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线粒体膜融合的分子机制。

Molecular mechanism of mitochondrial membrane fusion.

作者信息

Griffin Erik E, Detmer Scott A, Chan David C

机构信息

Division of Biology, California Institute of Technology, 1200 East California Blvd., MC114-96, Pasadena, CA 91125, USA.

出版信息

Biochim Biophys Acta. 2006 May-Jun;1763(5-6):482-9. doi: 10.1016/j.bbamcr.2006.02.003. Epub 2006 Mar 9.

Abstract

Mitochondrial fusion requires coordinated fusion of the outer and inner membranes. This process leads to exchange of contents, controls the shape of mitochondria, and is important for mitochondrial function. Two types of mitochondrial GTPases are essential for mitochondrial fusion. On the outer membrane, the fuzzy onions/mitofusin proteins form complexes in trans that mediate homotypic physical interactions between adjacent mitochondria and are likely directly involved in outer membrane fusion. Associated with the inner membrane, the OPA1 dynamin-family GTPase maintains membrane structure and is a good candidate for mediating inner membrane fusion. In yeast, Ugo1p binds to both of these GTPases to form a fusion complex, although a related protein has yet to be found in mammals. An understanding of the molecular mechanism of fusion may have implications for Charcot-Marie-Tooth subtype 2A and autosomal dominant optic atrophy, neurodegenerative diseases caused by mutations in Mfn2 and OPA1.

摘要

线粒体融合需要外膜和内膜的协同融合。这一过程导致内容物的交换,控制线粒体的形状,并且对线粒体功能至关重要。两种类型的线粒体GTP酶对于线粒体融合必不可少。在外膜上,模糊洋葱蛋白/线粒体融合蛋白形成反式复合物,介导相邻线粒体之间的同型物理相互作用,并且可能直接参与外膜融合。与内膜相关联,OPA1动力蛋白家族GTP酶维持膜结构,并且是介导内膜融合的良好候选者。在酵母中,Ugo1p与这两种GTP酶结合形成融合复合物,尽管在哺乳动物中尚未发现相关蛋白。对融合分子机制的理解可能对夏科-马里-图斯2A型和常染色体显性遗传性视神经萎缩(由Mfn2和OPA1突变引起的神经退行性疾病)具有重要意义。

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