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Condition-dependent functional shift of two Drosophila Mtmr lipid phosphatases in autophagy control

Myotubularin (MTM) and myotubularin-related (MTMR) lipid phosphatases catalyze the removal of a phosphate group from certain phosphatidylinositol derivatives. Because some of these substrates are required for macroautophagy/autophagy, during which unwanted cytoplasmic constituents are delivered into...

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Autores principales: Manzéger, Anna, Tagscherer, Kinga, Lőrincz, Péter, Szaker, Henrik, Lukácsovich, Tamás, Pilz, Petra, Kméczik, Regina, Csikós, George, Erdélyi, Miklós, Sass, Miklós, Kovács, Tibor, Vellai, Tibor, Billes, Viktor A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8726729/
https://www.ncbi.nlm.nih.gov/pubmed/33779490
http://dx.doi.org/10.1080/15548627.2021.1899681
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author Manzéger, Anna
Tagscherer, Kinga
Lőrincz, Péter
Szaker, Henrik
Lukácsovich, Tamás
Pilz, Petra
Kméczik, Regina
Csikós, George
Erdélyi, Miklós
Sass, Miklós
Kovács, Tibor
Vellai, Tibor
Billes, Viktor A.
author_facet Manzéger, Anna
Tagscherer, Kinga
Lőrincz, Péter
Szaker, Henrik
Lukácsovich, Tamás
Pilz, Petra
Kméczik, Regina
Csikós, George
Erdélyi, Miklós
Sass, Miklós
Kovács, Tibor
Vellai, Tibor
Billes, Viktor A.
author_sort Manzéger, Anna
collection PubMed
description Myotubularin (MTM) and myotubularin-related (MTMR) lipid phosphatases catalyze the removal of a phosphate group from certain phosphatidylinositol derivatives. Because some of these substrates are required for macroautophagy/autophagy, during which unwanted cytoplasmic constituents are delivered into lysosomes for degradation, MTM and MTMRs function as important regulators of the autophagic process. Despite its physiological and medical significance, the specific role of individual MTMR paralogs in autophagy control remains largely unexplored. Here we examined two Drosophila MTMRs, EDTP and Mtmr6, the fly orthologs of mammalian MTMR14 and MTMR6 to MTMR8, respectively, and found that these enzymes affect the autophagic process in a complex, condition-dependent way. EDTP inhibited basal autophagy, but did not influence stress-induced autophagy. In contrast, Mtmr6 promoted the process under nutrient-rich settings, but effectively blocked its hyperactivation in response to stress. Thus, Mtmr6 is the first identified MTMR phosphatase with dual, antagonistic roles in the regulation of autophagy, and shows conditional antagonism/synergism with EDTP in modulating autophagic breakdown. These results provide a deeper insight into the adjustment of autophagy. Abbreviations: Atg, autophagy-related; BDSC, Bloomington Drosophila Stock Center; DGRC, Drosophila Genetic Resource Center; EDTP, Egg-derived tyrosine phosphatase; FYVE, zinc finger domain from Fab1 (yeast ortholog of PIKfyve), YOTB, Vac1 (vesicle transport protein) and EEA1 cysteine-rich proteins; LTR, LysoTracker Red; MTM, myotubularin; MTMR, myotubularin-related; PI, phosphatidylinositol; Pi3K59F, Phosphotidylinositol 3 kinase 59F; PtdIns3P, phosphatidylinositol-3-phosphate; PtdIns(3,5)P(2), phosphatidylinositol-3,5-bisphosphate; PtdIns5P, phosphatidylinositol-5-phosphate; ref(2)P, refractory to sigma P; Syx17, Syntaxin 17; TEM, transmission electron microscopy; UAS, upstream activating sequence; Uvrag, UV-resistance associated gene; VDRC, Vienna Drosophila RNAi Center; Vps34, Vacuolar protein sorting 34.
