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Elife ; 62017 10 13.
Article in English | MEDLINE | ID: mdl-29027900

ABSTRACT

Numerous links exist between co-transcriptional RNA processing and the transcribing RNAPII. In particular, pre-mRNA splicing was reported to be associated with slowed RNAPII elongation. Here, we identify a site of ubiquitination (K1246) in the catalytic subunit of RNAPII close to the DNA entry path. Ubiquitination was increased in the absence of the Bre5-Ubp3 ubiquitin protease complex. Bre5 binds RNA in vivo, with a preference for exon 2 regions of intron-containing pre-mRNAs and poly(A) proximal sites. Ubiquitinated RNAPII showed similar enrichment. The absence of Bre5 led to impaired splicing and defects in RNAPII elongation in vivo on a splicing reporter construct. Strains expressing RNAPII with a K1246R mutation showed reduced co-transcriptional splicing. We propose that ubiquinitation of RNAPII is induced by RNA processing events and linked to transcriptional pausing, which is released by Bre5-Ubp3 associated with the nascent transcript.


Subject(s)
Catalytic Domain , RNA Polymerase II/metabolism , RNA Precursors/metabolism , Ubiquitination , Endopeptidases/metabolism , Models, Biological , Mutant Proteins/genetics , Mutant Proteins/metabolism , Mutation, Missense , RNA Polymerase II/genetics , Saccharomyces cerevisiae Proteins/metabolism
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