The Ubiquitin-Proteasome System Regulates Mitochondrial Intermembrane Space Proteins
Author(s) -
Piotr Brągoszewski,
Agnieszka Górnicka,
Malgorzata E. Sztolsztener,
Agnieszka Chacińska
Publication year - 2013
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.01579-12
Subject(s) - intermembrane space , mitochondrial intermembrane space , microbiology and biotechnology , biology , proteasome , mitochondrion , ubiquitin , mitochondrial biogenesis , cytosol , translocase of the inner membrane , biogenesis , biochemistry , inner mitochondrial membrane , mitochondrial membrane transport protein , bacterial outer membrane , escherichia coli , gene , enzyme
Mitochondrial precursor proteins are synthesized in the cytosol and subsequently imported into mitochondria. The import of mitochondrial intermembrane space proteins is coupled with their oxidative folding and governed by the mitochondrial intermembrane space import and assembly (MIA) pathway. The cytosolic steps that precede mitochondrial import are not well understood. We identified a role for the ubiquitin-proteasome system in the biogenesis of intermembrane space proteins. Interestingly, the function of the ubiquitin-proteasome system is not restricted to conditions of mitochondrial protein import failure. The ubiquitin-proteasome system persistently removes a fraction of intermembrane space proteins under physiological conditions, acting as a negative regulator in the biogenesis of this class of proteins. Thus, the ubiquitin-proteasome system plays an important role in determining the levels of proteins targeted to the intermembrane space of mitochondria.
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