Regulation of mitochondrial functions by protein phosphorylation and dephosphorylation
The mitochondria are double membrane-bound organelles found in most eukaryotic cells. They generate most of the cell's energy supply of adenosine triphosphate (ATP). Protein phosphorylation and dephosphorylation are critical mechanisms in the regulation of cell signaling networks and are essent...
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description | The mitochondria are double membrane-bound organelles found in most eukaryotic cells. They generate most of the cell's energy supply of adenosine triphosphate (ATP). Protein phosphorylation and dephosphorylation are critical mechanisms in the regulation of cell signaling networks and are essential for almost all the cellular functions. For many decades, mitochondria were considered autonomous organelles merely functioning to generate energy for cells to survive and proliferate, and were thought to be independent of the cellular signaling networks. Consequently, phosphorylation and dephosphorylation processes of mitochondrial kinases and phosphatases were largely neglected. However, evidence accumulated in recent years on mitochondria-localized kinases/phosphatases has changed this longstanding view. Mitochondria are increasingly recognized as a hub for cell signaling, and many kinases and phosphatases have been reported to localize in mitochondria and play important functions. However, the strength of the evidence on mitochondrial localization and the activities of the reported kinases and phosphatases vary greatly, and the detailed mechanisms on how these kinases/phosphatases translocate to mitochondria, their subsequent function, and the physiological and pathological implications of their localization are still poorly understood. Here, we provide an updated perspective on the recent advancement in this area, with an emphasis on the implications of mitochondrial kinases/phosphatases in cancer and several other diseases. |
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They generate most of the cell's energy supply of adenosine triphosphate (ATP). Protein phosphorylation and dephosphorylation are critical mechanisms in the regulation of cell signaling networks and are essential for almost all the cellular functions. For many decades, mitochondria were considered autonomous organelles merely functioning to generate energy for cells to survive and proliferate, and were thought to be independent of the cellular signaling networks. Consequently, phosphorylation and dephosphorylation processes of mitochondrial kinases and phosphatases were largely neglected. However, evidence accumulated in recent years on mitochondria-localized kinases/phosphatases has changed this longstanding view. Mitochondria are increasingly recognized as a hub for cell signaling, and many kinases and phosphatases have been reported to localize in mitochondria and play important functions. However, the strength of the evidence on mitochondrial localization and the activities of the reported kinases and phosphatases vary greatly, and the detailed mechanisms on how these kinases/phosphatases translocate to mitochondria, their subsequent function, and the physiological and pathological implications of their localization are still poorly understood. Here, we provide an updated perspective on the recent advancement in this area, with an emphasis on the implications of mitochondrial kinases/phosphatases in cancer and several other diseases.</description><identifier>ISSN: 2045-3701</identifier><identifier>EISSN: 2045-3701</identifier><identifier>DOI: 10.1186/s13578-016-0089-3</identifier><identifier>PMID: 27087918</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Adapter proteins ; Adenosine triphosphate ; Alzheimer's disease ; Apoptosis ; Cytochrome ; Cytoplasm ; Dehydrogenases ; Endoplasmic reticulum ; Kinases ; Leukemia ; Localization ; Medical research ; Mitochondria ; Mitochondrial DNA ; Muscle proteins ; Phosphatase ; Phosphatases ; Phosphorylation ; Phosphotransferases ; Physiological aspects ; Physiology ; Respiration ; Review ; Signal transduction</subject><ispartof>Cell & bioscience, 2016-04, Vol.6 (24), p.25-25, Article 25</ispartof><rights>COPYRIGHT 2016 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2016</rights><rights>Lim et al. 