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白细胞介素-2受体γ基因微缺失表明犬X连锁重症联合免疫缺陷病与人的该疾病是同源的。

IL-2R gamma gene microdeletion demonstrates that canine X-linked severe combined immunodeficiency is a homologue of the human disease.

作者信息

Henthorn P S, Somberg R L, Fimiani V M, Puck J M, Patterson D F, Felsburg P J

机构信息

Sections of Medical Genetics, Department of Clinical Studies-Philadelphia, University of Pennsylvania School of Veterinary Medicine 19104.

出版信息

Genomics. 1994 Sep 1;23(1):69-74. doi: 10.1006/geno.1994.1460.

Abstract

X-linked severe combined immunodeficiency (SCID) is characterized by profound defects in cellular and humoral immunity and, in humans, is associated with mutations in the gene for the gamma chain of the IL-2 receptor (IL-2R gamma). We have examined this gene in a colony of dogs established from a single X-linked SCID carrier female. Affected dogs have a 4-bp deletion in the first exon of the IL-2R gamma gene, which precludes the production of a functional protein, demonstrating that the canine disease is a true homologue of human X-linked SCID.

摘要

X连锁重症联合免疫缺陷病(SCID)的特征是细胞免疫和体液免疫存在严重缺陷,在人类中,它与白细胞介素2受体(IL-2Rγ)γ链基因的突变有关。我们在一个由一只X连锁SCID携带者雌性犬建立的犬群中研究了该基因。患病犬的IL-2Rγ基因第一外显子有一个4碱基对的缺失,这使得无法产生功能性蛋白质,表明犬类疾病是人类X连锁SCID的真正同源物。

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