Functional interactions between the transcription and mRNA 3′ end processing machineries mediated by Ssu72 and Sub1
Functional interactions between the transcription and mRNA 3′ end processing machineries mediated by Ssu72 and Sub1
Transcription and processing of pre-mRNA are coupled events. By using a combination of biochemical, molecular, and genetic methods, we have found that the phylogenetically conserved transcription factor Ssu72 is a component of the cleavage/polyadenylation factor (CPF) ofSaccharomyces cerevisiae. Our results demonstrate that Ssu72 is required for 3′ end cleavage of pre-mRNA but is dispensable for poly(A) addition and RNAP II termination. The in vitro cleavage defect caused by depletion of Ssu72 from cells can be rescued by addition of recombinant Ssu72. Ssu72 interacts physically and genetically with the Pta1 subunit of CPF. Overexpression ofPTA1causes synthetic lethality in anssu72-3mutant. Moreover, Sub1, which has been implicated in transcription initiation and termination, also interacts with Pta1, and overexpression ofSUB1suppresses the growth and processing defect of apta1mutation. Physical interactions of Ssu72 and Sub1 with Pta1 are mutually exclusive. Based on the interactions of Ssu72 and Sub1 with both the Pta1 of CPF and the TFIIB component of the initiation complex, we present a model describing how these novel connections between the transcription and 3′ end processing machineries might facilitate transitions in the RNAP II transcription cycle.
- Tufts University United States
Terminator Regions, Genetic, Saccharomyces cerevisiae Proteins, Recombinant Fusion Proteins, Saccharomyces cerevisiae, In Vitro Techniques, Polymerase Chain Reaction, Precipitin Tests, Chromatography, Affinity, Suppression, Genetic, Mutation, Escherichia coli, Mutagenesis, Site-Directed, Phosphoprotein Phosphatases, RNA Precursors, RNA Polymerase II, RNA Processing, Post-Transcriptional, Carrier Proteins, Poly A, 3' Untranslated Regions, DNA Primers
Terminator Regions, Genetic, Saccharomyces cerevisiae Proteins, Recombinant Fusion Proteins, Saccharomyces cerevisiae, In Vitro Techniques, Polymerase Chain Reaction, Precipitin Tests, Chromatography, Affinity, Suppression, Genetic, Mutation, Escherichia coli, Mutagenesis, Site-Directed, Phosphoprotein Phosphatases, RNA Precursors, RNA Polymerase II, RNA Processing, Post-Transcriptional, Carrier Proteins, Poly A, 3' Untranslated Regions, DNA Primers
11 Research products, page 1 of 2
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
chevron_left - 1
- 2
chevron_right
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).129 popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.Top 10% influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).Top 10% impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.Top 1%
