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生殖命运决定因素通过降低细胞分裂平面处的隔膜蛋白和肌球蛋白水平来保护生殖前体细胞的分裂。

Germ fate determinants protect germ precursor cell division by reducing septin and anillin levels at the cell division plane.

机构信息

Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY 10032.

Department of Biological Sciences, Columbia University, New York, NY 10027.

出版信息

Mol Biol Cell. 2024 Jul 1;35(7):ar94. doi: 10.1091/mbc.E24-02-0096-T. Epub 2024 May 2.

Abstract

Animal cell cytokinesis, or the physical division of one cell into two, is thought to be driven by constriction of an actomyosin contractile ring at the division plane. The mechanisms underlying cell type-specific differences in cytokinesis remain unknown. Germ cells are totipotent cells that pass genetic information to the next generation. Previously, using mutant 4-cell embryos, we found that the P2 germ precursor cell is protected from cytokinesis failure and can divide with greatly reduced F-actin levels at the cell division plane. Here, we identified two canonical germ fate determinants required for P2-specific cytokinetic protection: PIE-1 and POS-1. Neither has been implicated previously in cytokinesis. These germ fate determinants protect P2 cytokinesis by reducing the accumulation of septin and anillin at the division plane, which here act as negative regulators of cytokinesis. These findings may provide insight into the regulation of cytokinesis in other cell types, especially in stem cells with high potency.

摘要

动物细胞的胞质分裂,即将一个细胞分裂为两个的过程,被认为是由分裂平面处的肌动球蛋白收缩环的收缩驱动的。细胞类型特异性胞质分裂差异的机制尚不清楚。生殖细胞是具有全能性的细胞,可以将遗传信息传递给下一代。先前,使用突变体 4 细胞胚胎,我们发现 P2 生殖前体细胞免受胞质分裂失败的影响,并且可以在细胞分裂平面处以大大降低的 F-肌动蛋白水平进行分裂。在这里,我们确定了两个需要的典型生殖命运决定因素,以保护 P2 特有的胞质分裂:PIE-1 和 POS-1。以前都没有被牵连在胞质分裂中。这些生殖命运决定因素通过减少分裂平面处的隔蛋白和肌球蛋白的积累来保护 P2 的胞质分裂,在这里,它们作为胞质分裂的负调节剂。这些发现可能为其他细胞类型,特别是具有高潜能的干细胞的胞质分裂调节提供了新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81ae/11244169/ab9b2364e7b9/mbc-35-ar94-g001.jpg

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