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ROMO1 is a constituent of the human presequence translocase required for YME1L protease import.


ABSTRACT: The mitochondrial presequence translocation machinery (TIM23 complex) is conserved between the yeast Saccharomyces cerevisiae and humans; however, functional characterization has been mainly performed in yeast. Here, we define the constituents of the human TIM23 complex using mass spectrometry and identified ROMO1 as a new translocase constituent with an exceptionally short half-life. Analyses of a ROMO1 knockout cell line revealed aberrant inner membrane structure and altered processing of the GTPase OPA1. We show that in the absence of ROMO1, mitochondria lose the inner membrane YME1L protease, which participates in OPA1 processing and ROMO1 turnover. While ROMO1 is dispensable for general protein import along the presequence pathway, we show that it participates in the dynamics of TIM21 during respiratory chain biogenesis and is specifically required for import of YME1L. This selective import defect can be linked to charge distribution in the unusually long targeting sequence of YME1L. Our analyses establish an unexpected link between mitochondrial protein import and inner membrane protein quality control.

SUBMITTER: Richter F 

PROVIDER: S-EPMC6363466 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

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ROMO1 is a constituent of the human presequence translocase required for YME1L protease import.

Richter Frank F   Dennerlein Sven S   Nikolov Miroslav M   Jans Daniel C DC   Naumenko Nataliia N   Aich Abhishek A   MacVicar Thomas T   Linden Andreas A   Jakobs Stefan S   Urlaub Henning H   Langer Thomas T   Rehling Peter P  

The Journal of cell biology 20181231 2


The mitochondrial presequence translocation machinery (TIM23 complex) is conserved between the yeast <i>Saccharomyces cerevisiae</i> and humans; however, functional characterization has been mainly performed in yeast. Here, we define the constituents of the human TIM23 complex using mass spectrometry and identified ROMO1 as a new translocase constituent with an exceptionally short half-life. Analyses of a ROMO1 knockout cell line revealed aberrant inner membrane structure and altered processing  ...[more]

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