Classifications

• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
  • A01K67/00—Rearing or breeding animals, not otherwise provided for; New or modified breeds of animals
  • A01K67/027—New or modified breeds of vertebrates
  • A01K67/0275—Genetically modified vertebrates, e.g. transgenic
  • A01K67/0278—Knock-in vertebrates, e.g. humanised vertebrates
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
  • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
  • C07K14/52—Cytokines; Lymphokines; Interferons
  • C07K14/54—Interleukins [IL]
  • C07K14/5418—IL-7
• • C—CHEMISTRY; METALLURGY
  • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
  • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
  • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
  • C12N15/09—Recombinant DNA-technology
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
  • A01K2207/00—Modified animals
  • A01K2207/15—Humanized animals
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
  • A01K2217/00—Genetically modified animals
  • A01K2217/05—Animals comprising random inserted nucleic acids (transgenic)
  • A01K2217/052—Animals comprising random inserted nucleic acids (transgenic) inducing gain of function
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
  • A01K2217/00—Genetically modified animals
  • A01K2217/07—Animals genetically altered by homologous recombination
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
  • A01K2217/00—Genetically modified animals
  • A01K2217/07—Animals genetically altered by homologous recombination
  • A01K2217/072—Animals genetically altered by homologous recombination maintaining or altering function, i.e. knock in
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
  • A01K2227/00—Animals characterised by species
  • A01K2227/10—Mammal
  • A01K2227/105—Murine
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
  • A01K2267/00—Animals characterised by purpose
  • A01K2267/01—Animal expressing industrially exogenous proteins
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
  • A01K2267/00—Animals characterised by purpose
  • A01K2267/03—Animal model, e.g. for test or diseases
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
  • A01K2267/00—Animals characterised by purpose
  • A01K2267/03—Animal model, e.g. for test or diseases
  • A01K2267/0331—Animal model for proliferative diseases
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
  • A01K2267/00—Animals characterised by purpose
  • A01K2267/03—Animal model, e.g. for test or diseases
  • A01K2267/035—Animal model for multifactorial diseases
  • A01K2267/0387—Animal model for diseases of the immune system
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
  • A01K2267/00—Animals characterised by purpose
  • A01K2267/03—Animal model, e.g. for test or diseases
  • A01K2267/0393—Animal model comprising a reporter system for screening tests

