 4500 nucleotides, at least 4750 nucleotides, at least 5000 nucleotides at least 5250 nucleotides, at least 5500 nucleotides, at least 5750 nucleotides, at least 6000 nucleotides, at least 6250 nucleotides, at least 6500 nucleotides, or at least 6750 nucleotides. The length of DIVAC may be 100, 200, 300, 400, 500, 600, 700, 800, 900, 1000, 1250, 1500, 1750, 2000, 2250, 2500, 2750, 3000, 3250, 3500, 3750, 4000, 4250, 4500, 4750, 5000, 5250, 5500, 6000, 6250, 6500, 6750, or 7000 nucleotides.
Specific DIVAC fragments may be defined on the basis of the oligonucleotides listed in Table 2 that may be used for PCR amplification of individual fragments. DIVAC fragments may also be defined on the basis of the nucleotide positions within the 9.8 kb fragment (SEQ ID NO:1).
Thus, DIVAC may have the nucleotide sequence between positions 1-7099, 1-7799, 2184-9784, 3098-9784, 4102-9784, 5114-9784, 6107-9784, or 3098-7099 of SEQ ID NO:1. These sequences correspond to the fragments designated F, G, I, K, L, M, N and S, respectively, on
DIVAC can also be a functional homologue of SEQ ID NO:1 or a fragment thereof from the chicken Ig heavy chain (IgH) locus or from the immunoglobulin locus of other avian or mammalian species. It is preferred that the DIVAC homologue is derived from an organism that has the immunoglobulin locus organized similar to the chicken Ig locus. Thus, DIVAC may be a sequence corresponding to SEQ ID NO:1 or a fragment thereof from various birds. For example, DIVAC may be derived from the turkey IgL and have the sequence of SEQ ID NO:117 (homologue of the 9.8 kb fragment), or SEQ ID NO:115 (homologue of the ‘2.2-2.4’ fragment). Alternatively, DIVAC may be derived from the duck IgL and have the sequence SEQ ID NO:118 (homologue of the 9.8 kb fragment), or SEQ ID NO:116 or 119 (homologue of the ‘2.2-2.4’ fragment). It is preferred that DIVAC has the sequence between positions 6107-9784 (‘N’), 3098-7099 (‘S’), 5288-5485 (‘2.2-2.4’), or 9509-9802 (‘9.6-9.8’), corresponding to SEQ ID NO:1 in other organisms.
DIVAC may also be derived from the Ig locus of such organisms as pig, sheep, cow or rabbit, known to diversify their immunoglobulin genes by gene conversion. However, DIVAC may also be a functional homologue of SEQ ID NO:1 or fragment thereof from other mammals such as mouse or human that diversify their immunoglobulin genes by hypermutation.
According to the invention, the DIVAC function of activating diversification of a linked target nucleic acid is defined by an at least 5-fold, 10-fold, 20-fold, 50-fold or 100-fold increase of the diversification rate of the target nucleic acid in the presence of DIVAC compared to that in the absence of DIVAC.
DIVAC functional homologues may further be characterized by their structural homology to the 9.8 kb fragment (SEQ ID NO:1) or fragments thereof as defined above, whereby the homologue retains the DIVAC function of activating diversification of a nucleic acid linked thereto. For example, DIVAC of the invention shares at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, or at least 95% sequence identity with SEQ ID NO:1 of a fragment thereof. For example, the sequence homology between the duck and chicken ‘2.2-2.4’ fragments is about 85%.
To increase the rate of diversification, DIVACs of the invention may be combined. For this purpose, more than one copy of DIVAC may be provided to a recipient cell in form of tandem repeats. It is preferred that such sequences exhibit an additive effect. For example, a repeat may comprise two or more copies of the ‘2.2-2.4’ fragment (SEQ ID NOs: 114, 115, 116 or 119). Alternatively, different DIVAC sequences may be combined. It is preferred that such sequences exhibit a cumulative effect. For example, ‘S’ and ‘N’, ‘2.2-2.4’ and ‘3-4’, ‘3-4’ and a fragment between positions 8000-9000, ‘2.2-2.4’ and a fragment between positions 8000-9000, ‘2.2-2.4’ and ‘9.6-9.8’; ‘3-4’ and a fragment between positions 8000-9000 and ‘9.6-9.8’, a fragment between positions 2825-3625 and ‘0-4’, or a fragment between positions 2825-3626 and ‘0-4’ may be combined to increase the diversification activity.
