Cargando…

Members of the autophagy class III phosphatidylinositol 3-kinase complex I interact with GABARAP and GABARAPL1 via LIR motifs

Autophagosome formation depends on a carefully orchestrated interplay between membrane-associated protein complexes. Initiation of macroautophagy/autophagy is mediated by the ULK1 (unc-51 like autophagy activating kinase 1) protein kinase complex and the autophagy-specific class III phosphatidylinos...

Descripción completa

Detalles Bibliográficos
Autores principales: Birgisdottir, Åsa Birna, Mouilleron, Stephane, Bhujabal, Zambarlal, Wirth, Martina, Sjøttem, Eva, Evjen, Gry, Zhang, Wenxin, Lee, Rebecca, O’Reilly, Nicola, Tooze, Sharon A., Lamark, Trond, Johansen, Terje
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6613885/
https://www.ncbi.nlm.nih.gov/pubmed/30767700
http://dx.doi.org/10.1080/15548627.2019.1581009
_version_ 1783433103590555648
author Birgisdottir, Åsa Birna
Mouilleron, Stephane
Bhujabal, Zambarlal
Wirth, Martina
Sjøttem, Eva
Evjen, Gry
Zhang, Wenxin
Lee, Rebecca
O’Reilly, Nicola
Tooze, Sharon A.
Lamark, Trond
Johansen, Terje
author_facet Birgisdottir, Åsa Birna
Mouilleron, Stephane
Bhujabal, Zambarlal
Wirth, Martina
Sjøttem, Eva
Evjen, Gry
Zhang, Wenxin
Lee, Rebecca
O’Reilly, Nicola
Tooze, Sharon A.
Lamark, Trond
Johansen, Terje
author_sort Birgisdottir, Åsa Birna
collection PubMed
description Autophagosome formation depends on a carefully orchestrated interplay between membrane-associated protein complexes. Initiation of macroautophagy/autophagy is mediated by the ULK1 (unc-51 like autophagy activating kinase 1) protein kinase complex and the autophagy-specific class III phosphatidylinositol 3-kinase complex I (PtdIns3K-C1). The latter contains PIK3C3/VPS34, PIK3R4/VPS15, BECN1/Beclin 1 and ATG14 and phosphorylates phosphatidylinositol to generate phosphatidylinositol 3-phosphate (PtdIns3P). Here, we show that PIK3C3, BECN1 and ATG14 contain functional LIR motifs and interact with the Atg8-family proteins with a preference for GABARAP and GABARAPL1. High resolution crystal structures of the functional LIR motifs of these core components of PtdIns3K-C1were obtained. Variation in hydrophobic pocket 2 (HP2) may explain the specificity for the GABARAP family. Mutation of the LIR motif in ATG14 did not prevent formation of the PtdIns3K-C1 complex, but blocked colocalization with MAP1LC3B/LC3B and impaired mitophagy. The ULK-mediated phosphorylation of S29 in ATG14 was strongly dependent on a functional LIR motif in ATG14. GABARAP-preferring LIR motifs in PIK3C3, BECN1 and ATG14 may, via coincidence detection, contribute to scaffolding of PtdIns3K-C1 on membranes for efficient autophagosome formation. Abbreviations: ATG: autophagy-related; BafA1: bafilomycin A(1); GABARAP: GABA type A receptor-associated protein; GABARAPL1: GABA type A receptor associated protein like 1; GFP: enhanced green fluorescent protein; KO: knockout; LDS: LIR docking site; LIR: LC3-interacting region; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; PIK3C3: phosphatidylinositol 3-kinase catalytic subunit type 3; PIK3R4: phosphoinositide-3-kinase regulatory subunit 4; PtdIns3K: phosphatidylinositol 3-kinase; PtdIns3P: phosphatidylinositol-3-phosphate; SQSTM1/p62: sequestosome 1; VPS: Vacuolar protein sorting; ULK: unc-51 like autophagy activating kinase
format Online
Article
Text
id pubmed-6613885
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-66138852019-07-17 Members of the autophagy class III phosphatidylinositol 3-kinase complex I interact with GABARAP and GABARAPL1 via LIR motifs Birgisdottir, Åsa Birna Mouilleron, Stephane Bhujabal, Zambarlal Wirth, Martina Sjøttem, Eva Evjen, Gry Zhang, Wenxin Lee, Rebecca O’Reilly, Nicola Tooze, Sharon A. Lamark, Trond Johansen, Terje Autophagy Research Paper Autophagosome formation depends on a carefully orchestrated interplay between membrane-associated protein complexes. Initiation of macroautophagy/autophagy is mediated by the ULK1 (unc-51 like autophagy activating kinase 1) protein kinase complex and the autophagy-specific class III phosphatidylinositol 3-kinase complex I (PtdIns3K-C1). The latter contains PIK3C3/VPS34, PIK3R4/VPS15, BECN1/Beclin 1 and ATG14 and phosphorylates phosphatidylinositol to generate phosphatidylinositol 3-phosphate (PtdIns3P). Here, we show that PIK3C3, BECN1 and ATG14 contain functional LIR