Alternative Splicing Determines the Intracellular Localization of the Novel Nuclear Protein Nop30 and Its Interaction with the Splicing Factor SRp30c
| Autor: | Oliver Stoss, Thomas A. Cooper, Stefan Stamm, Franz-Werner Schwaiger |
|---|---|
| Rok vydání: | 1999 |
| Předmět: |
DNA
Complementary Molecular Sequence Data Muscle Proteins Biology Biochemistry Splicing factor Exon Protein splicing Complementary DNA Humans Amino Acid Sequence RNA Messenger Cloning Molecular Nuclear protein Molecular Biology Splice site mutation Base Sequence Serine-Arginine Splicing Factors Alternative splicing Chromosome Mapping Nuclear Proteins RNA-Binding Proteins Cell Biology Phosphoproteins Molecular biology Cell biology Alternative Splicing RNA splicing Apoptosis Regulatory Proteins Carrier Proteins Chromosomes Human Pair 16 Protein Binding |
| Zdroj: | Journal of Biological Chemistry. 274:10951-10962 |
| ISSN: | 0021-9258 |
| DOI: | 10.1074/jbc.274.16.10951 |
| Popis: | We report on the molecular cloning of a novel human cDNA by its interaction with the splicing factor SRp30c in a yeast two-hybrid screen. This cDNA is predominantly expressed in muscle and encodes a protein that is present in the nucleoplasm and concentrated in nucleoli. It was therefore termed Nop30 (nucleolar protein of 30 kDa). We have also identified a related cDNA with a different carboxyl terminus. Sequencing of the NOP gene demonstrated that both cDNAs are generated by alternative 5' splice site usage from a single gene that consists of four exons, spans at least 1800 nucleotides, and is located on chromosome 16q21-q23. The alternative 5' splice site usage introduces a frameshift creating two different carboxyl termini. The carboxyl terminus of Nop30 is rich in serines and arginines and has been found to target the protein into the nucleus, whereas its isoform is characterized by proline/glutamic acid dipeptides in its carboxyl terminus and is predominantly found in the cytosol. Interaction studies in yeast, in vitro protein interaction assays, and co-immunoprecipitations demonstrated that Nop30 multimerizes and binds to the RS domain of SRp30c but not to other splicing factors tested. Overexpression of Nop30 changes alternative exon usage in preprotachykinin and SRp20 reporter genes, suggesting that Nop30 influences alternative splice site selection in vivo. |
| Databáze: | OpenAIRE |
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