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spelling pubmed-87267292022-01-05 Condition-dependent functional shift of two Drosophila Mtmr lipid phosphatases in autophagy control Manzéger, Anna Tagscherer, Kinga Lőrincz, Péter Szaker, Henrik Lukácsovich, Tamás Pilz, Petra Kméczik, Regina Csikós, George Erdélyi, Miklós Sass, Miklós Kovács, Tibor Vellai, Tibor Billes, Viktor A. Autophagy Research Paper Myotubularin (MTM) and myotubularin-related (MTMR) lipid phosphatases catalyze the removal of a phosphate group from certain phosphatidylinositol derivatives. Because some of these substrates are required for macroautophagy/autophagy, during which unwanted cytoplasmic constituents are delivered into lysosomes for degradation, MTM and MTMRs function as important regulators of the autophagic process. Despite its physiological and medical significance, the specific role of individual MTMR paralogs in autophagy control remains largely unexplored. Here we examined two Drosophila MTMRs, EDTP and Mtmr6, the fly orthologs of mammalian MTMR14 and MTMR6 to MTMR8, respectively, and found that these enzymes affect the autophagic process in a complex, condition-dependent way. EDTP inhibited basal autophagy, but did not influence stress-induced autophagy. In contrast, Mtmr6 promoted the process under nutrient-rich settings, but effectively blocked its hyperactivation in response to stress. Thus, Mtmr6 is the first identified MTMR phosphatase with dual, antagonistic roles in the regulation of autophagy, and shows conditional antagonism/synergism with EDTP in modulating autophagic breakdown. These results provide a deeper insight into the adjustment of autophagy. Abbreviations: Atg, autophagy-related; BDSC, Bloomington Drosophila Stock Center; DGRC, Drosophila Genetic Resource Center; EDTP, Egg-derived tyrosine phosphatase; FYVE, zinc finger domain from Fab1 (yeast ortholog of PIKfyve), YOTB, Vac1 (vesicle transport protein) and EEA1 cysteine-rich proteins; LTR, LysoTracker Red; MTM, myotubularin; MTMR, myotubularin-related; PI, phosphatidylinositol; Pi3K59F, Phosphotidylinositol 3 kinase 59F; PtdIns3P, phosphatidylinositol-3-phosphate; PtdIns(3,5)P(2), phosphatidylinositol-3,5-bisphosphate; PtdIns5P, phosphatidylinositol-5-phosphate; ref(2)P, refractory to sigma P; Syx17, Syntaxin 17; TEM, transmission electron microscopy; UAS, upstream activating sequence; Uvrag, UV-resistance associated gene; VDRC, Vienna Drosophila RNAi Center; Vps34, Vacuolar protein sorting 34. Taylor & Francis 2021-03-28 /pmc/articles/PMC8726729/ /pubmed/33779490 http://dx.doi.org/10.1080/15548627.2021.1899681 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Research Paper
Manzéger, Anna
Tagscherer, Kinga
Lőrincz, Péter
Szaker, Henrik
Lukácsovich, Tamás
Pilz, Petra
Kméczik, Regina
Csikós, George
Erdélyi, Miklós
Sass, Miklós
Kovács, Tibor
Vellai, Tibor
Billes, Viktor A.
Condition-dependent functional shift of two Drosophila Mtmr lipid phosphatases in autophagy control
title Condition-dependent functional shift of two Drosophila Mtmr lipid phosphatases in autophagy control
title_full Condition-dependent functional shift of two Drosophila Mtmr lipid phosphatases in autophagy control
title_fullStr Condition-dependent functional shift of two Drosophila Mtmr lipid phosphatases in autophagy control
title_full_unstemmed Condition-dependent functional shift of two Drosophila Mtmr lipid phosphatases in autophagy control
title_short Condition-dependent functional shift of two Drosophila Mtmr lipid phosphatases in autophagy control
title_sort condition-dependent functional shift of two drosophila mtmr lipid phosphatases in autophagy control
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8726729/
https://www.ncbi.nlm.nih.gov/pubmed/33779490
http://dx.doi.org/10.1080/15548627.2021.1899681
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