Defining the interactome of the human mitochondrial ribosome identifies SMIM4 and TMEM223 as respiratory chain assembly factors

Author:

Dennerlein Sven1ORCID,Poerschke Sabine1,Oeljeklaus Silke23,Wang Cong1,Richter-Dennerlein Ricarda14,Sattmann Johannes1,Bauermeister Diana1,Hanitsch Elisa1,Stoldt Stefan456,Langer Thomas7,Jakobs Stefan4568ORCID,Warscheid Bettina23ORCID,Rehling Peter1489ORCID

Affiliation:

1. Department of Cellular Biochemistry, University Medical Center Göttingen

2. Biochemistry and Functional Proteomics, Institute of Biology II, University of Freiburg

3. Signalling Research Centres BIOSS and CIBSS, University of Freiburg

4. Cluster of Excellence "Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells" (MBExC), University of Göttingen

5. Department of NanoBiophotonics, Max Planck Institute for Biophysical Chemistry

6. Department of Neurology, University Medical Center Göttingen

7. Department of Mitochondrial Proteostasis, Max Planck Institute for Biology of Ageing

8. Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Translational Neuroinflammation and Automated Microscopy

9. Max Planck Institute for Biophysical Chemistry

Abstract

Human mitochondria express a genome that encodes thirteen core subunits of the oxidative phosphorylation system (OXPHOS). These proteins insert into the inner membrane co-translationally. Therefore, mitochondrial ribosomes engage with the OXA1L-insertase and membrane-associated proteins, which support membrane insertion of translation products and early assembly steps into OXPHOS complexes. To identify ribosome-associated biogenesis factors for the OXPHOS system, we purified ribosomes and associated proteins from mitochondria. We identified TMEM223 as a ribosome-associated protein involved in complex IV biogenesis. TMEM223 stimulates the translation of COX1 mRNA and is a constituent of early COX1 assembly intermediates. Moreover, we show that SMIM4 together with C12ORF73 interacts with newly synthesized cytochrome b to support initial steps of complex III biogenesis in complex with UQCC1 and UQCC2. Our analyses define the interactome of the human mitochondrial ribosome and reveal novel assembly factors for complex III and IV biogenesis that link early assembly stages to the translation machinery.

Funder

European Research Council

Deutsche Forschungsgemeinschaft

Max Planck Institute for Dynamics of Complex Technical Systems Magdeburg

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3