PTPN9-mediated dephosphorylation of VTI1B promotes ATG16L1 precursor fusion and autophagosome formation

Macroautophagy/autophagy is an evolutionarily conserved intracellular pathway for the degradation of cytoplasmic materials. Under stress conditions, autophagy is upregulated and double-membrane autophagosomes are formed by the expansion of phagophores. The ATG16L1 precursor fusion contributes to dev...

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Veröffentlicht in:Autophagy 2021-10, Vol.17 (10), p.2750-2765
Hauptverfasser: Chou, He-Yen, Lee, Yi-Tang, Lin, Yuchieh Jay, Wen, Jung-Kun, Peng, Wen-Hsin, Hsieh, Pei-Lien, Lin, Shu-Yu, Hung, Chin-Chun, Chen, Guang-Chao
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container_end_page 2765
container_issue 10
container_start_page 2750
container_title Autophagy
container_volume 17
creator Chou, He-Yen
Lee, Yi-Tang
Lin, Yuchieh Jay
Wen, Jung-Kun
Peng, Wen-Hsin
Hsieh, Pei-Lien
Lin, Shu-Yu
Hung, Chin-Chun
Chen, Guang-Chao
description Macroautophagy/autophagy is an evolutionarily conserved intracellular pathway for the degradation of cytoplasmic materials. Under stress conditions, autophagy is upregulated and double-membrane autophagosomes are formed by the expansion of phagophores. The ATG16L1 precursor fusion contributes to development of phagophore structures and is critical for the biogenesis of autophagosomes. Here, we discovered a novel role of the protein tyrosine phosphatase PTPN9 in the regulation of homotypic ATG16L1 vesicle fusion and early autophagosome formation. Depletion of PTPN9 and its Drosophila homolog Ptpmeg2 impaired autophagosome formation and autophagic flux. PTPN9 colocalized with ATG16L1 and was essential for homotypic fusion of ATG16L1 + vesicles during starvation-induced autophagy. We further identified the Q-SNARE VTI1B as a substrate target of PTPN9 phosphatase. Like PTPN9, the VTI1B nonphosphorylatable mutant but not the phosphomimetic mutant enhanced SNARE complex assembly and autophagic flux. Our findings highlight the important role of PTPN9 in the regulation of ATG16L1 + autophagosome precursor fusion and autophagosome biogenesis through modulation of VTI1B phosphorylation status. Abbreviations: csw: corkscrew; EBSS: Earle's balanced salt solution; ERGIC: ER-Golgi intermediate compartment; ESCRT: endosomal sorting complexes required for transport; mop: myopic; NSF: N-ethylmaleimide-sensitive factor; PAS: phagophore assembly site; PolyQ: polyglutamine; PtdIns3P: phosphatidylinositol-3-phosphate; PTK: protein tyrosine kinase; PTM: posttranslational modification; PTP: protein tyrosine phosphatase; PTPN23/HD-PTP: protein tyrosine phosphatase non-receptor type 23; SNARE: soluble N-ethylmaleimide sensitive factor attachment protein receptor; STX7: syntaxin 7; STX8: syntaxin 8; STX17: syntaxin 17; VAMP3: vesicle associated membrane protein 3; VAMP7: vesicle associated membrane protein 7; VTI1B: vesicle transport through interaction with t-SNAREs 1B; YKT6: YKT6 v-SNARE homolog; ZFYVE1/DFCP1: zinc finger FYVE-type containing 1.
