Eggert Ulrike S, Mitchison Timothy J, Field Christine M
Dana-Farber Cancer Institute and Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Annu Rev Biochem. 2006;75:543-66. doi: 10.1146/annurev.biochem.74.082803.133425.
The mechanism underlying cytokinesis, the final step in cell division, remains one of the major unsolved questions in basic cell biology. Thanks to advances in functional genomics and proteomics, we are now able to assemble a "parts list" of proteins involved in cytokinesis. In this review, we discuss how to relate this parts list to biological mechanism. For easier analysis, we split cytokinesis into discrete steps: cleavage plane specification, rearrangement of microtubule structures, contractile ring assembly, ring ingression, and completion. We report on the advances that have been made to understand these steps and how they can be integrated into a global understanding of cytokinesis. We also discuss the extent to which classic questions have been answered and identify major outstanding questions.
胞质分裂作为细胞分裂的最后一步,其潜在机制仍是基础细胞生物学中主要的未解决问题之一。得益于功能基因组学和蛋白质组学的进展,我们现在能够组装出参与胞质分裂的蛋白质“部件清单”。在本综述中,我们讨论如何将这份部件清单与生物学机制联系起来。为便于分析,我们将胞质分裂分为离散的步骤:分裂平面的确定、微管结构的重排、收缩环的组装、环的内陷以及完成。我们报告了在理解这些步骤方面所取得的进展,以及如何将它们整合到对胞质分裂的整体理解中。我们还讨论了经典问题已得到解答的程度,并确定了主要的悬而未决的问题。