Definitions

• Non-human animals e.g., mammals, e.g., rodents such as mice, rats, and hamsters
• a genetic modification comprising a replacement, at an endogenous locus, of a non- human IL-7 gene sequence with a human IL-7 gene sequence.
• Transgenic mice that have randomly inserted transgenes that contain a human IL-7 sequence are known in the art. However, most if not all of these transgenic mice are not optimal in one aspect or another. For example, most mice transgenic for human IL-7 exhibit abnormal levels and/or ratios of certain cells, including T cells, that are likely due to a dysregulation of immune cell development, e.g., T cell development.
• non-human animals that comprise human IL-7- encoding sequences, wherein the human IL-7 encoding sequences are at an endogenous non- human IL-7 locus, and for non-human animals that express human IL-7 under the control of endogenous non-human regulatory elements.
• non-human animals that express a human IL-7 wherein the non-human animals lack a significant abnormality in peripheral T cells, and/or in ratios of T cell subtypes.
• Non-human animals, cells, tissues, and nucleic acids comprise a human IL-7 genomic sequence at an endogenous non-human IL-7 locus.
• the non-human animals express a humanized IL-7 protein from a modified locus regulated by one or more endogenous non-human regulatory sequences of the modified endogenous IL-7 locus.
• the non-human animals are rodents, e.g., mice, rats, hamsters, etc.
• the rodent is a mouse or a rat.
• the non-human animals comprise a modified IL-7 gene in the germline of the non-human animal at a modified endogenous IL-7 locus, wherein the modified endogenous IL-7 locus comprises a humanization of at least a portion of the endogenous IL-7 gene.
• the mice are heterozygous or homozygous with respect to the modified IL-7 locus.
• a non-human animal is provided that comprises a lack of a first endogenous IL-7 allele and a humanization of a second endogenous IL-7 allele.
• the humanization is of one or more exons and/or introns.
• non-human animals having a modified IL-7 locus wherein one or both of an endogenous non-human 5 '-untranslated region and an endogenous non-human 3 '-untranslated region are retained in the modified animal.
• non-human animals of the present invention comprise a 5 '-untranslated region contained within SEQ ID NO: 1 In some aspects, non-human animals of the present invention comprise a 3 '-untranslated region contained within SEQ ID NO: 2. In some embodiments, non-human animals of the present invention comprises a 5 '-untranslated region contained within SEQ ID NO: 1 and a 3 '-untranslated region contained within SEQ ID NO: 2.
• non-human animals of the present invention comprise a 5 '-untranslated region that is SEQ ID NO: 1 In some aspects, non-human animals of the present invention comprise a 3 '-untranslated region that is SEQ ID NO: 2. In some aspects, non-human animals of the present invention comprise a 5 '-untranslated region that is SEQ ID NO: 1 and a 3'- untranslated region that is SEQ ID NO: 2.
• a humanized IL-7 gene of the present invention has a sequence that is at least 50% (e.g., 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more) identical to a continuous sequence comprising exons 2-6 of a human IL-7 gene.
• a human IL-7 gene of the present invention comprises SEQ ID NO: 3.
• a humanized IL-7 gene of the present invention has a sequence that reflects a humanization as set forth in Figure 1.
• a genetically modified rodent comprises a replacement at an endogenous rodent IL-7 locus of an endogenous rodent IL-7 genomic sequence with a human IL-7 genomic sequence.
• the genetically modified rodent comprises a first rodent regulatory sequence upstream (with respect to the direction of transcription of the IL-7 gene) of the human IL-7 genomic sequence and a second rodent regulatory sequence downstream of the human IL-7 genomic sequence.
• the first rodent regulatory sequence comprises a rodent promoter and/or enhancer
• the second rodent regulatory sequence comprises a 3'-UTR.
• the rodent is a mouse and comprises an endogenous mouse
• the endogenous mouse IL-7 gene locus having a mouse exon 1 and human exons 2, 3, 4, 5, and 6.
• the endogenous mouse IL-7 gene locus comprises, from upstream to downstream with respect to the direction of transcription, mouse exon 1, at least a portion of a first mouse intron, and a contiguous human genomic fragment comprising human exon 2 through human exon 6.
• the mouse further comprises a contiguous sequence of endogenous mouse DNA comprising an complete endogenous mouse IL-7 upstream (with respect to the direction of transcription of the IL-7 gene) promoter and regulatory region, wherein the contiguous mouse DNA is upstream of the human genomic fragment; and further comprises a contiguous sequence of endogenous mouse DNA 3'-UTR downstream of the human genomic fragment.
• the mouse comprises a mouse sequence that is at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% identical with a sequence selected from SEQ ID NO: 1, SEQ ID NO:2, and a combination thereof.
• the mouse comprises a mouse sequence selected from SEQ ID NO: l and SEQ ID NO:2.
• a genetically modified mouse comprises a replacement at an endogenous mouse IL-7 locus of an endogenous mouse IL-7 genomic sequence with a human IL-7 genomic sequence to form a modified locus, wherein the human IL-7 genomic sequence comprises at least one human exon, and the modified locus comprises a mouse sequence selected from a sequence of SEQ ID NO: l, SEQ ID NO:2, and a combination thereof.
• the replacement comprises a human genomic fragment comprising exons 2 through 6, and the human genomic fragment is linked to mouse exon 1 to form a modified endogenous mouse IL-7 locus, wherein the modified mouse IL-7 locus comprises a mouse sequence selected from SEQ ID NO: l, SEQ ID NO:2, and a combination thereof.
• a genetically modified rodent comprising an IL-7 gene that comprises a rodent exon 1 and at least a portion of a rodent intron 1 , and a human IL-7 gene sequence of human IL-7 exons 2, 3, 4, 5, and 6, wherein the rodent comprises a sequence selected from a rodent upstream IL-7 regulatory sequence, a rodent IL-7 3'-UTR, and a combination thereof.
• a genetically modified mouse comprising a sequence selected from SEQ ID NO: 1, SEQ ID NO:2, and a combination thereof; wherein the mouse lacks an endogenous sequence encoding exons 2 through 5 of a mouse IL-7 protein, and the mouse comprises a nucleic acid sequence at an endogenous mouse IL-7 locus wherein the nucleic acid sequence encodes human IL-7 exons 2, 3, 4, 5, and 6.
• a genetically modified rodent that expresses a human or humanized IL-7 protein from an endogenous rodent IL-7 locus that is modified to express at least one human IL-7 exon.
• the rodent IL-7 locus is modified to express a human or humanized IL-7 protein encoded by a sequence comprising at least two human IL-7 exons.
• the rodent IL-7 locus is modified to express a human or humanized IL-7 protein encoded by a sequence comprising at least three human IL-7 exons.
• the rodent IL-7 locus is modified to express a human or humanized IL-7 protein encoded by a sequence comprising at least human IL-7 exons 2, 3, 4, 5, and 6 (i.e., 2 through 6). In one embodiment, the rodent IL-7 locus is modified to express a human IL-7 protein. In some certain aspects, the rodent IL-7 locus is modified to express a human IL-7 protein whose sequence reflects a protein encoded by a locus as shown in Figure 1. In some certain aspects, the rodent IL-7 locus is modified to express a human IL-7 protein comprising a sequence encoded by exons 2-6 of a human IL-7 gene. In some certain aspects, the rodent IL-7 locus is modified to express a human IL-7 protein comprising a sequence encoded by exons 2-6 of a human IL-7 gene as set forth in SEQ ID NO: 3.
