首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Genetic analysis of the NZB contribution to lupus-like autoimmune disease in (NZB x NZW)F1 mice.
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Genetic analysis of the NZB contribution to lupus-like autoimmune disease in (NZB x NZW)F1 mice.

机译:NZB对(NZB x NZW)F1小鼠狼疮样自身免疫性疾病的遗传分析。

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摘要

Lupus-like autoimmunity in (NZB x NZW)F1 mice is frequently marked by the development of a severe and fatal renal disease. Genes from both NZB and NZW parents are required for the full expression of disease. We applied a mapping technique based on polymorphism in simple sequence repeats to the analysis of (NZB x NZW)F1 x NZW backcross mice to determine the NZB genetic contribution to disease. The results show that a single NZB locus or tightly linked group of loci on the distal part of chromosome 4 provides the strongest association with renal disease and death. This locus, designated here as nba-1 (New Zealand Black autoimmunity), lies distal to the locus elp-1, 60-70 centimorgans from the centromere. It is of interest that a gene encoding a receptor for tumor necrosis factor maps to the vicinity of this disease-associated gene.
机译:(NZB x NZW)F1小鼠的狼疮样自身免疫通常以严重和致命的肾脏疾病的发展为标志。完整表达疾病需要来自NZB和NZW父母的基因。我们将基于简单序列重复中的​​多态性的作图技术应用于(NZB x NZW)F1 x NZW回交小鼠的分析,以确定NZB对疾病的遗传贡献。结果显示,第4号染色体远端的单个NZB基因座或紧密连锁的基因座组与肾脏疾病和死亡的关联最强。该基因座在这里命名为nba-1(新西兰黑自身免疫性),位于着丝粒60-70厘摩器官elp-1的远端。令人感兴趣的是,编码肿瘤坏死因子受体的基因定位于该疾病相关基因的附近。

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