Target Nucleic Acid
A target nucleic acid of the invention is an arbitrary nucleic acid whose diversification is desired. In the method of the invention, the target nucleic acid is preferably transcribed. In one embodiment, the target nucleic acid encodes a protein. For example, a target nucleic acid encodes an immunoglobulin chain, a selection marker, a DNA-binding protein, an enzyme, a receptor protein, or parts thereof. It is preferred that the target nucleic acid is a human immunoglobulin gene. The method of the invention would thus allow to produce an immunoglobulin gene encoding an immunoglobulin with a specific binding activity such as high specificity and/or high affinity to an antigen. It is also preferred that the target nucleic acid is a fluorescent protein such as Green Fluorescent Protein (GFP) or Yellow Fluorescent Protein (YFP). In this embodiment, the method of the invention would allow to produce a fluorescent protein with a new and different absorption/emission wave length.
In another embodiment, the target nucleic acid possesses a regulatory activity. For example, the target nucleic acid may be a transcription regulatory element such as promoter or enhancer, or encode an interfering RNA molecule for use in specific gene suppression by RNA interference. In this embodiment, a reporter, which is influenced by the target nucleic acid, is required for the identification of a recombinant recipient cell bearing the target nucleic acid of interest.
In one embodiment, the target nucleic acid is an exogenous nucleic acid. An exogenous nucleic acid may be provided to the recipient cell together with DIVAC on the same genetic construct, or, alternatively, on a different genetic construct or constructs. In this embodiment, the genetic construct(s) preferably comprise(s) a selectable marker gene that allows for selection of cells comprising the transgene and/or DIVAC. The selectable marker gene may subsequently be removed by recombination, for example using a cre-recombinase system, or inactivated by other means. It is preferred that the target nucleic acid and DIVAC stably integrate into the cell chromosome. Alternatively, the target nucleic acid and DIVAC may remain in the recipient cell extrachromosomally, for example, on an autonomously replicating viral vector such as an EBV-derived vector.
In another embodiment, the target nucleic acid is a priori a part of the cell chromosome, i.e., an endogenous nucleic acid. It is preferred that the endogenous nucleic acid is not an immunoglobulin gene or a part thereof. In this embodiment, only DIVAC is provided to the cell and it is secured that DIVAC integrates into the cell chromosome in the vicinity of the target nucleic acid.
According to the invention, the target nucleic acid is linked to DIVAC. This implies that the two nucleic acids are on the same chromosome in a position relative to each other that ensures that DIVAC activates and directs the diversification of the target nucleic acid. Generally, it is understood that the diversification activity of DIVAC diminishes with the increase in the distance to the nucleic acid to be diversified. It is therefore preferred that the distance between DIVAC and the target nucleic acid is no more than 150 kb, preferably no more than 125 kb, preferably less than 120 kb, less than 100 kb, less than 70 kb, less than 50 kb, less than 30 kb, less than 10 kb, less than 5 kb, or less than 3 kb.
According to the invention, the target nucleic acid and/or DIVAC may be integrated into the chromosome of a recipient cell at a defined or random location. In one embodiment, a genetic construct comprising an exogenous target nucleic acid and DIVAC is integrated into the cell chromosome at a random location.
In another embodiment, a first genetic construct comprising an exogenous target nucleic acid, i.e., a transgene, is integrated at a defined chromosomal position and a second genetic construct comprising DIVAC is integrated at a chromosomal position that ensures that DIVAC activates and directs diversification of the transgene. It is preferred that DIVAC is integrated in the vicinity of the transgene, preferably not farther than 150 kb or 125 kb or 100 kb away therefrom, preferably less than 120 kb, less than 100 kb, less than 70 kb, less than 50 kb, less than 30 kb, less than 10 kb, less than 5 kb, or less than 3 kb.
