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Pex3p在过氧化物酶体形成和遗传中的双重功能。

A dual function for Pex3p in peroxisome formation and inheritance.

作者信息

Munck Joanne M, Motley Alison M, Nuttall James M, Hettema Ewald H

机构信息

Department of Molecular Biology and Biotechnology, University of Sheffield, Sheffield S10 2TN, England, UK.

出版信息

J Cell Biol. 2009 Nov 16;187(4):463-71. doi: 10.1083/jcb.200906161. Epub 2009 Nov 9.

Abstract

Saccharomyces cerevisiae Pex3p has been shown to act at the ER during de novo peroxisome formation. However, its steady state is at the peroxisomal membrane, where its role is debated. Here we show that Pex3p has a dual function: one in peroxisome formation and one in peroxisome segregation. We show that the peroxisome retention factor Inp1p interacts physically with Pex3p in vitro and in vivo, and split-GFP analysis shows that the site of interaction is the peroxisomal membrane. Furthermore, we have generated PEX3 alleles that support peroxisome formation but fail to support recruitment of Inp1p to peroxisomes, and as a consequence are affected in peroxisome segregation. We conclude that Pex3p functions as an anchor for Inp1p at the peroxisomal membrane, and that this function is independent of its role at the ER in peroxisome biogenesis.

摘要

酿酒酵母Pex3p已被证明在从头开始形成过氧化物酶体的过程中在内质网发挥作用。然而,其稳态位于过氧化物酶体膜上,其在该位置的作用存在争议。在此我们表明,Pex3p具有双重功能:一个在过氧化物酶体形成中,另一个在过氧化物酶体分离中。我们表明,过氧化物酶体保留因子Inp1p在体外和体内都与Pex3p发生物理相互作用,并且分裂GFP分析表明相互作用位点是过氧化物酶体膜。此外,我们已产生支持过氧化物酶体形成但不能支持Inp1p募集到过氧化物酶体的PEX3等位基因,因此在过氧化物酶体分离方面受到影响。我们得出结论,Pex3p在过氧化物酶体膜上作为Inp1p的锚定物发挥作用,并且该功能独立于其在内质网中在过氧化物酶体生物发生中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3efb/2779223/5843b07f2806/JCB_200906161_RGB_Fig1.jpg

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