A conserved myotubularin-related phosphatase regulates autophagy by maintaining autophagic flux

Author:

Allen Elizabeth A.1ORCID,Amato Clelia2,Fortier Tina M.1,Velentzas Panagiotis1ORCID,Wood Will2,Baehrecke Eric H.1ORCID

Affiliation:

1. Department of Molecular, Cell, and Cancer Biology, University of Massachusetts Medical School, Worcester, MA

2. Centre for Inflammation Research, The Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UK

Abstract

Macroautophagy (autophagy) targets cytoplasmic cargoes to the lysosome for degradation. Like all vesicle trafficking, autophagy relies on phosphoinositide identity, concentration, and localization to execute multiple steps in this catabolic process. Here, we screen for phosphoinositide phosphatases that influence autophagy in Drosophila and identify CG3530. CG3530 is homologous to the human MTMR6 subfamily of myotubularin-related 3-phosphatases, and therefore, we named it dMtmr6. dMtmr6, which is required for development and viability in Drosophila, functions as a regulator of autophagic flux in multiple Drosophila cell types. The MTMR6 family member MTMR8 has a similar function in autophagy of higher animal cells. Decreased dMtmr6 and MTMR8 function results in autophagic vesicle accumulation and influences endolysosomal homeostasis.

Funder

National Institutes of Health

Wellcome Trust

Publisher

Rockefeller University Press

Subject

Cell Biology

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