Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/245925
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dc.titleA Mitochondrial Encoded Messenger at the Nucleus
dc.contributor.authorYong, Cheryl Qian Ying
dc.contributor.authorTang, Bor Luen
dc.date.accessioned2023-11-14T04:30:04Z
dc.date.available2023-11-14T04:30:04Z
dc.date.issued2018-08
dc.identifier.citationYong, Cheryl Qian Ying, Tang, Bor Luen (2018-08). A Mitochondrial Encoded Messenger at the Nucleus. CELLS 7 (8). ScholarBank@NUS Repository.
dc.identifier.issn2073-4409
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/245925
dc.description.abstractMitochondria–nucleus (mitonuclear) retrograde signaling via nuclear import of otherwise mitochondrial targeted factors occurs during mitochondrial unfolded protein response (UPRmt), a mechanism that counters mitochondrial and cellular stresses. Other than nuclear encoded proteins, mitochondrial DNA (mtDNA)-encoded peptides, such as humanin, are known to have important pro-survival and metabolic regulatory functions. A recent report has indicated that another mtDNA-encoded peptide, the mitochondrial open reading frame of the 12S rRNA-c (MOTS-c), could translocate into the nucleus upon stress induction. In the nucleus, MOTS-c binds to DNA and regulates the transcription of stress response genes in concert with other transcription factors. This is the first clear example of a mitochondria-derived peptide (MDP) acting in the nucleus to affect transcriptional responses to stress. Thus, MOTS-c may bear some characteristics of a ‘mitokine’ factor that mediates mitohormesis, influencing cell survival as well as organismal health and longevity.
dc.language.isoen
dc.publisherMDPI
dc.sourceElements
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectCell Biology
dc.subjectAMP-activated protein kinase (AMPK)
dc.subjecthumanin
dc.subjectmitochondria
dc.subjectmitochondrial open reading frame of the 12S rRNA-c (MOTS-c)
dc.subjectmitochondrial unfolded protein response (UPRmt)
dc.subjectALZHEIMERS-DISEASE
dc.subjectREPERFUSION INJURY
dc.subjectPEPTIDE HUMANIN
dc.subjectSTRESS-RESPONSE
dc.subjectLONGEVITY
dc.subjectAMPK
dc.subjectHOMEOSTASIS
dc.subjectREGULATORS
dc.subjectAPOPTOSIS
dc.subjectISCHEMIA
dc.typeArticle
dc.date.updated2023-11-12T07:02:33Z
dc.contributor.departmentDEAN'S OFFICE (NGS FOR INTGR SCI & ENGG)
dc.contributor.departmentBIOCHEMISTRY
dc.description.sourcetitleCELLS
dc.description.volume7
dc.description.issue8
dc.published.statePublished
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