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酵母中的过氧化物酶体发育与 Pex3 依赖性过氧化物酶体-液泡接触位点的形成有关。

Peroxisome development in yeast is associated with the formation of Pex3-dependent peroxisome-vacuole contact sites.

机构信息

Molecular Cell Biology, University of Groningen, PO Box 11103, 9300, CC, Groningen, the Netherlands.

Molecular Cell Biology, University of Groningen, PO Box 11103, 9300, CC, Groningen, the Netherlands.

出版信息

Biochim Biophys Acta Mol Cell Res. 2019 Mar;1866(3):349-359. doi: 10.1016/j.bbamcr.2018.08.021. Epub 2018 Sep 1.

DOI:10.1016/j.bbamcr.2018.08.021
PMID:30595161
Abstract

Using electron and fluorescence microscopy techniques, we identified various physical contacts between peroxisomes and other cell organelles in the yeast Hansenula polymorpha. In exponential glucose-grown cells, which typically contain a single small peroxisome, contacts were only observed with the endoplasmic reticulum and the plasma membrane. Here we focus on a novel peroxisome-vacuole contact site that is formed when glucose-grown cells are shifted to methanol containing media, conditions that induce strong peroxisome development. At these conditions, the small peroxisomes rapidly increase in size, a phenomenon that is paralleled by the formation of distinct intimate contacts with the vacuole. Localization studies showed that the peroxin Pex3 accumulated in patches at the peroxisome-vacuole contact sites. In wild-type cells growing exponentially on medium containing glucose, peroxisome-vacuole contact sites were never observed. However, upon overproduction of Pex3 peroxisomes also associated to vacuoles at these growth conditions. Our observations strongly suggest a role for Pex3 in the formation of a novel peroxisome-vacuole contact site. This contact likely plays a role in membrane growth as it is formed solely at conditions of strong peroxisome expansion.

摘要

利用电子显微镜和荧光显微镜技术,我们在酵母 Hansenula polymorpha 中鉴定出了过氧化物酶体与其他细胞细胞器之间的各种物理接触。在指数生长期的葡萄糖培养细胞中,这些细胞通常只含有一个小的过氧化物酶体,仅观察到与内质网和质膜的接触。在这里,我们关注的是一种新型的过氧化物酶体-液泡接触位点,当葡萄糖培养的细胞被转移到含有甲醇的培养基中时,会形成这种接触位点,这种条件会强烈诱导过氧化物酶体的发育。在这些条件下,小的过氧化物酶体迅速增大,这一现象伴随着与液泡形成明显的紧密接触。定位研究表明,过氧化物酶体蛋白 Pex3 在过氧化物酶体-液泡接触部位积累成斑。在含有葡萄糖的培养基中指数生长的野生型细胞中,从未观察到过氧化物酶体-液泡接触位点。然而,当 Pex3 过氧化物酶体过量产生时,即使在这些生长条件下,过氧化物酶体也会与液泡结合。我们的观察结果强烈表明 Pex3 在形成新型过氧化物酶体-液泡接触位点中发挥作用。这个接触点很可能在膜生长中发挥作用,因为它仅在过氧化物酶体强烈扩张的条件下形成。

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