Abstract |
Subcellular compartmentalization of splicing factors has been proposed to play a role in the regulation of alternative splicing. In the present work we have addressed this issue using adenovirus-infected cells to visualize an alternative splicing switch at the single cell level. The adenovirus gene expression program requires the activation of distal alternative 3' splice sites during the late phase of infection in major late transcripts. We have established in situ hybridization conditions that allow for the specific detection of 3' alternatively spliced adenoviral mRNAs from the L1 transcript family. Results show that the switch from proximal to distal 3' splice sites correlates with a massive reorganization of splicing factors in the cell nucleus, involving their recruitment from nuclear speckles to sites of viral transcription. This observation raises the possibility that the subnuclear organization of splicing factors may be regulated in response to events that lead to the activation of alternative splicing programs.
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Authors | Margarida Gama-Carvalho, Inês Condado, Maria Carmo-Fonseca |
Journal | Experimental cell research
(Exp Cell Res)
Vol. 289
Issue 1
Pg. 77-85
(Sep 10 2003)
ISSN: 0014-4827 [Print] United States |
PMID | 12941606
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Nuclear Proteins
- RNA Splice Sites
- RNA, Messenger
- RNA, Viral
- RNA-Binding Proteins
- Viral Proteins
- Serine-Arginine Splicing Factors
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Topics |
- Adenoviridae
(genetics)
- Alternative Splicing
(genetics)
- Cell Nucleus
(metabolism, ultrastructure)
- Gene Expression Regulation
(genetics)
- Genetic Vectors
(genetics)
- HeLa Cells
- Humans
- In Situ Hybridization
(methods)
- Nuclear Proteins
(genetics)
- RNA Splice Sites
(genetics)
- RNA, Messenger
(biosynthesis, genetics)
- RNA, Viral
(genetics, metabolism)
- RNA-Binding Proteins
- Serine-Arginine Splicing Factors
- Viral Proteins
(genetics, metabolism)
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