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在C3H/HeJ小鼠模型中,成年期斑秃是一种复杂的多基因性状。

Adult-onset Alopecia areata is a complex polygenic trait in the C3H/HeJ mouse model.

作者信息

Sundberg John P, Silva Kathleen A, Li Renhua, Cox Gregory A, King Lloyd E

机构信息

The Jackson Laboratory, Bar Harbor, Maine 04609-1500, USA.

出版信息

J Invest Dermatol. 2004 Aug;123(2):294-7. doi: 10.1111/j.0022-202X.2004.23222.x.

Abstract

Alopecia areata (AA) is an autoimmune disease that targets actively growing (anagen) hair follicles in humans and other mammals. C3H/HeJ, but not C57BL/6J, mice spontaneously develop an adult-onset form of AA. A segregating population of C3HB6F2 female mice (n=1096), generated from crossing these two strains, was used for genome-wide linkage analysis to identify AA genetic susceptibility. Previous analysis identified susceptibility intervals on chromosomes 17 (Alaa1) and 9 (Alaa2). Using additional markers in these intervals and saturation mapping purported intervals on chromosomes 8 and 15, two additional regions were identified (Alaa3 and Alaa4, respectively). Human gene association studies identified specific human leukocyte antigen intervals comparable with those (major histocompatibility complex) found in Alaa1 in the mouse. Other human studies identified genes not found in this linkage study, but these human transcription factors are directly regulated by genes within Alaa1. These results indicate the necessity of integrating both gene association and genome-wide linkage studies in both mice and humans to understand the complex nature of these and other polygenic diseases.

摘要

斑秃(AA)是一种自身免疫性疾病,其靶向人类和其他哺乳动物中处于活跃生长期(生长期)的毛囊。C3H/HeJ小鼠而非C57BL/6J小鼠会自发发展出成年发病型斑秃。通过杂交这两个品系产生的一群C3HB6F2雌性小鼠(n = 1096)被用于全基因组连锁分析,以确定斑秃的遗传易感性。先前的分析在17号染色体(Alaa1)和9号染色体(Alaa2)上确定了易感区间。利用这些区间内的额外标记以及对8号和15号染色体上推测区间的饱和作图,又确定了另外两个区域(分别为Alaa3和Alaa4)。人类基因关联研究确定了与小鼠Alaa1中发现的特定人类白细胞抗原区间(主要组织相容性复合体)相当的区间。其他人类研究确定了在这项连锁研究中未发现的基因,但这些人类转录因子直接受Alaa1内的基因调控。这些结果表明,有必要将基因关联研究和全基因组连锁研究整合到小鼠和人类研究中,以了解这些及其他多基因疾病的复杂本质。

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