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Psip1/Ledgf p52 Binds Methylated Histone H3K36 and Splicing Factors and Contributes to the Regulation of Alternative Splicing

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    Rights statement: Copyright: © 2012 Pradeepa et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.1002717
Original languageEnglish
Article numbere1002717
Pages (from-to)e1002717
Number of pages15
JournalPLoS Genetics
Volume8
Issue number5
DOIs
StatePublished - May 2012

Abstract

Increasing evidence suggests that chromatin modifications have important roles in modulating constitutive or alternative splicing. Here we demonstrate that the PWWP domain of the chromatin-associated protein Psip1/Ledgf can specifically recognize tri-methylated H3K36 and that, like this histone modification, the Psip1 short (p52) isoform is enriched at active genes. We show that the p52, but not the long (p75), isoform of Psip1 co-localizes and interacts with Srsf1 and other proteins involved in mRNA processing. The level of H3K36me3 associated Srsf1 is reduced in Psip1 mutant cells and alternative splicing of specific genes is affected. Moreover, we show altered Srsf1 distribution around the alternatively spliced exons of these genes in Psip1 null cells. We propose that Psip1/p52, through its binding to both chromatin and splicing factors, might act to modulate splicing.

Research areas

  • GENE, PWWP DOMAIN, HIV-1 INTEGRASE, LEDGF/P75, SR PROTEINS, MYELOID-LEUKEMIA, MAMMALIAN-CELLS, IN-VIVO, TRANSCRIPTIONAL COACTIVATOR P75, CHROMATIN BINDING

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