内质网-线粒体相遇结构复合体协调辅酶Q生物合成。

Michal Eisenberg-Bord, Hui S Tsui, Diana Antunes, Lucía Fernández-Del-Río, Michelle C Bradley, Cory D Dunn, Theresa P T Nguyen, Doron Rapaport, Catherine F Clarke, Maya Schuldiner
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引用次数: 42

摘要

内质网(ER)-线粒体相遇结构(ERMES)复合物的缺失导致酵母内质网和线粒体之间接触部位的呼吸受损;然而,其原因尚不清楚。我们发现,在ERMES零突变体中,编码辅酶Q6 (CoQ6)生物合成酶的mrna水平增加,辅酶Q6是线粒体呼吸链的重要电子载体。我们发现,参与CoQ6生物合成的大型复合物(CoQ合成酶)在ERMES突变体中不稳定。这反过来又影响细胞内辅酶q6的水平和分布,导致线粒体辅酶q6减少。我们认为这些结果有助于在ERMES突变体中观察到的呼吸减少。荧光显微镜实验表明,CoQ合成体和ERMES之间非常接近,提示空间协调。er -线粒体接触位点参与调控CoQ6的生物发生,突出了这两个细胞器之间额外的交流水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The Endoplasmic Reticulum-Mitochondria Encounter Structure Complex Coordinates Coenzyme Q Biosynthesis.

Loss of the endoplasmic reticulum (ER)-mitochondria encounter structure (ERMES) complex that resides in contact sites between the yeast ER and mitochondria leads to impaired respiration; however, the reason for that is not clear. We find that in ERMES null mutants, there is an increase in the level of mRNAs encoding for biosynthetic enzymes of coenzyme Q6 (CoQ6), an essential electron carrier of the mitochondrial respiratory chain. We show that the mega complexes involved in CoQ6 biosynthesis (CoQ synthomes) are destabilized in ERMES mutants. This, in turn, affects the level and distribution of CoQ6 within the cell, resulting in reduced mitochondrial CoQ6. We suggest that these outcomes contribute to the reduced respiration observed in ERMES mutants. Fluorescence microscopy experiments demonstrate close proximity between the CoQ synthome and ERMES, suggesting a spatial coordination. The involvement of the ER-mitochondria contact site in regulation of CoQ6 biogenesis highlights an additional level of communication between these two organelles.

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