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c594t-f80f190147854aac32a2bdcb6490243388edd699d8871aa05050702d07896d43</citedby><cites>FETCH-LOGICAL-c594t-f80f190147854aac32a2bdcb6490243388edd699d8871aa05050702d07896d43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832502/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832502/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27087918$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lim, Sangbin</creatorcontrib><creatorcontrib>Smith, Kelly R</creatorcontrib><creatorcontrib>Lim, Ssang-Taek Steve</creatorcontrib><creatorcontrib>Tian, Rong</creatorcontrib><creatorcontrib>Lu, Jianrong</creatorcontrib><creatorcontrib>Tan, Ming</creatorcontrib><title>Regulation of mitochondrial functions by protein phosphorylation and dephosphorylation</title><title>Cell & bioscience</title><addtitle>Cell Biosci</addtitle><description>The mitochondria are double membrane-bound organelles found in most eukaryotic cells. They generate most of the cell's energy supply of adenosine triphosphate (ATP). Protein phosphorylation and dephosphorylation are critical mechanisms in the regulation of cell signaling networks and are essential for almost all the cellular functions. For many decades, mitochondria were considered autonomous organelles merely functioning to generate energy for cells to survive and proliferate, and were thought to be independent of the cellular signaling networks. Consequently, phosphorylation and dephosphorylation processes of mitochondrial kinases and phosphatases were largely neglected. However, evidence accumulated in recent years on mitochondria-localized kinases/phosphatases has changed this longstanding view. Mitochondria are increasingly recognized as a hub for cell signaling, and many kinases and phosphatases have been reported to localize in mitochondria and play important functions. However, the strength of the evidence on mitochondrial localization and the activities of the reported kinases and phosphatases vary greatly, and the detailed mechanisms on how these kinases/phosphatases translocate to mitochondria, their subsequent function, and the physiological and pathological implications of their localization are still poorly understood. Here, we provide an updated perspective on the recent advancement in this area, with an emphasis on the implications of mitochondrial kinases/phosphatases in cancer and several other diseases.</description><subject>Adapter proteins</subject><subject>Adenosine triphosphate</subject><subject>Alzheimer's disease</subject><subject>Apoptosis</subject><subject>Cytochrome</subject><subject>Cytoplasm</subject><subject>Dehydrogenases</subject><subject>Endoplasmic reticulum</subject><subject>Kinases</subject><subject>Leukemia</subject><subject>Localization</subject><subject>Medical research</subject><subject>Mitochondria</subject><subject>Mitochondrial DNA</subject><subject>Muscle proteins</subject><subject>Phosphatase</subject><subject>Phosphatases</subject><subject>Phosphorylation</subject><subject>Phosphotransferases</subject><subject>Physiological aspects</subject><subject>Physiology</subject><subject>Respiration</subject><subject>Review</subject><subject>Signal transduction</subject><issn>2045-3701</issn><issn>2045-3701</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNptkltrHCEUx6U0JCHNB8hLGehL-zDp8TKjvhRC6CUQCKShr-Kqs2uY0a3OhOy3r8NuLhvqQZRzfv_jhT9CZxjOMRbt14xpw0UNuK0BhKzpO3RMgDU15YDfv9ofodOc76EMJjHw5hAdEQ6CSyyO0Z9bt5x6PfoYqthVgx-jWcVgk9d91U3BzJVcLTbVOsXR-VCtVzGXmTY7lQ62su5N9gM66HSf3eluPUF3P77fXf6qr29-Xl1eXNemkWysOwEdloAZFw3T2lCiycKaRcskEEapEM7aVkorBMdaQ1OCA7HAhWwtoyfo27bteloMzhoXxqR7tU5-0GmjovZqvxL8Si3jg2KCkgZIafB51yDFv5PLoxp8Nq7vdXBxygpzQQhm5YIF_fQGvY9TCuV1hZItbaER7Qu11L1TPnSxnGvmpuqCMSk4L88q1Pl_qBLWDd7E4Dpf8nuCL3uCwozucVzqKWd19ft2n8Vb1qSYc3Ld839gULN11NY6qlhHzdZRs-bj6498VjwZhf4DWEi9pw</recordid><startdate>20160414</startdate><enddate>20160414</enddate><creator>Lim, Sangbin</creator><creator>Smith, Kelly R</creator><creator>Lim, Ssang-Taek Steve</creator><creator>Tian, Rong</creator><creator>Lu, Jianrong</creator><creator>Tan, Ming</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160414</creationdate><title>Regulation