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Comparison of Cell Wall Localization among Pir Family Proteins and Functional Dissection of the Region Required for Cell Wall Binding and Bud Scar Recruitment of Pir1p

机译:Pir家族蛋白之间的细胞壁定位和Pir1p细胞壁结合和芽疤痕招募所需区域的功能解剖的比较

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We examined the localization of the Pir protein family (Pir1 to Pir4), which is covalently linked to the cell wall in an unknown manner. In contrast to the other Pir proteins, a fusion of Pir1p and monomeric red fluorescent protein distributed in clusters in pir1Δ cells throughout the period of cultivation, indicating that Pir1p is localized in bud scars. Further microscopic analysis revealed that Pir1p is expressed inside the chitin rings of the bud scars. Stepwise deletion of the eight units of the repetitive sequence of Pir1p revealed that one unit is enough for the protein to bind bud scars and that the extent of binding of Pir1p to the cell wall depends on the number of these repetitive units. The localization of a chimeric Pir1p in which the repetitive sequence of Pir1p was replaced with that of Pir4p revealed the functional role of the different protein regions, specifically, that the repetitive sequence is required for binding to the cell wall and that the C-terminal sequence is needed for recruitment to bud scars. This is the first report that bud scars contain proteins like Pir1p as internal components.
机译:我们检查了Pir蛋白家族(Pir1至Pir4)的定位,该蛋白以未知方式共价连接到细胞壁。与其他Pir蛋白相反,在整个培养过程中,Pir1p和单体红色荧光蛋白的融合体分布在 pir1 Δ细胞的簇中,表明Pir1p定位于芽疤中。进一步的显微镜分析表明,Pir1p在芽疤的几丁质环内表达。 Pir1p重复序列的八个单元的逐步删除表明,一个单元足以使蛋白质结合芽疤痕,并且Pir1p与细胞壁结合的程度取决于这些重复单元的数量。嵌合的Pir1p的定位(其中Pir1p的重复序列被Pir4p的序列取代)揭示了不同蛋白质区域的功能,特别是,重复序列是结合细胞壁所必需的,并且C端序列需要招募来消除疤痕。这是第一个关于芽疤含有内在蛋白如Pir1p的报道。

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