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首页> 外文期刊>Molecular biology of the cell >The localization of inner centromeric protein (INCENP) at the cleavage furrow is dependent on Kif12 and involves interactions of the N terminus of INCENP with the actin cytoskeleton
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The localization of inner centromeric protein (INCENP) at the cleavage furrow is dependent on Kif12 and involves interactions of the N terminus of INCENP with the actin cytoskeleton

机译:在切割沟槽处的内焦蛋白(IncenCP)的定位依赖于KIF12,涉及与肌动蛋白细胞骨架的INCENP的N末端的相互作用

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摘要

The inner centromeric protein (INCENP) and other chromosomal passenger proteins are known to localize on the cleavage furrow and to play a role in cytokinesis. However, it is not known how INCENP localizes on the furrow or whether this localization is separable from that at the midbody. Here, we show that the association of Dictyostelium INCENP (DdINCENP) with the cortex of the cleavage furrow involves interactions with the actin cytoskeleton and depends on the presence of the kinesin-6-related protein Kif12. We found that Kif12 is found on the central spindle and the cleavage furrow during cytokinesis. Kif12 is not required for the redistribution of DdINCENP from centromeres to the central spindle. However, in the absence of Kif12, DdINCENP fails to localize on the cleavage furrow. Domain analysis indicates that the N terminus of DdINCENP is necessary and sufficient for furrow localization and that it binds directly to the actin cytoskeleton. Our data suggest that INCENP moves from the central spindle to the furrow of a dividing cell by a Kif12-dependent pathway. Once INCENP reaches the equatorial cortex, it associates with the actin cytoskeleton where it then concentrates toward the end of cytokinesis.
机译:已知内焦蛋白(INCENCP)和其他染色体乘客蛋白质定位在切割沟槽上并在细胞因子中发挥作用。但是,尚不知道在沟渠上造成的INCENP,或者该本地化是否与中间人的定位是如何分离的。在这里,我们表明,Dictyostelium Incenpp(DdincenP)与切割沟槽皮质的关联涉及与肌动蛋白细胞骨架的相互作用,并取决于Kinesin-6相关蛋白KIF12的存在。我们发现在Cytokinesis期间发现KIF12在中央主轴和切割沟槽上。从Centromeres到中央主轴的DDINCENP再分配不需要KIF12。然而,在没有KIF12的情况下,DDINCENP未能定位在切割沟槽上。结构域分析表明DDINCENP的N末端是必要的,并且足以用于沟槽定位,并且它直接与肌动蛋白细胞骨架结合。我们的数据表明,INVENP通过KIF12依赖性途径从中央主轴移动到划分单元的沟槽。一旦INCENCP到达赤道皮质,它就会与肌动蛋白细胞骨架相关,然后它将其朝向细胞因子末端浓缩。

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