Patent Grant
11034978
This application claims priority to EP Application No. 17155338.1, filed on Feb. 9, 2017, and EP Application No. 17163245.8, filed on Mar. 28, 2017. Each disclosure is incorporated herein by reference in its entirety.
This application contains a sequence listing, which is submitted electronically via EFS-Web as an ASCII formatted sequence listing with a file name “688097-442US Sequence Listing” and a creation date of Feb. 8, 2018, and having a size of 50 kB. The sequence listing submitted via EFS-Web is part of the specification and is herein incorporated by reference in its entirety.
The invention relates to the fields of biological research, medicine, and other applications related to heterologous gene expression. More in particular, the invention relates to a potent and short promoter for the expression of a heterologous gene in expression cassettes of plasmids, viral vectors and cell lines which can be used alone or in combination with commonly used promoters such as the hCMV promoter.
Recombinant expression vectors are used extensively in a variety of molecular biology applications for the expression of heterologous proteins, including, for example, mammalian gene expression systems for biological research, to produce cell lines for production of viral vectors, and as viral vectors for gene therapy and vaccination. For gene therapy and vaccination applications, vectors, including viral vectors, are used as carriers for a gene or genes of interest to be introduced into cells. For example, viral vectors can be used to express a gene or part thereof encoding a desired antigen to elicit an immune response.
The cis-acting elements that are part of expression vectors can have a great impact on the successful application of plasmids and viral vectors. Promoters are the major cis-acting elements that are placed in the expression cassettes of expression vectors and dictate the overall strength of expression. The promoter initiates the transcription and is therefore an important point of control for the expression of the cloned gene of interest. Promoter sequences commonly used in expression vectors are derived from viruses or eukaryotic gene regulatory sequences.
Some of the commonly used enhancer and promoter sequences in expression vectors and viral vectors are, for example, hCMV, CAG, SV40, mCMV, EF-1α and hPGK promoters. Due to its high potency and moderate size of ca. 0.8 kB, the hCMV promoter is one of the most commonly used of these promoters. The hPGK promoter is characterized by a small size (ca. 0.4 kB), but it is less potent than the hCMV promoter. On the other hand, the CAG promoter consisting of a cytomegalovirus early enhancer element, promoter, first exon and intron of chicken beta-actin gene, and splice acceptor of the rabbit beta-globin gene, can direct very potent gene expression that is comparable to the hCMV promoter, but its large size makes it less suitable in viral vectors where space constraints can be a significant concern, e.g., in adenoviral vectors (AdV), adeno-associated viral vectors (AAV) or lentiviral vectors (LVs).
In certain cases, it's desirable to express at least two antigens from one vector. In situations where two expression cassettes are placed in a vector in order to express two different genes, the size constraints for the expression cassettes in general and the promoter sequences in particular are especially important. In addition to size constraints, when placing two expression cassettes in a vector it is a disadvantage to use identical or even very similar promoter sequences because it can lead to genetic instability of the vector during production. Thus, it is desirable to use relatively small and relatively potent different heterologous promoter sequences that have little to no sequence identity with each other when two expression cassettes are placed in a vector in order to express two different genes.
When making cell lines for production of viral vectors it is also desirable to have a potent promoter with a sequence different from other promoters commonly used in the expression cassettes of the viral vectors, such as the commonly used hCMV promoter. Significant stretches of sequence identity between the genome of the cell line and the vector produced therein can lead to homologous recombination and therefore genetic instability or heterogeneity of the produced vector batches (e.g. Lochmüller et al, 1994), and therefore are preferably avoided (e.g. Fallaux et al, 1998; Murakami et al, 2002). Also for such applications, it would be desirable to use a potent promoter with little or no sequence identity with the commonly used hCMV promoter.
Thus, there remains a need to identify potent promoters, which preferably would be of short size and that would have little to no sequence identity with the hCMV promoter, for use in for instance plasmids, viral vectors and cell lines.
The present invention provides recombinant nucleic acid molecules comprising the major immediate early promoter region of Aotine herpesvirus-1 (AoHV-1 promoter) and vectors, including, for example, plasmid vectors, viral vectors, recombinant viruses, and recombinant cell lines comprising the AoHV-1 promoter operably linked to a transgene. The present invention also provides recombinant nucleic acid molecules comprising the AoHV-1 promoter operably linked to regulatory sequences that can be used to modulate transcription from the AoHV-1 promoter.
The general and preferred embodiments are defined, respectively, by the independent and dependent claims appended hereto, which for the sake of brevity are incorporated by reference herein. Other preferred embodiments, features, and advantages of the various aspects of the invention will become apparent from the detailed description below taken in conjunction with the appended drawing figures.
In one embodiment, the present invention provides an AoHV-1 promoter, wherein the AoHV-1 promoter is operably linked to a transgene for expression of the transgene with plasmid vectors, viral vectors or recombinant viruses, or in the genome of host cells comprising the AoHV-1 promoter.
In certain embodiments, the invention provides a plasmid vector comprising an AoHV-1 promoter, which plasmid vector comprises less than 1 kb of AoHV-1 DNA.
In certain embodiments, the invention provides an expression cassette, comprising an AoHV-1 promoter operably linked to a transgene, which transgene is heterologous to the AoHV-1 promoter, e.g., wherein the transgene is not operably linked to the AoHV-1 promoter in nature and/or the transgene does not originate from AoHV-1. The expression cassette may for instance be integrated into a plasmid, a vector, a viral genome, a cell line, etc. The invention also provides a method of making such an expression cassette, comprising constructing the expression cassette by recombinant means or by nucleic acid synthesis. The invention also provides a method for expressing a transgene, comprising expressing the transgene from the expression cassette of the invention, e.g. in a recombinant cell line.
In certain embodiments, the present invention provides recombinant cell lines comprising the AoHV-1 promoter, wherein the AoHV-1 promoter is operably linked to a transgene. In certain embodiments, the AoHV-1 promoter operably linked to a transgene may be present in the cell line embodied in e.g. plasmid vectors, viral vectors, or recombinant viruses for expression of the transgene therefrom. In certain embodiments, the AoHV-1 promoter operably linked to a transgene is integrated into the genome of the recombinant cell line, to express the transgene therefrom. In certain embodiments, the transgene is integrated into the genome of the cell line and encodes a tetracycline repressor (TetR) protein. In certain embodiments thereof, said cell line is a PER.C6 cell line.
In another embodiment, the present invention also provides a method for expressing a transgene in a cell, the method comprising providing a cell with a recombinant vector comprising the AoHV-1 promoter operably linked to a transgene.
In certain embodiments the invention also provides a method for producing a protein of interest, wherein the AoHV-1 promoter is operably linked to a transgene encoding the protein of interest, the method comprising providing a cell comprising an AoHV-1 protein operably linked to a nucleic acid sequence encoding the protein of interest, and expressing the protein of interest from the cell. In certain embodiments the method further comprises harvesting the protein of interest, e.g. from the cells or from culture medium or from the cells and culture medium. In certain embodiments, the method further comprises purifying the protein of interest. Preferably, the protein of interest is a protein that is not encoded by Aotine herpesvirus-1 in nature, i.e. it is a heterologous protein.
In certain embodiments, the present invention provides the AoHV-1 promoter operably linked to regulatory sequences that can be used to modulate transcription from the AoHV-1 promoter. In certain embodiments thereof, it can for instance be repressed by binding of a repressor to a repressor binding sequence that has been operably linked to the AoHV-1 promoter. In certain embodiments, the AoHV-1 promoter can be induced by removing a repressor or by providing an inducing signal or inducing agent.
In certain embodiments, the present invention provides the AoHV-1 promoter operably linked to one or more tetracycline operator sequences (tetO sites), such that expression can be reversibly controlled.
In another embodiment, the present invention also provides a method of producing a recombinant virus comprising the AoHV-1 promoter, the method comprising: preparing a construct comprising the AoHV-1 promoter operably linked to a transgene, and incorporating said construct into the genome of the recombinant virus.
In certain embodiments of the present invention, the AoHV-1 promoter is operably linked to a transgene encoding a protein of interest, wherein the protein of interest is a therapeutic protein or an antigen.
In certain embodiments, the viruses and viral vectors comprising the AoHV-1 promoter operably linked to a transgene are recombinant adenoviruses (rAd) and rAd vectors.
In certain embodiments, the invention relates to rAd and rAd vectors comprising the AoHV-1 promoter operably linked to a transgene, and to methods of making and/or using the rAd and rAd vectors, wherein the rAd and rAd vectors comprise a AoHV-1 promoter operably linked to a transgene.
In certain embodiments, a recombinant adenovirus of the invention has a deletion in the E1 region, and in certain embodiments comprises the AoHV-1 promoter operably linked to a transgene in this E1 region. Alternatively, other regions of the recombinant adenovirus could also be used. For example, the expression cassette comprising AoHV-1 promoter operably linked to a transgene could also be placed in the E3 region, or at the right end of the genome, between the E4 region and the right ITR of the recombinant adenovirus.
In certain embodiments, a rAd vector according to the invention is deficient in at least one essential gene function of the E1 region, e.g. the E1a region and/or the E1b region, of the adenoviral genome that is required for viral replication. In certain embodiments, an adenoviral vector according to the invention is deficient in at least part of the non-essential E3 region. In certain embodiments, the vector is deficient in at least one essential gene function of the E1 region and at least part of the non-essential E3 region. The adenoviral vector can be “multiply deficient,” meaning that the adenoviral vector is deficient in one or more essential gene functions in each of two or more regions of the adenoviral genome. For example, the aforementioned E1-deficient or E1-, E3-deficient adenoviral vectors can be further deficient in at least one essential gene of the E4 region and/or at least one essential gene of the E2 region (e.g., the E2A region and/or E2B region).
In another embodiment, the present invention also provides a recombinant DNA molecule comprising the genome of a recombinant adenovirus comprising the AoHV-1 promoter operably linked to a transgene.
Described herein are experimental results related to the identification, design, and testing of a new promoter derived from the immediate early enhancer/promoter region of Aotine herpesvirus-1 (AoHV-1 promoter). The results show that the AoHV-1 promoter provides potent expression of a transgene to which it is operably linked, based on transient transfection with plasmid vectors in different cell lines and viral infections with viruses comprising the AoHV-1 promoter operably linked to a transgene. The AoHV-1 promoter is also a relatively short promoter so it is suitable for use in many applications where size constraints are a concern. Thus, the AoHV-1 promoter of the present invention is suitable for use in applications where potent expression is a priority and/or where the small size of the AoHV-1 promoter is useful, e.g. to leave more space for transgenes in the limited size of the vector or viral genome, as compared to other, longer promoters. Furthermore, due to low sequence homology with other commonly used promoters like hCMV, the AoHV-1 promoter is also useful in applications where there is a concern about sequence identity between the two promoters being used together at the same time, e.g., when expressing two different transgenes from the same viral vector or when generating viruses with producer cell lines that also contain hCMV promoter sequences. The AoHV-1 promoter is also suitable for use with regulatory sequences that can be used to modulate transcription from the AoHV-1 promoter.
The present invention therefore relates to recombinant nucleic acid molecules comprising an AoHV-1 promoter operably linked to a transgene. In certain embodiments, the invention relates to using vectors and viruses comprising the AoHV-1 promoter operably linked to a transgene for expressing the transgene in a cell. In particular non-limiting embodiments, the vectors of the present invention may comprise a plasmid, a cosmid, a phagemid, a bacteriophage, a bacterial artificial chromosome, a yeast artificial chromosome, a human artificial chromosome, a retrovirus vector, a lentivirus vector, an adenovirus vector, an adeno-associated virus vector, an alphavirus vector, a herpes virus vector, an Epstein-Barr virus vector, a vaccinia virus vector, or combinations or chimerics thereof. Those of ordinary skill in the art will recognize that the AoHV-1 promoter of the present invention also will be useful in other vectors employed in the fields of gene expression and gene transfer, especially those in which potent expression is important and the overall size of the expression cassette is a relevant factor.
The present invention also relates to using vectors for enabling host cells to produce heterologous proteins, or other expression products of interest. For example, plasmid vectors comprising the AoHV-1 promoter operably linked to a transgene could be used for expressing a heterologous protein in the cell. Such plasmid vectors could be DNA sequences containing, for example, (1) the AoHV-1 promoter; (2) a Kozak consensus sequence for the transgene for initiation of translation; (3) a coding region for the transgene, e.g., a sequence of nucleotides which codes for a desired polypeptide; (4) a termination sequence for the transgene which permits translation to be terminated when the entire code for the transgene has been read; polyadenylation signals, and/or or intervening sequences and other elements known to those of ordinary skill in the art to express transgenes from certain vectors; and (6) optionally, if the vector is not directly inserted into the genome, an origin of replication which permits the entire vector to be reproduced once it is within the cell. The vector can be introduced into the host cell, for example by transfection, electroporation, or infection, and the host cells can be cultured to express the transgene.
Plasmid vectors of the present invention in certain embodiments also include one or more multiple cloning sites (MCS), also called polylinkers, which are short segments of DNA containing several restriction sites. These restriction sites within the MCS are typically unique, occurring only once within a given plasmid. MCSs are commonly used during procedures involving molecular cloning or subcloning and are extremely useful in biotechnology, bioengineering, and molecular genetics because they allow for insertion of a piece of DNA or several pieces of DNA into the region of the MCS, e.g., to insert an expression cassette, comprising an AoHV-1 promoter operably linked to a transgene encoding a protein of interest for expression in a cell.
