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6号染色体p21.3区域银屑病主要易感区域的特征分析。

Characterization of the major susceptibility region for psoriasis at chromosome 6p21.3.

作者信息

Balendran N, Clough R L, Arguello J R, Barber R, Veal C, Jones A B, Rosbotham J L, Little A M, Madrigal A, Barker J N, Powis S H, Trembath R C

机构信息

Center for Nephrology, Royal Free and University College Medical School of University College London, Royal Free Campus, UK.

出版信息

J Invest Dermatol. 1999 Sep;113(3):322-8. doi: 10.1046/j.1523-1747.1999.00710.x.

DOI:10.1046/j.1523-1747.1999.00710.x
PMID:10469328
Abstract

Psoriasis is a common inflammatory skin condition caused by genetic and environmental factors. Recent genome-wide linkage analyses have identified a locus encoding susceptibility to psoriasis and placed this gene in the 12 cM interval between markers D6S426 and D6S276 on chromosome 6p21.3. This is a broad region and encompasses the human major histocompatibility complex. We have sought to localize the susceptibility gene more precisely by exploiting the linkage, haplotype, and linkage disequilibrium information available through genotyping 118 affected sib pairs, their parents and other affected family members. A total of 14 highly polymorphic markers were genotyped, combining anonymous loci with the class I genes HLA-B and -C distributed across a genetic interval of approximately 14 cM including the entire major histocompatibility complex. Through the application of higher density mapping within the major histocompatibility complex, we identified those regions most commonly shared identical by descent in patients with psoriasis. Using the transmission-disequilibrium test, we found significant evidence of linkage and allelic association across an interval defined by the markers tn62 (p = 1.0 x 10(-7)), HLA-B (p = 4.0 x 10(-7)), and HLA-C (p = 2.7 x 10(-9)), a region encompassed within a 285 kb genomic DNA fragment. Hence these studies contribute to the refinement of the localization of a major psoriasis susceptibility gene and place the critical region near to HLA-C.

摘要

银屑病是一种由遗传和环境因素引起的常见炎症性皮肤病。最近的全基因组连锁分析确定了一个编码银屑病易感性的基因座,并将该基因定位在6号染色体p21.3上标记D6S426和D6S276之间的12厘摩区间内。这是一个广泛的区域,包含人类主要组织相容性复合体。我们试图通过利用对118对受累同胞对、他们的父母及其他受累家庭成员进行基因分型所获得的连锁、单倍型和连锁不平衡信息,更精确地定位该易感基因。总共对14个高度多态性标记进行了基因分型,将匿名基因座与I类基因HLA - B和 - C相结合,这些基因分布在一个约14厘摩的遗传区间内,包括整个主要组织相容性复合体。通过在主要组织相容性复合体内应用更高密度的图谱,我们确定了银屑病患者中最常见的同源相同区域。使用传递不平衡检验,我们发现了在由标记tn62(p = 1.0 x 10(-7))、HLA - B(p = 4.0 x 10(-7))和HLA - C(p = 2.7 x 10(-9))定义的区间内存在连锁和等位基因关联的显著证据,该区域包含在一个285 kb的基因组DNA片段内。因此,这些研究有助于细化主要银屑病易感基因的定位,并将关键区域定位在靠近HLA - C的位置。

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