• a genetically modified rodent that expresses a human or humanized IL-7 protein from an endogenous rodent IL-7 locus that is modified to comprise at least human IL-7 exons 2 through 6 in place of rodent IL-7 exons 2 through 5.
• a genetically modified rodent that expresses a human or humanized IL-7 protein from a humanized endogenous rodent IL-7 locus comprising a humanized endogenous rodent IL-7 coding region, wherein the humanized endogenous rodent IL-7 locus comprises all endogenous rodent regulatory elements that are present in a wild-type rodent upstream of a wild-type rodent IL-7 coding region and that are downstream of the wild- type rodent IL-7 coding region.
• a genetically modified rodent that expresses a human or humanized IL-7 protein from a humanized rodent IL-7 locus that comprises rodent regulatory regions upstream and downstream of a nucleic acid sequence encoding the human or humanized IL-7 protein, wherein the human or humanized IL-7 protein is expressed in an expression pattern that is about the same as the expression pattern of a rodent IL-7 protein in a wild-type rodent.
• the level of serum expression of the human or humanized IL-7 is about the same as the level of serum expression of a rodent IL-7 protein in a wild-type rodent.
• a genetically modified rodent that expresses a humanized IL-7 protein, wherein the lymphocyte population of the rodent is characterized by its B cell population that is about the same in number as a population of B cells in an age-matched wild-type mouse.
• the modified rodent is characterized by a population of mature B cells that is about the same in number as a population of mature B cells in an age- matched wild-type mouse.
• the humanized IL-7 protein is identical to a human IL-7 protein.
• the humanized IL-7 protein comprises human sequence encoded by at least exons 2 through 6 of a human IL-7 gene.
• a genetically modified rodent that expresses a humanized IL-7 protein, wherein the lymphocyte population of the rodent is characterized by a population of T cells that is about the same in number as a population of T cells in an age- matched wild-type mouse.
• the modified rodent exhibits a population of mature T cells that is about the same in number as a population of mature T cells in an age- matched wild-type mouse.
• the modified rodent exhibits a population of peripheral T cells that is about the same in number as the population of peripheral T cells in an age-matched wild-type mouse.
• the humanized IL-7 protein is identical to a human IL-7 protein.
• the humanized IL-7 protein comprises human sequence encoded by at least exons 2 through 6 of a human IL-7 gene.
• a genetically modified rodent that expresses a humanized IL-7 protein, wherein the lymphocyte population of the rodent is characterized by a T cell population that exhibits a CD4:CD8 ratio that is about the same as the CD4:CD8 ratio in the T cell population of an age-matched wild-type mouse.
• the humanized IL-7 protein is identical to a human IL-7 protein.
• the humanized IL-7 protein comprises human sequence encoded by at least exons 2 through 6 of a human IL-7 gene.
• a genetically modified rodent that expresses a humanized IL-7 protein, wherein the rodent comprises a characteristic selected from a lack of a propensity to develop a chronic colitis; lack of over-expression of IL-7 in colonic mucosal lymphocytes; normal, or wild-type, expression of IL-7 in colonic mucosal lymphocytes; lacks a severe dermatitis; lacks a dermatitis characterized by a massive dermal infiltration of mononuclear cells; exhibits a CD4:CD8 ratio in its T cell population that is about the same as the CD4:CD8 ratio of an age-matched wild-type mouse; exhibits an expression pattern of human IL-7 that is about the same as an expression pattern of mouse IL-7 in a wild-type mouse; and a combination thereof.
• a genetically modified rodent that expresses a humanized IL-7 protein, wherein the rodent lacks a propensity to develop a chronic colitis.
• a genetically modified rodent that expresses a humanized IL-7 protein, wherein the rodent does not exhibit over-expression of IL-7 in colonic mucosal lymphocytes.
• a genetically modified rodent that expresses a humanize IL-7 protein, wherein the rodent does not exhibit a dermatitis characterized by a massive dermal infiltration of mononuclear cells.
• a genetically modified rodent that expresses a humanized IL-7 protein, wherein the rodent does not exhibit a lymphoproliferation into dermis.
• a genetically modified rodent that expresses a humanized IL-7 protein, wherein the rodent does not exhibit B and/or T cell lymphomas at a higher frequency than an age-matched wild-type mouse.
• a genetically modified mouse that expresses a humanized IL-7 protein, or a human IL-7 protein, wherein the mouse is no more prone than a wild-type mouse to developing a pathology selected from colitis, chronic colitis, severe dermatitis, pathological and/or massive infiltration of the dermis by mononuclear cells, lympoproliferation of the dermis, B cell lymphomas, T cell lymphomas, reduction in the number of mature B and/or T cells, reduction in the number of peripheral B and/or T cells, abnormal numbers of CD4+ T cells, abnormal numbers of CD8+ T cells, and a combination thereof.
• a pathology selected from colitis, chronic colitis, severe dermatitis, pathological and/or massive infiltration of the dermis by mononuclear cells, lympoproliferation of the dermis, B cell lymphomas, T cell lymphomas, reduction in the number of mature B and/or T cells, reduction in the number of peripheral B and/or T cells,
• a genetically modified mouse that expresses a human IL-7 protein whose sequence reflects a replacement of a mouse IL-7 gene sequence with a human IL-7 gene sequence, wherein the human IL-7 gene sequence comprises exons 2-6 of a human IL-7 gene.
• the replacement is of a sequence comprising exons 2-5 of a mouse IL-7 gene.
• a human IL-7 gene comprises SEQ ID NO: 3.
• expression of the human IL-7 protein is under the control of mouse regulatory elements.
• a genetically modified mouse that does not detectably express a mouse IL-7 protein.
• the genome of a mouse as described herein comprises a deletion in whole or in part of a mouse IL-7 gene.
• the genome of a mouse as described herein comprises a deletion of an endogenous IL-7 gene sequence corresponding to exons 2-5.
• a genetically modified non-human animal comprising, in its germline, a replacement of at least one non-human IL-7 exon with at least one human IL-7 exon to form a human or humanized IL-7-encoding gene, wherein the replacement is at an endogenous non-human IL-7 locus, wherein the human or humanized IL-7-encoding gene is under control of endogenous non-human regulatory elements.
• the genetically modified non-human animal is a rodent.
• the rodent is selected from a rat and a mouse.
• the human or humanized IL-7-encoding gene comprises human exons selected from the group consisting of human exon 1, human exon 2, human exon 3, human exon 4, human exon 5, human exon 6, and a combination thereof. In one embodiment, the human or humanized IL-7-enconding gene comprises no more than five human exons.
• the genetically modified non-human animal is a rodent that is a mouse and the modified locus comprises a replacement of mouse exons 2, 3, 4, and 5 with a human genomic segment comprising human IL-7 exons 2, 3, 4, 5, and 6.
• the human or humanized IL-7-encoding gene comprises a cDNA encoding a human or humanized IL-7 protein.
• a genetically modified non-human animal comprising, in its germline, a transgene comprising a nucleic acid sequence encoding a human or humanized IL-7 gene, wherein the human or humanized IL-7 gene is flanked upstream and downstream with endogenous non-human regulatory sequences.