The present invention also provides cells transformed by the vectors described herein and recombinant cell lines comprising the AoHV-1 promoter, wherein the AoHV-1 promoter is operably linked to a transgene. In this context, transformation refers to any process by which heterologous nucleic acid material is introduced into and expressed within a cell. Thus, transformation as used herein includes “transient” and “stable” transfection procedures, including but not limited to those mediated by electroporation, cationic lipid/DNA complexes, protein/DNA complexes, calcium phosphate-mediated pinocytosis, virus vectors, etc., where a nucleic acid introduced into the host cell exists extrachromosomally or wherein the transfected nucleic acids have been integrated into the genome of the host cell. The transfection procedures can also include a second nucleic acid encoding a selectable marker (e.g. resistance to an antibiotic), which enables the positive selection of cells such that the transfected nucleic acid containing the AoHV-1 promoter is maintained. Thus the AoHV-1 promoter operably linked to a transgene may be present in the cell line embodied in e.g. plasmid vectors, viral vectors, and recombinant viruses for expression of the transgene therefrom. In certain embodiments, the AoHV-1 promoter operably linked to a transgene can be integrated into the genome of the recombinant cell line to express the transgene therefrom.
The present invention also provides a method for expressing a transgene in a cell, the transgene comprising, for example, a transgene encoding a protein of interest or a transgene comprising a non-coding sequence (e.g., regulatory RNA such as a microRNA, short interfering RNA (siRNA), or antisense RNA, etc.), the method comprising providing a cell with a vector comprising the AoHV-1 promoter operably linked to a transgene. In particular, in certain embodiments the invention provides a method for producing an expression product of interest in a cell, wherein the AoHV-1 promoter is operably linked to a transgene encoding the expression product of interest, the method comprising providing a cell comprising an AoHV-1 promoter operably linked to a nucleic acid sequence encoding the expression product of interest, and expressing the expression product of interest in the cell. In certain embodiments the expression product is a protein. In certain embodiments, the expression product is tetracycline repressor (TetR) protein. The method can further comprise harvesting the expression product, e.g. protein, of interest, e.g. from the cells or from the culture medium or from the cells and the culture medium. The method may also comprise purifying the protein for various purposes, including for example, diagnostic, therapeutic or prophylactic purposes, research, etc. Further the purified protein of interest can optionally be formulated into a pharmaceutical composition. Therapeutic proteins may include, for example, anticoagulants, blood clotting factors, growth factors, hormones, antibodies, Fc fusion proteins, bone morphogenetic proteins, engineered protein scaffolds, enzymes, and cytokines, e.g., chemokines, interferons, interleukins, lymphokines, and tumour necrosis factors, etc.
The invention also provides a method for producing a virus, comprising propagating the virus in a cell that expresses a gene that has a function in propagating said virus, wherein said gene is under control of an AoHV-1 promoter and wherein said gene encodes a nucleic acid (e.g. regulatory RNA) or protein, e.g. a protein that complements a deficiency in the viral replication cycle or other function of virus (e.g. infection). The virus can be a wild type virus, but preferably is a recombinant virus, e.g. with a deficiency that renders it replication deficient or infection deficient. Furthermore, said gene can be expressed from an extrachromosomal element or preferably from the genome of the cell (which cell then may be from a stable cell line) and the cell can be cultured in culture medium such that virus can be harvested and optionally purified and then used to infect other cells, or to formulate in pharmaceutical composition, etc.
A “cell” or a “host cell” according to the invention can be any cell wherein the AoHV-1 promoter can be active. In certain embodiments the cell is isolated from its normal tissue, and for instance can be cultured in a culture medium (in vitro). In certain embodiments, a cell or host cell according to the invention is an immortalized cell, e.g. from a cell line. In certain embodiments, a cell or host cell according to the invention is a mammalian or an avian cell, preferably a mammalian cell. Some non-limiting examples of cells or host cells according to the invention are rodent cells, human cells, simian cells, dog cells, chicken cells, etc. Some non-limiting examples of cells or host cells according to the invention are a Vero cell, an MDCK cell, a HEK293 cell, a PER.C6 cell, a CHO cell, a chicken embryonic fibroblast cell, a hybridoma cell, a baby hamster kidney (BHK) cell, a HeLa cell, an A549 cell, and the like. The skilled person will recognize that the AoHV-1 promoter can be used in many different cells to direct expression of an expression product of interest, and that the type of cell is not critical to the instant invention.
In certain aspects the invention provides a producer cell wherein an AoHV-1 promoter is operably linked to a nucleic acid sequence encoding a TetR protein, preferably wherein the AoHV-1 promoter and sequence encoding TetR are integrated into the genome of the producer cell, preferably wherein said cell is a mammalian cell, preferably a human cell, and in particularly preferred embodiments the producer cell is derived from a PER.C6 cell (see e.g., U.S. Pat. No. 5,994,128) by integration into the genome thereof of the AoHV-1 promoter and sequence encoding TetR. The invention thus also provides a PER.C6 cell comprising a transgene integrated into the genome of said cell, wherein the transgene comprises nucleic acid comprising an AoHV-1 promoter operably linked to a TetR-encoding sequence. In a non-limiting embodiment thereof, the transgene has a sequence as set forth in SEQ ID NO: 20. Such cells thus express TetR, and can for instance be used to produce recombinant adenovirus that encodes an expression product of interest under control of a promoter that can be regulated by TetR, e.g. a CMV or other promoter operably linked to one or more tetO sites, which can be particularly advantageous if the expression product of interest that is encoded by the adenovirus would be toxic to the producer cell or would reduce the stability or yield of the recombinant adenovirus when it would be produced during propagation of the adenovirus. The TetR can in such systems repress the tetO-regulated promoter, e.g. a tetO-regulated hCMV promoter, during production in the producer cell so that the expression product of interest is not or only at very low levels produced during propagation and production of the recombinant adenovirus, leading to improved yields and/or stability of the recombinant adenovirus during production. In one aspect the invention also provides a combination comprising: (i) a producer cell that comprises an AoHV-1 promoter operably linked to a sequence encoding TetR, and (ii) a recombinant adenovirus that comprises a sequence encoding an expression product of interest operably linked to a promoter that is operably linked to one or more tetO sites.
The present invention also provides methods for treating genetic, metabolic or acquired diseases with vectors and viruses comprising AoHV-1 promoter operably linked to a transgene. The method comprising contacting a cell with a sufficient amount of vector or virus of the present invention comprising the AoHV-1 promoter operably linked to a transgene wherein the cell is transformed such that the transgene is expressed in the cell. The cell can be transformed in vitro, ex vivo, or in vivo.
An important aspect of vectors, be it DNA vectors such as plasmid vectors or viral vectors such as adenoviral vectors, is the capacity of these vectors to accommodate desired transgene sequences. Such capacity may be limited by size constraints of the vectors, which may for instance become unstable or even impossible to produce if certain size limits are exceeded. The space taken up by a promoter is therefore an important consideration when designing new vectors, apart from the functional capabilities such promoters should have. The instant AoHV-1 promoter has the advantage that it is relatively short, meaning that at a certain size limit of a vector, more space remains for the transgene, e.g. allowing more epitopes to be included if a transgene is an immunogen or allowing expression of larger proteins, as compared to other promoters of larger size. A further advantage of the AoHV-1 promoter of the present invention is the possibility to combine it with the hCMV promoter in a system, e.g. both promoters on one nucleic acid molecule such as a vector, or one promoter in a cell line and the other promoter on a nucleic acid molecule such as a vector present in the cell line, with very limited to no risk of homologous recombination between the promoter sequences due to low sequence homology between theAoHV-1 promoter and the hCMV promoter.
As used herein, the terms “low sequence homology” and “low sequence identity” as they relate to the hCMV promoter sequence, refer to promoter sequences having less than about 50% identity with the hCMV promoter, and preferably having less than about 40% identify with the hCMV promoter. In addition, the promoter sequences with “low sequence homology” and “low sequence identity” preferably also do not have stretches of continuous identical alignment longer than about 15 nucleic acids, or more preferably no stretches of identical alignment longer than about 14 nucleic acids. In a certain preferred embodiment, the promoter is the AoHV-1 short promoter (SEQ ID NO:1 or SEQ ID NO:30) and the identity with the hCMV promoter is 36% and there are no stretches of continuous identical alignment longer than 14 nucleic acids. In other preferred embodiments, the promoter comprises a fragment of SEQ ID NO:1 or SEQ ID NO:30 having promoter activity, e.g. SEQ ID NO:25 or SEQ ID NO:26. As used herein, alignment refers to methods well known by those skilled in the art, e.g., using algorithms such as BLAST (Basic Local Alignment Search Tool) to align and compare different nucleotide or protein sequences (Altschul, Gish, Miller, Myers, & Lipman, 1990).
The present invention also provides cells or transgenic organisms transformed by vectors or viruses comprising the hCMV promoter and the AoHV-1 promoter, wherein the hCMV promoter and the AoHV-1 promoter are operably linked to transgenes, such that both transgenes are expressed in the cells or the transgenic organism. The hCMV promoter and the AoHV-1 promoter may be present on separate molecules (e.g. one promoter on a plasmid or in a virus and the other promoter in the genome of the cell, or both promoters on a different plasmid, or both promoters in the genome of the cell), or both promoters may be present in a single molecule (e.g. in one chromosome of the genome, or in one plasmid, or in one genome of a virus).
The invention also provides a method for producing a recombinant virus, wherein a transgene is potently expressed when the virus is introduced into a target cell, the method comprising: preparing a construct comprising an AoHV-1 promoter operably linked to a transgene, and incorporating said construct into the recombinant virus and then introducing the vector into the cell, e.g., by infection with the virus. The preparation of the construct as such encompasses the use of standard molecular cloning methods that are well known (see e.g. (Holterman et al., 2004; Lemckert et al., 2006; Vogels et al., 2003); Sambrook, Fritsch and Maniatis, Molecular Cloning: A Laboratory Manual, 2nd edition, 1989; Current Protocols in Molecular Biology, Ausubel F M, et al, eds, 1987; the series Methods in Enzymology (Academic Press, Inc.); PCR2: A Practical Approach, MacPherson M J, Hams B D, Taylor G R, eds, 1995), as known to the skilled person and routinely performed in the field of recombinant vector or recombinant virus technology, and exemplified herein. The AoHV-1 promoter has the features as described above, and in view of this disclosure, can be obtained by routine methods such as PCR or de novo nucleic acid synthesis. For convenience, the skilled person may manipulate a virus genome by cloning into smaller fragments, e.g. a first part for the left part of the genome of an adenovirus up to the E1 region for easy manipulation and introduction of the transgenes in plasmid form and a second, larger, part for the remainder of the genome that can upon recombination with the first part result in a complete adenovirus genome (see e.g. WO 99/55132).
“Heterologous nucleic acid” or a “heterologous gene” (also referred to herein as a “transgene”, or “gene of interest”), e.g. in vectors or viruses or cells of the invention is nucleic acid that is not naturally present in the vector or virus or cell, or that is not operably linked to the AoHV-1 promoter in nature. It is introduced into the vector or virus or cell for instance by standard molecular biology techniques. It may in certain embodiments encode a protein of interest or part thereof. In such cases, the protein of interest may be referred to as a “heterologous protein”, as it is not naturally encoded by a sequence operably linked to the AoHV-1 promoter in nature. A transgene can for instance be cloned into a plasmid vector or into a deleted E1 or E3 region of an adenoviral vector. In some embodiments of the invention, the expression cassette with an AoHV-1 promoter operably linked to a transgene is placed into the E1 region of an adenoviral genome. In some embodiments of the invention, the expression cassette with an AoHV-1 promoter operably linked to a transgene is placed into the E3 region of an adenoviral genome. In some embodiments of the invention, the expression cassette with an AoHV-1 promoter operably linked to a transgene is placed between the E4 region and the right ITR of an adenoviral genome. In other embodiments the expression cassette with an AoHV-1 promoter operably linked to a transgene is present in a plasmid vector. In other embodiments, the expression cassette with an AoHV-1 promoter operably linked to a transgene is integrated into the genome of a cell. Such cells or cell lines can be used to recombinantly express the transgene, e.g. by culturing the cells under conditions wherein the promoter is active (if the non-regulated version of the promoter is used, i.e. if no regulatory elements are added to the promoter, this expression will automatically happen upon culturing) and drives expression of the transgene.
As used herein, the terms “promoter” or “promoter region” or “promoter element” are used interchangeably, and refer to a segment of a nucleic acid sequence, typically but not limited to DNA, that controls the transcription of the nucleic acid sequence to which it is operatively linked. The promoter region includes specific sequences that are sufficient for RNA polymerase recognition, binding and transcription initiation. In addition, the promoter region can optionally include sequences which modulate this recognition, binding and transcription initiation activity of RNA polymerase. These sequences may be cis-acting or may be responsive to trans-acting factors. Furthermore, the promoters may be constitutive or regulated, depending upon the nature of the regulation.
The skilled person will be aware that promoters are built from stretches of nucleic acid sequences and often comprise elements or functional units in those stretches of nucleic acid sequences, such as a transcription start site, a binding site for RNA polymerase, general transcription factor binding sites, such as a TATA box, specific transcription factor binding sites, and the like. Further regulatory sequences may be present as well, such as enhancers, and sometimes introns at the end of a promoter sequence. Such functional units may be directly adjacent to each other but may also be separated by stretches of nucleic acid that do not have a direct role in the promoter function. The skilled person can refer to the examples herein for testing whether nucleotides in the stretch of nucleic acid are relevant for promoter function, and to test the effect of removing or adding nucleotides into a given promoter sequence by standard molecular biology methods, e.g. to minimize its length while retaining promoter activity or to optimize activity. Also mutations may be introduced into the promoter to reduce (stretches of) identity to other promoters (e.g. hCMV) if these promoters are intended to be present or used simultaneously in the same cell.
As used herein, the term “enhancer” refers to regulatory DNA sequences, e.g., 50-1500 bp, that can be bound by proteins (activator proteins) to stimulate or enhance transcription of a gene or several genes. These activator proteins, (a.k.a., transcription factors) interact with the mediator complex and recruit polymerase II and the general transcription factors which then begin transcribing the genes. Enhancers are generally cis-acting, but can be located either upstream or downstream from the start site of the gene or genes they regulate. Furthermore, an enhancer can be either in the forward or backward direction and doesn't need to be located near the transcription initiation site to affect transcription, as some have been found located several hundred thousand base pairs upstream or downstream of the start site. Enhancers can also be found within introns.