In a further embodiment, the target nucleic acid is endogenous, and a construct comprising DIVAC is integrated at a chromosomal position that ensures that DIVAC activates and directs diversification of the target nucleic acid. It is preferred that DIVAC is integrated in the vicinity of the target nucleic acid, preferably not farther than 150 kb or 125 kb or 100 kb away therefrom, preferably less than 120 kb, less than 100 kb, less than 70 kb, less than 50 kb, less than 30 kb, less than 10 kb, less than 5 kb, or less than 3 kb.
Integration at a defined chromosomal position (targeted integration) is achieved by including into the respective genetic construct nucleic acid fragments whose sequence is identical or homologous to the nucleic acid sequence at the integration site. The ability of a cell to integrate genetic constructs by targeted integration is an intrinsic property of the cell. Cells of different species and origins possess this property to a varying degree. For example, targeted integration is an infrequent event in a mouse cell. In contrast, the ALV-transduced chicken B cell line DT40 integrates genetic constructs preferably by targeted integration at a defined chromosomal position.
Recipient Cell
A recipient cell of the invention is a eukaryotic cell expressing activation-induced deaminase (AID) or a functional equivalent thereof. It is preferred that the recipient cell is a B lymphocyte from a vertebrate species, in particular an avian or mammalian B cell. For example, it is a B cell from chicken, rabbit, sheep, cow, pig, mouse or rat. It is further preferred that the recipient cell is a chicken B lymphocyte or derived thereof, in particular the ALV-transduced chicken B cell line DT40 or a derivative thereof.
A recombinant recipient cell of the invention is a recipient cell comprising a diversification activator of the invention as a transgenic (i.e., exogenous) nucleic acid, and a target nucleic acid.
In one embodiment, the recombinant recipient cell expresses the target nucleic acid in a manner that facilitates selection of cells comprising mutants of said target nucleic acids having a desired activity. The selection may be a direct selection for the activity encoded or otherwise determined by the target nucleic acid within the cell, on the cell surface or outside the cell. Alternatively, the selection is an indirect selection for the activity encoded by a reporter nucleic acid or otherwise determined by a reporter.
Trans-Acting Regulatory Factors
According to the invention, diversification of the target nucleic acid may be modulated by, a trans-acting regulatory factor. For example, the trans-acting regulatory factor may be a DNA repair or recombination factor, a DNA polymerase, a transcription factor, an uracil DNA glycosylase, a factor involved in chromosomal organization. The diversification process may also be initiated and terminated by a trans-acting regulatory factor such as activation-induced deaminase (AID). For example, AID may be conditionally expressed and its expression may be switched off once the targeted nucleic acid with a desired property is obtained. This would prevent further mutations that may result in a loss of the optimal property. Similarly, other regulatory factors may be added to or expressed in the recipient cell.
trans-acting factors may bind to respective motifs within a cis-regulatory diversification activation sequence such as DIVAC or by binding to other proteins within the diversification complex formed around the target gene. For example, DIVAC of the invention comprises E-Box, NF-kB and ISRE motifs. Alternatively, trans-regulatory factors may be targeted to the gene or locus of interest by tethering molecules fused thereto that would bind to their respective binding motif integrated within in the vicinity of the gene or within the locus.
Method of Preparing Nucleic Acids and Proteins with Desired Activity
In another aspect, the invention provides a method for preparing a target nucleic acid having a desired activity, comprising the steps of:
In one embodiment, steps (c) and (d) of the method are iteratively repeated.
In another embodiment, the method may include an additional step (e) comprising determining the sequence of the mutated target nucleic acid from the cells selected in (d).
In a further embodiment, the method additionally includes a step (f) comprising terminating the diversification. The diversification may, for example, be switched off by down-regulation of the expression of a trans-acting regulatory factor such as activation-induced deaminase (AID) or by the removal of the diversification activator. For this purpose, switchable promoters such as tet may be used.
In step (a), the nucleic acid constructs of the invention may be transfected into the recipient cell. Alternatively, the recipient cell may be transduced or infected with the construct.
In step (d), a variety of selection procedures may be applied for the isolation of mutants having a desired property. For example, cells expressing immunoglobulin molecules with improved or novel binding specificity may be selected by Fluorescence Activated Cell Sorting (FACS), cell separation using magnetic particles, antigen chromatography methods or other known cell separation techniques.
