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dc.contributor.authorFiorese, Christopher J.
dc.contributor.authorHaynes, Cole M.
dc.date2022-08-11T08:09:20.000
dc.date.accessioned2022-08-23T16:27:03Z
dc.date.available2022-08-23T16:27:03Z
dc.date.issued2017-06-01
dc.date.submitted2017-05-15
dc.identifier.citationCrit Rev Biochem Mol Biol. 2017 Jun;52(3):304-313. doi: 10.1080/10409238.2017.1291577. Epub 2017 Feb 22. <a href="https://doi.org/10.1080/10409238.2017.1291577">Link to article on publisher's site</a>
dc.identifier.issn1040-9238 (Linking)
dc.identifier.doi10.1080/10409238.2017.1291577
dc.identifier.pmid28276702
dc.identifier.urihttp://hdl.handle.net/20.500.14038/36695
dc.description.abstractMitochondrial function is central to many different processes in the cell, from oxidative phosphorylation to the synthesis of iron-sulfur clusters. Therefore, mitochondrial dysfunction underlies a diverse array of diseases, from neurodegenerative diseases to cancer. Stress can be communicated to the cytosol and nucleus from the mitochondria through many different signals, and in response the cell can effect everything from transcriptional to post-transcriptional responses to protect the mitochondrial network. How these responses are coordinated have only recently begun to be understood. In this review, we explore how the cell maintains mitochondrial function, focusing on the mitochondrial unfolded protein response (UPRmt), a transcriptional response that can activate a wide array of programs to repair and restore mitochondrial function.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=28276702&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttps://doi.org/10.1080/10409238.2017.1291577
dc.subjectMitochondrial unfolded protein response
dc.subjectintegrated stress response
dc.subjectmitochondria quality control
dc.subjectmitochondrial dysfunction
dc.subjectmitochondrial stress response
dc.subjectBiochemistry
dc.subjectCell Biology
dc.subjectCellular and Molecular Physiology
dc.subjectMolecular Biology
dc.titleIntegrating the UPRmt into the mitochondrial maintenance network
dc.typeJournal Article
dc.source.journaltitleCritical reviews in biochemistry and molecular biology
dc.source.volume52
dc.source.issue3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/metnet_pubs/63
dc.identifier.contextkey10167298
html.description.abstract<p>Mitochondrial function is central to many different processes in the cell, from oxidative phosphorylation to the synthesis of iron-sulfur clusters. Therefore, mitochondrial dysfunction underlies a diverse array of diseases, from neurodegenerative diseases to cancer. Stress can be communicated to the cytosol and nucleus from the mitochondria through many different signals, and in response the cell can effect everything from transcriptional to post-transcriptional responses to protect the mitochondrial network. How these responses are coordinated have only recently begun to be understood. In this review, we explore how the cell maintains mitochondrial function, focusing on the mitochondrial unfolded protein response (UPRmt), a transcriptional response that can activate a wide array of programs to repair and restore mitochondrial function.</p>
dc.identifier.submissionpathmetnet_pubs/63
dc.contributor.departmentUMass Metabolic Network
dc.contributor.departmentDepartment of Molecular, Cell and Cancer Biology
dc.source.pages304-313


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