Salmon E D, Cimini D, Cameron L A, DeLuca J G
Department of Biology, 607 Fordham Hall, University of North Carolina, Chapel Hill, NC 27599-3280, USA.
Philos Trans R Soc Lond B Biol Sci. 2005 Mar 29;360(1455):553-68. doi: 10.1098/rstb.2004.1610.
Merotelic kinetochore attachment is a major source of aneuploidy in mammalian tissue cells in culture. Mammalian kinetochores typically have binding sites for about 20-25 kinetochore microtubules. In prometaphase, kinetochores become merotelic if they attach to microtubules from opposite poles rather than to just one pole as normally occurs. Merotelic attachments support chromosome bi-orientation and alignment near the metaphase plate and they are not detected by the mitotic spindle checkpoint. At anaphase onset, sister chromatids separate, but a chromatid with a merotelic kinetochore may not be segregated correctly, and may lag near the spindle equator because of pulling forces toward opposite poles, or move in the direction of the wrong pole. Correction mechanisms are important for preventing segregation errors. There are probably more than 100 times as many PtK1 tissue cells with merotelic kinetochores in early mitosis, and about 16 times as many entering anaphase as the 1% of cells with lagging chromosomes seen in late anaphase. The role of spindle mechanics and potential functions of the Ndc80/Nuf2 protein complex at the kinetochore/microtubule interface is discussed for two correction mechanisms: one that functions before anaphase to reduce the number of kinetochore microtubules to the wrong pole, and one that functions after anaphase onset to move merotelic kinetochores based on the ratio of kinetochore microtubules to the correct versus incorrect pole.
在培养的哺乳动物组织细胞中,动粒的错向连接是染色体数目异常的一个主要来源。哺乳动物的动粒通常有大约20 - 25个动粒微管的结合位点。在前中期,如果动粒与来自相反两极的微管相连,而不是像正常情况那样只与一极相连,就会形成错向连接。错向连接支持染色体在中期板附近的双定向和排列,并且不会被有丝分裂纺锤体检查点检测到。在后期开始时,姐妹染色单体分离,但带有错向连接动粒的染色单体可能无法正确分离,并且可能由于向相反两极的拉力而滞留在纺锤体赤道附近,或者向错误的极移动。校正机制对于防止分离错误很重要。在有丝分裂早期,具有错向连接动粒的PtK1组织细胞数量可能比后期出现滞后染色体的细胞多100倍以上,进入后期的细胞数量约为后期末出现滞后染色体细胞数量的16倍。本文讨论了纺锤体力学的作用以及动粒/微管界面处Ndc80/Nuf2蛋白复合体的潜在功能,涉及两种校正机制:一种在后期之前起作用,减少与错误极相连的动粒微管数量;另一种在后期开始后起作用,根据动粒微管与正确极和错误极的比例移动错向连接的动粒。