Genome Plasticity Laboratory, Department of Cancer Biology, The Scripps Research Institute, Scripps Florida, Jupiter, FL 33458, USA.
Nucleic Acids Res. 2010 Apr;38(7):2346-54. doi: 10.1093/nar/gkp1251. Epub 2010 Jan 15.
Genome-wide analyses have suggested thousands of meiotic recombination hot spots across mammalian genomes. However, very few hot spots have been directly analyzed at a sub-kb scale for crossover (CO) activity. Using recombinant inbred strains as a CO library, here we report the identification and detailed characterization of seven new meiotic hot spots on mouse chromosome 19, more than doubling the number of currently available mouse hot spots. Although a shared feature is the narrow 1.5-2.5-kb width of these recombinogenic sites, these analyses revealed that hot spots have diverse sequence attributes and distinct symmetric and asymmetric CO profiles. Interestingly, CO molecules with discontinuous conversion tracts are commonly observed, contrasting with those found in human. Furthermore, unlike human hot spots, those present in the mouse do not necessarily have a quasi-normal CO distribution but harbor CO repulsion zones within recombinogenic cores. We propose a model where local chromatin landscape directs these repulsion zones.
全基因组分析表明,哺乳动物基因组中有数千个减数分裂重组热点。然而,很少有热点在亚千碱基尺度上直接分析其交叉(CO)活性。本研究利用重组近交系作为 CO 文库,报告了在小鼠 19 号染色体上鉴定和详细描述的七个新的减数分裂热点,使目前可用的小鼠热点数量增加了一倍以上。尽管这些重组性位点的共同特征是狭窄的 1.5-2.5kb 宽度,但这些分析表明热点具有不同的序列属性和不同的对称和不对称 CO 分布模式。有趣的是,通常观察到具有不连续转换片段的 CO 分子,与在人类中发现的 CO 分子不同。此外,与人类热点不同的是,存在于小鼠中的热点不一定具有准正态 CO 分布,而是在重组核心内具有 CO 排斥区。我们提出了一个模型,其中局部染色质景观指导这些排斥区的形成。