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Cotranscriptional coupling of splicing factor recruitment and precursor messenger RNA splicing in mammalian cells

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Listerman,  Imke
Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society;

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Neugebauer,  Karla M
Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society;

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Citation

Listerman, I., Sapra, A. K., & Neugebauer, K. M. (2006). Cotranscriptional coupling of splicing factor recruitment and precursor messenger RNA splicing in mammalian cells. Nature Structure and Molecular Biology, 13(9), 815-822.


Cite as: https://hdl.handle.net/21.11116/0000-0001-1029-F
Abstract
Coupling between transcription and RNA processing is a key gene regulatory mechanism. Here we use chromatin immunoprecipitation to detect transcription-dependent accumulation of the precursor mRNA (pre-mRNA) splicing factors hnRNP A1, U2AF65 and U1 and U5 snRNPs on the intron-containing human FOS gene. These factors were poorly detected on intronless heat-shock and histone genes, a result that opposes direct recruitment by RNA polymerase II (Pol II) or the cap-binding complex in vivo. However, an observed RNA-dependent interaction between U2AF65 and active forms of Pol II may stabilize U2AF65 binding to intron-containing nascent RNA. We establish chromatin-RNA immunoprecipitation and show that FOS pre-mRNA is cotranscriptionally spliced. Notably, the topoisomerase I inhibitor camptothecin, which stalls elongating Pol II, increased cotranscriptional splicing factor accumulation and splicing in parallel. This provides direct evidence for a kinetic link between transcription, splicing factor recruitment and splicing catalysis.