Greenwood Tiffany A, Rana Brinda K, Schork Nicholas J
Polymorphism Research Laboratory, Department of Psychiatry, University of California at San Diego, La Jolla, California 92093, USA.
Genome Res. 2004 Jul;14(7):1358-61. doi: 10.1101/gr.1540404.
The International Haplotype Map ("HapMap") Project is motivated, in part, by the belief that the organization of the human genome, the mechanics of recombination, and the population-level behavior of alleles at adjacent loci should allow researchers to parse the genome into small segments, or "blocks," that show strong linkage disequilibrium (LD) between alleles at loci within those segments. The discovery and evidence for these blocks is to be based solely on the observed LD strength and patterns between alleles at adjacent loci throughout the genome. Although there are many factors that contribute to LD strength, we assessed the correlation between block structure, in terms of length and percentage of the genome assembled into blocks within a region, and recombination rate obtained from two independent sources. We found evidence of a striking negative correlation between the average recombination rate and average block length, suggesting that recombination rate is a strong contributor to haplotype block structure within the genome. We discuss the potential implications of this negative correlation in the context of the organization, properties, and potential ubiquity of a block-like structure in the human genome.
国际单倍型图谱(“HapMap”)计划的部分动机在于,人们相信人类基因组的组织形式、重组机制以及相邻基因座上等位基因在群体水平的行为,应能使研究人员将基因组解析为小段,即“区块”,这些区块内的基因座上等位基因之间表现出强连锁不平衡(LD)。这些区块的发现和证据将完全基于全基因组中相邻基因座上等位基因间观察到的LD强度和模式。尽管有许多因素会影响LD强度,但我们评估了区块结构(就一个区域内组装成区块的基因组长度和百分比而言)与来自两个独立来源的重组率之间的相关性。我们发现平均重组率与平均区块长度之间存在显著的负相关证据,这表明重组率是基因组内单倍型区块结构的一个重要促成因素。我们在人类基因组中类似区块结构的组织、特性及潜在普遍性的背景下,讨论了这种负相关的潜在影响。