Center for Cell and Genome Sciences, University of Utah, Salt Lake City, UT 84112, USA.
School of Biological Sciences, University of Utah, Salt Lake City, UT 84112, USA.
J Cell Sci. 2021 May 15;134(10). doi: 10.1242/jcs.255745. Epub 2021 May 26.
The formation of crossovers between homologous chromosomes is key to sexual reproduction. In most species, crossovers are spaced further apart than would be expected if they formed independently, a phenomenon termed crossover interference. Despite more than a century of study, the molecular mechanisms implementing crossover interference remain a subject of active debate. Recent findings of how signaling proteins control the formation of crossovers and about the interchromosomal interface in which crossovers form offer new insights into this process. In this Review, we present a cell biological and biophysical perspective on crossover interference, summarizing the evidence that links interference to the spatial, dynamic, mechanical and molecular properties of meiotic chromosomes. We synthesize this physical understanding in the context of prevailing mechanistic models that aim to explain how crossover interference is implemented.
同源染色体之间交叉的形成是有性生殖的关键。在大多数物种中,交叉的间隔比独立形成时预期的要远,这种现象被称为交叉干扰。尽管已经研究了一个多世纪,但实施交叉干扰的分子机制仍然是一个活跃的争论话题。最近发现信号蛋白如何控制交叉的形成以及交叉形成的染色体间界面,为这一过程提供了新的见解。在这篇综述中,我们从细胞生物学和生物物理学的角度介绍了交叉干扰,总结了将干扰与减数分裂染色体的空间、动态、力学和分子特性联系起来的证据。我们将这种物理理解综合在旨在解释交叉干扰如何实施的流行机制模型的背景下。