秀丽隐杆线虫染色体内重组率的品系间差异

Dharani U. Matharage, Riley Cutler, Anamica Khadgi, Amy L. Dapper
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摘要

减数分裂重组是同源染色体之间遗传物质交换的结果。减数分裂重组的结果之一是产生新的等位基因组合。重组率在物种、种群、性别和个体内部和之间存在巨大差异。虽然 PRDM9 在染色体内交叉变异中的作用已被广泛研究,但由于重组景观的复杂性、重组的内在变异以及实验方法的有限性,人们对重组率的变异以及影响重组的细胞和进化动态还不甚了解。虽然目前关于秀丽隐杆线虫重组率变异的研究还很有限,但以往研究的观察结果表明,秀丽隐杆线虫有可能成为研究染色体内重组率变异的便捷系统,从而避免许多常见的陷阱。因此,我们在 IV 号染色体两个高重组区之一的两个不同的 elegans 群体中研究了染色体内重组率模式的变异。我们使用插入到IV号染色体中的表型荧光标记来估计两个基因差异最大的品系(N2和CB4856)的重组率。我们发现这两个品系的重组率在统计学上存在显著差异,CB4856 在该焦点区域的重组后代频率比 N2 高 3%。此外,我们没有发现任何证据表明重组率存在性别差异(heterochiasmy)。此外,我们还研究了两种秀丽隐杆线虫品系在应激条件下重组率的可塑性。在这里,我们观察到当暴露在应激条件下时,两个品系的重组率都会明显下降。这些结果为利用秀丽隐杆线虫研究重组率变异的进化和遗传学打开了大门。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inter-strain variation in intra-chromosomal rates of recombination in Caenorhabditis elegans
Meiotic recombination results in the exchange of genetic material between homologous chromosomes. One consequence of meiotic recombination is the production of novel combination of alleles. Recombination rate varies dramatically within and between species, populations, sexes and individuals. Although, the role of PRDM9 in intra-chromosomal variation in crossovers is extensively studied, variation in recombination rate and the cellular and evolutionary dynamics that influence recombination is not well understood due to the complexity of the recombination landscape, intrinsic variation in recombination, and the limited experimental approaches. Though, there has only been limited research regarding the variation in recombination rates in Caenorhabditis elegans, observations from previous studies bring out the potential of C. elegans to be a convenient system for studying intra-chromosomal variation in recombination rate that avoid many of the common pitfalls. Therefore, we investigated the variation in intra-chromosomal patterns of recombination rates in two distinct populations of C. elegans in one of the two high recombination regions of chromosome IV. We used phenotypic fluorescent markers which are inserted in chromosome IV to estimate the recombination rate of the two most genetically distinct strains, N2 and CB4856. We identified statistically significant differences in recombination rate between the two strains, with a 3% higher frequency of recombinant offspring in CB4856 in this focal region. Additionally, we did not find any evidence of sex differences in recombination rate (heterochiasmy). Moreover, we looked at the plasticity of recombination rate in response to stressful conditions in the two C. elegans strains. Here we observed a significant decrease in the recombination rate in both strains when exposed to stressful conditions. These results open the door to using C. elegans to study evolution and genetics of variation in recombination rate.
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