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Bro1对酿酒酵母中pH响应性Rim20定位的干预。

Intervention of Bro1 in pH-responsive Rim20 localization in Saccharomyces cerevisiae.

作者信息

Boysen Jacob H, Subramanian Shoba, Mitchell Aaron P

机构信息

Department of Microbiology, Columbia University, New York, New York 10032, USA.

出版信息

Eukaryot Cell. 2010 Apr;9(4):532-8. doi: 10.1128/EC.00027-10. Epub 2010 Feb 26.

Abstract

Yeast cells contain two Bro1 domain proteins: Bro1, which is required for endosomal trafficking, and Rim20, which is required for the response to the external pH via the Rim101 pathway. Rim20 associates with endosomal structures under alkaline growth conditions, when it promotes activation of Rim101 through proteolytic cleavage. We report here that the pH-dependent localization of Rim20 is contingent on the amount of Bro1 in the cell. Cells that lack Bro1 have increased endosomal Rim20-green fluorescent protein (GFP) under acidic conditions; cells that overexpress Bro1 have reduced endosomal Rim20-GFP under acidic or alkaline conditions. The novel endosomal association of Rim20-GFP in the absence of Bro1 requires ESCRT components including Vps27 but not specific Rim101 pathway components such as Dfg16. Vps27 influences the localization of Bro1 but is not required for RIM101 pathway activation in wild-type cells, thus suggesting that Rim20 enters the Bro1 localization pathway when a vacancy exists. Despite altered localization of Rim20, the lack of Bro1 does not bypass the need for signaling protein Dfg16 to activate Rim101, as evidenced by the expression levels of the Rim101 target genes RIM8 and SMP1. Therefore, endosomal association of Rim20 is not sufficient to promote Rim101 activation.

摘要

酵母细胞含有两种含Bro1结构域的蛋白质:参与内体运输所需的Bro1,以及通过Rim101途径响应外部pH值所需的Rim20。在碱性生长条件下,Rim20与内体结构相关联,此时它通过蛋白水解切割促进Rim101的激活。我们在此报告,Rim20的pH依赖性定位取决于细胞中Bro1的含量。缺乏Bro1的细胞在酸性条件下内体Rim20-绿色荧光蛋白(GFP)增加;过表达Bro1的细胞在酸性或碱性条件下内体Rim20-GFP减少。在没有Bro1的情况下,Rim20-GFP新的内体关联需要包括Vps27在内的ESCRT组件,但不需要特定的Rim101途径组件,如Dfg16。Vps27影响Bro1的定位,但在野生型细胞中RIM101途径激活不需要它,因此表明当有空位时,Rim20进入Bro1定位途径。尽管Rim20的定位发生了改变,但缺乏Bro1并不会绕过信号蛋白Dfg16激活Rim101的需求,Rim101靶基因RIM8和SMP1的表达水平证明了这一点。因此,Rim20的内体关联不足以促进Rim101的激活。

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