首页> 美国卫生研究院文献>Molecular and Cellular Biology >Presence of a Member of the Mitochondrial Carrier Family in Hydrogenosomes: Conservation of Membrane-Targeting Pathways between Hydrogenosomes and Mitochondria
【2h】

Presence of a Member of the Mitochondrial Carrier Family in Hydrogenosomes: Conservation of Membrane-Targeting Pathways between Hydrogenosomes and Mitochondria

机译:氢小体中线粒体载体家族成员的存在:氢小体和线粒体之间的膜靶向途径的养护。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

A number of microaerophilic eukaryotes lack mitochondria but possess another organelle involved in energy metabolism, the hydrogenosome. Limited phylogenetic analyses of nuclear genes support a common origin for these two organelles. We have identified a protein of the mitochondrial carrier family in the hydrogenosome of Trichomonas vaginalis and have shown that this protein, Hmp31, is phylogenetically related to the mitochondrial ADP-ATP carrier (AAC). We demonstrate that the hydrogenosomal AAC can be targeted to the inner membrane of mitochondria isolated from Saccharomyces cerevisiae through the Tim9-Tim10 import pathway used for the assembly of mitochondrial carrier proteins. Conversely, yeast mitochondrial AAC can be targeted into the membranes of hydrogenosomes. The hydrogenosomal AAC contains a cleavable, N-terminal presequence; however, this sequence is not necessary for targeting the protein to the organelle. These data indicate that the membrane-targeting signal(s) for hydrogenosomal AAC is internal, similar to that found for mitochondrial carrier proteins. Our findings indicate that the membrane carriers and membrane protein-targeting machinery of hydrogenosomes and mitochondria have a common evolutionary origin. Together, they provide strong evidence that a single endosymbiont evolved into a progenitor organelle in early eukaryotic cells that ultimately give rise to these two distinct organelles and support the hydrogen hypothesis for the origin of the eukaryotic cell.
机译:许多微需氧的真核生物缺乏线粒体,但具有参与能量代谢的另一个细胞器,即氢核小体。有限的核基因系统发育分析支持这两个细胞器的共同起源。我们已经在阴道毛滴虫的氢核小体中鉴定了线粒体载体家族的一种蛋白质,并表明该蛋白质Hmp31与线粒体ADP-ATP载体(AAC)在系统发育上相关。我们证明,通过用于线粒体载体蛋白组装的Tim9-Tim10导入途径,氢氧体AAC可以靶向从酿酒酵母分离的线粒体内膜。相反,酵母线粒体AAC可以靶向到氢体的膜中。氢氧体AAC含有一个可切割的N端预序列。然而,该序列对于将蛋白质靶向细胞器不是必需的。这些数据表明,与针对线粒体载体蛋白的信号相似,用于氢氧体AAC的膜靶向信号是内部的。我们的发现表明,脂质体和线粒体的膜载体和膜蛋白靶向机制具有共同的进化起源。它们在一起提供了强有力的证据,表明单个内共生体在早期的真核细胞中演变成祖细胞器,最终产生了这两个不同的细胞器,并支持了真核细胞起源的氢假说。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号