Sequences herein are provided in the 5′ to 3′ direction, as is customary in the art. Also note that the terms ‘upstream’ and ‘downstream’ are with respect to the direction of transcription as commonly used in the art. For example, by convention the terms upstream and downstream relate to the 5′ to 3′ direction in which RNA transcription takes place. Upstream is toward the 5′ end of the RNA molecule and downstream is toward the 3′ end. When considering double-stranded DNA, upstream is toward the 5′ end of the coding strand for the gene in question and downstream is toward the 3′ end. Due to the anti-parallel nature of DNA, this means the 3′ end of the template strand is upstream of the gene and the 5′ end is downstream.
An AoHV-1 promoter according to the invention preferably contains a TATA box sequence, such as a sequence located at positions 251 to 258 in SEQ ID NO: 25. A “TATA box” as defined herein is a DNA sequence that can be bound by TATA binding protein (TBP) and that has the consensus sequence TATAWAWR (where W is A or T, and R is A or G). It is usually located about 25-35 base pairs upstream of the transcription start site. In certain embodiments, an AoHV-1 promoter of the invention comprises TATA box sequence TATATAAG (positions 251-258 in SEQ ID NO: 25). The skilled person would appreciate that said TATA box sequence (i.e. TATATAAG) of an AoHV-1 promoter could be replaced by a similar canonical TATA box sequence, i.e. one that corresponds to the consensus sequence TATAWAWR (where W is A or T, and R is A or G), without an anticipated significant reduction of promoter activity.
An AoHV-1 promoter according to the invention may also contain a (putative) initiator element (Inr) such as located at positions 280 to 286 in SEQ ID NO: 25 (sequence: CCATTCG). In embodiments where an Inr is present, replacement of said Inr sequence (i.e. CCATTCG) of an AoHV-1 promoter by another sequence largely adhering to the Inr sequence YYANWYY (where Y is C or T; N is A, C, G, or T; and W is A or T) is not expected to significantly affect the activity of said promoter.
In certain embodiments wherein a putative Inr is present, an AoHV-1 promoter comprises a TATA box corresponding to positions 251-258, as well as the sequences up to about nt 286, in SEQ ID NO: 25. Without wishing to be bound by theory, it may be beneficial for certain embodiments of an AoHV-1 promoter of the invention to comprise both a TATA box and an Inr, wherein the Inr sequence is located about 25-40, e.g. about 29-36 nt downstream of the first nt of the TATA box.
Also in embodiments where no Inr is present, it is preferred to include at least about 25-35 base pairs downstream of the TATA box and upstream of the coding sequence of the operatively linked gene of interest. The present application includes at least one example of an AoHV-1 promoter that no longer comprises a consensus Inr sequence at the natural location of about 29-35 nt downstream of the first nt of the TATA-box, yet such promoter is still active, demonstrating that the Inr sequence at that position is not essential for a functional promoter.
An AoHV-1 promoter according to the invention is defined herein as a sequence having promoter activity and comprising a sequence having at least 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% identity, or being 100% identical, to a fragment of at least 50, 100, 150, 200, 250, 300, or 350 nucleotides of SEQ ID NO:25. Preferably, said fragment includes a fragment of at least 50 nt having at least 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91% 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% identity, or being 100% identical, to nt 237-286 of SEQ ID NO: 25, and preferably said at least 50 nt include a sequence TATAWAWR (TATA box consensus sequence) at a position corresponding to about nt 251-258 in SEQ ID NO: 25).
In certain preferred embodiments therefore, an AoHV-1 promoter of the invention comprises a sequence having at least 80% identity to nt 237-286 of SEQ ID NO: 25.
3′ truncations of AoHV-1 promoters of this invention can likely be made downstream of about nt 286 in SEQ ID NO: 25 (i.e. downstream of the putative Inr, which contains the expected transcription start site, which is expected to be at nucleotide 282 in this sequence) without strong effects on promoter activity, whereas larger 3′ truncations that remove the putative Inr/transcription start site or, especially, that remove both said putative Inr/transcription start site and said TATA box, are anticipated to result in significant reductions of promoter activity. Indeed, 3′ truncated versions of the AoHV-1 short promoter (SEQ ID NO: 30) that did not comprise AoHV-1 sequences downstream of nucleotide 399 (i.e. including only 1 AoHV-1 nucleotide downstream of the putative Inr, with reference to SEQ ID NO: 30, corresponding to nucleotide 287 in SEQ ID NO: 25) were shown to still be active as promoters.
It is demonstrated herein that a relatively short promoter fragment (SEQ ID NO: 26) comprising only 120 nucleotides upstream of its TATA box still has significant promoter activity, which can be increased somewhat further by addition of some further upstream sequences (as for example in SEQ ID NO: 25). By contrast, extension of the AoHV-1 short promoter (SEQ ID NO: 30) at its 3′ end (i.e. downstream of the putative Inr/transcription start site) by inclusion of certain further downstream sequences (as for example in SEQ ID NO: 27, SEQ ID NO:28, and SEQ ID NO:29) does not seem to add much activity.
In preferred embodiments, an AoHV-1 promoter of the invention comprises a fragment that is at least 95%, 96%, 97%, 98%, 99% identical, or is 100% identical, to nucleotides 201 to 286 of SEQ ID NO:25.
In more preferred embodiments, an AoHV-1 promoter of the invention comprises a fragment that is at least 95%, 96%, 97%, 98%, 99% identical, or is 100% identical, to nucleotides 187 to 286 of SEQ ID NO:25.
In more preferred embodiments, an AoHV-1 promoter of the invention comprises a fragment that is at least 95%, 96%, 97%, 98%, 99% identical, or is 100% identical, to nucleotides 137 to 286 of SEQ ID NO:25.
In more preferred embodiments, an AoHV-1 promoter of the invention comprises a fragment that is at least 95%, 96%, 97%, 98%, 99% identical, or is 100% identical, to nucleotides 131 to 286 of SEQ ID NO: 25.
In more preferred embodiments, an AoHV-1 promoter of the invention comprises a fragment that is at least 95%, 96%, 97%, 98%, 99% identical, or is 100% identical, to nucleotides 87 to 286 of SEQ ID NO:25.
In more preferred embodiments, an AoHV-1 promoter of the invention comprises a fragment that is at least 95%, 96%, 97%, 98%, 99% identical, or is 100% identical, to nucleotides 37 to 286 of SEQ ID NO:25.
In more preferred embodiments, an AoHV-1 promoter of the invention comprises a fragment that is at least 95%, 96%, 97%, 98%, 99% identical, or is 100% identical, to nucleotides 1 to 286 of SEQ ID NO:25.
In certain embodiments, an AoHV-1 promoter of the invention preferably comprises a sequence having at least 98% identity to at least 200 nucleotides of SEQ ID NO:26 (again preferably comprising at least the Inr and sequences upstream thereof including TATA box and sequences further upstream, e.g. at least about nt 87-286 of SEQ ID NO: 25), more preferably comprises a nucleotide sequence with at least 99% identity, or being 100% identical, to SEQ ID NO:26, still more preferably comprises a nucleotide sequence with at least 99% identity, or being 100% identical, to SEQ ID NO:25. In certain embodiments, the AoHV-1 promoter comprises a fragment of between 240 and 1500 nucleotides, preferably between 240 and 1000 nucleotides, more preferably between 240 and 500 nucleotides that is at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% identical, or is 100% identical, to a fragment of SEQ ID NO: 32, wherein said fragment of SEQ ID NO: 32 includes a fragment that is at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% identical, or is 100% identical, to nucleotides 201 to 286 of SEQ ID NO:25 (which correspond to nucleotides 1359 to 1444 of SEQ ID NO: 32).
The present invention provides a potent AoHV-1 promoter with a relatively small size, which can be highly advantageous in the context of size limitations of vectors carrying transgenes (i.e. larger transgenes can be accommodated and/or the vectors could remain more stable). Thus, the AoHV-1 promoter of the present invention is preferably less than 2000 nucleotides (2 kb) in length, preferably less than 1 kb, more preferably less than 0.8 kb. In certain preferred embodiments the AoHV-1 promoter is less than 700, less than 650, less than 600, less than 550, less than 500 nucleotides in length. In certain preferred embodiments, the AoHV-1 promoter is at least 200, at least 240, at least 250, at least 300, at least 350, at least 400 nucleotides in length. In certain preferred embodiments the AoHV-1 promoter is 200 to 500, e.g. 240 to 485, nucleotides in length. As shown herein, despite having a relatively short sequence, this novel AoHV-1 promoter was surprisingly capable of directing potent expression of the transgene to which it is operably linked.
A person skilled in the art will recognize that mutations can be made in the provided sequences and the resulting promoters can be tested for promoter activity by routine methods. Also variants of sequences may exist in nature, e.g. in different isolates of a virus, and thus such variants may have some differences in nucleotide sequence but keep the same functionality. Typically, a sequence having at least 90% identity with the indicated promoter sequences will still have functional activity and hence will be considered an AoHV-1 promoter. Thus, the AoHV-1 promoter of the present invention preferably comprises a sequence that has at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identity, or is 100% identical, to the preferred AoHV-1 promoter sequences provided herein, such as to any one of SEQ ID NO:1, 30, 25, or 26. The skilled person will also be aware that the length of the sequences of the different portions of the provided promoter sequences could be varied to some degree and essentially similar results could be obtained. Testing whether a fragment or mutant sequence of the promoter sequences exemplified herein still has promoter activity, can be performed without undue burden by a person skilled in the art with the information disclosed herein.
A preferred embodiment of an AoHV-1 promoter of the present invention is the AoHV-1 promoter comprising SEQ ID NO:26. The AoHV-1 promoter of the present invention preferably has at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identity to SEQ ID NO:26, or to a fragment thereof of at least 50, 100, 150, or 200 nucleotides. In a certain preferred embodiment the AoHV-1 promoter is 100% identical to SEQ ID NO:26 or to a fragment thereof of at least 50, 100, 150, or 200 nucleotides.
A further preferred AoHV-1 promoter of the present invention is the AoHV-1 promoter comprising SEQ ID NO:25. In certain embodiments, the AoHV-1 promoter of the present invention preferably has at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identity, or is 100% identical, to SEQ ID NO:25, or to a fragment thereof of at least 50, 100, 150, 200, 250, 300, or 350 nucleotides. In a certain preferred embodiment the AoHV-1 promoter is 100% identical to SEQ ID NO:25 or to a fragment thereof of at least 50, 100, 150, 200, 250, 300, or 350 nucleotides.
In a further embodiment, a preferred AoHV-1 promoter of the present invention is the AoHV-1 short promoter comprising SEQ ID NO:1 or SEQ ID NO:30. In certain embodiments, the AoHV-1 promoter of the present invention preferably has at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identity to SEQ ID NO:1, or to a fragment thereof of at least 50, 100, 150, 200, 250, 300, 350 or 400 nucleotides. In a certain preferred embodiment the AoHV-1 promoter is 100% identical to SEQ ID NO:1 or 100% identical to SEQ ID NO:30, or to a fragment of one of these of at least 50, 100, 150, 200, 250, 300, 350 or 400 nucleotides.
In other embodiments, an AoHV-1 promoter of the invention comprises a sequence having at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% identity, or that is 100% identical, to SEQ ID NO:22.
In other embodiments, an AoHV-1 promoter of the invention comprises a sequence having at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% identity, or that is 100% identical, to SEQ ID NO:23.
In other embodiments, an AoHV-1 promoter of the invention comprises a sequence having at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% identity, or that is 100% identical, to SEQ ID NO:27.
In other embodiments, an AoHV-1 promoter of the invention comprises a sequence having at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% identity, or that is 100% identical, to SEQ ID NO:28.
In other embodiments, an AoHV-1 promoter of the invention comprises a sequence having at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% identity, or that is 100% identical, to SEQ ID NO:29.
In certain other embodiments, an AoHV-1 promoter of the present invention comprises a core promoter (SEQ ID NO:31) operably linked with one or more operator sequences and/or enhancer sequences to modulate transcription, e.g., tetO sequences, operator sequences from the cumate operon, enhancers from naturally occurring enhancer-promoter pairs like SV40 or hCMV (Foecking & Hofstetter, 1986), synthetic enhancers (Schlabach, Hu, Li, & Elledge, 2010), or other regulatory sequences that are well known to those skilled in the art. As used herein, the term “core promoter” is intended to mean a minimum functional unit of the promoter with very low promoter activity on its own, but that can drive potent expression of a transgene when the core promoter is combined with one or more regulatory sequences to modulate transcription from the core promoter, e.g. tetO sequences that can be bound by tetracycline-controlled transactivator protein (tTA). See, for example (Smale, 2001), for a discussion on core promoter sequences.
