Cullen Michael, Perfetto Stephen P, Klitz William, Nelson George, Carrington Mary
Basic Research Program, SAIC-Frederick, National Cancer Institute, Frederick, MD 21702, USA.
Am J Hum Genet. 2002 Oct;71(4):759-76. doi: 10.1086/342973. Epub 2002 Sep 23.
Definitive characteristics of meiotic recombination events over large (i.e., >1 Mb) segments of the human genome remain obscure, yet they are essential for establishing the haplotypic structure of the genome and for efficient mapping of complex traits. We present a high-resolution map of recombination at the kilobase level across a 3.3-Mb interval encompassing the major histocompatibility complex (MHC). Genotyping of 20,031 single sperm from 12 individuals resulted in the identification and fine mapping of 325 recombinant chromosomes within genomic intervals as small as 7 kb. Several principal characteristics of recombination in this region were observed: (1) rates of recombination can differ significantly between individuals; (2) intense hot spots of recombination occur at least every 0.8 Mb but are not necessarily evenly spaced; (3) distribution in the location of recombination events can differ significantly among individuals; (4) between hot spots, low levels of recombination occur fairly evenly across 100-kb segments, suggesting the presence of warm spots of recombination; and (5) specific sequence motifs associate significantly with recombination distribution. These data provide a plausible model for recombination patterns of the human genome overall.
在人类基因组大片段(即>1 Mb)上减数分裂重组事件的明确特征仍不清楚,然而它们对于建立基因组的单倍型结构以及复杂性状的有效定位至关重要。我们展示了跨越3.3 Mb区间(包含主要组织相容性复合体(MHC))、分辨率达千碱基水平的重组图谱。对来自12个个体的20,031条单精子进行基因分型,结果在小至7 kb的基因组区间内鉴定并精细定位了325条重组染色体。观察到该区域重组的几个主要特征:(1)个体间的重组率可能有显著差异;(2)强烈的重组热点至少每隔0.8 Mb出现一次,但不一定均匀分布;(3)重组事件的位置分布在个体间可能有显著差异;(4)在热点之间,低水平的重组在100 kb片段上相当均匀地发生,表明存在重组温点;(5)特定的序列基序与重组分布显著相关。这些数据为人类基因组整体的重组模式提供了一个合理的模型。