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Pre-mRNA splicing is a determinant of histone H3K36 methylation.


ABSTRACT: A chromatin code appears to mark introns and exons with distinct patterns of nucleosome enrichment and histone methylation. We investigated whether a causal relationship exists between splicing and chromatin modification by asking whether splice-site mutations affect the methylation of histone H3K36. Deletions of the 3' splice site in intron 2 or in both introns 1 and 2 of an integrated ?-globin reporter gene caused a shift in relative distribution of H3K36 trimethylation away from 5' ends and toward 3' ends. The effects of splice-site mutations correlated with enhanced retention of a U5 snRNP subunit on transcription complexes downstream of the gene. In contrast, a poly(A) site mutation did not affect H3K36 methylation. Similarly, global inhibition of splicing by spliceostatin A caused a rapid repositioning of H3K36me3 away from 5' ends in favor of 3' ends. These results suggest that the cotranscriptional splicing apparatus influences establishment of normal patterns of histone modification.

SUBMITTER: Kim S 

PROVIDER: S-EPMC3158196 | biostudies-literature | 2011 Aug

REPOSITORIES: biostudies-literature

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Pre-mRNA splicing is a determinant of histone H3K36 methylation.

Kim Soojin S   Kim Hyunmin H   Fong Nova N   Erickson Benjamin B   Bentley David L DL  

Proceedings of the National Academy of Sciences of the United States of America 20110801 33


A chromatin code appears to mark introns and exons with distinct patterns of nucleosome enrichment and histone methylation. We investigated whether a causal relationship exists between splicing and chromatin modification by asking whether splice-site mutations affect the methylation of histone H3K36. Deletions of the 3' splice site in intron 2 or in both introns 1 and 2 of an integrated β-globin reporter gene caused a shift in relative distribution of H3K36 trimethylation away from 5' ends and t  ...[more]

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