A transgene operably linked to the AoHV-1 promoter can be potently expressed. As used herein, “potently expressed” or “potent expression” mean that the expression from the AoHV-1 promoter, as measured for example by one of different protein detection techniques such as Western Blot, FACS analysis, or other assays using luminescence or fluorescence, is at least about 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or preferably about 100%, or more than the expression from the hCMV promoter (having SEQ ID NO:4). Of note, the hCMV promoter is much stronger compared to other commonly used promoters such as hPGK, UBI C or RSV LTR promoters (Powell, Rivera-Soto, & Gray, 2015). The hCMV promoters are derived from the major immediate early (mIE) region of human cytomegalovirus and are frequently used for potent gene expression in vaccine and gene therapy vectors. For example, a hCMV promoter sequence can be derived from the hCMV AD169 strain mIE locus (X03922) and include NF1 binding sites, the enhancer region, TATA box and part of the first exon. Other hCMV promoter sequences are known which can be shorter (e.g. only containing the enhancer and promoter region and lacking NF1 binding sites) or longer (e.g. including additional cellular factor binding sites and the first intron sequence). These hCMV promoters which differ in length were all found to be potent ubiquitously active promoters. Examples of truncated hCMV promoters are disclosed in U.S. Pat. No. 7,407,801, incorporated by reference herein. As used herein, a “hCMV promoter” comprises a sequence having at least 80%, preferably at least 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% sequence identity to nt 578-736, preferably to nt 564-736, of SEQ ID NO: 4. A fragment of nt 578-736 of SEQ ID NO: 4 was shown to have promoter activity in experiments in our laboratory (not shown), and a sequence with some mismatches to nt 564-736 of SEQ ID NO: 4 has been shown to provide good expression levels by others (e.g. U.S. Pat. No. 7,407,801 B2, SEQ ID NO: 1 therein). In certain embodiments, a hCMV promoter comprises a sequence having at least 80%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% sequence identity to SEQ ID NO: 4. For the comparisons of expression levels as described herein, the hCMV promoter sequence was SEQ ID NO:4. For example, the expression level from the AoHV-1 promoter of the present invention in a vector is preferably at least about 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or preferably about 100%, or more of the expression level from a vector where the transgene is under control of a hCMV promoter of SEQ ID NO:4. Furthermore, it is known from rAd expressing an antigen under the control of an hCMV promoter that the expression is sufficient to generate significant T-cell and B-cell immune responses. Similarly, expression of a transgene expressed by an AoHV-1 promoter of the present invention from a rAd is expected to generate a significant T-cell and B-cell immune response to the transgene. For example, if the transgene encoded an antigen to elicit an immune response when administered to a subject, potent expression of the transgene is expected to generate a measurable immune response against the antigen.
The term ‘about’ for numerical values as used in the present disclosure means the value ±10%.
The terms “coding sequence”, “sequence encoding”, or “encoding” are used interchangeably herein, and refer to the nucleic acid sequence which is transcribed (DNA) and translated (mRNA) into a polypeptide in vitro or in vivo when operably linked to appropriate regulatory sequences.
A polyadenylation signal, for example the bovine growth hormone polyA signal (U.S. Pat. No. 5,122,458) or an SV40 polyA signal, may be present behind the transgenes.
Further regulatory sequences may also be added to constructs comprising the AoHV-1 promoter of the present invention. The term “regulatory sequence” is used interchangeably with “regulatory element” herein and refers to a segment of nucleic acid, typically but not limited to DNA, that modulate the transcription of the nucleic acid sequence to which it is operatively linked, and thus acts as a transcriptional modulator. This modulation of expression can be especially useful in cases where expression of a protein is toxic to the host cell, e.g., where expression is lethal to a host cell or negatively affects cell growth and/or reduces or eliminates protein production. Furthermore, modulation of expression can also be useful in cases where expression causes vector instability or where timing of expression is a consideration for an experiment done in vitro or in vivo. A regulatory sequence often comprises nucleic acid sequences that are recognized by the nucleic acid-binding domains of transcriptional proteins and/or transcription factors that activate or repress transcription. For example, a regulatory sequence could include one or more (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, etc.) tetracycline operator sequences (tetO sites), such that expression is inhibited in the presence of the tetracycline repressor protein (tetR), see e.g. WO 1999/000510 A1. An example of a single tetO sequence is CCCTATCAGTGATAGAG (SEQ ID NO:14). In the absence of tetracycline, the tetR protein is able to bind to the tetO sites and repress transcription of a gene operably linked to the tetO sites. In the presence of tetracycline, however, a conformational change in the tetR protein prevents it from binding to the operator sequences, allowing transcription of operably linked genes to occur. In certain embodiments, a vector or rAd of the present invention can optionally include one or more tetO sites operatively linked to the AoHV-1 promoter, such that expression of one or more transgenes is inhibited in the vectors that are produced in the producer cell line in which tetR protein is expressed. Subsequently, expression would not be inhibited if the vector is introduced into a subject or into cells that do not express the tetR protein (see e.g., WO 07/073513). In certain other embodiments, vectors of the present invention can optionally include a cumate gene-switch system, in which regulation of expression is mediated by the binding of the repressor (CymR) to the operator site (CuO), operably linked, e.g. by placing it close to the transcription start site of the promoter (see e.g., (Mullick et al., 2006)). In other embodiments, the well-known lac repressor system is combined with the promoter of the invention, wherein one or more lac operator sites are operably linked to the promoter, so that binding of lac repressor protein can be used to regulate expression.
As used herein, the term “repressor” refers to entities (e.g., proteins or other molecules) having the capacity to inhibit, interfere, retard and/or repress the production of heterologous protein product of a recombinant expression vector. For example, by interfering with a binding site at an appropriate location along the expression vector, such as in an expression cassette. Examples of repressors include tetR, CymR, the lac repressor, the trp repressor, the gal repressor, the lambda repressor, and other appropriate repressors known in the art.
The terms “operably linked”, or “operatively linked” are used interchangeably herein, and refer to the functional relationship of the nucleic acid sequences with regulatory sequences of nucleotides, such as promoters, enhancers, repressor sequences, transcriptional and translational stop sites, and other signal sequences and indicates that two or more DNA segments are joined together such that they function in concert for their intended purposes. For example, operative linkage of nucleic acid sequences, typically DNA, to a regulatory sequence or promoter region refers to the physical and functional relationship between the DNA and the regulatory sequence or promoter such that the transcription of such DNA is initiated from the regulatory sequence or promoter, by an RNA polymerase that specifically recognizes, binds and transcribes the DNA. In order to optimize expression and/or in vitro transcription, it may be possible to modify the regulatory sequence for the expression of the nucleic acid or DNA in the cell type for which it is expressed. The desirability of, or need of, such modification may be empirically determined.
The invention also provides a method for expressing a transgene in a cell, the method comprising providing the cell with a recombinant virus, e.g. a recombinant adenovirus, comprising an AoHV-1 promoter operably linked to a transgene. Providing a cell with a recombinant adenovirus can be done via administration of the adenovirus to a subject, or via introduction (e.g. infection) of the adenovirus in vitro or ex vivo into a cell. In certain embodiments the invention provides a recombinant adenoviral vector for use in expressing a transgene in a cell, e.g. by administering the recombinant adenovirus to a subject.
The present invention also provides a method for expressing a transgene in a cell, the method comprising providing the cell with a recombinant virus, e.g. a recombinant adenovirus, comprising the AoHV-1 promoter operably linked to a transgene encoding an expression product such as a protein of interest, for instance wherein the protein of interest is a therapeutic protein or an antigen.
The invention also provides a method for inducing an immune response against an antigen, comprising administering to a subject a vector, e.g. a recombinant adenovirus comprising an AoHV-1 promoter operably linked to a transgene. The invention also provides a vector or a recombinant adenovirus according to the invention for use in inducing an immune response against an antigen.
The AoHV-1 promoter of the invention can in certain embodiments for instance be used to drive expression of an antigen, with the aim of generating an immune response to the antigens in a vaccine application. The identity of the transgene is not material for the instant invention, which is suitable for example with vectors or adenoviruses comprising any transgene. Suitable transgenes are well known to the skilled person, and for instance may include transgene open reading frames, for instance open reading frames coding for polypeptides that have a therapeutic effect, e.g. for gene therapy purposes, or polypeptides against which an immune response is desired when the vector, e.g. rAd vector, is used for vaccination purposes. Particularly preferred heterologous nucleic acids are genes of interest encoding antigenic determinants towards which an immune response needs to be raised. Such antigenic determinants are also typically referred to as antigens. When the recombinant vector is administered to a subject, an immune response will be raised against the antigen(s). Any desired antigen can be encoded by the vector. In typical embodiments according to the invention, antigens are peptides, polypeptides or proteins from organisms that may cause a disease or condition. Therefore, in a further preferred embodiment, said heterologous nucleic acid of interest encodes an immunogenic (or antigenic) determinant. More preferably, said immunogenic determinant is an antigen from a bacterium, a virus, yeast or a parasite. The diseases caused by such organisms are generally referred to as ‘infectious disease’ (and are thus not limited to organisms that ‘infect’ but also include those that enter the host and cause a disease). So-called ‘self-antigens’, e.g. tumour antigens, also form part of the state of the art, and may be encoded by heterologous nucleic acids in the recombinant vectors according to the present invention. Non-limiting examples from which the antigenic determinants (or antigens) are taken are malaria-causing organisms, such as Plasmodium falciparum, tuberculosis-causing organism such as Mycobacterium tuberculosis, yeasts, or viruses. In other preferred embodiments, antigens from viruses such as flaviviruses (e.g., West Nile Virus, Hepatitis C Virus, Japanese Encephalitis Virus, Dengue Virus, Zika Virus), Ebola virus, Human Immunodeficiency Virus (HIV), and Marburg virus may be used in compositions according to the present invention. Exemplary non-limiting embodiments of antigens are the CS protein or immunogenic part thereof from P. falciparum, a protein of one antigen-, or a fusion protein of several antigens fromM tuberculosis, such as the Ag85A, Ag85B and/or the TB10.4 proteins or immunogenic part(s) thereof, a viral glycoprotein or immunogenic part thereof, such as GP from a filovirus, such as Ebola virus or Marburg virus, an HIV protein such as gag, pol, env, nef, or variants thereof, or a HA, NA, M, or NP protein, or immunogenic part of any of these, from influenza virus, or a respiratory syncytial virus (RSV) antigen, e.g. RSV F protein or RSV G protein, or both, or other RSV proteins, a human papillomavirus or other virus antigen, etc. The recombinant vector, e.g. rAd may encode one antigen, but may also optionally encode two different antigens from the same organism, or optionally combinations of antigens from different organisms, e.g. a first antigen from a first organism and second antigen from a second organism. It is also possible to encode an antigen and for instance an adjuvant into the same vector such as rAd vector, e.g. an antigen and a Toll-Like-Receptor (TLR) agonist, such as a TLR3 agonist, such as dsRNA or a mimetic thereof or the like (e.g. WO 2007/100908). In certain embodiments, the recombinant vector, e.g. recombinant adenovirus, encodes two different antigens, one under control of the AoHV-1 promoter and one under the control of a different promoter, e.g., the hCMV promoter. In other embodiments, the vector or recombinant virus encodes an antigen and an immune modulator, one of which is under control of the AoHV-1 promoter and the other is under control of a different promoter, e.g., the hCMV promoter. In certain embodiments, further heterologous sequences or transgenes may be present in the vector or recombinant virus, besides the transgene that is under control of the AoHV-1 promoter.
The invention also provides a recombinant DNA molecule comprising the AoHV-1 promoter of the present invention operably linked to a transgene. The invention also provides the genome of a recombinant adenovirus comprising the AoHV-1 promoter operably linked to a transgene. The skilled person will be aware that this may also be a combination of at least two different recombinant DNA molecules that together can form the single recombinant DNA molecule of the invention. Such molecules are useful in manipulating the genome and creating novel recombinant adenoviruses. The genome encodes the proteins that are required for adenovirus replication and packaging in permissive cells.
The term ‘recombinant’ for a recombinant adenovirus, as used herein implicates that it has been modified by the hand of man as opposed to wild-type adenoviruses, e.g. it comprises a heterologous gene, genes, or parts thereof and an AoHV-1 promoter operably linked to a transgene.
Adenoviral vectors, methods for construction thereof and methods for propagating thereof, are well known in the art and are described in, for example, U.S. Pat. Nos. 5,559,099, 5,837,511, 5,846,782, 5,851,806, 5,994,106, 5,994,128, 5,965,541, 5,981,225, 6,040,174, 6,020,191, 6,113,913, and 8,932,607, and Thomas Shenk, “Adenoviridae and their Replication” M. S. Horowitz, “Adenoviruses”, Chapters 67 and 68, respectively, in Virology, B. N. Fields et al., eds 3d ed., Raven Press, Ltd., New York (1996), and other references mentioned herein. Typically, construction of adenoviral vectors involves the use of standard molecular biological techniques that are well known in the art, such as those described in, for example, Sambrook et al., Molecular Cloning, a Laboratory Manual, 2d ed., Cold Spring Harbor Press, Cold Spring Harbor, N.Y. (1989), Watson et al., Recombinant DNA, 2d ed., Scientific American Books (1992), and Ausubel et al., Current Protocols in Molecular Biology, Wiley Interscience Publishers, NY (1995), and other references mentioned herein.
An adenovirus according to the invention belongs to the family of the Adenoviridae and preferably is one that belongs to the genus Mastadenovirus. It can be a human adenovirus, but also an adenovirus that infects other species, including but not limited to a bovine adenovirus (e.g. bovine adenovirus 3, BAdV3), a canine adenovirus (e.g. CAdV2), a porcine adenovirus (e.g. PAdV3 or 5), or a simian adenovirus (which includes a monkey adenovirus and an ape adenovirus, such as a chimpanzee adenovirus or a gorilla adenovirus). Preferably, the adenovirus is a human adenovirus (HAdV, or AdHu; in the present invention a human adenovirus is meant if referred to Ad without indication of species, e.g. the brief notation “Ad5” means the same as HAdV5, which is human adenovirus serotype 5), or a simian adenovirus such as chimpanzee or gorilla adenovirus (ChAd, AdCh, or SAdV), or a rhesus monkey adenovirus (RhAd).
Most advanced studies have been performed using human adenoviruses, and human adenoviruses are preferred according to certain aspects of the invention. In certain preferred embodiments, the recombinant adenovirus according to the invention is based upon a human adenovirus. In preferred embodiments, the recombinant adenovirus is based upon a human adenovirus serotype 5, 11, 26, 34, 35, 48, 49 or 50. According to a particularly preferred embodiment of the invention, an adenovirus is a human adenovirus of one of the serotypes 26 and 35. An advantage of these serotypes is a low seroprevalence and/or low pre-existing neutralizing antibody titers in the human population. Preparation of rAd26 vectors is described, for example, in WO 2007/104792 and in (Abbink et al., 2007). Exemplary genome sequences of Ad26 are found in GenBank Accession EF 153474 and in SEQ ID NO:1 of WO 2007/104792. Preparation of rAd35 vectors is described, for example, in U.S. Pat. No. 7,270,811, in WO 00/70071, and in (Vogels et al., 2003). Exemplary genome sequences of Ad35 are found in GenBank Accession AC_000019 and in FIG. 6 of WO 00/70071.
