Asakawa Kazuhide, Toya Mika, Sato Masamitsu, Kanai Muneyoshi, Kume Kazunori, Goshima Tetsuya, Garcia Miguel Angel, Hirata Dai, Toda Takashi
Laboratory of Cell Regulation, Cancer Research UK, London Research Institute, Lincoln's Inn Fields Laboratories, 44 Lincoln's Inn Fields, London WC2A 3PX, UK.
EMBO Rep. 2005 Dec;6(12):1194-200. doi: 10.1038/sj.embor.7400540.
Bipolar microtubule attachment is central to genome stability. Here, we investigate the mitotic role of the fission yeast EB1 homologue Mal3. Mal3 shows dynamic inward movement along the spindle, initial emergence at the spindle pole body (SPB) and translocation towards the equatorial plane, followed by sudden disappearance. Deletion of Mal3 results in early mitotic delay, which is dependent on the Bub1, but not the Mad2, spindle checkpoint. Consistently, Bub1, but not Mad2, shows prolonged kinetochore localization. Double mutants between mal3 and a subset of checkpoint mutants, including bub1, bub3, mad3 and mph1, but not mad1 or mad2, show massive chromosome mis-segregation defects. In mal3bub1 mutants, both sister centromeres tend to remain in close proximity to one of the separating SPBs. Further analysis indicates that mis-segregated centromeres are exclusively associated with the mother SPB. Mal3, therefore, has a role in preventing monopolar attachment in cooperation with the Bub1/Bub3/Mad3/Mph1-dependent checkpoint.
双极微管附着对于基因组稳定性至关重要。在此,我们研究了裂殖酵母EB1同源物Mal3在有丝分裂中的作用。Mal3沿纺锤体呈现动态向内移动,最初出现在纺锤体极体(SPB)并向赤道平面移位,随后突然消失。缺失Mal3会导致有丝分裂早期延迟,这依赖于Bub1,但不依赖于Mad2纺锤体检查点。一致地,Bub1而非Mad2显示出在动粒上的定位延长。mal3与包括bub1、bub3、mad3和mph1但不包括mad1或mad2的一部分检查点突变体之间的双突变体显示出大量染色体错分离缺陷。在mal3bub1突变体中,两个姐妹着丝粒往往保持与其中一个分离的SPB紧密相邻。进一步分析表明,错分离的着丝粒仅与母本SPB相关。因此,Mal3在与Bub1/Bub3/Mad3/Mph1依赖性检查点协同作用中具有防止单极附着的作用。