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Aim44p调节Hof1p的磷酸化,以促进芽殖酵母胞质分裂过程中收缩环的闭合。

Aim44p regulates phosphorylation of Hof1p to promote contractile ring closure during cytokinesis in budding yeast.

作者信息

Wolken Dana M Alessi, McInnes Joseph, Pon Liza A

机构信息

Department of Pathology and Cell Biology, Columbia University, New York, NY 10027 School of Engineering and Science, Jacobs University Bremen, 28759 Bremen, Germany.

出版信息

Mol Biol Cell. 2014 Mar;25(6):753-62. doi: 10.1091/mbc.E13-06-0317. Epub 2014 Jan 22.

Abstract

Whereas actomyosin and septin ring organization and function in cytokinesis are thoroughly described, little is known regarding the mechanisms by which the actomyosin ring interacts with septins and associated proteins to coordinate cell division. Here we show that the protein product of YPL158C, Aim44p, undergoes septin-dependent recruitment to the site of cell division. Aim44p colocalizes with Myo1p, the type II myosin of the contractile ring, throughout most of the cell cycle. The Aim44p ring does not contract when the actomyosin ring closes. Instead, it forms a double ring that associates with septin rings on mother and daughter cells after cell separation. Deletion of AIM44 results in defects in contractile ring closure. Aim44p coimmunoprecipitates with Hof1p, a conserved F-BAR protein that binds both septins and type II myosins and promotes contractile ring closure. Deletion of AIM44 results in a delay in Hof1p phosphorylation and altered Hof1p localization. Finally, overexpression of Dbf2p, a kinase that phosphorylates Hof1p and is required for relocalization of Hof1p from septin rings to the contractile ring and for Hof1p-triggered contractile ring closure, rescues the cytokinesis defect observed in aim44 cells. Our studies reveal a novel role for Aim44p in regulating contractile ring closure through effects on Hof1p.

摘要

虽然在胞质分裂中肌动球蛋白和隔膜蛋白环的组织和功能已得到充分描述,但关于肌动球蛋白环与隔膜蛋白及相关蛋白相互作用以协调细胞分裂的机制却知之甚少。在此,我们表明YPL158C的蛋白产物Aim44p在隔膜蛋白依赖的情况下被募集到细胞分裂位点。在细胞周期的大部分时间里,Aim44p与收缩环的II型肌球蛋白Myo1p共定位。当肌动球蛋白环关闭时,Aim44p环不会收缩。相反,它会形成一个双环,在细胞分离后与母细胞和子细胞上的隔膜蛋白环相关联。删除AIM44会导致收缩环关闭出现缺陷。Aim44p与Hof1p共免疫沉淀,Hof1p是一种保守的F-BAR蛋白,它既能结合隔膜蛋白又能结合II型肌球蛋白,并促进收缩环关闭。删除AIM44会导致Hof1p磷酸化延迟并改变Hof1p的定位。最后,Dbf2p的过表达(Dbf2p是一种使Hof1p磷酸化的激酶,是Hof1p从隔膜蛋白环重新定位到收缩环以及Hof1p触发收缩环关闭所必需的)挽救了在aim44细胞中观察到的胞质分裂缺陷。我们的研究揭示了Aim44p通过对Hof1p的作用在调节收缩环关闭方面的新作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/661d/3952846/5b73fc5e9001/753fig1.jpg

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