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年轻人群中的连锁不平衡分析:假性维生素D缺乏性佝偻病与法裔加拿大人的奠基者效应

Linkage disequilibrium analysis in young populations: pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians.

作者信息

Labuda M, Labuda D, Korab-Laskowska M, Cole D E, Zietkiewicz E, Weissenbach J, Popowska E, Pronicka E, Root A W, Glorieux F H

机构信息

Genetics Unit, Shriners Hospital for Crippled Children, Montreal, Quebec, Canada.

出版信息

Am J Hum Genet. 1996 Sep;59(3):633-43.

Abstract

Pseudo-vitamin D-deficiency rickets (PDDR) was mapped close to D12S90 and between proximal D12S312 and distal (D12S305, D12S104) microsatellites that were subsequently found on a single YAC clone. Analysis of a complex haplotype in linkage disequilibrium (LD) with the disease discriminated among distinct founder effects in French Canadian populations in Acadia and in Charlevoix-Saguenay-Lac-Saint-Jean (Ch-SLSJ), as well as an earlier one in precolonial Europe. A simple demographic model suggested the historical age of the founder effect in Ch-SLSJ to be approximately 12 generations. The corresponding LD data are consistent with this figure when they are analyzed within the framework of Luria-Delbrück model, which takes into account the population growth. Population sampling due to a limited number of first settlers and the rapid demographic expansion appear to have played a major role in the founding of PDDR in Ch-SLSJ and, presumably, other genetic disorders endemic to French Canada. Similarly, the founder effect in Ashkenazim, coinciding with their early settlement in medieval Poland and subsequent expansion eastward, could explain the origin of frequent genetic diseases in this population.

摘要

假性维生素D缺乏性佝偻病(PDDR)被定位在靠近D12S90的位置,且位于近端D12S312和远端(D12S305、D12S104)微卫星之间,这些微卫星后来在一个单一的酵母人工染色体(YAC)克隆上被发现。对与该疾病处于连锁不平衡(LD)状态的复杂单倍型进行分析,区分了阿卡迪亚法裔加拿大人群以及沙勒沃伊 - 萨格奈 - 圣让湖地区(Ch - SLSJ)与前殖民时期欧洲的不同奠基者效应。一个简单的人口统计学模型表明,Ch - SLSJ奠基者效应的历史年代约为12代。当在考虑了人口增长的卢里亚 - 德尔布吕克模型框架内分析相应的LD数据时,与这一数字相符。由于首批定居者数量有限以及人口的快速增长,人口抽样似乎在Ch - SLSJ地区PDDR的形成以及大概在法裔加拿大特有的其他遗传疾病的形成中起到了主要作用。同样,德系犹太人的奠基者效应,与其在中世纪波兰的早期定居以及随后向东扩张相吻合,能够解释该人群中常见遗传疾病的起源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c6e/1914903/575e21e34056/ajhg00022-0150-a.jpg

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