In one embodiment, the target nucleic acid and DIVAC(s) are on the same nucleic acid construct. Alternatively, the target nucleic acid and DIVAC(s) are on different constructs. In this embodiment, the genetic locus containing the target nucleic acid to be diversified may be constructed by more than one round of transfection. In a further embodiment, the target nucleic acid is part of the cell chromosome and the construct or constructs comprise(s) one or more DIVACs.
Recombinant Nucleic Acid Construct
In a third aspect, the invention provides a recombinant nucleic acid construct comprising a diversification activator of the invention. The construct may be a plasmid, a virus, a virus-derived vector such as an integrating or autonomously replicating vector. The construct may comprise one or more copies of DIVAC or a combination of different DIVACs.
Recombinant Cell
In a fourth aspect, the invention provides a recombinant cell comprising a diversification activator of the invention as a transgenic (exogenous) sequence. In one embodiment, the cell is a B lymphocyte. A B cell maybe from a vertebrate species such as bird, pig, cow, sheep, rabbit, mouse, or human. It is preferred that a B cell is from chicken. It is highly preferred that the recombinant cell of the invention is a cell of the DT40 cell line.
Excluded from the scope of the invention are highly unlikely embodiment, wherein the diversification activator is integrated into the chromosome of a cell and replaced part of the chromosome identical to the diversification activator, such that the resulting cell is not distinguishable from a natural cell.
The invention is illustrated by the following examples.
Inventors previously demonstrated that a GFP transgene in DT40 rapidly accumulated mutations, if integrated at the position of the promoter of the rearranged IgL [Arakawa et al., 2008]. The hypermutation activity depended on AID expression and could be visualized by the appearance of cells displaying decreased green fluorescence due to detrimental GFP mutations.
To exploit this phenomenon a new expression cassette named GFP2 was designed which consisted of the strong RSV promoter followed by the GFP coding region, an internal ribosome entry site (IRES), the blasticidin resistance gene (P19997) and the SV40 polyadenylation signal. GFP2 was incorporated into the targeting construct pIgLGFP2 (
Transfection of pIgLGFP2 into the conditionally AID expressing clone AIDR2 yielded a number of transfectants named IgLGFP2 in which targeted integration had substituted the IgL promoter by the GFP2 transgene. Fluorescence activated cell sorting (FACS) analysis of subclones from two independent primary transfectants revealed median values of 12.8% and 14.5% decreased green fluorescence (
Targeted integration was used to insert the GFP2 reporter at various distances from the IgL locus into chromosome 15 [International Chicken Genome Sequencing Consortium, 2004] (
Since surrounding sequences should not influence the post-transcriptional processing and translation of GFP2 transcripts, GFP2 transcription would be reflected by the green fluorescence of the cells independent of the transgene insertion site. Even for mutating transgenes, GFP2 transcription levels could be deduced from the average green fluorescence of the major cell populations which most likely expressed the non-mutated GFP sequence. As seen by FACS analysis, the average green fluorescence of the major cell populations varied slightly among the primary transfectants (
The effects observed in Examples 1 and 2 could be explained by the presence of a cis-acting sequence that activated hypermutation in a distance-dependent manner. This putative regulatory sequence was designated Diversification Activator (DIVAC). Mapping of DIVAG was done by combining insertions of the GFP2 reporter with deletions of the IgL locus.