doi_str_mv 10.1080/15548627.2020.1838117
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Under stress conditions, autophagy is upregulated and double-membrane autophagosomes are formed by the expansion of phagophores. The ATG16L1 precursor fusion contributes to development of phagophore structures and is critical for the biogenesis of autophagosomes. Here, we discovered a novel role of the protein tyrosine phosphatase PTPN9 in the regulation of homotypic ATG16L1 vesicle fusion and early autophagosome formation. Depletion of PTPN9 and its Drosophila homolog Ptpmeg2 impaired autophagosome formation and autophagic flux. PTPN9 colocalized with ATG16L1 and was essential for homotypic fusion of ATG16L1 + vesicles during starvation-induced autophagy. We further identified the Q-SNARE VTI1B as a substrate target of PTPN9 phosphatase. Like PTPN9, the VTI1B nonphosphorylatable mutant but not the phosphomimetic mutant enhanced SNARE complex assembly and autophagic flux. Our findings highlight the important role of PTPN9 in the regulation of ATG16L1 + autophagosome precursor fusion and autophagosome biogenesis through modulation of VTI1B phosphorylation status. Abbreviations: csw: corkscrew; EBSS: Earle's balanced salt solution; ERGIC: ER-Golgi intermediate compartment; ESCRT: endosomal sorting complexes required for transport; mop: myopic; NSF: N-ethylmaleimide-sensitive factor; PAS: phagophore assembly site; PolyQ: polyglutamine; PtdIns3P: phosphatidylinositol-3-phosphate; PTK: protein tyrosine kinase; PTM: posttranslational modification; PTP: protein tyrosine phosphatase; PTPN23/HD-PTP: protein tyrosine phosphatase non-receptor type 23; SNARE: soluble N-ethylmaleimide sensitive factor attachment protein receptor; STX7: syntaxin 7; STX8: syntaxin 8; STX17: syntaxin 17; VAMP3: vesicle associated membrane protein 3; VAMP7: vesicle associated membrane protein 7; VTI1B: vesicle transport through interaction with t-SNAREs 1B; YKT6: YKT6 v-SNARE homolog; ZFYVE1/DFCP1: zinc finger FYVE-type containing 1.</description><identifier>ISSN: 1554-8627</identifier><identifier>EISSN: 1554-8635</identifier><identifier>DOI: 10.1080/15548627.2020.1838117</identifier><identifier>PMID: 33112705</identifier><language>eng</language><publisher>United States: Taylor &amp; Francis</publisher><subject>ATG16l1 ; Autophagosome ; Autophagosomes - metabolism ; Autophagy - physiology ; Autophagy-Related Proteins - metabolism ; HeLa Cells ; Humans ; Macroautophagy ; Membrane Fusion ; Protein Tyrosine Phosphatases, Non-Receptor - genetics ; Protein Tyrosine Phosphatases, Non-Receptor - metabolism ; PTPN9 ; Qb-SNARE Proteins - metabolism ; Research Paper ; SNARE ; VTI1B</subject><ispartof>Autophagy, 2021-10, Vol.17 (10), p.2750-2765</ispartof><rights>2020 Informa UK Limited, trading as Taylor &amp; Francis Group 2020</rights><rights>2020 Informa UK Limited, trading as Taylor &amp; Francis Group 2020 Informa UK Limited, trading as Taylor &amp; Francis Group</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c468t-64a85bc5ec02d5dcc218a47467542d7114094d102d19ac4b6183577fb09568663</citedby><cites>FETCH-LOGICAL-c468t-64a85bc5ec02d5dcc218a47467542d7114094d102d19ac4b6183577fb09568663</cites><orcidid>0000-0002-4980-4718</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8526009/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8526009/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33112705$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chou, He-Yen</creatorcontrib><creatorcontrib>Lee, Yi-Tang</creatorcontrib><creatorcontrib>Lin, Yuchieh