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过氧化物酶体在多形汉逊酵母中的再导入需要 Pex25 和 Rho1。

Peroxisome reintroduction in Hansenula polymorpha requires Pex25 and Rho1.

机构信息

Molecular Cell Biology, Groningen Biomolecular Sciences and Biotechnology Institute, Kluyver Centre for Genomics of Industrial Fermentation, University of Groningen, 9700 CC Groningen, Netherlands.

出版信息

J Cell Biol. 2011 May 30;193(5):885-900. doi: 10.1083/jcb.201012083. Epub 2011 May 23.

Abstract

We identified two proteins, Pex25 and Rho1, which are involved in reintroduction of peroxisomes in peroxisome-deficient yeast cells. These are, together with Pex3, the first proteins identified as essential for this process. Of the three members of the Hansenula polymorpha Pex11 protein family-Pex11, Pex25, and Pex11C-only Pex25 was required for reintroduction of peroxisomes into a peroxisome-deficient mutant strain. In peroxisome-deficient pex3 cells, Pex25 localized to structures adjacent to the ER, whereas in wild-type cells it localized to peroxisomes. Pex25 cells were not themselves peroxisome deficient but instead contained a slightly increased number of peroxisomes. Interestingly, pex11 pex25 double deletion cells, in which both peroxisome fission (due to the deletion of PEX11) and reintroduction (due to deletion of PEX25) was blocked, did display a peroxisome-deficient phenotype. Peroxisomes reappeared in pex11 pex25 cells upon synthesis of Pex25, but not of Pex11. Reintroduction in the presence of Pex25 required the function of the GTPase Rho1. These data therefore provide new and detailed insight into factors important for de novo peroxisome formation in yeast.

摘要

我们鉴定出两种蛋白质,Pex25 和 Rho1,它们参与了过氧化物酶体缺陷酵母细胞中过氧化物酶体的重新引入。这两种蛋白质与 Pex3 一起,是首次被鉴定为该过程所必需的蛋白质。在汉逊酵母 Pex11 蛋白家族的三个成员(Pex11、Pex25 和 Pex11C)中,只有 Pex25 是过氧化物酶体缺陷突变株中过氧化物酶体重新引入所必需的。在过氧化物酶体缺陷的 pex3 细胞中,Pex25 定位于 ER 附近的结构中,而在野生型细胞中,它定位于过氧化物酶体中。Pex25 细胞本身并不缺乏过氧化物酶体,而是含有稍微增加数量的过氧化物酶体。有趣的是,pex11pex25 双缺失细胞(由于 PEX11 的缺失导致过氧化物酶体分裂,由于 PEX25 的缺失导致过氧化物酶体重新引入都被阻断)确实表现出过氧化物酶体缺陷表型。在合成 Pex25 后,pex11pex25 细胞中的过氧化物酶体重新出现,但 Pex11 没有出现。在有 Pex25 的存在下的重新引入需要 GTPase Rho1 的功能。因此,这些数据为酵母中从头合成过氧化物酶体的重要因素提供了新的详细见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6573/3105547/9b7169e4754f/JCB_201012083_RGB_Fig1.jpg

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