• the genetically modified non-human animal is a rodent.
• the rodent is selected from the group consisting of a mouse, a rat, and a hamster.
• the genetically modified non-human animal comprises a human exon selected from the group consisting of human exon 1, human exon 2, human exon 3, human exon 4, human exon 5, human exon 6, and a combination thereof.
• the human or humanized IL-7 gene comprises at least five human exons.
• a humanized IL-7 locus comprising, a non-human exon 1, a human exon 2, a human exon 3, a human exon 4, a human exon 5 and a human exon 6.
• the humanized IL-7 locus further comprises 5' and 3 ' non-human untranslated regions flanking non-human exon 1 and human exon 6.
• the humanized IL-7 locus comprises a 3 ' human untranslated region, or portion thereof, that is contiguous with a non-human 3 ' untranslated region.
• the humanized IL-7 locus comprises a 5' non-human untranslated region, or portion thereof, and non-human exon 1 that is contiguous with a human exon 2.
• a humanized IL-7 locus comprises the structure set forth in Figure 1.
• a humanized IL-7 locus comprising human exons 2-6 of a human IL-7 gene operably linked to non-human IL-7 regulatory sequences.
• a humanized IL-7 locus of the present invention comprises a non-human IL-7 exon 1.
• a humanized IL-7 locus of the present invention comprises a non-human IL-7 exon 1 and a non-human IL-7 intron 1.
• a humanized IL-7 locus of the present invention comprises a 3' human IL-7 untranslated region, or portion thereof, that is contiguous with a non-human IL-7 3 ' untranslated region, or portion thereof.
• a humanized IL-7 locus of the present invention comprises a 5' non-human untranslated region, or portion thereof, and non-human exon 1 that is contiguous with a human IL-7 exon 2.
• a humanized IL-7 locus comprising a sequence that encodes an IL-7 protein that is substantially human.
• a humanized IL-7 locus of the present invention comprises a sequence that is at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 98% identical to SEQ ID NO: 3.
• a humanized IL-7 locus of the present invention comprises SEQ ID NO: 3.
• an IL-7 protein of the present invention is encoded by a sequence that is at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 98% identical to SEQ ID NO: 3.
• an IL-7 protein of the present invention is encoded by SEQ ID NO: 3.
• a method for making a non-human animal with a human or humanized IL-7-encoding gene comprising modifying the germline of the non-human animal to comprise a human or humanized IL-7-encoding gene flanked upstream and downstream with endogenous non-human IL-7 regulatory sequences.
• the modification is at an endogenous non- human IL-7 locus.
• the non-human animal is a rodent.
• the rodent is selected from the group consisting of a mouse, a rat, and a hamster.
• a genetically modified non-human animal that is genetically modified to express human IL-7 in an expression pattern that is the same expression pattern as observed for a wild-type non-human animal of the same genus and species.
• the non-human animal is a rodent.
• the rodent is selected from a mouse and a rat.
• the level of human IL-7 expressed in the non-human animal is about the same as the level of non-human IL-7 in a corresponding wild-type mouse.
• the non-human animal is a rodent.
• the rodent is selected from a mouse and a rat.
• a DNA construct comprising from 5' to 3' with respect to direction of transcription, a nucleic acid sequence homologous to a mouse IL-7 5' noncoding sequence, a human genomic fragment encoding a human IL-7 protein but not comprising a human regulatory sequence upstream or downstream of sequence encoding the human IL-7 protein, and a nucleic acid sequence homologous to a mouse IL-7 3' noncoding sequence.
• a DNA construct comprising from 5' to 3' with respect to direction of transcription, a nucleic acid sequence that comprises a region of homology to a mouse IL-7 exon 1 sequence, a human genomic fragment encoding a human IL-7 protein but not comprising a human regulatory sequence upstream or downstream of sequence encoding the human IL-7 protein, and a nucleic acid sequence homologous to a mouse IL-7 3' noncoding sequence.
• a genetically modified rodent comprising a DNA construct as described herein.
• rodent or rodent cell that expresses a human IL-7 protein
• the rodent or rodent cell does not detectably express a rodent IL-7 protein.
• a genetically modified rodent cell comprising a replacement at an endogenous rodent IL-7 locus of a gene sequence encoding a rodent IL-7 with a human genomic sequence encoding a human IL-7.
• the replacement is made with DNA construct as described herein.
• the rodent cell is a rat cell.
• the rodent cell is a mouse cell.
• the human genomic sequence comprises a contiguous human nucleic acid sequence spanning human IL-7 exons 2 through human IL-7 exon 6.
• the genetically modified rodent comprises a mouse IL-7 promoter at the endogenous rodent IL-7 locus.
• the cell is selected from a pluripotent cell, an induced pluripotent cell, a totipotent cell, an ES cell, and an ovum.
• the cell secretes human IL-7.
• the cell that secretes human IL-7 is selected from an epithelial cell (e.g., an intestinal epithelial cell), a hepatocyte, a keratinocyte, a dendritic cell, and a follicular dendritic cell.
• the rodent cell is a bone marrow dendritic cell.
• the cell that secretes human IL-7 is a thymic stromal cell; in a specific embodiment, the thymic stromal cell is a cortical epithelial cell.
• a rodent embryo comprising at least one rodent donor cell (e.g., an ES cell, a pluripotent cell, a totipotent cell, etc.) comprising a replacement of an endogenous rodent IL-7-encoding nucleic acid sequence with a nucleic acid sequence encoding a human IL-7 at the endogenous rodent IL-7 locus.
• the donor cell is a mouse ES cell and the embryo is a host mouse embryo that is a pre-morula, a morula, or a blastocyst.
• a rodent tissue that comprises a humanized IL-7 gene at an endogenous rodent IL-7 locus is provided, wherein the rodent tissue is selected from thymic, splenic, epidermal, and intestinal.
• a genetically modified mouse is provided that comprises a DNA sequence that encodes a human IL-7, wherein the mouse does not express a mouse IL-7, and wherein the mouse exhibits a T cell population that is about the same size as the T cell population of a wild-type mouse.
• the mouse exhibits a peripheral T cell population that is about the same size as a peripheral T cell population of a wild-type mouse.
• the T cell population is a mouse T cell population.
• the mouse is not more prone than a wild-type mouse to develop a B cell tumor comprising a pro-B or a pre-B cell.
• the mouse is not more prone than a wild-type mouse to develop a lymphoid tumor.
• the mouse does not exhibit a lymphoproliferative disorder in the absence of a known lymphoproliferative causative agent.
• the mouse does not exhibit a pathologic infiltration of T cell in a skin layer. In one embodiment, the mouse does not exhibit a symptom of alopecia.
• the majority of T cells of the genetically modified mouse are about the same in size distribution as in an age-matched wild-type mouse.
• the genetically modified mouse does not exhibit an enlargement of T cell
• a rodent that expresses a humanized or human IL-7 protein from an endogenous modified rodent IL-7 locus, wherein the serum concentration of human IL-7 in the rodent is physiologically normal.
• a humanized rodent that expresses a humanized IL-7 gene in the serum of the rodent at a physiologically normal concentration.
• the rodent is selected from a mouse and a rat.
