Service S K, Ophoff R A, Freimer N B
Center for Neurobehavioral Genetics, UCLA, Gonda Center, Room 3506, 695 Charles E. Young Drive South, Box 951761, Los Angeles, CA 90095-1761, USA.
Hum Mol Genet. 2001 Mar 1;10(5):545-51. doi: 10.1093/hmg/10.5.545.
Recent interest in using association studies to investigate complex traits has focused attention on understanding linkage disequilibrium (LD) in the human genome. We examined the genome-wide distribution and magnitude of such background LD (BLD) using 1036 densely spaced microsatellites, in a sample from the demographically well characterized population of the Central Valley of Costa Rica. High levels of BLD were found between linked markers several centiMorgans apart, and although BLD was significantly related to genetic distance between markers it was not spread uniformly throughout the genome. Understanding the forces governing the distribution of BLD in the genome will require similar investigations using a standard set of markers in other populations.
近期,利用关联研究来探究复杂性状的兴趣,已将注意力集中在了解人类基因组中的连锁不平衡(LD)上。我们在来自人口统计学特征明确的哥斯达黎加中央山谷人群的样本中,使用1036个密集分布的微卫星,研究了这种背景LD(BLD)在全基因组范围内的分布和程度。在相隔几个厘摩的连锁标记之间发现了高水平的BLD,并且尽管BLD与标记之间的遗传距离显著相关,但它并非在整个基因组中均匀分布。要了解控制基因组中BLD分布的力量,需要在其他人群中使用一组标准标记进行类似的研究。