The long term objectives of this research proposal are to understand the mechanisms involved in the processing and modification of pre-messenger RNA. Experiments are proposed to address three aspects of RNA processing: 1. The regulation of alternative splicing. 2. The recognition and pairing of splice sites in constitutively spliced pre- mRNA. 3. The editing of pre-mRNA by site-specific adenosine deamination. Pre-mRNA splicing is a critical step in the pathway of normal gene expression. Defects in splicing are the cause of numerous human genetic diseases and they are correlated with certain types of human cancer. The editing of pre-mRNA results in the production of proteins with amino acid sequences distinct from these encoded in genomic DNA. Defects in this process would have a profound effect on the function of the encoded proteins. The problem of regulated alternative splicing will be approached by a detailed functional and structural analysis of a well characterized splicing enhancer complex from the Drosophila doublesex pre-mRNA AN essential component of this complex is a member of the serine/arginine(SR) family of splicing factors which are highly conserved from flies to man. These proteins are thought to mediate interactions between the 5' and 3' splice site in constitutively spliced RNA and the interaction between splicing enhancer complexes and the basic splicing apparatus in alternatively spliced RNAs. A novel hybrid protein approach will be used to determine the function of the arginine-serine-rich region of SR proteins in alternative and constitutive splicing. This approach involves the use of low molecular weight reversible protein dimerizers that can be used to tightly control activity of hybrid SR protein during the splicing reaction. The role of exon sequences in splice site recognition will be approached by determining whether novel enhancer sequences recognized by specific members of the SR family of proteins correspond to conserved regions in the exons of beta-globin pre-mRNAs. In addition, UV crosslinking and mutagenesis studies will be carried out to identify and characterize the function of SR protein binding sites in the beta-globin exons The mechanism of pre-mRNA editing will be approached by studying interactions between a specific editing enzyme and two highly structured editing sites in GluR-B pre-mRNA. In addition, a novel immunoaffinity selection method will be employed to identify and characterize new targets for editing by site-specific adenosine deamination. When completed, the proposed studies will significantly advance the understanding of the mechanisms of RNA splicing and editing.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM042231-21
Application #
6385920
Study Section
Molecular Biology Study Section (MBY)
Program Officer
Rhoades, Marcus M
Project Start
1981-04-01
Project End
2002-03-31
Budget Start
2001-04-01
Budget End
2002-03-31
Support Year
21
Fiscal Year
2001
Total Cost
$504,274
Indirect Cost
Name
Harvard University
Department
Microbiology/Immun/Virology
Type
Schools of Arts and Sciences
DUNS #
071723621
City
Cambridge
State
MA
Country
United States
Zip Code
02138
Buchanan, Sean M; Schalm, Stefanie S; Maniatis, Tom (2010) Proteolytic processing of protocadherin proteins requires endocytosis. Proc Natl Acad Sci U S A 107:17774-9
Ribich, Scott; Tasic, Bosiljka; Maniatis, Tom (2006) Identification of long-range regulatory elements in the protocadherin-alpha gene cluster. Proc Natl Acad Sci U S A 103:19719-24
Ibrahim, El Cherif; Schaal, Thomas D; Hertel, Klemens J et al. (2005) Serine/arginine-rich protein-dependent suppression of exon skipping by exonic splicing enhancers. Proc Natl Acad Sci U S A 102:5002-7
Tasic, Bosiljka; Nabholz, Christoph E; Baldwin, Kristin K et al. (2002) Promoter choice determines splice site selection in protocadherin alpha and gamma pre-mRNA splicing. Mol Cell 10:21-33
Graveley, B R; Hertel, K J; Maniatis, T (2001) The role of U2AF35 and U2AF65 in enhancer-dependent splicing. RNA 7:806-18
Wu, Q; Zhang, T; Cheng, J F et al. (2001) Comparative DNA sequence analysis of mouse and human protocadherin gene clusters. Genome Res 11:389-404
Gaur, R K; Beigelman, L; Haeberli, P et al. (2000) Role of adenine functional groups in the recognition of the 3'-splice-site AG during the second step of pre-mRNA splicing. Proc Natl Acad Sci U S A 97:115-20
Wu, Q; Maniatis, T (2000) Large exons encoding multiple ectodomains are a characteristic feature of protocadherin genes. Proc Natl Acad Sci U S A 97:3124-9
Wu, Q; Maniatis, T (1999) A striking organization of a large family of human neural cadherin-like cell adhesion genes. Cell 97:779-90
Schaal, T D; Maniatis, T (1999) Selection and characterization of pre-mRNA splicing enhancers: identification of novel SR protein-specific enhancer sequences. Mol Cell Biol 19:1705-19

Showing the most recent 10 out of 27 publications