Department of Molecular and Cell Biology, University of California, Berkeley, CA, 94720 USA.
Curr Opin Cell Biol. 2020 Jun;64:43-49. doi: 10.1016/j.ceb.2020.02.003. Epub 2020 Mar 6.
As a cell prepares to divide, its genetic material changes dramatically in both form and function. During interphase, a dynamic interplay between DNA compartmentalization and transcription functions to program cell identity. During mitosis, this purpose is put on hold and instead chromosomes function to facilitate their accurate segregation to daughter cells. Chromatin loops are rearranged, stacked, and compressed to form X-shaped chromosomes that are neatly aligned at the center of the mitotic spindle and ready to withstand the forces of anaphase. Many factors that contribute to mitotic chromosome assembly have now been identified, but how the plethora of molecular mechanisms operate in concert to give rise to the distinct form and physical properties of mitotic chromosomes at the cellular scale remains under active investigation. In this review, we discuss recent work that addresses a major challenge for the field: How to connect the molecular-level activities to large-scale changes in whole-chromosome architecture that determine mitotic chromosome size, shape, and function.
当一个细胞准备分裂时,其遗传物质在形式和功能上都发生了巨大的变化。在间期,DNA 区室化和转录功能之间的动态相互作用有助于编程细胞的身份。在有丝分裂过程中,这个目的被搁置,取而代之的是染色体发挥作用,以促进它们准确地分配到子细胞中。染色质环被重新排列、堆叠和压缩,形成 X 形染色体,整齐地排列在有丝分裂纺锤体的中心,准备承受后期的力。现在已经确定了许多有助于有丝分裂染色体组装的因素,但是众多的分子机制如何协同作用,在细胞尺度上产生有丝分裂染色体的独特形态和物理特性,仍然是一个活跃的研究领域。在这篇综述中,我们讨论了最近的工作,这些工作解决了该领域的一个主要挑战:如何将分子水平的活动与决定有丝分裂染色体大小、形状和功能的整个染色体结构的大规模变化联系起来。