性染色体之间的抑制重组的进化和进化层的长度
Colin Olito1, Jessica K Abbott1
1Department of Biology, Division of Biodiversity and Evolution, Lund University, Lund, Sweden.
概括
性对抗性选择可能驱动性染色体进化,但证据是混合的. 这项研究模拟了反转大小如何揭示选择的模型.
科学领域:
- 进化遗传学的进化遗传学
- 人口遗传学 人口遗传学
- 性染色体的进化性染色体的进化
背景情况:
- 理论上,性对抗性 (SA) 选择驱动性染色体上的重组抑制.
- 将SA选择与重组停止联系起来的实证证据是模两可的.
- 对于重组抑制的替代假设仍未得到充分发展.
研究的目的:
- 调查由反向扩大非重组性相关区域 (SLR) 形成的进化层长度是否表明选择在固定中的作用.
- 模拟反转长度和有害突变负载如何影响不同选择模式下的固定概率.
主要方法:
- 开发了种群遗传模型来模拟反向固定.
- 分析了逆转大小,链接和有害突变负载的影响.
- 对于中性,有益和SA-locus-capturing反转的不同固定概率.
主要成果:
- 捕捉SA位点在与祖先SLR的链接不平衡中的倒置有利于小的倒置大小.
- 中性,有益和无关的SA-locus-capturing反向有利于更大的尺寸.
- 有害突变负载,祖先的SLR位置和反转长度分布影响进化层的大小.
结论:
- 进化层的大小可以作为推动性染色体进化的选择制度的信息足迹.
- 在SA选择,突变负载和物理联系之间的相互作用形成了重组抑制.
- 需要进一步的经验研究来验证这些模型预测.
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