首页> 外文期刊>Journal of Molecular Biology >A New Yeast Peroxin, Pex36, a Functional Homolog of Mammalian PEX16, Functions in the ER-to-Peroxisome Traffic of Peroxisomal Membrane Proteins
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A New Yeast Peroxin, Pex36, a Functional Homolog of Mammalian PEX16, Functions in the ER-to-Peroxisome Traffic of Peroxisomal Membrane Proteins

机译:一种新的酵母过氧化辛,Pex36,哺乳动物Pex16的功能同源物,在过氧化合物血型膜蛋白的ER-过氧缺氧血症中的作用

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Abstract Peroxisomal membrane proteins (PMPs) traffic to peroxisomes by two mechanisms: direct insertion from the cytosol into the peroxisomal membrane and indirect trafficking to peroxisomes via the endoplasmic reticulum (ER). In mammals and yeast, several PMPs traffic via the ER in a Pex3- and Pex19-dependent manner. In Komagataella phaffii (formerly called Pichia pastoris ) specifically, the indirect traffic of Pex2, but not of Pex11 or Pex17, depends on Pex3, but all PMPs tested for indirect trafficking require Pex19. In mammals, the indirect traffic of PMPs also requires PEX16, a protein that is absent in most yeast species. In this study, we isolated PEX36 , a new gene in K. phaffii , which encodes a PMP. Pex36 is required for cell growth in conditions that require peroxisomes for the metabolism of certain carbon sources. This growth defect in cells lacking Pex36 can be rescued by the expression of human PEX16, Saccharomyces cerevisiae Pex34, or by overexpression of the endogenous K. phaffii Pex25. Pex36 is not an essential protein for peroxisome proliferation, but in the absence of the functionally redundant protein, Pex25, it becomes essential and less than 20% of these cells show import-incompetent, peroxisome-like structures (peroxisome remnants). In the absence of both proteins, peroxisome biogenesis and the intra-ER sorting of Pex2 and Pex11C are seriously impaired, likely by affecting Pex3 and Pex19 function. Graphical abstract Display Omitted Highlights ? Characterization of a new peroxisomal membrane protein, Pex36 in K. phaffii ? Pex36 shares some functional homology with human Pex16 and S. cerevisiae Pex34. ? Pex25 and Pex36 are redundant proteins and cells lacking both are synthetic lethal. ? Pex25 and Pex36 are required for the ER-to-peroxisome targeting of Pex2 and Pex11C. ? The complex between Pex3 and Pex19 is impaired in the absence of both Pex25 and Pex36.
机译:摘要过氧硅烷膜蛋白(PMP)通过两种机制到过氧化物的流量:通过内质网(ER)直接插入过氧硅醇进入过氧硅烷膜和间接贩运过氧化物体。在哺乳动物和酵母中,通过ER以PEX3和PEX19依赖方式通过ER的几个PMP流量。在Komagataella Phaffii(以前称为Pichia Pastoris),特别是Pex2,但不是Pex11或Pex17的间接流量取决于PEX3,但所有对间接贩运的PMP都需要PEX19。在哺乳动物中,PMP的间接流量也需要PEX16,蛋白质在大多数酵母种类中缺席。在本研究中,我们分离Pex36,Pex36是Phaffii的新基因,其编码PMP。 PEX36是细胞生长所必需的,在需要过氧缺氧的条件下进行某些碳源的代谢。缺乏PEX36的细胞中的这种生长缺陷可以通过人pex16,酿酒酵母酿酒酵母pex34或通过内源性K. phaffii pex25的过表达来抵押。 Pex36不是过氧化物组织增殖的必需蛋白质,而是在没有功能冗余蛋白质的情况下,Pex25的情况下,这些细胞的必要性且小于20%显示进口无能的过氧化物样结构(过氧化物残留物)。在没有两种蛋白质的情况下,通过影响PEX3和PEX19功能可能会受到严重损害过氧化物体生物发生和PEX2和PEX11C的intra-ER分选。图形抽象显示省略了亮点?新过氧甲基硅烷蛋白,Pex36在K.Phaffii中的表征? PEX36与人PEX16和S. CEREVISIAE PEX34分享一些功能性同源性。还是PEX25和PEX36是冗余蛋白质,缺乏两者的细胞是合成致命的。还是PEX2和PEX11C的ER-TO-过氧缺位需要PEX25和PEX36。还是在没有Pex25和Pex36的情况下,PEX3和PEX19之间的复合物受损。

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