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分选连接蛋白 9 将网格蛋白重链募集到有丝分裂纺锤体上,以实现染色体的对准和分离。

Sorting nexin 9 recruits clathrin heavy chain to the mitotic spindle for chromosome alignment and segregation.

机构信息

Children's Medical Research Institute, the University of Sydney, Westmead, New South Wales, Australia.

出版信息

PLoS One. 2013 Jul 5;8(7):e68387. doi: 10.1371/journal.pone.0068387. Print 2013.

Abstract

Sorting nexin 9 (SNX9) and clathrin heavy chain (CHC) each have roles in mitosis during metaphase. Since the two proteins directly interact for their other cellular function in endocytosis we investigated whether they also interact for metaphase and operate on the same pathway. We report that SNX9 and CHC functionally interact during metaphase in a specific molecular pathway that contributes to stabilization of mitotic spindle kinetochore (K)-fibres for chromosome alignment and segregation. This function is independent of their endocytic role. SNX9 residues in the clathrin-binding low complexity domain are required for CHC association and for targeting both CHC and transforming acidic coiled-coil protein 3 (TACC3) to the mitotic spindle. Mutation of these sites to serine increases the metaphase plate width, indicating inefficient chromosome congression. Therefore SNX9 and CHC function in the same molecular pathway for chromosome alignment and segregation, which is dependent on their direct association.

摘要

分选连接蛋白 9(SNX9)和网格蛋白重链(CHC)在有丝分裂中期都有各自的作用。由于这两种蛋白在细胞内吞作用中通过直接相互作用发挥其他功能,我们研究了它们是否在中期也相互作用,并在同一途径上发挥作用。我们报告称,SNX9 和 CHC 在特定的分子途径中在功能上相互作用,该途径有助于稳定有丝分裂纺锤体动粒(K)-纤维,以实现染色体的排列和分离。这个功能与它们的内吞作用无关。网格蛋白结合的低复杂度结构域中的 SNX9 残基对于 CHC 结合以及将 CHC 和转化酸性卷曲螺旋蛋白 3(TACC3)靶向有丝分裂纺锤体是必需的。将这些位点突变为丝氨酸会增加中期板的宽度,表明染色体的内聚效率降低。因此,SNX9 和 CHC 在同一分子途径中发挥作用,用于染色体的排列和分离,这取决于它们的直接相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2036/3702553/17e48a89fdce/pone.0068387.g001.jpg

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