Park Jae-Sook, Okumura Yuuya, Tachikawa Hiroyuki, Neiman Aaron M
Department of Biochemistry and Cell biology, Stony Brook University, Stony Brook, New York, USA.
Eukaryot Cell. 2013 Nov;12(11):1530-7. doi: 10.1128/EC.00239-13. Epub 2013 Sep 13.
The creation of haploid gametes in yeast, termed spores, requires the de novo formation of membranes within the cytoplasm. These membranes, called prospore membranes, enclose the daughter nuclei generated by meiosis. Proper growth and closure of prospore membranes require the highly conserved Vps13 protein. Mutation of SPO71, a meiosis-specific gene first identified as defective in spore formation, was found to display defects in membrane morphogenesis very similar to those seen in vps13Δ cells. Specifically, prospore membranes are smaller than in the wild type, they fail to close, and membrane vesicles are present within the prospore membrane lumen. As in vps13Δ cells, the levels of phophatidylinositol-4-phosphate are reduced in the prospore membranes of spo71Δ cells. SPO71 is required for the translocation of Vps13 from the endosome to the prospore membrane, and ectopic expression of SPO71 in vegetative cells results in mislocalization of Vps13. Finally, the two proteins can be coprecipitated from sporulating cells. We propose that Spo71 is a sporulation-specific partner for Vps13 and that they act in concert to regulate prospore membrane morphogenesis.
酵母中称为孢子的单倍体配子的产生需要在细胞质内重新形成膜。这些膜称为前孢子膜,包裹着减数分裂产生的子核。前孢子膜的正常生长和闭合需要高度保守的Vps13蛋白。SPO71是一个首次被鉴定为在孢子形成中有缺陷的减数分裂特异性基因,其突变显示出与vps13Δ细胞中所见非常相似的膜形态发生缺陷。具体而言,前孢子膜比野生型小,无法闭合,并且在前孢子膜腔内存在膜泡。与vps13Δ细胞一样,spo71Δ细胞的前孢子膜中磷脂酰肌醇-4-磷酸水平降低。SPO71是Vps13从内体转运到前孢子膜所必需的,并且SPO71在营养细胞中的异位表达导致Vps13定位错误。最后,可以从产孢细胞中共沉淀这两种蛋白质。我们提出Spo71是Vps13的孢子形成特异性伙伴,它们共同作用以调节前孢子膜的形态发生。