Evidence map›Paper›PMID 27506791›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Disruption of promoter memory by synthesis of a long noncoding RNA.

Yaxin Yu, Robert M Yarrington, Edward B Chuong, Nels C Elde, David J Stillman

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Long Non-Coding RNAs inFrontiers in cellular and infection microbiology · 2022
    Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
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  12. Article
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  14. Article
  15. A current view on long noncoding RNAs in yeast and filamentous fungi.Applied microbiology and biotechnology · 2018
    Review
  16. Article
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

5 authors at 1 institution in 1 country.

Yaxin YuDepartment of Pathology, University of Utah Health Sciences Center, Salt Lake City, UT 84112;
Robert M YarringtonDepartment of Pathology, University of Utah Health Sciences Center, Salt Lake City, UT 84112;
Edward B ChuongDepartment of Human Genetics, University of Utah Health Sciences Center, Salt Lake City, UT 84112.
Nels C EldeDepartment of Human Genetics, University of Utah Health Sciences Center, Salt Lake City, UT 84112.
David J StillmanDepartment of Pathology, University of Utah Health Sciences Center, Salt Lake City, UT 84112; david.stillman@path.utah.edu.ORCID 0000-0002-5268-2416
University of Utah · US

Funding

RESEARCH TRAINING IN HEMATOLOGYT32DK007115 · NIDDK · UNIVERSITY OF UTAH · PI LEIBOLD, ELIZABETH ANN, PRCHAL, JOSEF T · 1986 to 2020
$8.4M
MOLECULAR MECHANISMS IN TRANSCRIPTIONAL REGULATIONR01GM039067 · NIGMS · UNIVERSITY OF UTAH · PI STILLMAN, DAVID J · 1988 to 2013
$3.9M
Mechanisms of mimicry underlying the evolution of a model poxvirusR01GM114514 · NIGMS · UNIVERSITY OF UTAH · PI ELDE, NELS C. · 2015 to 2019
$1.6M
NIDDK NIH HHS T32 DK007115NIGMS NIH HHS R01 GM039067NIGMS NIH HHS R01 GM114514
6 · The paper itself

Abstract

The yeast HO endonuclease is expressed in late G1 in haploid mother cells to initiate mating-type interconversion. Cells can be arrested in G1 by nutrient deprivation or by pheromone exposure, but cells that resume cycling after nutrient deprivation or cyclin-dependent kinase (CDK) inactivation express HO in the first cell cycle, whereas HO is not expressed until the second cycle after release from pheromone arrest. Here, we show that transcription of a long noncoding RNA (lncRNA) mediates this differential response. The SBF and Mediator factors remain bound to the inactive promoter during arrest due to CDK inactivation, and these bound factors allow the cell to remember a transcriptional decision made before arrest. If the presence of mating pheromone indicates that this decision is no longer appropriate, a lncRNA originating at -2700 upstream of the HO gene is induced, and the transcription machinery displaces promoter-bound SBF, preventing HO transcription in the subsequent cell cycle. Further, we find that the displaced SBF is blocked from rebinding due to incorporation of its recognition sites within nucleosomes. Expressing the pHO-lncRNA in trans is ineffective, indicating that transcription in cis is required. Factor displacement during lncRNA transcription could be a general mechanism for regulating memory of previous events at promoters.

Indexed as

Gene Expression Regulation, FungalPromoter Regions, GeneticBase SequenceBinding SitesEndonucleasesG1 Phase Cell Cycle CheckpointsMediator ComplexNucleosomesProtein BindingRNA, FungalRNA, Long NoncodingSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTranscription FactorsTranscription, GeneticEndonucleasesMediator ComplexNucleosomesRNA, FungalRNA, Long NoncodingSaccharomyces cerevisiae ProteinsSBF protein, S cerevisiaeTranscription Factorschromatingene regulationlncRNAnucleosomespromoter memory

Identifiers

PMID27506791
PMCPMC5003236
OpenAlexW2516953906

What OpenQuestion holds

Textmetadata
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.