Literature DB >> 28396559

An mRNA Capping Enzyme Targets FACT to the Active Gene To Enhance the Engagement of RNA Polymerase II into Transcriptional Elongation.

Rwik Sen1, Amala Kaja1, Jannatul Ferdoush1, Shweta Lahudkar1, Priyanka Barman1, Sukesh R Bhaumik2.   

Abstract

We have recently demonstrated that an mRNA capping enzyme, Cet1, impairs promoter-proximal accumulation/pausing of RNA polymerase II (Pol II) independently of its capping activity in Saccharomyces cerevisiae to control transcription. However, it is still unknown how Pol II pausing is regulated by Cet1. Here, we show that Cet1's N-terminal domain (NTD) promotes the recruitment of FACT (facilitates chromatin transcription that enhances the engagement of Pol II into transcriptional elongation) to the coding sequence of an active gene, ADH1, independently of mRNA-capping activity. Absence of Cet1's NTD decreases FACT targeting to ADH1 and consequently reduces the engagement of Pol II in transcriptional elongation, leading to promoter-proximal accumulation of Pol II. Similar results were also observed at other genes. Consistently, Cet1 interacts with FACT. Collectively, our results support the notion that Cet1's NTD promotes FACT targeting to the active gene independently of mRNA-capping activity in facilitating Pol II's engagement in transcriptional elongation, thus deciphering a novel regulatory pathway of gene expression.
Copyright © 2017 American Society for Microbiology.

Entities:  

Keywords:  Cet1; FACT; RNA polymerase II; mRNA capping; transcription

Mesh:

Substances:

Year:  2017        PMID: 28396559      PMCID: PMC5472824          DOI: 10.1128/MCB.00029-17

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  64 in total

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Review 5.  The role of FACT in making and breaking nucleosomes.

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  8 in total

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2.  An F-Box Protein, Mdm30, Interacts with TREX Subunit Sub2 To Regulate Cellular Abundance Cotranscriptionally in Orchestrating mRNA Export Independently of Splicing and Mitochondrial Function.

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3.  FACT is recruited to the +1 nucleosome of transcribed genes and spreads in a Chd1-dependent manner.

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4.  Genome-Wide Regulations of the Preinitiation Complex Formation and Elongating RNA Polymerase II by an E3 Ubiquitin Ligase, San1.

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8.  Interplay of mRNA capping and transcription machineries.

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  8 in total

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