Equipment Supplement: Ubiquitin-Dependent Protein Regulation and Quality Control of the Lysosomal Membrane

Information

  • Research Project
  • 10387872
  • ApplicationId
    10387872
  • Core Project Number
    R01GM133873
  • Full Project Number
    3R01GM133873-03S1
  • Serial Number
    133873
  • FOA Number
    PA-20-272
  • Sub Project Id
  • Project Start Date
    9/13/2019 - 4 years ago
  • Project End Date
    8/31/2024 - 3 months from now
  • Program Officer Name
    GAILLARD, SHAWN R
  • Budget Start Date
    9/1/2021 - 2 years ago
  • Budget End Date
    8/31/2022 - a year ago
  • Fiscal Year
    2021
  • Support Year
    03
  • Suffix
    S1
  • Award Notice Date
    9/17/2021 - 2 years ago

Equipment Supplement: Ubiquitin-Dependent Protein Regulation and Quality Control of the Lysosomal Membrane

Project Summary The lysosome is an essential organelle responsible for the digestion and recycling of materials delivered by endocytosis and autophagy. It also plays important roles in nutrient sensing and control of cell growth by regulating the localization and activity of mTORC1 signaling complex. Because of its importance, lysosome dysfunction leads to ~ 50 types of lysosomal storage diseases (LSDs) and contributes to many aging-related neurodegenerative diseases such as Alzheimer's, Huntington's, and Parkinson's diseases. Despite exhaustive research on how proteins are delivered to lysosomes, how lysosomes regulate their own membrane proteins remains poorly understood. However, studying this question will reveal how cells maintain a healthy lysosome during stresses and aging. Our long-term goal is to understand these fundamental questions using both yeast and mammalian cells as model systems. Recently, we discovered a ubiquitin- and ESCRT- dependent down-regulation pathway for lysosome (vacuole) membrane proteins in yeast. Follow-up investigations in our laboratory led us to hypothesize that the ubiquitin- and ESCRT- dependent degradation pathway is a general conserved mechanism to regulate the lysosome membrane composition from yeast to human. Consistently, recent proteomic studies identified multiple E3 ubiquitin ligases on the human lysosome membrane. Furthermore, the ESCRT machinery was shown to be recruited to the human lysosome membrane. In this proposed research, we plan to expand our initial findings by pursuing three specific aims. Our Aim 1 will investigate how TORC1 regulates the vacuole membrane proteome via the ubiquitin- and ESCRT-dependent pathway in yeast. Our Aim 2 will study how yeast vacuole membrane E3 ligases recognize their membrane substrates at both structure and function level. Our Aim 3 will study how human lysosomes turnover their membrane proteins. Our research will shed light on the development of new treatment strategies for LSDs and lysosome-related neurodegenerative diseases.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R01
  • Administering IC
    GM
  • Application Type
    3
  • Direct Cost Amount
    209964
  • Indirect Cost Amount
  • Total Cost
    209964
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    859
  • Ed Inst. Type
    SCHOOLS OF ARTS AND SCIENCES
  • Funding ICs
    NIGMS:209964\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    MBPP
  • Study Section Name
    Membrane Biology and Protein Processing Study Section
  • Organization Name
    UNIVERSITY OF MICHIGAN AT ANN ARBOR
  • Organization Department
    BIOCHEMISTRY
  • Organization DUNS
    073133571
  • Organization City
    ANN ARBOR
  • Organization State
    MI
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    481091276
  • Organization District
    UNITED STATES