• the physiologically normal serum concentration of human is physiologically normal serum concentration of human
• IL-7 is less than 10 picograms/mL. In one embodiment, the physiologically normal serum concentration of human IL-7 is less than 5 picograms/mL. In one embodiment, the
• physiologically normal serum concentration of human IL-7 in the rodent is about 2
• the physiologically normal serum concentration of human IL-7 in the rodent serum is about 2.4 picograms/mL to about 3.2 picograms/mL.
• a method for making a human IL-7 protein comprising inserting into the germline of the non-human animal a human or humanized IL-7 coding gene under control of endogenous non-human regulatory elements, allowing the non-human animal to make the human or humanized IL-7, and isolating from the non-human animal (e.g., a mammal, e.g., a rodent such as, e.g., a mouse or rat or hamster) human or humanized IL-7.
• a non-human animal e.g., a mammal, e.g., a rodent such as, e.g., a mouse or rat or hamster
• a method for making a human IL-7 protein comprising isolating from a non-human animal as described herein (e.g., a mammal, e.g., a rodent such as, e.g., a mouse or rat or hamster).
• a non-human animal as described herein (e.g., a mammal, e.g., a rodent such as, e.g., a mouse or rat or hamster).
• a method for making a non-human animal that comprises a human or humanized IL-7 gene in its germline comprising inserting into the germline of the non-human animal a human or humanized IL-7-encoding nucleic acid sequence or fragment thereof, wherein the human or humanized IL-7-coding nucleic acid sequence or fragment thereof is under regulatory control of endogenous non-human regulatory elements.
• the human or humanized IL-7 gene is at an endogenous non-human IL-7 locus (i.e., inserted between upstream and downstream non-human regulatory elements at the endogenous non-human IL-7 locus, wherein the human or humanized IL-7-coding nucleic acid sequence replaces the wild-type existing non-human IL-7 coding sequence in whole or in part).
• the non-human animal is a mammal, e.g., rodent.
• the rodent is selected from a mouse, a rat, and a hamster.
• a method for making a non-human animal that comprises a human or humanized IL-7 gene comprising inserting a DNA construct comprising exons 2- 6 of a human IL-7 gene into an endogenous non-human IL-7 gene of a non-human cell.
• a method for isolating from a non-human animal a T cell that has been exposed to a human or humanized IL-7 protein comprising a step of isolating a T cell from a non-human animal as described herein.
• the non-human animal is a mouse or a rat.
• the T cell is a non-human T cell, e.g., a rodent T cell, e.g., a T cell of a mouse or a rat.
• the T cell is selected from a T cell in the thymus and a peripheral T cell.
• IL-7 is provided, comprising a step of administering an agent to a genetically modified rodent as described herein, determining an effect of the agent on a human IL-7-mediated function in the rodent, and identifying the agent as an IL-7 antagonist if it antagonizes the function of human IL-7 in the genetically modified rodent.
• a genetically modified rodent as described herein for identifying an agent that is an antagonist of human IL-7 comprising of
• the agent comprises an immunoglobulin variable domain that binds IL-7.
• the agent specifically binds human IL-7 but not rodent IL-7.
• the agent is an antibody.
• a method for determining whether an agent reduces IL-7-mediated peripheral T cell population comprising a step of administering to a genetically modified rodent as described herein an IL-7 antagonist for a period of time, measuring peripheral T cell population number of the rodent at one or more time periods following administration, and determining whether the IL-7 antagonist reduces the peripheral T cell population.
• a genetically modified rodent as described herein for determining whether an agent reduces IL-7-mediated peripheral T cell population comprising administering to the genetically modified rodent an IL-7 antagonist for a period of time, measuring peripheral T cell population number of the rodent at one or more time periods following administration, and determining whether the IL-7 antagonist reduces the peripheral T cell population.
• the genetically modified non-human animal is heterozygous for a human or humanized IL-7-encoding gene.
• the non-human animal is unable to express an endogenous IL-7 protein.
• the non-human animal comprises a knockout of both endogenous IL-7 alleles.
• Figure 1 depicts (not to scale) a schematic of a wild-type mouse IL7 gene locus
• top and a humanized endogenous mouse IL-7 locus (bottom).
• Open symbols indicate human sequence; closed symbols indicate mouse sequence; shaded items indicate untranslated regions; stippled region indicates other sequence.
• Figure 2 depicts human IL-7 concentration in serum of wild-type mice that has a genetic background of 75% C57B6 and 25% 129/SvJ (75/25 WT) and mice heterozygous for a humanized endogenous IL-7 locus as described herein (5148 Het).
• non-human animals are described that comprise the genetic modification(s) described herein.
• the genetically modified non-human animal may be selected from a group consisting of a mouse, rat, rabbit, pig, bovine (e.g., cow, bull, buffalo), deer, sheep, goat, chicken, cat, dog, ferret, primate (e.g., marmoset, rhesus monkey).
• bovine e.g., cow, bull, buffalo
• deer sheep, goat
• chicken cat
• cat dog
• ferret e.g., marmoset, rhesus monkey
• other methods are employed to make a non-human animal comprising the genetic
• the non-human animal is a mammal.
• the non-human animal is a small mammal, e.g., of the superfamily Dipodoidea or Muroidea. In one
• the genetically modified animal is a rodent.
• the rodent is selected from a mouse, a rat, and a hamster.
• the rodent is selected from the superfamily Muroidea.
• the genetically modified animal is from a family selected from Calomyscidae (e.g., mouse-like hamsters), Cricetidae (e.g., hamster, New World rats and mice, voles), Muridae (true mice and rats, gerbils, spiny mice, crested rats), Nesomyidae (climbing mice, rock mice, with-tailed rats, Malagasy rats and mice), Platacanthomyidae (e.g., spiny dormice), and Spalacidae (e.g., mole rates, bamboo rats, and zokors).
• Calomyscidae e.g., mouse-like hamsters
• Cricetidae e.g., ham
• the genetically modified rodent is selected from a true mouse or rat (family Muridae), a gerbil, a spiny mouse, and a crested rat.
• the genetically modified mouse is from a member of the family Muridae.
• the animal is a rodent.
• the rodent is selected from a mouse and a rat.
• the non-human animal is a mouse.
• C57BL strain selected from C57BL/A, C57BL/An, C57BL/GrFa, C57BL/KaLwN, C57BL/6, C57BL/6J, C57BL/6ByJ, C57BL/6NJ, C57BL/10, C57BL/10ScSn, C57BL/10Cr, and
• the genetically modified mouse is a mix of an aforementioned 129 strain and an aforementioned C57BL/6 strain.
• the mouse is a mix of aforementioned 129 strains, or a mix of aforementioned BL/6 strains.
• the 129 strain of the mix is a 129S6 (129/SvEvTac) strain.
• the mouse is a BALB strain, e.g., BALB/c strain.
• the mouse is a mix of a BALB strain and another aforementioned strain.
• the non-human animal is a rat.
• the rat is selected from a Wistar rat, an LEA strain, a Sprague Dawley strain, a Fischer strain, F344, F6, and Dark Agouti.
• the rat strain is a mix of two or more strains selected from the group consisting of Wistar, LEA, Sprague Dawley, Fischer, F344, F6, and Dark Agouti.
• exemplary flanking genomic sequences of a humanized IL-7 gene of the present invention are provided in SEQ ID NO: 1 (5' flanking sequence) and SEQ ID NO: 2 (3' flanking sequence).
