Vitart Veronique, Biloglav Zrinka, Hayward Caroline, Janicijevic Branka, Smolej-Narancic Nina, Barac Lovorka, Pericic Marijana, Klaric Irena Martinovic, Skaric-Juric Tatjana, Barbalic Maja, Polasek Ozren, Kolcic Ivana, Carothers Andrew, Rudan Pavao, Hastie Nick, Wright Alan, Campbell Harry, Rudan Igor
Human Genetics Unit, Medical Research Council, Western General Hospital, Edinburgh, Scotland, UK.
Eur J Hum Genet. 2006 Apr;14(4):478-87. doi: 10.1038/sj.ejhg.5201589.
Communities with increased shared ancestry represent invaluable tools for genetic studies of complex traits. "1001 Dalmatians" research program collects biomedical information for genetic epidemiological research from multiple small isolated populations ('metapopulation') in the islands of Dalmatia, Croatia. Random samples of 100 individuals from 10 small island settlements (n<2000 inhabitants) were collected in 2002 and 2003. These island communities were carefully chosen to represent a wide range of distinct and well-documented demographic histories. Here, we analysed their genetic make-up using 26 short tandem repeat (STR) markers, at least 5 cM apart. We found a very high level of differentiation between most of these island communities based on Wright's fixation indexes, even within the same island. The model-based clustering algorithm, implemented in STRUCTURE, defined six clusters with very distinct genetic signatures, four of which corresponded to single villages. The extent of background LD, assessed with eight linked markers on Xq13-21, paralleled the extent of differentiation and was also very high in most of the populations under study. For each population, demographic history was characterised and 12 "demographic history" variables were tentatively defined. Following stepwise regression, the demographic history variable that most significantly predicted the extent of LD was the proportion of locally born grandparents. Strong isolation and endogamy are likely to be the main forces maintaining this highly structured overall population.
具有更多共同祖先的群体是复杂性状基因研究的宝贵工具。“1001只斑点狗”研究项目从克罗地亚达尔马提亚群岛的多个小型孤立种群(“集合种群”)收集生物医学信息用于遗传流行病学研究。2002年和2003年从10个小岛屿定居点(居民人数n<2000)中随机抽取了100个人的样本。这些岛屿社区经过精心挑选,以代表广泛的、有详细记录的不同人口历史。在这里,我们使用26个短串联重复(STR)标记(彼此间隔至少5厘摩)分析了它们的基因组成。基于赖特固定指数,我们发现这些岛屿社区中的大多数之间存在非常高的分化水平,即使在同一个岛屿内也是如此。STRUCTURE中实施的基于模型的聚类算法定义了六个具有非常独特基因特征的聚类,其中四个对应于单个村庄。用Xq13 - 21上的八个连锁标记评估的背景连锁不平衡程度与分化程度平行,并且在大多数研究人群中也非常高。对于每个人群,我们描述了其人口历史,并初步定义了12个“人口历史”变量。经过逐步回归,最能显著预测连锁不平衡程度的人口历史变量是当地出生的祖父母的比例。强烈的隔离和近亲通婚可能是维持这种高度结构化总体人群的主要力量。