Defining Translational Reprogramming in Tuberous Sclerosis Complex
Abstract
Tuberous sclerosis complex (TSC) is an autosomal dominant disease characterized by benign tumors in various tissues. The genes mutated in this disease, TSC1 and TSC2, encode tumor suppressors that are associated in a complex. The TSC1/2 complex, through its Rheb-GAP activity, is a critical negative regulator of mTORC1 under physiological conditions. Activation of mTORC1 positively stimulates cap-dependent mRNA translation via its downstream substrates S6K and 4E-BP. In our previous study, we demonstrated that TSC-mTORC1 signaling regulates the balance between cap-dependent and cap-independent translation. In this project, we aim to (1) Dissect the molecular linkage between mTORC1 and protein homeostasis; (2) Define the role of mTORC1 in ribosome dynamics and translational re-programming.
Document Details
- Document Type
- Technical Report
- Publication Date
- Jul 01, 2015
- Accession Number
- ADA621822
Entities
People
- Shu-Bing Qian
Organizations
- Cornell University