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Mitophagy receptor FUNDC1 regulates mitochondrial dynamics and mitophagy
Mitochondrial fragmentation due to imbalanced fission and fusion of mitochondria is a prerequisite for mitophagy, however, the exact "coupling" of mitochondrial dynamics and mitophagy remains unclear. We have previously identified that FUNDC1 recruits MAP1LC3B/LC3B (LC3) through its LC3-in...
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Published in: | Autophagy 2016-04, Vol.12 (4), p.689-702 |
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container_title | Autophagy |
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creator | Chen, Ming Chen, Ziheng Wang, Yueying Tan, Zheng Zhu, Chongzhuo Li, Yanjun Han, Zhe Chen, Linbo Gao, Ruize Liu, Lei Chen, Quan |
description | Mitochondrial fragmentation due to imbalanced fission and fusion of mitochondria is a prerequisite for mitophagy, however, the exact "coupling" of mitochondrial dynamics and mitophagy remains unclear. We have previously identified that FUNDC1 recruits MAP1LC3B/LC3B (LC3) through its LC3-interacting region (LIR) motif to initiate mitophagy in mammalian cells. Here, we show that FUNDC1 interacts with both DNM1L/DRP1 and OPA1 to coordinate mitochondrial fission or fusion and mitophagy. OPA1 interacted with FUNDC1 via its Lys70 (K70) residue, and mutation of K70 to Ala (A), but not to Arg (R), abolished the interaction and promoted mitochondrial fission and mitophagy. Mitochondrial stress such as selenite or FCCP treatment caused the disassembly of the FUNDC1-OPA1 complex while enhancing DNM1L recruitment to the mitochondria. Furthermore, we observed that dephosphorylation of FUNDC1 under stress conditions promotes the dissociation of FUNDC1 from OPA1 and association with DNM1L. Our data suggest that FUNDC1 regulates both mitochondrial fission or fusion and mitophagy and mediates the "coupling" across the double membrane for mitochondrial dynamics and quality control. |
doi_str_mv | 10.1080/15548627.2016.1151580 |
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We have previously identified that FUNDC1 recruits MAP1LC3B/LC3B (LC3) through its LC3-interacting region (LIR) motif to initiate mitophagy in mammalian cells. Here, we show that FUNDC1 interacts with both DNM1L/DRP1 and OPA1 to coordinate mitochondrial fission or fusion and mitophagy. OPA1 interacted with FUNDC1 via its Lys70 (K70) residue, and mutation of K70 to Ala (A), but not to Arg (R), abolished the interaction and promoted mitochondrial fission and mitophagy. Mitochondrial stress such as selenite or FCCP treatment caused the disassembly of the FUNDC1-OPA1 complex while enhancing DNM1L recruitment to the mitochondria. Furthermore, we observed that dephosphorylation of FUNDC1 under stress conditions promotes the dissociation of FUNDC1 from OPA1 and association with DNM1L. Our data suggest that FUNDC1 regulates both mitochondrial fission or fusion and mitophagy and mediates the "coupling" across the double membrane for mitochondrial dynamics and quality control.</description><identifier>ISSN: 1554-8627</identifier><identifier>EISSN: 1554-8635</identifier><identifier>DOI: 10.1080/15548627.2016.1151580</identifier><identifier>PMID: 27050458</identifier><language>eng</language><publisher>United States: Taylor & Francis</publisher><subject>Amino Acid Sequence ; Basic Research Paper ; Casein Kinase II - metabolism ; DNM1L/DRP1 ; Gene Knockdown Techniques ; GTP Phosphohydrolases - metabolism ; HeLa Cells ; Humans ; Membrane Proteins - chemistry ; Membrane Proteins - metabolism ; Microtubule-Associated Proteins - metabolism ; Mitochondria - metabolism ; Mitochondrial Degradation ; Mitochondrial Dynamics ; Mitochondrial Proteins - chemistry ; Mitochondrial Proteins - metabolism ; mitophagy ; mitophagy receptor ; OPA1 ; Phosphorylation ; Protein Binding</subject><ispartof>Autophagy, 2016-04, Vol.12 (4), p.689-702</ispartof><rights>2016 Taylor & Francis 2016</rights><rights>2016 Taylor & Francis 2016 Taylor & Francis</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c468t-a65d6be69f7e2d67e9b8140ec4a460bfa0417859fd16dbb5c1a4754d891afa3b3</citedby><cites>FETCH-LOGICAL-c468t-a65d6be69f7e2d67e9b8140ec4a460bfa0417859fd16dbb5c1a4754d891afa3b3</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/PMC4836026/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4836026/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,27906,27907,53773,53775</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27050458$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Ming</creatorcontrib><creatorcontrib>Chen, Ziheng</creatorcontrib><creatorcontrib>Wang, Yueying</creatorcontrib><creatorcontrib>Tan, Zheng</creatorcontrib><creatorcontrib>Zhu, Chongzhuo</creatorcontrib><creatorcontrib>Li, Yanjun</creatorcontrib><creatorcontrib>Han, Zhe</creatorcontrib><creatorcontrib>Chen, Linbo</creatorcontrib><creatorcontrib>Gao, Ruize</creatorcontrib><creatorcontrib>Liu, Lei</creatorcontrib><creatorcontrib>Chen, Quan</creatorcontrib><title>Mitophagy receptor FUNDC1 regulates mitochondrial dynamics and mitophagy</title><title>Autophagy</title><addtitle>Autophagy</addtitle><description>Mitochondrial fragmentation due to imbalanced fission and fusion of mitochondria is a prerequisite for mitophagy, however, the exact "coupling" of mitochondrial dynamics and mitophagy remains unclear. 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Our data suggest that FUNDC1 regulates both mitochondrial fission or fusion and mitophagy and mediates the "coupling" across the double membrane for mitochondrial dynamics and quality control.</description><subject>Amino Acid Sequence</subject><subject>Basic Research Paper</subject><subject>Casein Kinase II - metabolism</subject><subject>DNM1L/DRP1</subject><subject>Gene Knockdown Techniques</subject><subject>GTP Phosphohydrolases - metabolism</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Membrane Proteins - chemistry</subject><subject>Membrane Proteins - metabolism</subject><subject>Microtubule-Associated Proteins - metabolism</subject><subject>Mitochondria - metabolism</subject><subject>Mitochondrial Degradation</subject><subject>Mitochondrial Dynamics</subject><subject>Mitochondrial Proteins - chemistry</subject><subject>Mitochondrial Proteins - metabolism</subject><subject>mitophagy</subject><subject>mitophagy receptor</subject><subject>OPA1</subject><subject>Phosphorylation</subject><subject>Protein Binding</subject><issn>1554-8627</issn><issn>1554-8635</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp9kctOwzAQRS0EglL4BFCWbFrsxK9sEKhQisRjA2trYjutURIXOwX170npQ7BhZXvm3DsjX4TOCB4SLPElYYxKnophigkfEsIIk3gP9Vb1geQZ29_dU3GEjmN8xzjjMk8P0VEqMMOUyR6aPLnWz2cwXSbBajtvfUjGb8-3I9K9p4sKWhuTumP0zDcmOKgSs2ygdjom0Jif1o_8BB2UUEV7ujn76G189zqaDB5f7h9GN48DTblsB8CZ4YXleSlsariweSEJxVZToBwXJWBKhGR5aQg3RcE0ASoYNTInUEJWZH10tfadL4raGm2bNkCl5sHVEJbKg1N_O42bqan_VFRmHKe8M7jYGAT_sbCxVbWL2lYVNNYvoiJC5DLHRNIOZWtUBx9jsOVuDMFqlYLapqBWKahNCp3u_PeOO9X22zvgeg24pvShhi8fKqNaWFY-lAEa7aLK_p_xDZk9mIA</recordid><startdate>20160402</startdate><enddate>20160402</enddate><creator>Chen, Ming</creator><creator>Chen, Ziheng</creator><creator>Wang, Yueying</creator><creator>Tan, Zheng</creator><creator>Zhu, Chongzhuo</creator><creator>Li, Yanjun</creator><creator>Han, Zhe</creator><creator>Chen, Linbo</creator><creator>Gao, Ruize</creator><creator>Liu, Lei</creator><creator>Chen, Quan</creator><general>Taylor & Francis</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160402</creationdate><title>Mitophagy receptor FUNDC1 regulates mitochondrial dynamics and mitophagy</title><author>Chen, Ming ; Chen, Ziheng ; Wang, Yueying ; Tan, Zheng ; Zhu, Chongzhuo ; Li, Yanjun ; Han, Zhe ; Chen, Linbo ; Gao, Ruize ; Liu, Lei ; Chen, Quan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c468t-a65d6be69f7e2d67e9b8140ec4a460bfa0417859fd16dbb5c1a4754d891afa3b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Amino Acid Sequence</topic><topic>Basic Research Paper</topic><topic>Casein Kinase II - metabolism</topic><topic>DNM1L/DRP1</topic><topic>Gene Knockdown Techniques</topic><topic>GTP Phosphohydrolases - metabolism</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Membrane Proteins - chemistry</topic><topic>Membrane Proteins - metabolism</topic><topic>Microtubule-Associated Proteins - metabolism</topic><topic>Mitochondria - metabolism</topic><topic>Mitochondrial Degradation</topic><topic>Mitochondrial Dynamics</topic><topic>Mitochondrial Proteins - chemistry</topic><topic>Mitochondrial Proteins - metabolism</topic><topic>mitophagy</topic><topic>mitophagy receptor</topic><topic>OPA1</topic><topic>Phosphorylation</topic><topic>Protein Binding</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Ming</creatorcontrib><creatorcontrib>Chen, Ziheng</creatorcontrib><creatorcontrib>Wang, Yueying</creatorcontrib><creatorcontrib>Tan, Zheng</creatorcontrib><creatorcontrib>Zhu, Chongzhuo</creatorcontrib><creatorcontrib>Li, Yanjun</creatorcontrib><creatorcontrib>Han, Zhe</creatorcontrib><creatorcontrib>Chen, Linbo</creatorcontrib><creatorcontrib>Gao, Ruize</creatorcontrib><creatorcontrib>Liu, Lei</creatorcontrib><creatorcontrib>Chen, Quan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Autophagy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Ming</au><au>Chen, Ziheng</au><au>Wang, Yueying</au><au>Tan, Zheng</au><au>Zhu, Chongzhuo</au><au>Li, Yanjun</au><au>Han, Zhe</au><au>Chen, Linbo</au><au>Gao, Ruize</au><au>Liu, Lei</au><au>Chen, Quan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mitophagy receptor FUNDC1 regulates mitochondrial dynamics and mitophagy</atitle><jtitle>Autophagy</jtitle><addtitle>Autophagy</addtitle><date>2016-04-02</date><risdate>2016</risdate><volume>12</volume><issue>4</issue><spage>689</spage><epage>702</epage><pages>689-702</pages><issn>1554-8627</issn><eissn>1554-8635</eissn><abstract>Mitochondrial fragmentation due to imbalanced fission and fusion of mitochondria is a prerequisite for mitophagy, however, the exact "coupling" of mitochondrial dynamics and mitophagy remains unclear. We have previously identified that FUNDC1 recruits MAP1LC3B/LC3B (LC3) through its LC3-interacting region (LIR) motif to initiate mitophagy in mammalian cells. Here, we show that FUNDC1 interacts with both DNM1L/DRP1 and OPA1 to coordinate mitochondrial fission or fusion and mitophagy. OPA1 interacted with FUNDC1 via its Lys70 (K70) residue, and mutation of K70 to Ala (A), but not to Arg (R), abolished the interaction and promoted mitochondrial fission and mitophagy. Mitochondrial stress such as selenite or FCCP treatment caused the disassembly of the FUNDC1-OPA1 complex while enhancing DNM1L recruitment to the mitochondria. Furthermore, we observed that dephosphorylation of FUNDC1 under stress conditions promotes the dissociation of FUNDC1 from OPA1 and association with DNM1L. 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subjects | Amino Acid Sequence Basic Research Paper Casein Kinase II - metabolism DNM1L/DRP1 Gene Knockdown Techniques GTP Phosphohydrolases - metabolism HeLa Cells Humans Membrane Proteins - chemistry Membrane Proteins - metabolism Microtubule-Associated Proteins - metabolism Mitochondria - metabolism Mitochondrial Degradation Mitochondrial Dynamics Mitochondrial Proteins - chemistry Mitochondrial Proteins - metabolism mitophagy mitophagy receptor OPA1 Phosphorylation Protein Binding |
title | Mitophagy receptor FUNDC1 regulates mitochondrial dynamics and mitophagy |
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