Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School and Howard Hughes Medical Institute, 250 Longwood Avenue, Boston, MA 02115, USA.
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School and Howard Hughes Medical Institute, 250 Longwood Avenue, Boston, MA 02115, USA.
Trends Cell Biol. 2018 Jan;28(1):22-33. doi: 10.1016/j.tcb.2017.09.002. Epub 2017 Oct 3.
During a single human lifetime, nearly one quintillion chromosomes separate from their sisters and transit to their destinations in daughter cells. Unlike DNA replication, chromosome segregation has no template, and, unlike transcription, errors frequently lead to a total loss of cell viability. Rapid progress in recent years has shown how kinetochores enable faithful execution of this process by connecting chromosomal DNA to microtubules. These findings have transformed our idea of kinetochores from cytological features to immense molecular machines and now allow molecular interpretation of many long-appreciated kinetochore functions. In this review we trace kinetochore protein connectivity from chromosomal DNA to microtubules, relating new findings to important points of regulation and function.
在人类的一生中,几乎有五分之一的染色体与其姐妹染色体分离,并转移到子细胞的目的地。与 DNA 复制不同,染色体分离没有模板;与转录不同,错误常常导致细胞完全失去活力。近年来的快速进展表明,动粒如何通过将染色体 DNA 连接到微管上来实现这一过程的忠实执行。这些发现将我们对动粒的认识从细胞学特征转变为巨大的分子机器,并使我们现在能够对许多长期以来被认可的动粒功能进行分子解释。在这篇综述中,我们从染色体 DNA 到微管追踪动粒蛋白的连接,将新发现与重要的调节和功能点联系起来。