Jay</creatorcontrib><creatorcontrib>Wen, Jung-Kun</creatorcontrib><creatorcontrib>Peng, Wen-Hsin</creatorcontrib><creatorcontrib>Hsieh, Pei-Lien</creatorcontrib><creatorcontrib>Lin, Shu-Yu</creatorcontrib><creatorcontrib>Hung, Chin-Chun</creatorcontrib><creatorcontrib>Chen, Guang-Chao</creatorcontrib><title>PTPN9-mediated dephosphorylation of VTI1B promotes ATG16L1 precursor fusion and autophagosome formation</title><title>Autophagy</title><addtitle>Autophagy</addtitle><description>Macroautophagy/autophagy is an evolutionarily conserved intracellular pathway for the degradation of cytoplasmic materials. Under stress conditions, autophagy is upregulated and double-membrane autophagosomes are formed by the expansion of phagophores. The ATG16L1 precursor fusion contributes to development of phagophore structures and is critical for the biogenesis of autophagosomes. Here, we discovered a novel role of the protein tyrosine phosphatase PTPN9 in the regulation of homotypic ATG16L1 vesicle fusion and early autophagosome formation. Depletion of PTPN9 and its Drosophila homolog Ptpmeg2 impaired autophagosome formation and autophagic flux. PTPN9 colocalized with ATG16L1 and was essential for homotypic fusion of ATG16L1 + vesicles during starvation-induced autophagy. We further identified the Q-SNARE VTI1B as a substrate target of PTPN9 phosphatase. Like PTPN9, the VTI1B nonphosphorylatable mutant but not the phosphomimetic mutant enhanced SNARE complex assembly and autophagic flux. Our findings highlight the important role of PTPN9 in the regulation of ATG16L1 + autophagosome precursor fusion and autophagosome biogenesis through modulation of VTI1B phosphorylation status. Abbreviations: csw: corkscrew; EBSS: Earle's balanced salt solution; ERGIC: ER-Golgi intermediate compartment; ESCRT: endosomal sorting complexes required for transport; mop: myopic; NSF: N-ethylmaleimide-sensitive factor; PAS: phagophore assembly site; PolyQ: polyglutamine; PtdIns3P: phosphatidylinositol-3-phosphate; PTK: protein tyrosine kinase; PTM: posttranslational modification; PTP: protein tyrosine phosphatase; PTPN23/HD-PTP: protein tyrosine phosphatase non-receptor type 23; SNARE: soluble N-ethylmaleimide sensitive factor attachment protein receptor; STX7: syntaxin 7; STX8: syntaxin 8; STX17: syntaxin 17; VAMP3: vesicle associated membrane protein 3; VAMP7: vesicle associated membrane protein 7; VTI1B: vesicle transport through interaction with t-SNAREs 1B; YKT6: YKT6 v-SNARE homolog; ZFYVE1/DFCP1: zinc finger FYVE-type containing 1.</description><subject>ATG16l1</subject><subject>Autophagosome</subject><subject>Autophagosomes - metabolism</subject><subject>Autophagy - physiology</subject><subject>Autophagy-Related Proteins - metabolism</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Macroautophagy</subject><subject>Membrane Fusion</subject><subject>Protein Tyrosine Phosphatases, Non-Receptor - genetics</subject><subject>Protein Tyrosine Phosphatases, Non-Receptor - metabolism</subject><subject>PTPN9</subject><subject>Qb-SNARE Proteins - metabolism</subject><subject>Research