Vitre Benjamin, Gudimchuk Nikita, Borda Ranier, Kim Yumi, Heuser John E, Cleveland Don W, Grishchuk Ekaterina L
Ludwig Institute for Cancer Research and Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA 92093.
Physiology Department, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
Mol Biol Cell. 2014 Aug 1;25(15):2272-81. doi: 10.1091/mbc.E14-01-0698. Epub 2014 Jun 11.
Centromere protein E (CENP-E) is a highly elongated kinesin that transports pole-proximal chromosomes during congression in prometaphase. During metaphase, it facilitates kinetochore-microtubule end-on attachment required to achieve and maintain chromosome alignment. In vitro CENP-E can walk processively along microtubule tracks and follow both growing and shrinking microtubule plus ends. Neither the CENP-E-dependent transport along microtubules nor its tip-tracking activity requires the unusually long coiled-coil stalk of CENP-E. The biological role for the CENP-E stalk has now been identified through creation of "Bonsai" CENP-E with significantly shortened stalk but wild-type motor and tail domains. We demonstrate that Bonsai CENP-E fails to bind microtubules in vitro unless a cargo is contemporaneously bound via its C-terminal tail. In contrast, both full-length and truncated CENP-E that has no stalk and tail exhibit robust motility with and without cargo binding, highlighting the importance of CENP-E stalk for its activity. Correspondingly, kinetochore attachment to microtubule ends is shown to be disrupted in cells whose CENP-E has a shortened stalk, thereby producing chromosome misalignment in metaphase and lagging chromosomes during anaphase. Together these findings establish an unexpected role of CENP-E elongated stalk in ensuring stability of kinetochore-microtubule attachments during chromosome congression and segregation.
着丝粒蛋白E(CENP-E)是一种高度细长的驱动蛋白,在有丝分裂前期染色体向赤道板移动的过程中负责运输靠近纺锤体极的染色体。在中期,它促进着丝粒与微管末端的端对端附着,这是实现和维持染色体排列所必需的。在体外,CENP-E可以沿着微管轨道持续移动,并追踪微管不断生长和收缩的正端。无论是CENP-E依赖的沿微管运输还是其末端追踪活性,都不需要CENP-E异常长的卷曲螺旋茎。现在,通过创建茎显著缩短但具有野生型马达和尾部结构域的“盆景”CENP-E,已经确定了CENP-E茎的生物学作用。我们证明,除非通过其C末端尾部同时结合货物,否则盆景CENP-E在体外无法结合微管。相比之下,没有茎和尾部的全长和截短的CENP-E在有或没有货物结合的情况下都表现出强大的运动能力,这突出了CENP-E茎对其活性的重要性。相应地,在CENP-E茎缩短的细胞中,着丝粒与微管末端的附着被证明会受到破坏,从而在中期产生染色体排列错误,并在后期产生滞后染色体。这些发现共同确立了CENP-E细长茎在确保染色体向赤道板移动和分离过程中着丝粒-微管附着稳定性方面的意外作用。