of mitochondrial functions by protein phosphorylation and dephosphorylation</title><author>Lim, Sangbin ; Smith, Kelly R ; Lim, Ssang-Taek Steve ; Tian, Rong ; Lu, Jianrong ; Tan, Ming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c594t-f80f190147854aac32a2bdcb6490243388edd699d8871aa05050702d07896d43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adapter proteins</topic><topic>Adenosine triphosphate</topic><topic>Alzheimer's disease</topic><topic>Apoptosis</topic><topic>Cytochrome</topic><topic>Cytoplasm</topic><topic>Dehydrogenases</topic><topic>Endoplasmic reticulum</topic><topic>Kinases</topic><topic>Leukemia</topic><topic>Localization</topic><topic>Medical research</topic><topic>Mitochondria</topic><topic>Mitochondrial DNA</topic><topic>Muscle proteins</topic><topic>Phosphatase</topic><topic>Phosphatases</topic><topic>Phosphorylation</topic><topic>Phosphotransferases</topic><topic>Physiological aspects</topic><topic>Physiology</topic><topic>Respiration</topic><topic>Review</topic><topic>Signal transduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lim, Sangbin</creatorcontrib><creatorcontrib>Smith, Kelly R</creatorcontrib><creatorcontrib>Lim, Ssang-Taek Steve</creatorcontrib><creatorcontrib>Tian, Rong</creatorcontrib><creatorcontrib>Lu, Jianrong</creatorcontrib><creatorcontrib>Tan, Ming</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cell & bioscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lim, Sangbin</au><au>Smith, Kelly R</au><au>Lim, Ssang-Taek Steve</au><au>Tian, Rong</au><au>Lu, Jianrong</au><au>Tan, Ming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulation of mitochondrial functions by protein phosphorylation and dephosphorylation</atitle><jtitle>Cell & bioscience</jtitle><addtitle>Cell Biosci</addtitle><date>2016-04-14</date><risdate>2016</risdate><volume>6</volume><issue>24</issue><spage>25</spage><epage>25</epage><pages>25-25</pages><artnum>25</artnum><issn>2045-3701</issn><eissn>2045-3701</eissn><abstract>The mitochondria are double membrane-bound organelles found in most eukaryotic cells. They generate most of the cell's energy supply of adenosine triphosphate (ATP). Protein phosphorylation and dephosphorylation are critical mechanisms in the regulation of cell signaling networks and are essential for almost all the cellular functions. For many decades, mitochondria were considered autonomous organelles merely functioning to generate energy for cells to survive and proliferate, and were thought to be independent of the cellular signaling networks. Consequently, phosphorylation and dephosphorylation processes of mitochondrial kinases and phosphatases were largely neglected. However, evidence accumulated in recent years on mitochondria-localized kinases/phosphatases has changed this longstanding view. Mitochondria are increasingly recognized as a hub for cell signaling, and many kinases and phosphatases have been reported to localize in mitochondria and play important functions. However, the strength of the evidence on mitochondrial localization and the activities of the reported kinases and phosphatases vary greatly, and the detailed mechanisms on how these kinases/phosphatases translocate to mitochondria, their subsequent function, and the physiological and pathological implications of their localization are still poorly understood. Here, we provide an updated perspective on the recent advancement in this area, with an emphasis on the implications of mitochondrial kinases/phosphatases in cancer and several other diseases.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>27087918</pmid><doi>10.1186/s13578-016-0089-3</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adapter proteins Adenosine triphosphate Alzheimer's disease Apoptosis Cytochrome Cytoplasm Dehydrogenases Endoplasmic reticulum Kinases Leukemia Localization Medical research Mitochondria Mitochondrial DNA Muscle proteins Phosphatase Phosphatases Phosphorylation Phosphotransferases Physiological aspects Physiology Respiration Review Signal transduction |
title | Regulation of mitochondrial functions by protein phosphorylation and dephosphorylation |
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