The sequences of most of the human and non-human adenoviruses mentioned above are known, and for others can be obtained using routine procedures.
A recombinant adenovirus according to the invention may be replication-competent or replication-deficient.
In certain embodiments, the adenovirus is replication deficient, e.g. because it contains a deletion in the E1 region of the genome. A “deletion in the E1 region” means a deletion in this region as compared to a wild-type adenovirus, and means a deletion in at least one of the E1A, E1B 55K or E1B 21K coding regions, preferably a deletion of E1A, E1B 55K and E1B21K coding regions. As known to the skilled person, in case of deletions of essential regions from the adenovirus genome, the functions encoded by these regions have to be provided in trans, preferably by the producer cell, i.e. when parts or whole of E1, E2 and/or E4 regions are deleted from the adenovirus, these have to be present in the producer cell, for instance integrated in the genome thereof, or in the form of so-called helper adenovirus or helper plasmids. The adenovirus may also have a deletion in the E3 region, which is dispensable for replication, and hence such a deletion does not have to be complemented.
A producer cell (sometimes also referred to in the art and herein as ‘packaging cell’ or ‘complementing cell’) that can be used can be any producer cell wherein a desired adenovirus can be propagated. For example, the propagation of recombinant adenovirus vectors is done in producer cells that complement deficiencies in the adenovirus. Such producer cells preferably have in their genome at least an adenovirus E1 sequence, and thereby are capable of complementing recombinant adenoviruses with a deletion in the E1 region. Any E1-complementing producer cell can be used, such as human retina cells immortalized by E1, e.g. 911 or PER.C6 cells (see, e.g., U.S. Pat. No. 5,994,128), E1-transformed amniocytes (See, e.g., EP 1230354), E1-transformed A549 cells (see e.g. WO 98/39411, U.S. Pat. No. 5,891,690), GH329:HeLa cells (Gao, Engdahl, & Wilson, 2000), 293 cells, and the like. In certain embodiments, the producer cells are for instance HEK293 cells, or PER.C6 cells, or 911 cells, or IT293SF cells, and the like.
In addition to adenoviruses, those skilled in the art will recognize that other viruses are also suitable for use as viral vectors using the AoHV-1 promoter of the present invention. For example, adeno-associated viruses (AAV), herpes simplex virus (HSV), paramyxoviruses such as measles virus, alphaviruses, EBNA virus, retroviruses, poxvirus and lentivirus, and the like, can also be engineered to include the AoHV-1 promoter of the present invention. See, for example, reviews about different vectors as discussed in (Heilbronn & Weger, 2010; Robbins & Ghivizzani, 1998; Walther & Stein, 2000).
For administering to humans, one may employ pharmaceutical compositions for instance comprising a vector, a recombinant virus, or a recombinant protein expressed using methods of the present invention, e.g., rAd or a recombinant protein expressed using AoHV-1 promoter of the present invention, and a pharmaceutically acceptable carrier or excipient. In the present context, the term “Pharmaceutically acceptable” means that the carrier or excipient, at the dosages and concentrations employed, will not cause unwanted or harmful effects in the subjects to which they are administered. Such pharmaceutically acceptable carriers and excipients are well known in the art (see Remington's Pharmaceutical Sciences, 18th edition, A. R. Gennaro, Ed., Mack Publishing Company [1990]; Pharmaceutical Formulation Development of Peptides and Proteins, S. Frokjaer and L. Hovgaard, Eds., Taylor & Francis [2000]; and Handbook of Pharmaceutical Excipients, 3rd edition, A. Kibbe, Ed., Pharmaceutical Press [2000]). A purified vector, e.g. rAd, or protein, preferably is formulated and administered as a sterile solution although it is also possible to utilize lyophilized preparations. Sterile solutions are prepared by sterile filtration or by other methods known per se in the art. The solutions are then lyophilized or filled into pharmaceutical dosage containers. The pH of the solution generally is in the range of pH 3.0 to 9.5, e.g. pH 5.0 to 7.5. A vector or rAd or protein typically is in a solution having a suitable buffer, and the solution may also contain a salt. Optionally stabilizing agent may be present, such as albumin. In certain embodiments, detergent is added. In certain embodiments, vector, rAd or protein may be formulated into an injectable preparation. These formulations contain effective amounts of the pharmaceutical ingredient, e.g. vector, rAd, or protein, are either sterile liquid solutions, liquid suspensions or lyophilized versions and optionally contain stabilizers or excipients. The pharmaceutical preparations can be prepared for different routes of administration, e.g. intramuscular or intradermal injection, inhalation, intravenous administration, oral administration, etc.
Examples of adenovirus formulations are the Adenovirus World Standard (Hoganson et al., 2002): 20 mM Tris pH 8, 25 mM NaCl, 2.5% glycerol; or 20 mM Tris, 2 mM MgCl2, 25 mM NaCl, sucrose 10% w/v, polysorbate-80 0.02% w/v; or 10-25 mM citrate buffer pH 5.9-6.2, 4-6% (w/w) hydroxypropyl-beta-cyclodextrin (HBCD), 70-100 mM NaCl, 0.018-0.035% (w/w) polysorbate-80, and optionally 0.3-0.45% (w/w) ethanol. Obviously, many other buffers can be used, and several examples of suitable formulations for the storage and for pharmaceutical administration of purified pharmaceutical preparations are known.
In certain embodiments a composition comprising a vector or recombinant virus of the invention, e.g., rAd, further comprises one or more adjuvants. Adjuvants are known in the art to further increase the immune response to an applied antigenic determinant, and pharmaceutical compositions comprising adenovirus and suitable adjuvants are for instance disclosed in WO 2007/110409, incorporated by reference herein. The terms “adjuvant” and “immune stimulant” are used interchangeably herein, and are defined as one or more substances that cause stimulation of the immune system. In this context, an adjuvant is used to enhance an immune response to the adenovirus vectors of the invention. Examples of suitable adjuvants include aluminium salts such as aluminium hydroxide and/or aluminium phosphate; oil-emulsion compositions (or oil-in-water compositions), including squalene-water emulsions, such as MF59 (see e.g. WO 90/14837); saponin formulations, such as for example QS21 and Immunostimulating Complexes (ISCOMS) (see e.g. U.S. Pat. No. 5,057,540; and WO 90/03184, WO 96/11711, WO 2004/004762, WO 2005/002620); bacterial or microbial derivatives, examples of which are monophosphoryl lipid A (MPL), 3-O-deacylated MPL (3dMPL), CpG-motif containing oligonucleotides, ADP-ribosylating bacterial toxins or mutants thereof, such as E. coli heat labile enterotoxin LT, cholera toxin CT, and the like. It is also possible to use vector-encoded adjuvant, e.g. by using heterologous nucleic acid that encodes a fusion of the oligomerization domain of C4-binding protein (C4 bp) to the antigen of interest (Ogun, Dumon-Seignovert, Marchand, Holder, & Hill, 2008), or heterologous nucleic acid encoding a toll-like receptor (TLR) agonist, such as a TLR3 agonist such as dsRNA (see e.g. WO 2007/100908), or heterologous nucleic acid encoding an immunostimulating cytokine, e.g. an interleukin, e.g. IL-12 (see e.g. U.S. Pat. No. 5,723,127), or the like.
A pharmaceutical composition according to the invention may in certain embodiments be a vaccine.
Administration of a vector or recombinant virus of the invention, e.g., adenovirus compositions, can be performed using standard routes of administration. Non-limiting embodiments include parenteral administration, such as by injection, e.g. intradermal, intramuscular, etc, or subcutaneous or transcutaneous, or mucosal administration, e.g. intranasal, oral, and the like. The skilled person knows the various possibilities to administer a composition, e.g. a vaccine in order to induce an immune response to the antigen(s) in the vaccine.
Adenovirus compositions may be administered to a subject, e.g. a human subject. The total dose of the adenovirus provided to a subject during one administration can be varied as is known to the skilled practitioner, and is generally between 1×107 viral particles (vp) and 1×1012 vp, preferably between 1×108 vp and 1×1011 vp, for instance between 3×108 and 5×1010 vp, for instance between 109 and 3×1010 vp.
A subject as used herein preferably is a mammal, for instance a rodent, e.g. a mouse, or a non-human-primate, or a human. Preferably, the subject is a human subject.
It is also possible to provide one or more booster administrations of one or more vaccines. If a boosting vaccination is performed, typically, such a boosting vaccination will be administered to the same subject at a moment between one week and one year, preferably between two weeks and four months, after administering the composition to the subject for the first time (which is in such cases referred to as ‘priming vaccination’). In alternative boosting regimens, it is also possible to administer different vectors, e.g. one or more adenoviruses of different serotype, or other vectors such as MVA, or DNA, or protein, to the subject as a priming or boosting vaccination.
Various publications, which may include patents, published applications, technical articles and scholarly articles, are cited throughout the specification in parentheses, and full citations of each may be found at the end of the specification. Each of these cited publications is incorporated by reference herein, in its entirety.
Embodiment 1 is a recombinant nucleic acid molecule comprising an Aotine Herpesvirus major immediate early promoter (AoHV-1 promoter) operably linked to a heterologous transgene.
Embodiment 2 is a plasmid vector comprising an AoHV-1 promoter followed by a multiple cloning site.
Embodiment 3 is the recombinant nucleic acid molecule of embodiment 1 or a plasmid vector of embodiment 2, wherein the AoHV-1 promoter is operably linked to a regulatory sequence that modulates transcription from the AoHV-1 promoter.
Embodiment 4 is the recombinant nucleic acid molecule of embodiment 1 or a plasmid vector of embodiment 2, wherein the AoHV-1 promoter is operably linked to a regulatory sequence comprising one or more tetracycline operator sequences (tetO sites).
Embodiment 5 is a recombinant vector or a recombinant virus, comprising a recombinant nucleic acid molecule according to any one of embodiments 1, 3, or 4.
Embodiment 6 is a recombinant vector according to embodiment 5, wherein the vector is a plasmid vector.
Embodiment 7 is a recombinant virus according to embodiment 5, wherein the virus is an adenovirus.
Embodiment 8 is the recombinant adenovirus according to embodiment 7, wherein the adenovirus has a deletion in a region of its genome.
Embodiment 9 is the recombinant adenovirus of embodiment 8, wherein the deletion is in the E1 region, in the E3 region, or in the E1 region and in the E3 region.
Embodiment 10 is a cell comprising a recombinant nucleic acid molecule according to embodiment 1, 3 or 4, a plasmid vector according to embodiment 2, 3 or 4, or a recombinant vector or recombinant virus according to any one of embodiments 5-9.
Embodiment 11 is a cell comprising a recombinant nucleic acid molecule comprising an AoHV-1 promoter in its genome, preferably wherein said promoter is operably linked to a nucleic acid encoding a protein of interest.
Embodiment 12 is a cell comprising: (i) a recombinant nucleic acid molecule comprising an AoHV-1 promoter operably linked to a first transgene, and (ii) a recombinant nucleic acid molecule comprising a hCMV promoter operably linked to a second transgene.
Embodiment 13 is a vector comprising: (i) a recombinant nucleic acid molecule comprising an AoHV-1 promoter operably linked to a first transgene, and (ii) a recombinant nucleic acid molecule comprising a hCMV promoter operably linked to a second transgene.
Embodiment 14 is a method of producing a recombinant adenovirus comprising an AoHV-1 promoter operably linked to a transgene, wherein the transgene is potently expressed when the adenovirus infects a target cell, the method comprising:
Embodiment 15 is a method of producing a recombinant nucleic acid molecule comprising an AoHV-1 promoter operably linked to a transgene encoding a protein of interest, the method comprising molecular cloning of the transgene in operable linkage to an AoHV-1 promoter.
Embodiment 16 is a recombinant DNA molecule comprising the genome of a recombinant adenovirus according to any one of embodiments 7-9.
Embodiment 17 is a method for making the cell of embodiment 11, comprising introducing an AoHV-1 promoter into the cell and integrating the AoHV-1 promoter into the genome, preferably wherein said promoter is operably linked to a nucleic acid encoding a protein of interest.
Embodiment 18 is a method for producing an expression product of interest, comprising expressing a transgene encoding the expression product of interest in a host cell, wherein the transgene is operably linked to an AoHV-1 promoter.
Embodiment 19 is the method of embodiment 18, wherein the expression product is a protein.
Embodiment 20 is a method for expressing a transgene of interest, comprising expressing in a host cell the transgene from the recombinant nucleic acid molecule according to any one of embodiments 1, 3, 4, 5 or 6,
Embodiment 21 is the method of embodiment 20, wherein the transgene of interest encodes a protein of interest that is expressed in the host cell.
Embodiment 22 is the method of embodiment 19 or 21, further comprising harvesting the protein of interest from the host cell or from a culture medium wherein the host cell is cultured, or from both the host cell and the culture medium.
Embodiment 24 is a method for producing a virus, comprising propagating the virus in a cell that expresses a gene that has a function in propagating said virus, wherein said gene is under control of an AoHV-1 promoter.
Embodiment 25 is the method of embodiment 24, wherein said virus does not produce said gene in functional form from its own genome, and wherein said gene is essential for replication of said virus.
Embodiment 26 is a pharmaceutical composition comprising a recombinant vector or a recombinant virus according to any one of embodiments 5-9 and a pharmaceutically acceptable carrier or excipient.
Embodiment 27 is a cell according to embodiment 11, wherein the AoHV-1 promoter in the genome is operably linked to nucleic acid that encodes a tetracycline repressor (TetR) protein.
Embodiment 28 is a cell according to embodiment 12, wherein the first transgene encodes TetR.
Embodiment 29 is a cell according to embodiment 28, that further comprises a recombinant adenovirus which comprises the recombinant nucleic acid molecule comprising a hCMV promoter operably linked to the second transgene.
