UK Home Academics Athletics Medical Center Research Site Index Search UK
CTW and Gill Heart Buildings at Rose and Limestone UK College of Medicine Department Logo filler image to complete the header
click here to view a link
UK COBRE: Subproject Description - Qingjun Wang


Center of Biomedical Research Excellence in the Molecular Basis of Human Disease

National Institutes of Health, Center of Biomedical Research Excellence (COBRE)

COBRE Homepage | COBRE Pilot Grant Program | Forms | Internal Advisory Board |
External Advisory Board | Investigators
| Announcements | Cores | Awards and Projects | Grant Submission Information | Meetings | New Publications | Data Sharing

MOLECULAR MECHANISM OF MAMMALIAN AUTOPHAGY

Project Summary

As a ubiquitous lysosomal pathway essential for degrading and recycling proteins and organelles, autophagy has been implicated in a broad spectrum of human disease including cancer, infection, liver disease, myopathy and neurodegeneration. However, the molecular machinery comprising the mammalian autophagy pathway and the molecular mechanism of how this machinery functions are largely unknown. Our long-term goal is to understand the molecular mechanism of the mammalian autophagy pathway and its relevance to human disease, for discovering much needed early diagnostic biomarkers and therapeutic targets. To achieve this goal, our overall objective is to first identify novel protein-protein interactions in the mammalian autophagy pathway and subsequently to determine the functions of these novel interactors. Among the 12 known mammalian autophagy proteins, Beclin 1 plays an important positive role in autophagy regulation and has been implicated in a variety of human physiology and pathology, including tumor suppression, neurodegeneration, development and aging. Therefore, for this proposal, we will investigate Beclin 1-mediated autophagy regulation so as to begin deciphering the molecular mechanism of mammalian autophagy. Guided by strong preliminary data, three specific aims will be pursued using a combination of a novel integrated mouse genetic-proteomic approach as well as biochemical and cell biological studies. In Aim 1, we will establish the framework of a mammalian autophagy interactome through identifying Beclin 1-interacting proteins from living animals (i.e., Becn1-EGFP/+;Becn1-/- mice); in Aim 2, we will elucidate the molecular details of autophagy regulation by two novel Beclin 1-interacting proteins, Atg14L and Rubicon; and in Aim 3, we will explore the molecular details of autophagy regulation by a third novel Beclin 1-interactor and its cancer relevance. By establishing the framework of the mammalian autophagy interactome and unraveling the molecular details of autophagy regulation by Beclin 1 and its interacting proteins, this proposed work will not only provide insight into the role of autophagy in mammals but also generate novel potential targets for preventive and therapeutic interventions that may ultimately aid patients suffering from autophagy-related human disease.


.

Search COM
 
Comments to fish@uky.edu, Last Modified: Friday, September 04, 2009
Copyright © 2004, University of Kentucky Chandler Medical Center
Terms, Conditions & Privacy Statement
An Equal Opportunity University