4.8 Article

H3K36 Methylation and the Chromodomain Protein Eaf3 Are Required for Proper Cotranscriptional Spliceosome Assembly

Journal

CELL REPORTS
Volume 27, Issue 13, Pages 3760-+

Publisher

CELL PRESS
DOI: 10.1016/j.celrep.2019.05.100

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Funding

  1. National Institute of General Medical Sciences [GM-085474]
  2. Cellular and Molecular Biology Training Program Ruth L. Kirschstein National Research Service Award [GM007185]
  3. Whitcome Predoctoral Fellowship
  4. UCLA Dissertation Year Fellowship
  5. Russian Foundation for Basic Research [17-29-06056, 18-29-01027]
  6. Russian Science Foundation [19-44-02027]
  7. Russian Science Foundation [19-44-02027] Funding Source: Russian Science Foundation

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In the eukaryotic cell, spliceosomes assemble onto pre-mRNA cotranscriptionally. Spliceosome assembly takes place in the context of the chromatin environment, suggesting that the state of the chromatin may affect splicing. The molecular details and mechanisms through which chromatin affects splicing, however, are still unclear. Here, we show a role for the histone methyltransferase Set2 and its histone modification, H3K36 methylation, in pre-mRNA splicing through high-throughput sequencing. Moreover, the effect of H3K36 methylation on pre-mRNA splicing is mediated through the chromodomain protein Eaf3. We find that Eaf3 is recruited to intron-containing genes and that Eaf3 interacts with the splicing factor Prp45. Eaf3 acts with Prp45 and Prp19 after formation of the precatalytic B complex around the time of splicing activation, thus revealing the step in splicing that is regulated by H3K36 methylation. These studies support a model whereby H3K36 facilitates recruitment of an adapter protein to support efficient, constitutive splicing.

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