Evidence map›Paper›PMID 28190770›Full record

ArticleMolecular cell2017

Nuclear RNA Decay Pathways Aid Rapid Remodeling of Gene Expression in Yeast.

Stefan Bresson, Alex Tuck, Desislava Staneva, David Tollervey

Open access · hybridAbstract read
In one paragraph

Article in Molecular cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
5.0field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 74 citations in OpenAlex.

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  12. Quiescence inAnnual review of genetics · 2022
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 2 countries.

Stefan BressonWellcome Trust Centre for Cell Biology, University of Edinburgh, Michael Swann Building, King's Buildings, Edinburgh EH9 3BF, Scotland.
Alex TuckFriedrich Miescher Institute for Biomedical Research, Maulbeerstrasse 66, 4058 Basel, Switzerland; European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SD, UK.
Desislava StanevaWellcome Trust Centre for Cell Biology, University of Edinburgh, Michael Swann Building, King's Buildings, Edinburgh EH9 3BF, Scotland.
David TollerveyWellcome Trust Centre for Cell Biology, University of Edinburgh, Michael Swann Building, King's Buildings, Edinburgh EH9 3BF, Scotland. Electronic address: d.tollervey@ed.ac.uk.
Wellcome Centre for Cell Biology · GBEuropean Bioinformatics Institute · GBUniversity of Edinburgh · GB

Funding

Wellcome Trust 077248Wellcome Trust 092076Wellcome Trust 103977
6 · The paper itself

Abstract

In budding yeast, the nuclear RNA surveillance system is active on all pre-mRNA transcripts and modulated by nutrient availability. To test the role of nuclear surveillance in reprogramming gene expression, we identified transcriptome-wide binding sites for RNA polymerase II and the exosome cofactors Mtr4 (TRAMP complex) and Nab3 (NNS complex) by UV crosslinking immediately following glucose withdrawal (0, 4, and 8 min). In glucose, mRNA binding by Nab3 and Mtr4 was mainly restricted to promoter-proximal sites, reflecting early transcription termination. Following glucose withdrawal, many growth-related mRNAs showed reduced transcription but increased Nab3 binding, accompanied by downstream recruitment of Mtr4, and oligo(A) tailing. We conclude that transcription termination is followed by TRAMP-mediated RNA decay. Upregulated transcripts evaded increased surveillance factor binding following glucose withdrawal. Some upregulated genes showed use of alternative transcription starts to bypass strong NNS binding sites. We conclude that nuclear surveillance pathways regulate both positive and negative responses to glucose availability.

Indexed as

Gene Expression Regulation, FungalRNA Processing, Post-TranscriptionalRNA StabilityTranscription, GeneticAdaptation, PhysiologicalBinding SitesCell NucleusDEAD-box RNA HelicasesGlucoseNuclear ProteinsProtein BindingRNA-Binding ProteinsRNA, FungalRNA, MessengerRNA, NuclearRNA Polymerase IIDEAD-box RNA HelicasesGlucoseMTR4 protein, S cerevisiaeNAB3 protein, S cerevisiaeNuclear ProteinsRNA-Binding ProteinsRNA, FungalRNA, MessengerRNA, NuclearRNA Polymerase IISaccharomyces cerevisiae Proteinsgene expressionRNA exosomeRNA polymerase IIRNA surveillance

Identifiers

PMID28190770
PMCPMC5344683
OpenAlexW2587668290

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.