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Mitochondrial import efficiency of ATFS-1 regulates mitochondrial UPR activation.


ABSTRACT: To better understand the response to mitochondrial dysfunction, we examined the mechanism by which ATFS-1 (activating transcription factor associated with stress-1) senses mitochondrial stress and communicates with the nucleus during the mitochondrial unfolded protein response (UPR(mt)) in Caenorhabditis elegans. We found that the key point of regulation is the mitochondrial import efficiency of ATFS-1. In addition to a nuclear localization sequence, ATFS-1 has an N-terminal mitochondrial targeting sequence that is essential for UPR(mt) repression. Normally, ATFS-1 is imported into mitochondria and degraded. However, during mitochondrial stress, we found that import efficiency was reduced, allowing a percentage of ATFS-1 to accumulate in the cytosol and traffic to the nucleus. Our results show that cells monitor mitochondrial import efficiency via ATFS-1 to coordinate the level of mitochondrial dysfunction with the protective transcriptional response.

SUBMITTER: Nargund AM 

PROVIDER: S-EPMC3518298 | biostudies-literature | 2012 Aug

REPOSITORIES: biostudies-literature

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Mitochondrial import efficiency of ATFS-1 regulates mitochondrial UPR activation.

Nargund Amrita M AM   Pellegrino Mark W MW   Fiorese Christopher J CJ   Baker Brooke M BM   Haynes Cole M CM  

Science (New York, N.Y.) 20120614 6094


To better understand the response to mitochondrial dysfunction, we examined the mechanism by which ATFS-1 (activating transcription factor associated with stress-1) senses mitochondrial stress and communicates with the nucleus during the mitochondrial unfolded protein response (UPR(mt)) in Caenorhabditis elegans. We found that the key point of regulation is the mitochondrial import efficiency of ATFS-1. In addition to a nuclear localization sequence, ATFS-1 has an N-terminal mitochondrial target  ...[more]

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