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外排型Rabs蛋白Ypt3和Ypt2调控裂殖酵母中孢子质膜生物合成的早期步骤。

The exocytic Rabs Ypt3 and Ypt2 regulate the early step of biogenesis of the spore plasma membrane in fission yeast.

作者信息

Imada Kazuki, Nakamura Taro

机构信息

Department of Biology, Graduate School of Science, Osaka City University, Sumiyoshi-ku, Osaka 558-8585, Japan.

Department of Biology, Graduate School of Science, Osaka City University, Sumiyoshi-ku, Osaka 558-8585, Japan

出版信息

Mol Biol Cell. 2016 Nov 1;27(21):3317-3328. doi: 10.1091/mbc.E16-03-0162. Epub 2016 Sep 14.

DOI:10.1091/mbc.E16-03-0162
PMID:27630265
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5170864/
Abstract

During fission yeast sporulation, a membrane compartment called the forespore membrane (FSM) is newly formed on the spindle pole body (SPB). The FSM expands by membrane vesicle fusion, encapsulates the daughter nucleus resulting from meiosis, and eventually matures into the plasma membrane of the spore. Although many of the genes involved in FSM formation have been identified, its molecular mechanism is not fully understood. Here a genetic screen for sporulation-deficient mutations identified Ypt3, a Rab-family small GTPase known to function in the exocytic pathway. The ypt3-ki8 mutant showed defects in both the initiation of FSM biogenesis and FSM expansion. We also show that a mutation in Ypt2, another Rab protein that may function in the same pathway as Ypt3, compromises the initiation of FSM formation. As meiosis proceeds, both GFP-Ypt3 and GFP-Ypt2 are observed at the SPB and then relocalize to the FSM. Their localizations at the SPB precede FSM formation and depend on the meiotic SPB component Spo13, a putative GDP/GTP exchange factor for Ypt2. Given that Spo13 is essential for initiating FSM formation, these results suggest that two exocytic Rabs, Ypt3 and Ypt2, regulate the initiation of FSM formation on the SPB in concert with Spo13.

摘要

在裂殖酵母形成孢子的过程中,一种称为前孢子膜(FSM)的膜性区室在纺锤体极体(SPB)上重新形成。FSM通过膜泡融合而扩张,包裹减数分裂产生的子细胞核,并最终成熟为孢子的质膜。尽管已经鉴定出许多参与FSM形成的基因,但其分子机制仍未完全了解。在这里,通过对孢子形成缺陷突变进行遗传筛选,鉴定出Ypt3,一种已知在胞吐途径中发挥作用的Rab家族小GTP酶。ypt3-ki8突变体在FSM生物发生的起始和FSM扩张方面均表现出缺陷。我们还表明,Ypt2(另一种可能与Ypt3在同一途径中发挥作用的Rab蛋白)中的突变会损害FSM形成的起始。随着减数分裂的进行,在SPB处观察到绿色荧光蛋白标记的Ypt3(GFP-Ypt3)和绿色荧光蛋白标记的Ypt2(GFP-Ypt2),然后它们重新定位到FSM。它们在SPB处的定位先于FSM形成,并依赖于减数分裂SPB组分Spo13(一种推测的Ypt2的GDP/GTP交换因子)。鉴于Spo13对于启动FSM形成至关重要,这些结果表明,两种胞吐Rab蛋白Ypt3和Ypt2与Spo13协同调节SPB上FSM形成的起始。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/d31eb4518413/3317fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/d264826ce91f/3317fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/b2892a136ac8/3317fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/61ac7a83225d/3317fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/544e0dcc7bbe/3317fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/c3766806664d/3317fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/a7bd764a51f0/3317fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/f04964ba8972/3317fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/39451d749a6c/3317fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/017869a3f0a6/3317fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/d31eb4518413/3317fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/d264826ce91f/3317fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/b2892a136ac8/3317fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/61ac7a83225d/3317fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/544e0dcc7bbe/3317fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/c3766806664d/3317fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/a7bd764a51f0/3317fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/f04964ba8972/3317fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/39451d749a6c/3317fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/017869a3f0a6/3317fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e763/5170864/d31eb4518413/3317fig10.jpg

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