Embodiment 30 is a cell according to embodiment 29, wherein the hCMV promoter can be regulated by TetR, e.g. by being operably linked to one or more tetO sites.
Embodiment 31 is a cell according to embodiment 27, 28, 29, or 30, wherein the cell is a PER.C6 cell.
Embodiment 32 is a method according to embodiment 20, wherein the transgene encodes TetR.
Embodiment 33 is a method according to embodiment 32, wherein the cell is a PER.C6 cell.
Embodiment 34 is a method for propagating a recombinant adenovirus, the method comprising propagating a recombinant adenovirus that encodes a transgene under control of a hCMV promoter that is operably linked to one or more tetO sites in a cell according to embodiment 27, 29, or 31, and preferably isolating the recombinant adenovirus.
Embodiment 35 is any one of the preceding embodiments, wherein the AoHV-1 promoter comprises a sequence having at least 80% identity to nt 237-286 of SEQ ID NO: 25.
Embodiment 36 is any one of the preceding embodiments, wherein the AoHV-1 promoter comprises a sequence having at least 86% identity, preferably at least 90% identity, preferably at least 96% identity, preferably at least 98% identity, more preferably 100% identity, to nt 237-286 of SEQ ID NO: 25.
Embodiment 37 is any one of the preceding embodiments, wherein the AoHV-1 promoter comprises a sequence having at least 90% identity to nt 131-286 of SEQ ID NO: 25.
Embodiment 38 is any one of the preceding embodiments, wherein the AoHV-1 promoter comprises a sequence that is at least 95% identical to SEQ ID NO:31.
Embodiment 39 is any one of the preceding embodiments, wherein the AoHV-1 promoter comprises between 240 and 1500 nucleotides, preferably between 240 and 1000 nucleotides, more preferably between 240 and 500 nucleotides of SEQ ID NO:32.
Embodiment 40 is any one of the preceding embodiments, wherein the AoHV-1 promoter comprises SEQ ID NO:26.
Embodiment 41 is any one of the preceding embodiments, wherein the AoHV-1 promoter comprises a sequence that is at least 95% identical to a fragment of at least 300 nucleotides of SEQ ID NO:25.
Embodiment 42 is any one of the preceding embodiments, wherein the AoHV-1 promoter comprises SEQ ID NO:25.
Embodiment 43 is any of the preceding embodiments, wherein the AoHV-1 promoter comprises a sequence that is at least 95% identical to a fragment of at least 400 nucleotides of SEQ ID NO:1.
Embodiment 44 is embodiment 43, wherein the AoHV-1 promoter comprises SEQ ID NO:1 or SEQ ID NO:30.
Embodiment 45 is a cell comprising a transgene that comprises SEQ ID NO: 20, preferably within the genome of the cell.
Embodiment 46 is a cell according to embodiment 45, wherein the cell is a PER.C6 cell.
Without further description, it is believed that one of ordinary skill in the art can, using the preceding description and the following illustrative methods and examples, make and utilize the present invention and practice the claimed methods. The following working examples therefore, specifically point out certain embodiments, features, and advantages of the present invention, and are not to be construed as limiting in any way the remainder of the disclosure. The examples merely serve to clarify the invention.
Methods
Cell Culture:
HEK293 cells were maintained in Dulbecco's modified Eagle's medium (DMEM) with 10% fetal bovine serum (FBS). Vero cells were cultured in Minimal Essential Medium (MEM, Life Technologies) supplemented with 5% fetal bovine serum (FBS). PER.C6 cells (Fallaux et al., 1998) were cultured in DMEM with 10% fetal bovine serum (FBS), supplemented with 10 mM MgCl2.
PER.C6-hCMV.TetR cells (described herein) were cultured in similar medium as described above for PER.C6 cells but supplemented with 2 ug/ml Blasticidin (Gibco A11139-03).
Subculturing of above cells was performed according to standard protocols using TrypLE Select Enzyme (ThermoFisher, Cat. No.: 12563011) to detach cells.
Padapt35 Plasmids:
Different promoter constructs were cloned into pAdApt35 (Vogels et al. 2007) using AvrII and HindIII restriction sites. A gene encoding for firefly luciferase was inserted using HindIII and XbaI restriction sites, resulting in pAdapt plasmids in which the Luc gene is expressed under the different tested promoters (pAdapt35.P.Luc). These plasmids were used in Example 1.
Expression Analysis in Transiently Transfected HEK293 Cells.
HEK293 cells were plated in multiwell 6 Poly-L-Lysine (PLL) coated plates and transfected with 1 μg pAdapt.P.Luc plasmids using Lipofectamine according to the instructions provided by the manufacturer (Life Technologies). Subsequently the plates were incubated 24 hours in 37° C., 10% CO2. Luciferase activity was measured 24 h post transfection in cell lysates in presence with 0.1% DTT (1M), in Luminoskan™ Ascent Microplate Luminometer. As a control of transfection efficiency, a plasmid encoding secreted embryonic Alkaline Phosphatase was co-transfected (80 ng/well). SEAP levels were measured using the Clontech Great EscAPe™ SEAP Chemoluminescence Kit 2.0 and a Trilux Microbeta workstation. Expression analysis in transiently transfected HEK293 cells is used in Example 1.
Expression Analysis of Gaussia Luciferase Under Control of the tTA-Responsive Artificial Promoter “7xTetO-AoHV-1” in Transiently Transfected Vero Cells
Vero cells were seeded in multiwell 96 plates with a seeding density of 1.25×104 cells/well. Cells were transfected 1 day post seeding with a pDualLuc-derived plasmid containing the Gaussia luciferase gene under control of 7xtetO-AoHV-1. Besides the Luciferase plasmid, cells were co-transfected with a plasmid encoding the tetracycline-controlled transactivator (tTA) protein, or with a negative control plasmid (pBluescript). Cell transfection was performed using Lipofectamine 3000 according to manufacturer's protocol (Life Technologies). Luciferase activity was measured at 24 hours post transfection using the Pierce Gaussia-Firefly Luciferase Dual Assay kit (Thermo Scientific) in a Luminoskan™ Ascent Microplate Luminometer. To control for transfection efficiency, the measured Gaussia Luciferase units were normalized to levels of Red Firefly luciferase (for which the expression cassette, driven by AoHV-1 short, was located on the same pDualLuc plasmid). Expression analysis in transiently transfected Vero cells was performed in Example 2.
Expression Analysis of Gaussia Luciferase Under Control of AoHV-1 Promoter Variants in Transiently Transfected PER.C6 Cells
PER.C6 cells were seeded in multiwell 96 plates with a seeding density of 5×104 cells/well. Cells were transfected 1 day post seeding using the pDualLuc plasmids containing the Gaussia luciferase gene under control of different AoHV-1 promoter variants, as described in Example 6. Cell transfection was performed using Lipofectamine 2000 CD according to manufacturer's protocol (Life Technologies). Luciferase activity was measured on cells lysed at 24 hours post transfection using the Pierce Gaussia-Firefly Luciferase Dual Assay kit (Thermo Scientific) and a Luminoskan™ Ascent Microplate Luminometer. To control for transfection efficiency, the measured Gaussia Luciferase units were normalized to levels of Red Firefly luciferase (for which the expression cassette, driven by AoHV-1 short, was located on the same pDualLuc plasmid). This methods section is applicable for Example 6.
PER.C6-hCMV.TetR and PER.C6-AoHV.TetR Cells
Two types of PER.C6 cells stably expressing TetR were generated and used herein. First, PER.C6-hCMV.TetR cells, which express TetR under control of a hCMV promoter, were generated by stable transfection of PER.C6 cells with plasmid pCDNA6/TR (Thermo Fisher Scientific Cat. No.: V102520) according to standard procedures described in the manufacturer's protocol.
Second, PER.C6-AoHV.TetR cells, which express TetR under control of the AoHV-1 short promoter, were generated by stable transfection of PER.C6 cells with plasmid pC_AoHV_TetR according to procedures described in Example 5 (and the methods section referred to therein).
Cell Clone Generation of PER.C6-hCMV.TetR Cells Expressing an Additional Gene of Interest Under Control of a TetR-Regulated AoHV-1 Short Promoter
PER.C6-hCMV.TetR cells were seeded 1 day before transfection in a T80 culture flask. The plasmid used for transfection carried a gene of interest (GOI) under control of the AoHV.2xtetO promoter (SEQ ID NO:7). Additionally it contains a neomycin phosphotransferase II gene expression cassette controlled by the SV40-derived promoter. The plasmid was constructed by replacement, via several cloning steps, of the hCMV promoter-containing MfeI-XbaI fragment of pcDNA2004Neo(−) (GenBank accession FB674876) by a fragment comprising AoHV.2xtetO followed by the coding sequence of the GOI. Transfection was done with Lipofectamin 2000 according to the manufacturer's protocol (Invitrogen). The day after transfection, the cells were subcultured and seeded 1:2, 1:4, 1:8 and 1:16 in 10-cm culture dishes. One day after seeding, the cell culture medium was replaced with PER.C6-hCMV.TetR medium supplemented with 0.5 mg/ml Geneticin (Gibco 10131-019). Medium was replaced 2× per week. Clones were picked 2-3 weeks post transfection. This methods section is applicable for Example 3.
Western Blot to Analyse Expression of a Gene of Interest
Seeded cells were incubated for 2 days with or without Doxycycline (1 μg/ml) and harvested in RIPA buffer (150 mM NaCl, 1% triton X100, 0.5% Doxycholate, 0.1% SDS 50 mM tris-HCL).
Samples were loaded on a 10% bis-tris gel (Invitrogen NP0301PK2) and run in MOPS buffer (Invitrogen NP0001). The SDS gel was blotted in a iBlot2 system (Invitrogen) and proteins were transferred to a nitrocellulose membrane (Invitrogen IB23001). The membrane was blocked overnight at 4° C. in blocking buffer (LI-COR 927-40000). The Western blot membrane was incubated with primary antibody (1:200 mouse polyclonal against Ad35 virus (in-house)) in blocking buffer for 2 hours and washed with TBST. Western blot was incubated with secondary antibody (1:5000 Goat anti-mouse-800CW) in blocking buffer for 1 hour and washed multiple times with TBST. Visualization was done on the LI-COR Odessey Imager. This methods section is applicable for Example 3.
Generation of Dual Luciferase Plasmid pDualLuc
pDualLuc (SEQ ID NO:21) is a plasmid carrying two expression cassettes: a first expression cassette expressing Gaussia luciferase (Gluc) under control of the human cytomegalovirus (hCMV) promoter, and a second cassette expressing red firefly luciferase (RFL) under control the AoHV-1 short promoter. Within pDualLuc, the Gluc and RFL expression cassettes are positioned in a tail-to-tail orientation relative to each other.
pDualLuc was generated by several gene synthesis and subcloning steps performed at GeneArt (Life Technologies). First, synthetic fragments “CMV_GLuc_SV” (SEQ ID NO:17) and “AoHV1_RFL_BGH” (SEQ ID NO:19), which carry the respective expression cassettes, were generated and cloned in a standard GeneArt plasmid (pMK-RQ). Subsequently, synthetic fragment AoHV1_RFL_BGH was further subcloned into the CMV_GLuc_SV-containing construct, using MluI and NsiI restriction sites.
The Gaussia luciferase-driving CMV promoter sequence of pDualLuc is flanked by unique restriction sites Xhol and HindIII, allowing for the replacement of this promoter by alternative promoter sequences, as was done herein in Examples 2 and 6.
Generation of Ad26 Vector Genome Plasmid pAd26.dE1.dE3.5orf6
pAd26.dE1.dE3.5orf6 is a plasmid containing a full-length Ad26 vector genome that carries an E1 deletion, an E3 deletion, and a replacement of Ad26 E4 orf6 by that of Ad5, as described for previously generated Ad26-based vectors (Abbink et al., 2007). The plasmid backbone of pAd26.dE1.dE3.5orf6 comprises a pMB1 origin of replication and an ampicillin resistance gene, and is derived from pBR322 (GenBank accession J01749.1). pAd26.dE1.dE3.5orf6 further contains a unique AsiSI restriction site in place of the E1 deletion of the vector genome, and a unique Pad restriction site in between the E4 region and the right inverted terminal repeat (RITR) of the vector genome. These sites can be used to insert transgene cassettes at the respective locations. Finally, the adenovirus vector genome within pAd26.dE1.dE3.5orf6 is flanked at each of its termini by a SwaI restriction site, allowing for its release from the plasmid backbone by SwaI digestion.
Construction of pAd26.dE1.dE3.5orf6 involved several synthesis and cloning steps. A 2-kb sequence (SEQ ID NO:16) containing a left-end and a right-end fragment of the (desired) Ad26 vector genome was synthesized at GeneArt/LifeTechnologies. The left-end vector genome fragment of this sequence spans from the left inverted terminal repeat (LITR) of the vector genome up to and including the SfiI site that corresponds to the SfiI site at positions 3755 to 3767 of the (wild type) Ad26 viral genome (GenBank accession EF153474.1). The right-end viral genome fragment spans from the NheI site corresponding to the NheI site at positions 34079 to 34084 of the wild type Ad26 viral genome up to and including the right ITR (RITR). The synthesized sequence was designed to carry the E1 deletion (from position 472 to 3365 of Ad26, GenBank accession EF153474.1) as well as the restriction sites mentioned above (i.e. the AsiSI site in place of E1 deletion, the Pad site between E4 and RITR, and the two SwaI sites directly flanking the vector genome sequences). The gene synthesis fragment further contained two outer restriction sites to facilitate cloning: an MfeI site was included at the left-end side, while an AseI site was included at the right-end side. The synthesized fragment was ligated, as an MfeI-AseI restriction fragment, into EcoRI- and NdeI-digested pBR322 (GenBank accession J01749.1) (thereby replacing the 2.3-kb, tetracyclin resistance gene-containing EcoRI-NdeI fragment of pBR322), leading to the abolishment of the restriction sites that had been digested to generate the respective ligation fragments. The resulting plasmid, carrying the left and right ends of the vector genome, was finally used to construct pAd26.dE1.dE3.5orf6 by two sequential cloning steps. First, a 12.7-kb SfiI-NheI Ad26 vector genome restriction fragment derived from of pWE.Ad26.dE3.5orf6 (Abbink et al., 2007) was ligated into the “left-end/right-end” plasmid digested by SfiI and NheI. Second, a 13.7-kb SfiI-SfiI Ad26 vector genome restriction fragment derived from pWE.Ad26.dE3.5orf6 was inserted into the SfiI site of the resultant partial vector genome plasmid.