• SEQ ID NO: 3 An exemplary human IL-7 gene of the present invention is provided in SEQ ID NO: 3.
• IL-7 is a cytokine that is essential for development of immature B and T cells and, to some degree, mature T cells; IL-7 knockout mice display a severe depletion of mature B and T cells (von Freeden-Jeffry U. et al. (1995) Lymphopenia in interleukin (IL)-7 gene-deleted mice identifies IL-7 as a nonredundant cytokine, J. Exp. Med. 181 : 1519-1526).
• IL-7 is produced by epithelial cells in the thymus and intestine, in keratinocytes, liver, and dendritic cells— but not by normal lymphocytes (reviewed, e.g., in Fry T.J. and Mackall, C.L. (2002) Interleukin-7: from bench to clinic, Blood 99(1 1):3892-3904).
• IL-7 increases T cell number and enhances T cell function (see, e.g.,
• IL-7 Administration Alters the CD4:CD8 Ratio Increases T Cell Numbers, and Increases T Cell Function in the Absence of Activation, J. Immunol. 166:3019- 3027; see also, Tan J.T. et al. (2001) IL-7 is critical for homeostatic proliferation and survival of naive T cells, Proc. Natl. Acad. Sci. USA 98(15):8732-8737).
• IL-7 is necessary for both early and late stage T cell regulation. IL-7 is not expressed by T cells, which must encounter IL-7 that is released by non-thymic cells in the periphery and that is believed to be responsible for peripheral T cell proliferation and maintenance (reviewed, e.g., in Guimond, M (2005) Cytokine Signals in T-Cell Homeostasis, J. Immunother. 28(4):289-294). IL-7 starvation results in severely impaired T cell development and survival of naive T cells.
• IL-7 also appears to be necessary for the survival of mature T cells; mature T cells acquired through adoptive transfer into IL-7 -deficient mice enter apoptosis where the mice lack an IL-7 gene, but not in mice that express IL-7 that lack an IL-7R gene (Schluns, K.S. et al. (2000) Interleukin-7 mediates the homeostasis of naive and memory CD8 T cells in vivo, Nat. Immunol. l(5):426-432. Loss of IL-7 function results in a SCID-like phenotype in mice (Puel, A. and Leonard, W.J.
• the human IL-7 gene comprises 6 exons that extend over 33 kb and is located on chromosome 8 at 8ql2-13.
• Mouse IL-7 comprises 5 exons (there is no counterpart in mouse to human exon 5) and is about 80% homologous to the human gene; analysis of non-coding sequences of the human and the mouse genes revealed a paucity of recognizable regulatory motifs responsible for transcription and regulation of gene expression (Lupton, S.D. et al. (1990) Characterization of the Human and Murine IL-7 Genes, J. Immunol. 144(9):3592-3601), suggesting that regulation of IL-7 expression may be complex.
• mice BAC fragments comprising a reporter gene at the hIL-7 locus have been expressed in mice to successfully ascertain expression patterns of IL-7 in mice (see, e.g., Avles, N.L. et al. (2009) Characterization of the thymic IL-7 niche in vivo, Proc. Natl. Acad. Sci. USA 106(5): 1512- 1517; Mazzucchelli, R.I. (2009) Visualization and Identification of IL-7 Producing Cells in Reporter Mice, PLoS ONE 4(l l):e7637; Repas, J.F. et al.
• IL7-hCD25 and IL7-Cre BAC transgenic mouse lines new tools for analysis of IL-7 expressing cells, Genesis 47:281-287).
• a BAC-based replacement of an IL-7 exon with a reporter required the entire 43 kb IL-7 locus as well as 96 kb of 5' flanking sequence and 17 kb of 3 ' flanking sequence in the hope of faithfully recapitulating IL-7 expression of wild-type mice (Repass, J.F. et al.
• mice that express abnormally or poorly regulated human IL-7 exhibit a panoply of pathologies or syndromes.
• Mice transgenic for a murine IL-7 cDNA under control of mouse Ig heavy chain enhancer, ⁇ light chain enhancer, and light chain promoter) to target expression in the lymphoid compartment exhibit significantly enhanced numbers of B cell precursors and an overall expansion of all subsets of thymocytes in the thymus and peripheral T cells (Samaridis, J. et al. (1991) Development of lymphocytes in interleukin 7-transgenic mice, Eur. J. Immunol. 21 :453-460).
• Transgenic mice that express IL-7 from a mouse cDNA under control of an SRa promoter develop a panoply of pathologies, including a chronic colitis that histopathologically mimics chronic colitis in humans, and is characterized by at least a transient over-expression of IL-7 in colonic mucosal lymphocytes (but not colonic epithelial cells) and its apparent accumulation in mucus of goblet cells of the colonic mucosa (Watanabe, M. et al. (1998) Interleukin 7 Transgenic Mice Develop Chronic Colitis with Decreased Interleukin 7 Protein Accumulation in the Colonic Mucosa, J. Exp Med. 187(3):389-402; Takebe, Y.
• sR alpha promoter an efficient and versatile mammalian cDNA expression system composed of the simian virus 40 early promoter and the R-U5 segment of human T-cell leukemia virus type 1 long terminal repeat, Mol. Cell Biol. 8(l):466-472).
• Constitutive expression of mouse IL-7 driven by the same promoter in transgenic mice also develop a severe dermatitis characterized by gross deformities and a massive dermal infiltration of mononuclear cells that are mostly TCRyS cells (Uehira, M. et al. The development of dermatitis infiltrated by yd T cells in IL-7 transgenic mice, Intl. Immunol. 5(12): 1619-1627).
• mice expressing a murine IL-7 cDNA driven by a murine heavy chain promoter and enhancer also exhibited dermatitis and lymphoproliferation into the dermis, but reportedly of TCRaP cells and cells that express Thy-1, CD3, and CD5 but lack CD4 and CD 8 (CD4+/CD8+ thymocytes are virtually absent from these transgenic mice); these mice also developed B and T cell lymphomas, presumably associated with a prolonged lymphoproliferation observed in these mice (see, Rich, B.E. et al. (1993) Cutaneous lymphoproliferation and lymphomas in interleukin 7 transgenic mice, J. Exp. Med. 177:305-316).
• mice expressing transgenic mouse IL-7 under control of the MHC class II Ea promoter are highly prone to lymphoid tumors (see, e.g., Fisher, A.G. et al. (1995) Lymphoproliferative disorders in IL-7 transgenic mice: expansion of immature B cells which retain macrophage potential, Int. Immunol. 7(3):414-423; see, also, Ceredig, R. et al. (1999) Effect of deregulated IL-7 transgene expression on B lymphocyte development in mice expressing mutated pre-B cell receptors, Eur. J. Immunol. 29(9):2797-2807).
• T cell sizes are also larger in the transgenic mice, and a polyclonal T cell expansion is observed (predominantly CD8+, indicating a perturbed regulation in these mice) (Mertsching, E. et al. IL-7 transgenic mice: analysis of the role of IL-7 in the differentiation of thymocytes in vivo and in vitro, Intl. Immunol. 7(3):401-414).
• mice that over-express mIL-7 (by about 25-50-fold) through the MHC class II Ea promoter appear grossly healthy (but for a low incidence of B cell tumors) and exhibit a 10-20- fold increase in T cell number over wild-type mice, characterized by large numbers of CD8+ cells that are also CD44 hi and CD122 hi (Kieper W.C. et al. (2002) Overexpression of Interleukin (IL)-7 Leads to IL- 15 -independent Generation of Memory Phenotype CD8+ T Cells, J. Exp. Med. 195(12): 1533-1539).
• IL-7 Interleukin
• MHC class II Ea promoter selectively expand IL-7-responsive early B cells, and are a good source of tumors comprising pro-B and pre-B cells.
• Mice that express IL-7 driven by a human K14 promoter develop a lymphoproliferative response that results in T cell infiltrates of skin that resemble alopecia.
• CD8- precursor cells in thymus presumably due to depletion of IL-7 by the large number of double positive thymocytes in the transgenic mice, suggesting that IL-7 levels must be extraordinarly controlled to promote normal thymocyte development (see, e.g., Malek, T.R. (2004) IL-7: a limited resource during thymopoiesis, Blood, 104(13):2842).