motifs and interact with the Atg8-family proteins with a preference for GABARAP and GABARAPL1. High resolution crystal structures of the functional LIR motifs of these core components of PtdIns3K-C1were obtained. Variation in hydrophobic pocket 2 (HP2) may explain the specificity for the GABARAP family. Mutation of the LIR motif in ATG14 did not prevent formation of the PtdIns3K-C1 complex, but blocked colocalization with MAP1LC3B/LC3B and impaired mitophagy. The ULK-mediated phosphorylation of S29 in ATG14 was strongly dependent on a functional LIR motif in ATG14. GABARAP-preferring LIR motifs in PIK3C3, BECN1 and ATG14 may, via coincidence detection, contribute to scaffolding of PtdIns3K-C1 on membranes for efficient autophagosome formation. Abbreviations: ATG: autophagy-related; BafA1: bafilomycin A(1); GABARAP: GABA type A receptor-associated protein; GABARAPL1: GABA type A receptor associated protein like 1; GFP: enhanced green fluorescent protein; KO: knockout; LDS: LIR docking site; LIR: LC3-interacting region; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; PIK3C3: phosphatidylinositol 3-kinase catalytic subunit type 3; PIK3R4: phosphoinositide-3-kinase regulatory subunit 4; PtdIns3K: phosphatidylinositol 3-kinase; PtdIns3P: phosphatidylinositol-3-phosphate; SQSTM1/p62: sequestosome 1; VPS: Vacuolar protein sorting; ULK: unc-51 like autophagy activating kinase Taylor & Francis 2019-03-04 /pmc/articles/PMC6613885/ /pubmed/30767700 http://dx.doi.org/10.1080/15548627.2019.1581009 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Birgisdottir, Åsa Birna
Mouilleron, Stephane
Bhujabal, Zambarlal
Wirth, Martina
Sjøttem, Eva
Evjen, Gry
Zhang, Wenxin
Lee, Rebecca
O’Reilly, Nicola
Tooze, Sharon A.
Lamark, Trond
Johansen, Terje
Members of the autophagy class III phosphatidylinositol 3-kinase complex I interact with GABARAP and GABARAPL1 via LIR motifs
title Members of the autophagy class III phosphatidylinositol 3-kinase complex I interact with GABARAP and GABARAPL1 via LIR motifs
title_full Members of the autophagy class III phosphatidylinositol 3-kinase complex I interact with GABARAP and GABARAPL1 via LIR motifs
title_fullStr Members of the autophagy class III phosphatidylinositol 3-kinase complex I interact with GABARAP and GABARAPL1 via LIR motifs
title_full_unstemmed Members of the autophagy class III phosphatidylinositol 3-kinase complex I interact with GABARAP and GABARAPL1 via LIR motifs
title_short Members of the autophagy class III phosphatidylinositol 3-kinase complex I interact with GABARAP and GABARAPL1 via LIR motifs
title_sort members of the autophagy class iii phosphatidylinositol 3-kinase complex i interact with gabarap and gabarapl1 via lir motifs
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6613885/
https://www.ncbi.nlm.nih.gov/pubmed/30767700
http://dx.doi.org/10.1080/15548627.2019.1581009
work_keys_str_mv AT birgisdottirasabirna membersoftheautophagyclassiiiphosphatidylinositol3kinasecomplexiinteractwithgabarapandgabarapl1vialirmotifs
AT mouilleronstephane membersoftheautophagyclassiiiphosphatidylinositol3kinasecomplexiinteractwithgabarapandgabarapl1vialirmotifs
AT bhujabalzambarlal membersoftheautophagyclassiiiphosphatidylinositol3kinasecomplexiinteractwithgabarapandgabarapl1vialirmotifs
AT wirthmartina membersoftheautophagyclassiiiphosphatidylinositol3kinasecomplexiinteractwithgabarapandgabarapl1vialirmotifs
AT sjøttemeva membersoftheautophagyclassiiiphosphatidylinositol3kinasecomplexiinteractwithgabarapandgabarapl1vialirmotifs
AT evjengry membersoftheautophagyclassiiiphosphatidylinositol3kinasecomplexiinteractwithgabarapandgabarapl1vialirmotifs
AT zhangwenxin membersoftheautophagyclassiiiphosphatidylinositol3kinasecomplexiinteractwithgabarapandgabarapl1vialirmotifs
AT leerebecca membersoftheautophagyclassiiiphosphatidylinositol3kinasecomplexiinteractwithgabarapandgabarapl1vialirmotifs
AT oreillynicola membersoftheautophagyclassiiiphosphatidylinositol3kinasecomplexiinteractwithgabarapandgabarapl1vialirmotifs
AT toozesharona membersoftheautophagyclassiiiphosphatidylinositol3kinasecomplexiinteractwithgabarapandgabarapl1vialirmotifs
AT lamarktrond membersoftheautophagyclassiiiphosphatidylinositol3kinasecomplexiinteractwithgabarapandgabarapl1vialirmotifs
AT johansenterje membersoftheautophagyclassiiiphosphatidylinositol3kinasecomplexiinteractwithgabarapandgabarapl1vialirmotifs