Generation of Ad26 Vector Genome Plasmids pAd26.CMV_GLuc.AoHV1_RFL and pAd26.CMVtetO_GLuc.AoHV1_RFL
pAd26.CMV_GLuc.AoHV1_RFL is a plasmid containing the Ad26 vector genome of pAd26.dE1.dE3.5orf6 (see above), modified to carry two transgene expression cassettes: (1) a human cytomegalovirus (hCMV) promoter-driven Gaussia luciferase (Gluc) expression cassette inserted in the (deleted) E1 region, and (2) an AoHV-1 promoter-driven red firefly luciferase (RFL) expression cassette inserted in between E4 and the RITR.
pAd26.CMVtetO_GLuc.AoHV1_RFL is identical to pAd26.CMV_GLuc.AoHV1_RFL except that it additionally carries two tetracycline operator (tetO) sequences within the hCMV promoter of the GLuc expression cassette.
Construction of plasmids pAd26.CMV_GLuc.AoHV1_RFL and pAd26.CMVtetO_GLuc.AoHV1_RFL involved the generation of intermediate constructs carrying the required expression cassettes, followed by insertion of these cassettes into the Ad26 vector genome of pAd26.dE1.dE3.5orf6 by Gibson assembly (Gibson et al., 2009). Intermediate constructs carrying synthetic sequences “CMV_GLuc_SV” (SEQ ID NO:17), “CMVtetO_GLuc_SV” (SEQ ID NO:18), and “AoHV1_RFL_BGH” (SEQ ID NO:19) were generated at gene synthesis service provider GeneArt (LifeTechnologies). Sequence CMV_GLuc_SV contains an expression cassette for the expression of GLuc. It comprises a human cytomegalovirus (hCMV) promoter (SEQ ID NO:4), a Gluc coding sequence, and an SV40-derived polyadenylation signal sequence. Sequence CMVtetO_GLuc_SV differs from sequence CMV_GLuc_SV in that it carries, within its hCMV promoter-derived promoter, CMVtetO (SEQ ID NO:15), a 54-bp insertion containing two tetracycline operator (tetO) sequences. Sequence AoHV1_RFL_BGH contains an expression cassette for the expression of RFL. It comprises AoHV-1 short (SEQ ID NO:30), an RFL coding sequence, and a bovine growth hormone gene-derived polyadenylation signal sequence. Sequences CMV_GLuc_SV and CMVtetO_Gluc_SV were designed to additionally contain short flanking sequences corresponding to sequences directly flanking the AsiSI site of pAd26.dE1.dE3.5orf6. These flanking sequences allow for insertion of the concerning expression cassettes into the AsiSI site of pAd26.dE1.dE3.5orf6 (i.e. at the location of the E1 deletion of the Ad vector genome) by way of in vitro assembly (IVA) methods (as for instance described by Gibson et al. (Gibson et al., 2009). Similarly, sequence AoHV1_RFL_BGH contains flanking sequences that allow for the insertion of the concerning expression cassette into the PacI site of pAd26.dE1.dE3.5orf6 (i.e. in between the E4 region and the RITR of the vector genome) by IVA. All three sequences were further equipped with flanking outer restriction sites meant to release these sequences from their respective plasmid backbones (in which they are provided by the gene synthesis service supplier). pAd26.CMV_GLuc.AoHV1_RFL was constructed by performing a 4-fragment Gibson assembly reaction (New England Biolabs) between plasmid pAd26.dE1.dE3.5orf6, digested by both AsiSI and Pad, and synthesized sequences CMV_GLuc_SV and AoHV1_RFL_BGH, which were released from their respective plasmid backbones by digestion by, respectively, Pm1I and PshAI. pAd26.CMVtetO_GLuc.AoHV1_RFL was generated in the same way as pAd26.dE1.dE3.5orf6, but using synthesized sequence CMVtetO_GLuc_SV instead of CMV_Gluc_SV in the Gibson assembly reaction.
Primers for Analysis of Transgene Cassette Integrity
“E1 PCR” primer pair sequences:
“E4 PCR1” primer pair sequences:
“E4 PCR2” primer pair sequences:
The plasmids described in this sections are used in Example 4.
TetR-Expression Plasmid pC_AoHV_TetR
To construct pC_AoHV_TetR, a 1.3-Kbp DNA (SEQ ID NO:20) fragment comprising AoHV-1 short (SEQ ID NO:30) followed by a codon-optimized TetR-coding sequence was synthesized (at GeneArt/LifeTechnolgies) and subsequently subcloned into pcDNA2004Neo(−) (GenBank accession FB674876) using MfeI and XbaI restriction sites.
PER.C6-AoHV.TetR Cell Line Generation Procedures
PER.C6-AoHV.TetR stable cell lines were generated by standard cell line generation procedures. Briefly, serum-free grown, suspension-adapted PER.C6 cells (Fallaux et al., 1998) grown in CDM4 PerMAb medium (HyClone) supplemented with 4 mM L-Glutamine (Lonza) were transfected with plasmid pC_AoHV_TetR by electroporation using a BioRad electroporator. After recovery and antibiotic selection in “PerMab selection medium”, i.e. CDM4 PerMAb medium supplemented with 4 mM L-Glutamine and 125 ug/mL Geneticin (Gibco), the transfected cells were seeded for single cell cloning in MW96 plates at 1 viable cell per well in MAb medium (SAFC) supplemented with 4 mM L-Glutamine and 125 ug/mL Geneticin. Upon formation of cell colonies, isolated clones were expanded for several passages in static cultures in PerMAb selection medium. 100 clones were subsequently analyzed for ability to express TetR by a flow cytometry intracellular staining procedure using an anti-TetR antibody (Tet03, MoBiTec). In this first screen, 94 of the 100 tested clones were found to be TetR-positive. 47 of these TetR-positive clones were selected and, after adaptation to growth in Permexcis medium (Lonza) supplemented with 4 mM L-Glutamine and 125 ug/mL Geneticin, tested again for TetR expression by flow cytometry intracellular staining procedure, as well as for TetR activity by a TetR functionality assay (described in the methods section herein). 24 TetR-positive clones were then selected that displayed population doubling times of 30 hours or lower, and that represented a broad range of TetR activity levels. These clones, denoted PER.C6-AoHV.TetR clones #1 to #24, were (re-)adapted to growth in shaker flasks after which they were finally cryopreserved in small-scale research cell banks. This methods section is applicable for Example 5.
Stability of TetR Expression from PER.C6-AoHV.TetR Clones
Analysis of the stability of TetR expression by PER.C6-AoHV.TetR cell clones upon extended passaging. PER.C6-AoHV.TetR cell clones were grown in shaker flasks, with and without antibiotic selection, for multiple passages until approximately 60 population doublings (or generations) were reached. TetR expression was analyzed by flow cytometry intracellular staining at generations 20, 40, and 60. At each of these timepoints, cells of each clone were subjected to a flow cytometry intracellular double-staining protocol to detect both TetR and Tubulin. The staining was according to standard flow cytometry intracellular procedures and included two antibody incubation steps: a first with an anti-TetR mouse monoclonal antibody (Tet03, MoBiTec), and a second with an anti-mouse IgG-FITC conjugate (554001, BD Biosciences) in combination with an anti-Tubulin antibody-Alexa Fluor 647 conjugate (ab195884, Abcam). Per clone, the fractions of TetR-positive and -negative cells were determined within a stringent Tubulin-positive gate. This methods section is applicable for Example 5.
TetR Functionality Assay
The TetR functionality assay was performed after extended passaging of the PER.C6-AoHV.TetR cell clones. PER.C6-AoHV.TetR cell clones were grown in shaker flasks, with and without antibiotic selection, for multiple passages until approximately 60 population doublings (or generations) were reached. Then, PER.C6-AoHV.TetR cell clones and control PER.C6 cells were seeded in Poly-L-Lysine-coated multiwell 96 plates in Permexcis medium supplemented with 4 mM L-Glutamine, and, after 2 hours of incubation, infected in quadruplicates by the vectors Ad26.CMV_GLuc.AoHV1_RFL and Ad26.CMVtetO_GLuc.AoHV1_RFL (described in Example 4). At one day post infection, the infected cells were harvested in Luciferase Cell Lysis Buffer (Pierce/Thermo Scientific). Using separate aliquots of each cell lysate, GLuc and RFL activities were subsequently measured according the manufacturers' instructions using, respectively, BioLux Gaussia Luciferase Assay Kit (NEB) and Luciferase Glow Assay Kit (Pierce/Thermo Scientific) reagents, and the Luminoskan Ascent Microplate Luminometer (Thermo Scientific). Per infection replicate, Gluc activity was normalized by RFL activity. This methods section is applicable for Example 5.
Often, promoters derived from viruses or animal/human genomes are used for heterologous protein expression, e.g. in expression cassettes in plasmid vectors or viral vectors for expressing a gene of interest in cells or a host organism. A promoter commonly used for this purpose is a promoter derived from the immediate early region of human cytomegalovirus (hCMV) (Powell et al., 2015). Several cytomegaloviruses (CMVs) that infect other hosts are also known. They infect, for example, rhesus monkeys (rhCMV) (Barry, Alcendor, Power, Kerr, & Luciw, 1996; Chan, Chiou, Huang, & Hayward, 1996; Chang et al., 1993; Hansen, Strelow, Franchi, Anders, & Wong, 2003), and chimpanzees (chCMV) (Chan et al. 1996).
In order to identify a promoter that is preferably potent and short and also has low sequence identity with the commonly used hCMV promoter, several putative promoter sequences were identified and tested. Several putative promoters that we tested and that were derived from herpesviruses more distantly related to hCMV showed very low or no promoter activity at all. For some other promoters derived from different CMV species and that were known to be potent promoters, we confirmed promoter activity, but unfortunately such promoters often display one of the following disadvantages: either they are characterized by larger size due to e.g. inclusion of enhancer and intron sequences and/or they display considerable homology to the hCMV promoter sequence.
The aotine herpesvirus 1 (AoHV-1) is tentatively classified as a cytomegalovirus. Interestingly, while the complete genome sequence of the AoHV-1 is published and the open reading frames (ORFs) are annotated in the sequence, no major immediate early promoter has been described so far. We tested two different designs of differing length of a region of the AoHV-1 genome, and called the respective putative promoter sequences AoHV-1 long and AoHV-1 short. Based on results described below, where we demonstrate promoter activity for these sequences, we refer to these and their derivatives as the AoHV-1 major immediate early promoter, or briefly to AoHV-1 promoter.
In order to test the identified putative promoter sequences for potency of heterologous gene expression, we had the putative promoter sequences synthesized at GeneArt LifeTechnologies and subcloned into pAdapt35.Luc plasmids via AvrII and HindIII restriction sites upstream of the Firefly Luciferase reporter gene. Firefly luciferase levels were measured in transfected HEK293 cells 24 h post transfection and compared to the Firefly luciferase expression induced by the hCMV promoter (SEQ ID NO:4).
Selecting from a panel of possible promoters, we chose some potent promoters (data not shown), of which chCMV short and AoHV-1 short would be preferred due to their very small size and potency. Results of potency testing for selected promoter AoHV-1 short (SEQ ID NO:1), AoHV-1 long (SEQ ID NO:2), chCMV short (SEQ ID NO:3) and hCMV promoter are shown in
However, as shown in
In conclusion, the AoHV-1 short promoter is preferred because it showed very good potency, in the range of the gold standard hCMV, while at the same time having a very short sequence (484 bp) and low sequence identity with the hCMV promoter.
Inducible expression of genes can have high applicability in the field of biotechnology, in particular for the transient expression of toxic gene products. Certain well-established systems for heterologous gene regulation in mammalian cells make use of artificial promoters consisting of multiple copies of the Tet operator (TetO) sequence linked to the hCMV core promoter (Gossen & Bujard, 1992; Gossen et al., 1995). In these systems, said artificial promoters, which display no or very low basal transcriptional activity, can become activated by the specific binding to their TetO sequences of certain recombinant transcription factors known as the tetracycline-controlled transactivator protein (tTA) or the reverse tetracycline-controlled transactivator protein (rtTA). Here we tested whether a similar such tTA/rtTA-responsive artificial promoter could be generated using, instead of the hCMV core promoter, a sequence element of the AoHV-1 promoter.
To this end, a promoter was constructed where only the putative minimal (core) AoHV-1 promoter was placed immediately downstream of seven Tet operators (7xTetO-AoHV-1, SEQ ID NO:5). The promoter sequence was synthesized at GeneArt LifeTechnologies and subcloned into plasmid pDualLuc, described in the Methods section herein, via Xhol and HindIII restriction sites, thereby replacing the CMV promoter controlling the Gaussia Luciferase reporter gene of this plasmid. Gaussia luciferase levels were measured in transfected Vero cells 24 h post transfection and compared to the Gaussia luciferase expression by the same promoter in the presence of the transactivator protein tTA. Expression data was normalized for transfection efficiency via measurement of Red Firefly Luciferase (RFL) under control of AoHV-1 short promoter, for which the expression cassette was located on the same pDualLuc plasmid.
In conclusion, a putative core promoter-comprising sequence derived from the AoHV-1 promoter can be used to construct an artificial promoter that is responsive to a tetracycline-controlled transactivator protein. Application of this sequence in this context proved to allow for tightly controlled regulation of the expression of a gene of interest. Said sequence therefore represents a true “core promoter” as defined herein as having very low promoter activity on its own, but being able to drive potent gene expression when combined with other regulatory sequences, such as binding sites for natural or artificial transcription factors.
