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Genetic characterization of FLA, the cat major histocompatibility complex.

作者信息

Winkler C, Schultz A, Cevario S, O'Brien S

机构信息

Laboratory of Viral Carcinogenesis, National Cancer Institute-Frederick Cancer Research Facility, MD 21701.

出版信息

Proc Natl Acad Sci U S A. 1989 Feb;86(3):943-7. doi: 10.1073/pnas.86.3.943.

DOI:10.1073/pnas.86.3.943
PMID:2492667
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC286595/
Abstract

The major histocompatibility complex (MHC) of the domestic cat (termed FLA) has been refractile to genetic and serological definition largely because of repeated failure to detect cytotoxic antibodies in multiparous cats or to elicit antibody following allogeneic lymphocyte immunization. We have developed a protocol for producing cytotoxic alloantisera in the cat following rejection of multiple surgical skin grafts. Of 59 cats subjected to grafting, 13 produced lymphocytotoxic antisera which had varying specificities among a panel of outbred cat cells. A population cluster analysis of the 13 alloantisera permitted the identification of six clusters of overlapping FLA specificities. Serological analysis of cells from 12 cat kindreds led to the definition of 24 allogeneic haplotypes, which segregate as a single Mendelian complex. Feline FLA antisera were characterized as class I or class II specific by immunoprecipitation of FLA gene products on lymphocyte cell surfaces. Abundant antigenic polymorphisms for both class I and class II MHC determinants were discovered, a result consistent with precedence in other species and the common expectation of the adaptive value of MHC variation. Development of feline MHC typing reagents and the definition of haplotypes for the cat hold promise for experimental analysis of valuable feline models for virus-induced immune deficiencies.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7276/286595/0750c1b70dc0/pnas00243-0198-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7276/286595/3b241481c20e/pnas00243-0198-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7276/286595/0750c1b70dc0/pnas00243-0198-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7276/286595/3b241481c20e/pnas00243-0198-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7276/286595/0750c1b70dc0/pnas00243-0198-b.jpg

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Comparative genome organization of the major histocompatibility complex: lessons from the Felidae.

本文引用的文献

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Preliminary studies of the feline histocompatibility system.猫组织相容性系统的初步研究。
Immunogenetics. 1982;16(4):339-47. doi: 10.1007/BF00372305.
2
Major histocompatibility antigens: the human (HLA-A, -B, -C) and murine (H-2K, H-2D) class I molecules.主要组织相容性抗原:人类(HLA - A、- B、- C)和小鼠(H - 2K、H - 2D)I类分子。
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Exchanges of short polymorphic DNA segments predating speciation in feline major histocompatibility complex class I genes.猫主要组织相容性复合体I类基因中物种形成之前的短多态性DNA片段交换。
J Mol Evol. 1994 Jul;39(1):22-33. doi: 10.1007/BF00178246.
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DNA variation of the mammalian major histocompatibility complex reflects genomic diversity and population history.哺乳动物主要组织相容性复合体的DNA变异反映了基因组多样性和种群历史。
Proc Natl Acad Sci U S A. 1990 Jan;87(2):836-40. doi: 10.1073/pnas.87.2.836.
7
DNA recombination and natural selection pressure sustain genetic sequence diversity of the feline MHC class I genes.DNA重组和自然选择压力维持了猫科动物主要组织相容性复合体I类基因的遗传序列多样性。
J Exp Med. 1990 Aug 1;172(2):621-30. doi: 10.1084/jem.172.2.621.
8
Feline immune system.猫科动物免疫系统。
Comp Immunol Microbiol Infect Dis. 1992 Jan;15(1):1-11. doi: 10.1016/0147-9571(92)90097-b.
Transplantation. 1983 Dec;36(6):712-8. doi: 10.1097/00007890-198336060-00025.
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Correction of feline arylsulphatase B deficiency (mucopolysaccharidosis VI) by bone marrow transplantation.通过骨髓移植纠正猫的芳基硫酸酯酶B缺乏症(粘多糖贮积症VI型)
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