Autophagy plays important and diverse roles in muscle biology, including a role in glycogen metabolism and muscle homeostasis. In particular, several myopathies are associated with accumulation of autophagic and lysosomal vesicles containing glycogen, but for most of them it remains unclear how glycogen metabolism connects to the pathology of the diseases. In addition, the role of the autophagy-lysosome pathway in muscle wasting is not clear, especially whether it contributes to pathogenesis or serves a protective role. The overall goal of this project is to characterize the mechanisms underlying autophagy in Drosophila muscles and the role autophagy plays during muscle wasting. A high level of conservation with higher organisms makes the Drosophila muscle an attractive system to study the role of autophagy in vivo. We have established two Drosophila models that allow us to: 1) study glycogen autophagy in skeletal muscle and 2) study muscle degeneration. We have made the surprising finding that glycogen synthase (GlyS) is a critical regulator of glycogen autophagy, possibly acting as an autophagic cargo receptor for the glycogen particle, and linking glycogen metabolism to the lysosomal pathway.
In Aim 1, we propose to determine if GlyS is a cargo receptor, identify sites or regions on GlyS that are required for binding (direct o indirect) to autophagosomes, determine what signaling pathways regulate glycophagy, and determine whether GlyS function is conserved in mammalian cells.
In Aim 2, we will identify other factors involved in the transport of glycogen to lysosomes using proteomic approaches and will distinguish between factors involved specifically in selective glycogen autophagy, and factors involved in other types of autophagy that occur in muscles.
In Aim 3, we will characterize, using our Drosophila wasting model, the role of the autophagy-lysosome pathway in degradation of muscle proteins. Altogether, these studies will provide fundamental insights into the role of autophagy in muscles and its regulation.

Public Health Relevance

The overall goal of this project is to characterize the mechanisms underlying autophagy in Drosophila muscles and the role autophagy plays during muscle wasting. The studies are relevant to several myopathies that are associated with accumulation of autophagic and lysosomal vesicles containing glycogen, and to muscle wasting associated with a number of human diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
2R01AR057352-06
Application #
8884138
Study Section
Skeletal Muscle Biology and Exercise Physiology Study Section (SMEP)
Program Officer
Boyce, Amanda T
Project Start
2009-08-01
Project End
2020-06-30
Budget Start
2015-07-01
Budget End
2016-06-30
Support Year
6
Fiscal Year
2015
Total Cost
Indirect Cost
Name
Harvard Medical School
Department
Genetics
Type
Schools of Medicine
DUNS #
047006379
City
Boston
State
MA
Country
United States
Zip Code
Tang, Hong-Wen; Hu, Yanhui; Chen, Chiao-Lin et al. (2018) The TORC1-Regulated CPA Complex Rewires an RNA Processing Network to Drive Autophagy and Metabolic Reprogramming. Cell Metab 27:1040-1054.e8
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Song, Wei; Owusu-Ansah, Edward; Hu, Yanhui et al. (2017) Activin signaling mediates muscle-to-adipose communication in a mitochondria dysfunction-associated obesity model. Proc Natl Acad Sci U S A :
Droujinine, Ilia A; Perrimon, Norbert (2016) Interorgan Communication Pathways in Physiology: Focus on Drosophila. Annu Rev Genet 50:539-570
Kuhn, Hallie; Sopko, Richelle; Coughlin, Margaret et al. (2015) The Atg1-Tor pathway regulates yolk catabolism in Drosophila embryos. Development 142:3869-78
Zirin, Jonathan; Nieuwenhuis, Joppe; Samsonova, Anastasia et al. (2015) Regulators of autophagosome formation in Drosophila muscles. PLoS Genet 11:e1005006
Kwon, Young; Song, Wei; Droujinine, Ilia A et al. (2015) Systemic organ wasting induced by localized expression of the secreted insulin/IGF antagonist ImpL2. Dev Cell 33:36-46
Demontis, Fabio; Patel, Vishal K; Swindell, William R et al. (2014) Intertissue control of the nucleolus via a myokine-dependent longevity pathway. Cell Rep 7:1481-1494
Owusu-Ansah, Edward; Perrimon, Norbert (2014) Modeling metabolic homeostasis and nutrient sensing in Drosophila: implications for aging and metabolic diseases. Dis Model Mech 7:343-50
Piccirillo, Rosanna; Demontis, Fabio; Perrimon, Norbert et al. (2014) Mechanisms of muscle growth and atrophy in mammals and Drosophila. Dev Dyn 243:201-15

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