As mentioned in example 2, regulated expression of for instance a toxic gene of interest in a cell line can be essential for recombinant production of proteins or viral vectors. In case a viral vector is used that already contains an expression cassette with an hCMV promoter, it is desirable to use a strong promoter with a different sequence for expression of a gene of interest (GOI) in the production cell line. In order to identify an alternative to the hCMV promoter, AoHV-1 short promoter and the human phosphoglycerate kinase 1 (hPGK) promoter (another promoter described for use in biotechnology expression systems) were tested for transient expression of eGFP in PER.C6 cells. In line with results of example 1, the AoHV-1 short promoter again showed to be a potent promoter for expression of a heterologous gene, driving eGFP expression levels similar to hCMV (of SEQ ID NO:4), and much higher than by the hPGK promoter (SEQ ID NO:6) (
In the following, the AoHV-1 short promoter, which is normally constitutively active (see example 1 and first part of this example), was designed as a tetracycline repressor protein (TetR)-regulated promoter by insertion of two Tet operators downstream of the TATA box and upstream of the transcription start site (TSS) of the AoHV-1 short promoter (AoHV.2xtetO, SEQ ID NO:7). This design was previously shown to work for the hCMV promoter (e.g. see WO 1999/000510 A1). The promoter is active in cells that do not express TetR. In this design, promoter activity is repressed in presence of TetR, e.g. in cell lines expressing TetR. The repression can be alleviated by addition of Doxycyclin (Dox) which has a high affinity for TetR protein.
To establish stable cell clones displaying TetR-regulated expression of a gene of interest, PER.C6-hCMV.TetR cells, which express TetR under control of a hCMV promoter, were transfected with a plasmid expressing the gene of interest under control of AoHV.2xtetO. Eighty-five clones were selected using antibiotic selection media. Two clones were selected for testing of inducible expression of the gene of interest (GOI) in this experiment.
An alternative bacterial repressor-regulated promoter in which the cumate operator sequence (CuO) was placed directly downstream of the (putative) initiator element of the AoHV-1 short promoter was also designed and tested, and also proved to be functional (data not shown). In this promoter design, the CymR repressor protein can bind the CuO sequences and thereby inhibit expression.
In addition, analogous to the described TetR- and CymR-regulated AoHV1-promoter-based systems, a Lac operator (LacO)-containing AoHV-1 short promoter was generated and proved to be strongly repressible by the Lac repressor (LacR) (data not shown).
In conclusion, this example confirms the high potency of AoHV-1 short promoter in comparison to other commonly used promoters for heterologous gene expression. Furthermore, TetR-, CymR-, and LacR-regulated versions of the AoHV-1 promoter were generated that allow for regulated expression of GOIs in mammalian cells. This can for instance be used for expression of proteins that are toxic for the cell or for expression of proteins that lead to instability of the cells or vectors.
The AoHV-1 short promoter (AoHV-1 short) can be applied in viral vectors to drive the expression of vaccine antigens or other proteins of interest. This is illustrated herein by the application of AoHV-1 short in the context of adenoviral vectors Ad26.CMV_GLuc.AoHV1_RFL and Ad26.CMVtetO_GLuc.AoHV1_RFL. These are two Ad26-based recombinant adenoviral vectors that both carry two expression cassettes, a first cassette encoding Gaussia Luciferase (GLuc) inserted in place of the (deleted) E1 region, and a second cassette encoding red firefly luciferase (RFL) located in between the E4 region and the right inverted terminal repeat (RITR). The Gluc expression cassettes of the two viruses are driven by the hCMV promoter (SEQ ID NO:4) and CMVtetO (SEQ ID NO:15), respectively. CMVtetO differs from the hCMV promoter in that it carries an insertion of a sequence containing two tetracycline operator (TetO) sequence motifs, making that this promoter is repressible by the tetracycline repressor (TetR) protein. In both viruses the RFL expression cassette is under control of AoHV-1 short (SEQ ID NO:30). See
The above two vectors were generated by transfection of full-genome plasmids pAd26.CMV_GLuc.AoHV1_RFL and pAd26.CMVtetO_GLuc.AoHV1_RFL, described in the Methods section herein, into PER.C6 cells. These transfections were performed according to standard procedures using Lipofectamine 2000 transfection reagent (Invitrogen) and 4 ug of SwaI-digested plasmid DNA per transfection in a T25 tissue culture flask seeded with 3×106 PER.C6 cells per flask the day before. (The SwaI digestion serves to release the adenoviral vector genome from the plasmid backbone). After harvesting of the viral rescue transfections, the viruses were further amplified by several successive infection rounds on PER.C6 cells until large-scale virus production infections were performed at viral passage number (VPN) 5 after transfection. The viruses were purified from crude viral harvests using a two-step cesium chloride (CsCl) density gradient ultracentrifugation procedure as described before (Havenga et al., 2006). Viruses were quantified by a spectrophotometry-based procedure to determine the viral particle (VP) titer, and by a TCID50 assay to determine the infectious unit (IU) titer, in both cases as described previously (Maize′, White, & Scharff, 1968).
VP and IU quantification results for the purified batches of Ad26.CMV_GLuc.AoHV1_RFL and Ad26.CMVtetO_GLuc.AoHV1_RFL are shown in Table 1. The viral yields as well as the VP-to-IU ratios obtained for the two batches are in the same range of those that are routinely obtained for standard, single transgene expression cassette-containing Ad26-based vectors. For example, the VP-to-IU ratios obtained for the batches of Ad26.CMV_GLuc.AoHV1_RFL and Ad26.CMVtetO_GLuc.AoHV1_RFL, i.e. 23 and 14, both fall within the range of VP-to-IU ratios of 18, 11, 24, 10, 12, and 26 that were reported previously for a panel of Ad26-based vectors with different (single) transgene expression cassettes (Zahn et al., 2012).
It has been previously reported that use of two identical promoters for expression of two transgenes from the E1 region of an adenovirus can give rise to genetic instability, presumably by homologous recombination (see, e.g. (Belousova et al., 2006) and example 2 of WO2016166088A1). To check whether this can be solved by using a combination of the AoHV-1 promoter of the invention in the same system as the hCMV promoter in the E1 and E4_rITR position respectively, we tested transgene cassette integrity for this combination. Transgene (TG) cassette integrity was confirmed for the two purified batches of Ad26.CMV_GLuc.AoHV1_RFL and Ad26.CMVtetO_GLuc.AoHV1_RFL by PCR-based amplification followed by sequencing of the transgene cassette insertion regions (
Finally, the Ad26.CMV_GLuc.AoHV1_RFL and Ad26.CMVtetO_GLuc.AoHV1_RFL purified batches were tested for their abilities to express the two luciferases that they encode. To this end, the human cell line A549 was infected at different multiplicities of infections by the two viruses, and GLuc and RFL activities were detected in samples harvested two days later. The results show that both vectors were able to express both GLuc and RFL (
In conclusion, AoHV-1 short can be applied as a promoter to drive the expression of a protein of interest from transgene expression cassettes inserted in a viral vector. This is exemplified above where AoHV-1 short was employed to express RFL in the context of two adenoviral vectors each comprising two separate transgene expression cassettes inserted at different locations within the adenoviral vector genome. These adenoviral vectors were readily generated and proved producible to high-titer purified vector batches displaying good VP-to-IU ratios and harboring genetically and functionally intact transgene expression cassettes.
The AoHV-1 promoter can be applied to drive the expression of heterologous genes in stable cell lines. This is illustrated herein by the generation of TetR-expressing cell lines using pC_AoHV_TetR, a plasmid in which TetR gene expression is driven by the AoHV-1 promoter.
pC_AoHV_TetR is depicted in
As further detailed in the Methods section herein under “PER.C6-AoHV.TetR cell line generation procedures”, pC_AoHV_TetR was employed for stable transfections into human cell line PER.C6. This resulted, after single cell cloning, in the efficient generation of multiple TetR-expressing “PER.C6-AoHV.TetR” cell clones. It was found that 94 out of the 100 tested Geneticin-resistant clones were positive for TetR expression in a first screening step based on a flow cytometry intracellular staining protocol to detect TetR (data not shown). After a second screening step on 47 of these TetR-positive clones (data not shown), a selection of 24 clones was cryopreserved in small-scale research cell banks.
Twelve of the cryopreserved PER.C6-AoHV.TetR clones were subjected to further evaluation of their post-thaw growth performance in shaker flasks and their ability to express (functional) TetR upon extended passaging (up to 60 populations doublings), both in the presence and in the absence of Geneticin selection. It was found that all clones grew at least as efficient, and with similar viabilities, as the parental suspension PER.C6 control cell line (data not shown). Analysis of TetR expression by flow cytometry intracellular staining further demonstrated that the TetR-positive cell fraction remained high (i.e. 97% or higher) throughout the extended passaging experiment. This is shown in
In conclusion, stable sPER.C6-AoHV.TetR cell lines in which TetR expression is driven by the AoHV1 promoter were successfully generated. This is one, non-limiting, example of the stable expression of a protein of interest after integration of a transgene operably linked to the AoHV-1 promoter according to the invention into the genome of a host cell.
In order to map the essential parts of the AoHV-1 major immediate early regulatory region for expression of heterologous genes, a panel of different versions of the AoHV-1 promoter was made. The different designs are presented in
Tested promoter versions are named version v00-v09 and are listed below:
v00: SEQ ID NO:30 (with native AvrII site)
v01: SEQ ID NO:22
v02: SEQ ID NO:23
v03: SEQ ID NO:24
v04: SEQ ID NO:25
v05: SEQ ID NO:26
v06: SEQ ID NO:1 (AvrII site eliminated with single nucleotide insertion of cytosine (c) at nucleotide position 360)
v07: SEQ ID NO:27
v08: SEQ ID NO:28
v09: SEQ ID NO:29
Promoter activity was tested using transient transfection of plasmids into PER.C6 cells. The different promoter versions drive expression of Gaussia luciferase in the pDualLuc plasmid described in the methods section herein.
Interestingly, the truncated version 04 shows promoter activity comparable to AoHV-1 short (version 00 and 06). This version 04 has a length of only 371 nucleotides. In contrast, the further truncated version 05 with a length of 241 nucleotides shows reduced activity compared to AoHV-1 short, which may be explained by the absence of several predicted cellular factor binding sites. This promoter version 05 can still be considered a potent promoter. The activity of the promoter is expected to decrease gradually with further truncations.
The potencies of most other promoter versions, which all contain extensions compared to AoHV-1 short promoter, are in the range of AoHV-1 short promoter. Of these extended AoHV-1 promoter variants only v03 (data not shown) shows a major drop in promoter activity compared to AoHV-1 short, but this may be explained by the presence of an incomplete intron sequence in v03: while v03 carries within its extension a predicted splice donor site it lacks any of the predicted splice acceptor sites located further downstream. By contrast, extended AoHV-1 promoter variants v07, v08 and v09, which each do carry at least one predicted splice acceptor site downstream of (any of) their predicted splice donor sites, each showed expression in the range of AoHV-1 short promoter. Sequence v09 is a deletion mutant of v07; compared to v07, v09 carries an internal deletion that leaves intact certain predicted splice donor and acceptor sequences. The data show that v09 is an example of a short but potent AoHV-1 promoter variant harbouring a predicted intron. It can be envisioned that a similarly short but potent, intron-containing promoter can be generated by applying a similar deletion (as said internal deletion applied to v07) to AoHV-1 promoter variant v08.
Two additional AoHV-1 promoter sequences, SEQ ID NO: 33 and SEQ ID NO: 34, were also designed and tested for the ability to drive the expression of a gene of interest. Compared to AoHV-1 short (i.e. SEQ ID NO: 30), these two sequences each carry an 84-bp long 3′ truncation and, furthermore, respectively carry 2 and 7 single-nucleotide substitutions within their AoHV-1 promoter core region. Due to said 3′ truncation, both SEQ ID NO: 33 and SEQ ID NO: 34 comprise only 1 AoHV-1 nucleotide downstream of the putative initiator sequence of the AoHV-1 promoter.
SEQ ID NO: 33 was operably linked to a TetR-encoding sequence by inserting it as part of a synthesized gene fragment into plasmid pC_AoHV_TetR (described in the Methods section herein), replacing the AoHV-1 short promoter of that plasmid. Transient transfections into PER.C6 cells followed by immunoblotting of cell lysates using anti-TetR monoclonal antibody (TetR03, MoBiTec) subsequently demonstrated that promoter activity of SEQ ID NO:33 was similar to that of AoHV-1 short (data not shown).
SEQ ID NO: 34 was operably linked to an RFL-encoding sequence by cloning of a synthesized gene fragment into pDualLuc (described in the Methods section herein) using AvrII and AscI restriction sites. Transient transfection experiments into PER.C6 cells followed by RFL activity measurement in cell lysates subsequently demonstrated that SEQ ID NO:34 is a functional promoter sequence (data not shown).
The activity of these promoter variants demonstrates that for promoter activity, it is not required to include AoHV-1 sequences downstream of the first nucleotide 3′ of the putative Inr (i.e., nucleotide 399 in SEQ ID NO: 30, corresponds to nucleotide 287 in SEQ ID NO: 25).
As described supra, a short and potent promoter was identified from Aotine herpesvirus-1. The AoHV-1 promoter has a short sequence and it has potency that is comparable to the hCMV promoter. These features make the AoHV-1 promoter an ideal promoter to use as a substitute in any situation where the hCMV promoter is used. Furthermore, the AoHV-1 promoter has comparatively low sequence identity with the hCMV promoter, which makes it suitable for use in combination with the hCMV promoter when expressing two different transgenes from the same viral vector or when generating viruses with producer cell lines that may also contain similar sequences. The AoHV-1 promoter is also suitable for use with regulatory sequences that can be used to modulate transcription from the AoHV-1 promoter.
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| Number | Date | Country | |
|---|---|---|---|
| 20180223314 A1 | Aug 2018 | US |
