The alpha-globin polyC binding proteins (alpha CPs) comprise a widely distributed and highly abundant family of RNA-binding proteins. The complex formed by the interaction of alphaCP with its target RNA has been implicated in various post-transcriptional controls, including mRNA stability and translation. The goal of the proposed research is to define the full spectrum of mRNA targets and roles of alphaCPs in the post-transcriptional controls of gene expression.
Aim I will optimize and verify a co-purification approach for the isolation of mRNAs that interact with alpha-CPs in vivo.
Aim II will utilize a genome wide screen to identify the sets of mRNAs that associates with specific alphaCP isoforms.
Aim III will consist of two parts: (A) the alpha CP binding site(s) within representative numbers of target mRNAs will be mapped and then mutated in order to disrupt the alphaCP-mRNA, which will be followed by (B) studies designed to determine the function(s) of the defined alphaCP-mRNA interaction(s).

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32GM063396-01A1
Application #
6445779
Study Section
Cell Development and Function Integrated Review Group (CDF)
Program Officer
Wolfe, Paul B
Project Start
2002-03-01
Project End
Budget Start
2002-03-01
Budget End
2003-02-28
Support Year
1
Fiscal Year
2002
Total Cost
$48,148
Indirect Cost
Name
University of Pennsylvania
Department
Genetics
Type
Schools of Medicine
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Waggoner, Shelly A; Liebhaber, Stephen A (2003) Identification of mRNAs associated with alphaCP2-containing RNP complexes. Mol Cell Biol 23:7055-67
Waggoner, Shelly A; Liebhaber, Stephen A (2003) Regulation of alpha-globin mRNA stability. Exp Biol Med (Maywood) 228:387-95