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驱动蛋白6家族成员Subito参与有丝分裂纺锤体组装并与有丝分裂调节因子相互作用。

Kinesin 6 family member Subito participates in mitotic spindle assembly and interacts with mitotic regulators.

作者信息

Cesario Jeff M, Jang Janet K, Redding Bethany, Shah Nishit, Rahman Taslima, McKim Kim S

机构信息

Waksman Institute and Department of Genetics, Rutgers, The State University of New Jersey, Piscataway, NJ 08854-8020, USA.

出版信息

J Cell Sci. 2006 Nov 15;119(Pt 22):4770-80. doi: 10.1242/jcs.03235. Epub 2006 Oct 31.

Abstract

Drosophila Subito is a kinesin 6 family member and ortholog of mitotic kinesin-like protein (MKLP2) in mammalian cells. Based on the previously established requirement for Subito in meiotic spindle formation and for MKLP2 in cytokinesis, we investigated the function of Subito in mitosis. During metaphase, Subito localized to microtubules at the center of the mitotic spindle, probably interpolar microtubules that originate at the poles and overlap in antiparallel orientation. Consistent with this localization pattern, subito mutants improperly assembled microtubules at metaphase, causing activation of the spindle assembly checkpoint and lagging chromosomes at anaphase. These results are the first demonstration of a kinesin 6 family member with a function in mitotic spindle assembly, possibly involving the interpolar microtubules. However, the role of Subito during mitotic anaphase resembles other kinesin 6 family members. Subito localizes to the spindle midzone at anaphase and is required for the localization of Polo, Incenp and Aurora B. Genetic evidence suggested that the effects of subito mutants are attenuated as a result of redundant mechanisms for spindle assembly and cytokinesis. For example, subito double mutants with ncd, polo, Aurora B or Incenp mutations were synthetic lethal with severe defects in microtubule organization.

摘要

果蝇Subito是一种驱动蛋白6家族成员,是哺乳动物细胞中有丝分裂驱动蛋白样蛋白(MKLP2)的直系同源物。基于先前确定的Subito在减数分裂纺锤体形成中的需求以及MKLP2在胞质分裂中的需求,我们研究了Subito在有丝分裂中的功能。在中期,Subito定位于有丝分裂纺锤体中心的微管上,可能是起源于两极并以反平行方向重叠的极间微管。与这种定位模式一致,subito突变体在中期微管组装不当,导致纺锤体组装检查点激活和后期染色体滞后。这些结果首次证明了驱动蛋白6家族成员在有丝分裂纺锤体组装中具有功能,可能涉及极间微管。然而,Subito在有丝分裂后期的作用类似于其他驱动蛋白6家族成员。Subito在后期定位于纺锤体中间区,是Polo、Incenp和Aurora B定位所必需的。遗传证据表明,由于纺锤体组装和胞质分裂的冗余机制,subito突变体的影响减弱。例如,具有ncd、polo、Aurora B或Incenp突变的subito双突变体是合成致死的,在微管组织方面存在严重缺陷。

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