To address the role of the ψV locus, a GFP2 construct (FIG. 2A, upper part) was transfected into the clone ψV−AIDR1 [Arakawa et al., 2008] in which the entire 20 kb of the ψV locus had been deleted. The transfectants ψV−IgLGFP2 expressed the GFP2 reporter at the position of the IgL promoter in the absence of the ψV locus (
ψV−IgLGFP2 still contained a 9.8 kb fragment (referred to in the following as fragment ‘W’) of the rearranged IgL locus extending from the IgL transcription start site to the 3′ end of the carbonic anhydrase gene. To test the relevance of this fragment, a GFP2 construct was transfected into the clone ψV−IgL− in which the entire rearranged IgL locus had been replaced by the puromycin resistance gene (P42670). The resulting transfectants ψV−IgL−,GFP2 had inserted the GFP2 reporter at the position of the deleted IgL locus (
Controls confirmed that the appearance of cells with decreased green fluorescence reflected hypermutation in the GFP2 gene. As expected, the decrease of green fluorescence in ψV−IgLGFP2 cultures depended on AID, because subclones of the AID negative transfectant ψV−IgLGFP2AID−/− showed only very low medians of 0.001% decreased green fluorescence (
Mapping of the ‘W’ Fragment
A new series of targeting constructs was transfected into ψV−IgL− to characterize the ‘W’ fragment by step-wise deletions (
The average green fluorescence in the main population of ψV−IgLW,GFP2 was increased compared to ψV−IgL−,GFP2 (
Mapping of the ‘S’ Fragment
As described supra, an approximately 4 kb segment of the rearranged DT40 IgL locus (‘S’ fragment) was essential for AID-mediated hypermutation. The DNA fragment spans 2 kb sequence upstream and 1.6 kb sequence downstream of the already identified enhancer. To locate an active core (or cores) of the ‘S’ fragment which might serve as platform for the assembly of a putative hypermutation machinery and is locating AID to the Ig locus, a detailed deletion analysis of the 4 kb region was conducted. The 5′ starting point of the ‘S’ fragment (further referred to as ‘0-4’ fragment) was defined as zero point and the sequence was divided into four 1 kb regions (
The ‘0-4’ fragment itself produced a median decrease of green fluorescence of 2.7% and 1.7%. The median green fluorescence decrees of the deletion constructs was compared to the ‘0-4’ control and p-values were calculated using Mann-Whitney U-test. Only values of p<0.001 were accepted as significant.
Deletions starting from the 3′ end showed that the last 1 kb region (‘3-4’) had no significant relevance for AID recruitment, since the median green fluorescence decrease of the ‘0-3’ fragment was still 3.7% and 1.7%. Deleting an additional 1 kb from the 3′ end (‘0-2’) clearly reduced mutations to 0.1% and 0.3%, suggesting that ‘2-3’, which includes the complete enhancer sequence, plays a role in the hypermutation process. Deletions starting from the 5′ end supported this theory. The fragment ‘2-4’ ranged with 1.5% and 1.3% in the same level as ‘0-4’, but with removing ‘2-3’, the median GFP mutation level of ‘3-4’ dropped to significantly decreased values of 0.4% and 0.1%. Accordingly, deletion from both ends of the ‘0-4’ fragment supported a role of ‘2-3’ for AID recruitment.
Examination of the 1 kb fragment ‘2-3’ confirmed the result, as it was the only 1 kb fragment with a hypermutation enhancing effect (0.9% and 1.3%). Neither of ‘0-1’ (0.1% both), ‘1-2’ (0% and 0.3%) and ‘3-4’ initiated hypermutation to a significant degree although diversification activity in these clones was still above the background level if compared to the IgL This result spoke against an additive effect (i.e., an enhancing effect on their own) of ‘0-1’, ‘1-2’ and ‘3-4’ on hypermutation. However, there could be some cumulative effect of these fragments, as hypermutation level increases slightly if one of the fragments was added to ‘2-3’. The ‘2-3’ fragment appears to include the core cis-element responsible for targeting the hypermutation. The results also indicated an important role of the enhancer, which resides within ‘2-3’ in the hypermutation activation process.
Fine Mapping of the ‘0-4’ Fragment
A deletion analysis of internal deletions in ‘0-4’ is useful in defining a smaller active fragment. At the same time, it would help to identify single acting sequences or elements which act in cooperative way, even if they are distant from each other. A drop in the somatic hypermutation frequency would indicate that an essential element involved in AID-mediated diversification is deleted.
Fine mapping of the ‘0-4’ fragment was performed with help of a series of 200 bp deletions (
Mapping of the ‘2-3’ Fragment
As typical protein binding sites are in range of 10-20 bp, a more detailed deletion analysis was performed in the ‘2-3’ fragment to define specific protein binding regions. A combination of 50 bp internal deletions and 50 bp serial deletions from both ends is useful to identify redundant motifs or a repetition of motifs.