• human IL-7 can induce proliferation of murine pre-B cells (Goodwin, R.G. et al. (1989) Human interleukin 7: Molecular cloning and growth factor activity on human and murine B-lineage lines, Proc. Natl. Acad. Sci. USA 86:302-306). Although expressed in certain chronic lymphocytic leukemia cells, expression of mouse IL-7 in tumor cells implanted in mice induce inflammation and reduced tumorigenicity, yet paradoxically mice transgenic for IL-7 are prone to lymphomas (reviewed in Foss, H.-D. et al.
• mice that express human IL-7 but not mouse IL-7) from endogenous mouse IL-7 loci in a physiologically relevant fashion, in particular but not limited to mice that comprise human or mouse tumors, e.g., lymphocytic tumors.
• mice that express human IL-7 in a physiologically relevant manner are also useful for evaluating anti-tumor properties of putative therapeutics (including human IL-7 and analogs thereof) in xenograft models of human solid tumors in mice.
• SCID mice implanted with HT29 human colon adenocarcinoma and tested under a variety of conditions (e.g., ablation of native T cells and addition of human T cells; addition of recombinant human IL-7, etc.) (see, Murphy, W.J. et al. (1993) Antitumor Effects of Interleukin-7 and Adoptive Immunotherapy on Human Colon Carcinoma Xenografts, J. Clin. Invest. 92: 1918-1924). That study found that human IL-7 when administered with human T cells resulted in a significantly prolonged survival than in the absence of human IL-7 (Id.).
• mice that express human IL-7 in particular mice that are capable of supporting a xenograft (e.g., a human tumor), such as, e.g., immunodeficient mice, have a specific and a well-established utility.
• IL-7 signaling has been shown to be necessary for development and survival of human T-cell acute lymphoblastic leukemias (T-ALL) in vitro and in vivo.
• T-ALL T-cell acute lymphoblastic leukemias
• Interleukin-7 is a growth factor of precursor B and T acute lymphoblastic leukemia.
• T-ALL is an aggressive hematological cancer with poor prognosis; the understanding of mechanisms driving proliferation and survival of T- ALL cells remains relatively poor due to lack of xenograft models that can support the growth of patient derived tumors in vivo.
• an immunodeficient animal expressing human IL-7 can serve as an invaluable in vivo system for testing pharmaceutical compositions against such T- cell related malignancies, e.g., testing the efficacy of a pharmaceutical composition to target IL- 7-mediated signaling in a mouse that expresses human IL-7 and has an implanted T-cell derived tumor, wherein the tumor requires IL-7 signaling for development and survival.
• Mouse ES cells were modified to replace mouse IL-7 gene sequences with human IL-7 gene sequences at the endogenous mouse IL-7 locus, under control of mouse IL-7 regulatory elements, using VELOCIGENE® genetic engineering technology, to produce a humanized locus as shown in FIG. 1.
• Targeting Construct Bacterial homologous recombination (BHR) is performed to construct a large targeting vector (LTVEC) containing the human IL-7 gene for targeting to the mouse IL-7 locus using standard BHR techniques (see, e.g., Valenzuela et al. (2003) High- throughput engineering of the mouse genome coupled with high-resolution expression analysis, Nature Biotech. 21(6):652-659).
• Linear fragments are generated by ligating PCR-generated homology boxes to cloned cassettes followed by gel isolation of ligation products and electroporation into BHR-competent bacteria harboring the target bacterial artificial chromosome (BAC).
• Mouse BAC bMQ-271gl 8 is used as the source of mouse sequence; human BAC RPl 1-625K1 is used as the source of human sequence.
• a large targeting vector (LTVEC) containing the homology arms and human IL-7 gene sequences was made.
• Mouse ES cells were electroporated with the LTVEC constructs, grown on selection medium, and used as donor ES cells to make humanized IL-7 mice.
• mouse IL-7 gene (mouse Gene ID: 96561 ; Ref Seq transcript:
• NM_008371.4 is modified by deleting exons 2 through 5 (deletion coordinates
• the human genomic IL-7 sequence is provided in SEQ ID NO: 3 (NC#166E2F2).
• mouse genomic IL-7 locus is known and reported as a 41,351 nt sequence under accession number NC0000696 (hereby incorporated by reference); relevant 5' and 3' sequences of the mouse IL-7 genomic locus are provided in SEQ ID NO: l (5' flanking) and SEQ ID NO:2 (3' flanking).
• the LTVEC comprising the humanized IL-7 gene had a 48 kb upstream mouse targeting arm flanked upstream with a NotI site, and a 77 kb downstream mouse targeting arm flanked downstream with a NotI site.
• the LTVEC was linearized with NotI for electroporation.
• nucleotide sequence of the LTVEC was obtained across the mouse/human 5' junction, which included, from 5' (mouse) to 3' (human), the following sequence with the mouse/human junction nucleotides in parenthesis: 5' - TGCAAGCACC AAAAAGGTGA CCACACTTCA CATTGGCGAT CGC(GG)GTTTC TATCTGAGGA TGTGAATTTA TTTACAGA - 3' (SED ID NO: 4).
• Nucleotide sequence of the LTVEC across the junction of the human insertion and the 5' end of the cassette was determined and included the following sequence having, from 5' to 3', human sequence/restriction site/loxp/cassette sequence with the human sequence/restriction site junction nucleotides in parenthesis: 5' - GTTATGTGCT
• Nucleotide sequence of the LTVEC across the junction of the end of the cassette and the beginning of mouse sequence was determined and included the following sequence having, from 5' to 3', cassette sequence/restriction site/mouse sequence with the junction nucleotides in parenthesis: 5' - GTATGCTATA CGAAGTTATG CTAGTAACTA
• a loss of native allele assay (see, e.g., Valenzuela et al. (2003)) is performed to detect loss of endogenous IL-7 sequence due to the targeting.
• Primer pairs, fragment sizes, and TAQMANTM probes are as shown in Table 1.
• the CI probe binds the mouse IL-7 genomic sequence (NC0000696) at nts 9,635-9,664; the C2 probe binds the mouse IL-7 genomic sequence (NC0000696) at nts 39,793-39,825.
• the C3 probe binds the human IL-7 genomic sequence (NC#166E2F2) at nts 29,214-29,242.
• Donor mouse ES cells comprising a humanized IL-7 locus are introduced into early stage mouse embryos by the VELOCIMOUSE® method (Poueymirou et al. (2007) F0 generation mice fully derived from gene-targeted embryonic stem cells allowing immediate phenotypic analyses, Nat Biotechnol 25:91-99).
• F0 mice fully derived from donor ES cells were obtained that were heterozygous for humanization of the endogenous mouse IL-7 locus.
• F0 mice are bred to homozygosity with respect to the humanization. Homozygous mice are genotyped to confirm homozygosity. All mouse studies were overseen and approved by Regeneron's Institutional Animal Care and Use Committee (IACUC).
• mice humanized for the IL-7 gene and their non-humanized littermate controls were bled and serum concentrations of human IL-7 were measured using QuantikineHS Human IL-7 Immunoassay kit from R&D Systems, Inc. Data was analyzed using Microsoft Excel and plotted using Prism statistical analysis software. Mice heterozygous for the humanized IL-7 locus (designated MAID 5148 het) expressed human IL-7 in serum at a physiologically relevant concentration. This is in contrast to transgenic human IL-7 mice bearing lentivirally transduced human IL-7 in double knockout mice, which mice exhibit unphysiologically and potentially seriously detrimental high levels of human IL-7 in serum (10 to 100 pg/mL) (O'Connell, R.M.
• mice heterozygous for a humanized endogenous IL-7 locus exhibited about 2.4 to about 3.2 pg/mL in serum (FIG. 2), reflecting normal, or physiologically appropriate, levels of IL-7.