Paper</subject><subject>SNARE</subject><subject>VTI1B</subject><issn>1554-8627</issn><issn>1554-8635</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9Uctu2zAQJIoEdR79hAY69qKUpPjSpagTNK4BI8nB7ZWgScpWIGlVUmrhvy8dO0ZyyYFYYnZ29jEIfSb4mmCFvxLOmRJUXlNME6QKRYj8gM52eK5EwU-Ofyon6DzGJ4wLoUr6EU2KghAqMT9D68fl432Zt97VZvAuc77fQEwvbBsz1NBlUGW_l3Nyk_UBWhh8zKbLGRELkgBvxxAhZNUYd1TTucyMA_Qbs4YIrc8qCO2zzCU6rUwT_adDvEC_7n4sb3_mi4fZ_Ha6yC0TasgFM4qvLPcWU8edtZQowyQTkjPqJCEMl8yRlCSlsWwl0uJcymqFSy6UEMUF-rbX7cdVWsr6bgim0X2oWxO2Gkyt32a6eqPX8FcrTgXGZRL4chAI8Gf0cdBtHa1vGtN5GKOmjHPFcIFlovI91QaIMfjq2IZgvTNJv5ikdybpg0mp7ur1jMeqF1cS4fueUHfPB_wHoXF6MNsGQhVMZ-uoi_d7_AeEXaFw</recordid><startdate>20211003</startdate><enddate>20211003</enddate><creator>Chou, He-Yen</creator><creator>Lee, Yi-Tang</creator><creator>Lin, Yuchieh Jay</creator><creator>Wen, Jung-Kun</creator><creator>Peng, Wen-Hsin</creator><creator>Hsieh, Pei-Lien</creator><creator>Lin, Shu-Yu</creator><creator>Hung, Chin-Chun</creator><creator>Chen, Guang-Chao</creator><general>Taylor &amp; 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Under stress conditions, autophagy is upregulated and double-membrane autophagosomes are formed by the expansion of phagophores. The ATG16L1 precursor fusion contributes to development of phagophore structures and is critical for the biogenesis of autophagosomes. Here, we discovered a novel role of the protein tyrosine phosphatase PTPN9 in the regulation of homotypic ATG16L1 vesicle fusion and early autophagosome formation. Depletion of PTPN9 and its Drosophila homolog Ptpmeg2 impaired autophagosome formation and autophagic flux. PTPN9 colocalized with ATG16L1 and was essential for homotypic fusion of ATG16L1 + vesicles during starvation-induced autophagy. We further identified the Q-SNARE VTI1B as a substrate target of PTPN9 phosphatase. Like PTPN9, the VTI1B nonphosphorylatable mutant but not the phosphomimetic mutant enhanced SNARE complex assembly and autophagic flux. Our findings highlight the important role of PTPN9 in the regulation of ATG16L1 + autophagosome precursor fusion and autophagosome biogenesis through modulation of VTI1B phosphorylation status. Abbreviations: csw: corkscrew; EBSS: Earle's balanced salt solution; ERGIC: ER-Golgi intermediate compartment; ESCRT: endosomal sorting complexes required for transport; mop: myopic; NSF: N-ethylmaleimide-sensitive factor; PAS: phagophore assembly site; PolyQ: polyglutamine; PtdIns3P: phosphatidylinositol-3-phosphate; PTK: protein tyrosine kinase; PTM: posttranslational modification; PTP: protein tyrosine phosphatase; PTPN23/HD-PTP: protein tyrosine phosphatase non-receptor type 23; SNARE: soluble N-ethylmaleimide sensitive factor attachment protein receptor; STX7: syntaxin 7; STX8: syntaxin 8; STX17: syntaxin 17; VAMP3: vesicle associated membrane protein 3; VAMP7: vesicle associated membrane protein 7; VTI1B: vesicle transport through interaction with t-SNAREs 1B; YKT6: YKT6 v-SNARE homolog; ZFYVE1/DFCP1: zinc finger FYVE-type containing 1.</abstract><cop>United States</cop><pub>Taylor &amp; Francis</pub><pmid>33112705</pmid><doi>10.1080/15548627.2020.1838117</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0002-4980-4718</orcidid><oa>free_for_read</oa></addata></record>
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subjects ATG16l1
Autophagosome
Autophagosomes - metabolism
Autophagy - physiology
Autophagy-Related Proteins - metabolism
HeLa Cells
Humans
Macroautophagy
Membrane Fusion
Protein Tyrosine Phosphatases, Non-Receptor - genetics
Protein Tyrosine Phosphatases, Non-Receptor - metabolism
PTPN9
Qb-SNARE Proteins - metabolism
Research Paper
SNARE
VTI1B
title PTPN9-mediated dephosphorylation of VTI1B promotes ATG16L1 precursor fusion and autophagosome formation
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