Mapping of the ‘2-3’ fragment was performed by analyzing 50 bp end and internal deletions of the ‘2-3’ fragment (
The 50 bp progressively increasing deletion series starting from the 5′ end displayed a drop of GFP expression from ‘2.2-3.0’ with 0.6% to ‘2.25-3.0’ with 0.2% (
In the 3′ end deletion series, a drop of GFP decrease associated with ‘2-2.75’ and ‘2-2.8’ could additionally be detected (
Thus, the 50 bp internal deletions showed no significant reduction of GFP expression. As random deletions were produced, it is tempting to speculate that only parts of sequence motifs were deleted, without deleting the conserved parts. Additionally, the ‘2-3’ fragment might contain redundant elements which could substitute for each other.
Reconstitution and multimerization of the ‘2.2-2.4’ fragment Deleting ‘2.2-2.4’ in the ‘0-4’ fragment led to a five-fold reduction of decreased GFP expression. To find out if ‘2.2-2.4’, similar to ‘2-3’, was not only necessary but also sufficient for hypermutation, the ‘2.2-2.4’ fragment was reconstituted in ψV−IgL−. A median decrease of GFP expression of 0.6% could be detected. This result confirmed that ‘2.2-2.4’ contained one or several elements sufficient for hypermutation. However, the number of GFP negative cells was lower than in ‘2-3’ (0.9%, 1.3%) and significantly lower than in ‘0-4’ (2.7%, 1.7%).
To find out whether this effect was due to additive elements or to repetitive motives, the ‘2.2-2.4’ fragment was multimerized (
‘W’ (9.8 kb) Fragment
To confirm that the GFP2 reporter on its own is stably expressed at non-Ig loci, six loci on five different chromosomes [International Chicken Genome Sequencing Consortium, 2004] were targeted by transfection of GFP2 constructs into ψV−AIDR1 (
GFP2 was then inserted together with the ‘W’ fragment into the respective AID, BACH2 (NC—006090) and RDM1 (BAC02561) loci of ψV−AIDR1 (
‘2.2-2.4’ Fragment
The mapping of the DIVAC sequence indicated that ‘2.2-2.4’ acted like a true hypermutation core element (“HyCorE”) that is capable of starting hypermutation. Multimerization of this element had an additive effect. The ability of ‘2.2-2.4’ to target hypermutation to a specific, non-Ig locus was tested. In analogy with the experiments described in this example for the ‘W’ fragment in different non-Ig loci, hypermutation activity of the ‘2.2-2.4’ fragment was tested in the BACH2 locus (
Insertion of the GFP2 reporter alone at the position of the BACH2 locus of ψV−AIDR1 (AIDR1IgL−BACH2+/GFP2) did not lead to mutations in the GFP transgene. When combined with the ‘2.2-2.4’ fragment, however, GFP2 became a target for mutations with a median of about 1% decrease in green fluorescence. This is somewhat higher than in “IgL 2.2-2.4”, where the fragment was inserted at the position of the deleted IgL locus. At the same time, both values were significantly different from “IgL−”, a cell line in which the GFP2 reporter is not hypermutating due to the deletion of the entire IgL locus.
These results demonstrate that the ‘2.2-2.4’ fragment is able to trigger hypermutation at non-Ig loci, indicating that it is both necessary and sufficient for activating hypermutation.
Homologous of the ‘2.2-2.4’ fragment in duck and turkey were cloned and sequenced. Sequence homology between the three species is very high, with the homology of the duck sequence of 85%, and that of the turkey sequence of 92% (
A bioinformatical analysis of the about 9.8 kb ‘W’ fragment was performed with the purpose of identifying positions of important protein binding motifs. A motif analysis of the 9.8 kb fragment, considering the motifs E-Box, NF-kB and ISRE is illustrated in
The coordinates of the deletion fragments on the 9.8 kb scale are indicated in Table 3.
It is thus likely that the ‘W’ fragment is composed of multiple redundant motifs with high similarity to that of ‘2.2-2.4’. Results of multimerization (Example 4;
The analysis supports of a theory according to which the “hypermutation motif” has an A-B-B-A structure. The first 800 bp of the 9.8 kb fragment (2825-3625) correspond to motif A. Mofif A is a motif, which is an enhancer of a core motif, or motif B. Motif B is for example, the ‘2.2-2.4’ fragment. The two core elements (B) have definite motif homology as do the two enhancing elements (A). It is known that defects in NEMO stop the process even with AID present. This points to a very definite activating core element where signal transduction is interpreted into somatic hypermutation, gene conversion and class switch recombination activity. While the elements listed above are likely the main ones, possible enhancing motif factors such as SP1, AP1, E2A/Thing1, PAX 2/4/5 family may also play a role.