Landscapes

• Life Sciences & Earth Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical & Material Sciences (AREA)
• Zoology (AREA)
• Organic Chemistry (AREA)
• General Health & Medical Sciences (AREA)
• Environmental Sciences (AREA)
• Engineering & Computer Science (AREA)
• Genetics & Genomics (AREA)
• Biotechnology (AREA)
• Biophysics (AREA)
• Molecular Biology (AREA)
• Biochemistry (AREA)
• Veterinary Medicine (AREA)
• Animal Behavior & Ethology (AREA)
• Animal Husbandry (AREA)
• Biodiversity & Conservation Biology (AREA)
• Proteomics, Peptides & Aminoacids (AREA)
• Medicinal Chemistry (AREA)
• Gastroenterology & Hepatology (AREA)
• Toxicology (AREA)
• Biomedical Technology (AREA)
• General Engineering & Computer Science (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Wood Science & Technology (AREA)
• Physics & Mathematics (AREA)
• Plant Pathology (AREA)
• Microbiology (AREA)
• Micro-Organisms Or Cultivation Processes Thereof (AREA)
• Preparation Of Compounds By Using Micro-Organisms (AREA)
• Peptides Or Proteins (AREA)
• Investigating Or Analysing Biological Materials (AREA)
• Catching Or Destruction (AREA)

Priority Applications (17)

Applications Claiming Priority (6)

Publications (1)

Family

ID=49757275

Family Applications (1)

Country Status (27)

Cited By (8)

Families Citing this family (24)

Citations (1)

Family Cites Families (8)

• 2013
  • 2013-03-12 US US13/795,765 patent/US8962913B2/en not_active Expired - Fee Related
  • 2013-06-14 CN CN201610168011.XA patent/CN105779467A/zh active Pending
  • 2013-06-14 PL PL14195502T patent/PL2859793T3/pl unknown
  • 2013-06-14 SG SG10201609576YA patent/SG10201609576YA/en unknown
  • 2013-06-14 BR BR112014029892A patent/BR112014029892A2/pt not_active Application Discontinuation
  • 2013-06-14 DK DK14195502.1T patent/DK2859793T3/en active
  • 2013-06-14 SG SG11201407370QA patent/SG11201407370QA/en unknown
  • 2013-06-14 LT LTEP14195502.1T patent/LT2859793T/lt unknown
  • 2013-06-14 AU AU2013277457A patent/AU2013277457B2/en not_active Ceased
  • 2013-06-14 SM SM20170313T patent/SMT201700313T1/it unknown
  • 2013-06-14 SG SG10201609569PA patent/SG10201609569PA/en unknown
  • 2013-06-14 SI SI201330664A patent/SI2859793T1/sl unknown
  • 2013-06-14 MX MX2014015679A patent/MX363540B/es unknown
  • 2013-06-14 HU HUE14195502A patent/HUE034592T2/en unknown
  • 2013-06-14 RU RU2014148107A patent/RU2654565C2/ru not_active IP Right Cessation
  • 2013-06-14 HK HK15104315.3A patent/HK1203761A1/xx unknown
  • 2013-06-14 EP EP14195502.1A patent/EP2859793B1/en active Active
  • 2013-06-14 EP EP13739875.6A patent/EP2861063A1/en not_active Withdrawn
  • 2013-06-14 NZ NZ702943A patent/NZ702943A/en not_active IP Right Cessation
  • 2013-06-14 JP JP2015517447A patent/JP6174134B2/ja not_active Expired - Fee Related
  • 2013-06-14 WO PCT/US2013/045788 patent/WO2013192030A1/en not_active Ceased
  • 2013-06-14 PT PT141955021T patent/PT2859793T/pt unknown
  • 2013-06-14 ES ES14195502.1T patent/ES2626965T3/es active Active
  • 2013-06-14 KR KR1020147035047A patent/KR20150027752A/ko not_active Ceased
  • 2013-06-14 RS RS20170543A patent/RS56039B1/sr unknown
  • 2013-06-14 CN CN201380031333.4A patent/CN104378976B/zh not_active Expired - Fee Related
  • 2013-06-14 CA CA2873134A patent/CA2873134A1/en not_active Abandoned
• 2014
  • 2014-11-18 IL IL235773A patent/IL235773B/en active IP Right Grant
  • 2014-11-24 US US14/551,538 patent/US9232776B2/en not_active Expired - Fee Related
  • 2014-11-28 IN IN10189DEN2014 patent/IN2014DN10189A/en unknown
• 2015
  • 2015-11-10 US US14/937,270 patent/US20160052986A1/en not_active Abandoned
• 2016
  • 2016-11-21 US US15/357,021 patent/US9737059B2/en not_active Expired - Fee Related
• 2017
  • 2017-05-31 CY CY20171100577T patent/CY1119071T1/el unknown
  • 2017-06-27 HR HRP20170974TT patent/HRP20170974T1/hr unknown
  • 2017-07-14 US US15/649,797 patent/US9974291B2/en not_active Expired - Fee Related
• 2018
  • 2018-04-24 US US15/960,642 patent/US10314298B2/en not_active Expired - Fee Related
  • 2018-06-25 IL IL260250A patent/IL260250B/en not_active IP Right Cessation
• 2019
  • 2019-05-01 US US16/400,074 patent/US20190343093A1/en not_active Abandoned
  • 2019-08-13 IL IL26867419A patent/IL268674A/en unknown

Patent Citations (1)

Non-Patent Citations (39)

Also Published As

Similar Documents

Legal Events