McNally Karen, Audhya Anjon, Oegema Karen, McNally Francis J
Section of Molecular and Cellular Biology, University of California, Davis, CA 95616, USA.
J Cell Biol. 2006 Dec 18;175(6):881-91. doi: 10.1083/jcb.200608117.
Accurate control of spindle length is a conserved feature of eukaryotic cell division. Lengthening of mitotic spindles contributes to chromosome segregation and cytokinesis during mitosis in animals and fungi. In contrast, spindle shortening may contribute to conservation of egg cytoplasm during female meiosis. Katanin is a microtubule-severing enzyme that is concentrated at mitotic and meiotic spindle poles in animals. We show that inhibition of katanin slows the rate of spindle shortening in nocodazole-treated mammalian fibroblasts and in untreated Caenorhabditis elegans meiotic embryos. Wild-type C. elegans meiotic spindle shortening proceeds through an early katanin-independent phase marked by increasing microtubule density and a second, katanin-dependent phase that occurs after microtubule density stops increasing. In addition, double-mutant analysis indicated that gamma-tubulin-dependent nucleation and microtubule severing may provide redundant mechanisms for increasing microtubule number during the early stages of meiotic spindle assembly.
纺锤体长度的精确控制是真核细胞分裂的一个保守特征。有丝分裂纺锤体的延长有助于动物和真菌有丝分裂期间的染色体分离和胞质分裂。相比之下,纺锤体缩短可能有助于雌性减数分裂期间卵细胞细胞质的保留。katanin是一种微管切断酶,在动物的有丝分裂和减数分裂纺锤体极处富集。我们发现,抑制katanin会减缓用诺考达唑处理的哺乳动物成纤维细胞和未处理的秀丽隐杆线虫减数分裂胚胎中纺锤体缩短的速率。野生型秀丽隐杆线虫减数分裂纺锤体缩短过程经历一个早期不依赖katanin的阶段,其特征是微管密度增加,以及第二个依赖katanin的阶段,该阶段发生在微管密度停止增加之后。此外,双突变分析表明,γ-微管蛋白依赖性成核和微管切断可能为减数分裂纺锤体组装早期增加微管数量提供冗余机制。