Targeting constructs. The GFP2 construct was made by combining the RSV promoter—GFP open reading frame of pHypermut2 [20] with a PCR amplicon including an IRES [Arakawa et al., 2004], the blasticidin resistance gene and the SV40 polyadenylation signal [Arakawa et al., 2001]. The PCR was performed using the primers described in the Supplementary table 2. GFP2 was flanked by unique BamHI restriction sites for easy cloning into the targeting vectors.
All targeting constructs except the ones belonging to the series of ‘W’ fragment deletions and reconstitutions were made by cloning the arms sequences into pBluescriptKS+ (Stratagene, CA) and then inserting GFP2 either into unique BamHI or BglII sites as shown in
Since the ‘W’ fragment was difficult to amplify as a single sequence, it was sequentially cloned by combining upstream and downstream PCR amplicons with a 2.2 kb AvrII/SpeI restriction fragment excised from the rearranged IgL targeting construct ‘Construct R’ [Buerstedde and Takeda, 1991]. The sequence of the AvrII/SpeI restriction fragment is A/T rich and localized between the J segment and the C region. The assembled ‘W’ fragment was sequenced and deposited into Genbank under the accession number bankit FJ482234. Constructs belonging to ‘W’ fragment deletion series were made by cloning GFP2 between the target arms and then inserting the ‘W’ fragment or parts thereof into unique NheI/SpeI sites. A BamHI fragment containing GFP2 and the ‘W’ fragment was incorporated into the AID, BACH2 and RDM1 targeting vectors to test the activity of the ‘W’ fragment in non-Ig loci.
Cell culture. Cells were cultured in chicken medium (RPMI-1640 or DMEM/F-12 with 10% fetal bovine serum, 1% chicken serum, 2 mM L-glutamine, 0.1 μM β-mercaptoethanol and penicillin/streptomycin) at 41° C. with 5% CO2. Transfections were performed by electroporation, using 40 μg of linearized plasmid DNA with a Gene Pulser Xceil (BIO-RAD) at 25 μF and 700 V. Stable transfectants were selected by culturing in 15 μg/ml of blasticidin. Transfectants having integrated the transgenic constructs by targeted integration were identified by PCR using an inside primer from the SV40 polyadenylation signal sequence of GFP2 together with a primer derived from the sequence outside the target arm (Table 2). In case of insertions into the IgL locus, targeted integration into the rearranged allele was verified by amplifying the VJ intervening sequence of the unrearranged locus. The AID reconstituted clone AIDR2 was generated from the AID deleted clone AID−/− [Arakawa et al., 2002] by transfection of a construct which targeted an AID cDNA expression cassette into one of the deleted AID loci. The AID negative transfectants were produced by transfecting ψV−AID−/− [Arakawa et al., 2004].
Flow cytometry. The phenotype of each mutation was determined by FACS analysis of at least two independent targeted transfectants and twenty-four subclones of each. The primary transfectants were analyzed by FACS about three weeks after transfection and the subclones two weeks after subcloning. As the green fluorescence levels in the main populations varied slightly among the transfectants, the gates to separate the main population of green fluorescent cells from cells showing decreased or lost green fluorescence were adapted accordingly. At least 50% events falling into the live cell gate were collected for each primary transfectant or subclone. Subclones in which more than 50% of the live cell events fell into the gates for decreased or lost green fluorescence were excluded from the analysis as they might represent the expansion of a precursor cell already expressing a mutated GFP2 transgene at the time of subcloning.
GFP Gene Sequencing. To minimize PCR-introduced mutations, Pfu Ultra hotstart polymerase (Stratagene) was used for the amplifications of the GFP open reading frames prior to sequencing. Sequencing and sequence analysis were performed as previously described [Arakawa et al., 2004].
| Number | Date | Country | Kind |
|---|---|---|---|
| 08007120.2 | Apr 2008 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP09/02680 | 4/9/2009 | WO | 00 | 6/2/2011 |
