Suppr超能文献

扫描17号染色体寻找银屑病易感性:缺乏17q远端位点的证据。

Scanning chromosome 17 for psoriasis susceptibility: lack of evidence for a distal 17q locus.

作者信息

Nair R P, Guo S W, Jenisch S, Henseler T, Lange E M, Terhune M, Westphal E, Christophers E, Voorhees J J, Elder J T

机构信息

Department of Dermatology, School of Medicine, University of Michigan, Ann Arbor, USA.

出版信息

Hum Hered. 1995 Jul-Aug;45(4):219-30. doi: 10.1159/000154293.

Abstract

Evidence for a genetically heterogeneous psoriasis susceptibility locus on distal human chromosome 17q has recently been reported [Science 1994;264:1141]. Making use of an independently ascertained collection of 24 multiplex psoriasis kindreds, we have performed a genotyping scan of chromosome 17 using 12 microsatellite markers and analyzed the data using parametric (lod score) as well as novel nonparametric methods. Pairwise lod scores revealed no evidence for linkage to the previously implicated marker D17S784 under any of eight models varying in mode of inheritance, penetrance, and sporadic cases. Homogeneous linkage to D17S784 could be excluded under all four autosomal dominant models tested (Z < - 5.8 at theta = 0.05), and there was no evidence for genetic heterogeneity. All other chromosome 17 markers tested also failed to detect evidence for linkage in any of the kindreds under either a dominant or a recessive model. Although further analysis using affected sib pair methods provided no statistically significant evidence for linkage to any chromosome 17 marker, a cluster of three distal 17q loci displayed a trend towards greater than expected allele-sharing values (observed/expected = 1.10-1.14). These results do not formally confirm the existence of a psoriasis susceptibility locus on the distal long arm of human chromosome 17, but are suggestive of its possible involvement under a polygenic model, warranting its further investigation in familial psoriasis.

摘要

最近有报道称在人类远端17号染色体q臂上存在一个具有遗传异质性的银屑病易感基因座[《科学》,1994年;264:1141]。我们利用独立确定的24个多发型银屑病家系样本,使用12个微卫星标记对17号染色体进行了基因分型扫描,并使用参数法(对数优势分数)以及新的非参数法对数据进行了分析。成对的对数优势分数显示,在八种不同遗传模式、外显率和散发病例的模型中,均没有证据表明与先前涉及的标记D17S784存在连锁关系。在所有测试的四种常染色体显性模型下(在θ = 0.05时,Z < - 5.8),可以排除与D17S784的均匀连锁关系,并且没有遗传异质性的证据。在显性或隐性模型下,对所有其他测试的17号染色体标记进行检测,也未在任何家系中发现连锁证据。尽管使用患病同胞对方法进行的进一步分析没有提供与任何17号染色体标记连锁的统计学显著证据,但17q远端的三个位点组成的一个簇显示出等位基因共享值高于预期的趋势(观察值/预期值 = 1.10 - 1.14)。这些结果并未正式证实人类17号染色体长臂远端存在银屑病易感基因座,但提示其可能在多基因模型中发挥作用,因此有必要在家族性银屑病中对其进行进一步研究。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验