Evidence map›Paper›PMID 16420678›Full record

ArticleGenome biology2005

The undertranslated transcriptome reveals widespread translational silencing by alternative 5' transcript leaders.

G Lynn Law, Kellie S Bickel, Vivian L MacKay, David R Morris

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

37 citing papers in PubMed, 49 citations in OpenAlex.

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  9. Disruption of promoter memory by synthesis of a long noncoding RNA.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  10. Article
  11. Nonsense-mediated RNA decay--a switch and dial for regulating gene expression.BioEssays : news and reviews in molecular, cellular and developmental biology · 2015
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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 2 institutions in 1 country.

G Lynn LawDepartment of Biochemistry, University of Washington, Seattle, WA 98195, USA. gllaw@u.washington.edu
Kellie S Bickel
Vivian L MacKay
David R Morris
Seattle University · USUniversity of Washington · US

Funding

TRAINING IN MOLECULAR AND CELLULAR BIOLOGYT32GM007270 · NIGMS · UNIVERSITY OF WASHINGTON · PI RAIBLE, DAVID W · 1985 to 2020
$21.0M
DEVELOPMENT OF TRANSLATION STATE ARRAY ANALYSISR33CA089807 · NCI · UNIVERSITY OF WASHINGTON · PI MORRIS, DAVID R · 2001 to 2003
$2.2M
TRANSLATIONAL CONTROL OF ONCOPROTEIN MDM2 SYNTHESISR01CA071453 · NCI · UNIVERSITY OF WASHINGTON · PI MORRIS, DAVID R · 1999 to 2003
$946k
NCI NIH HHS CA71453NCI NIH HHS CA89807NCI NIH HHS R01 CA071453NCI NIH HHS R33 CA089807NIGMS NIH HHS T32 GM007270NIGMS NIH HHS T32 GM07270
6 · The paper itself

Abstract

backgroundTranslational efficiencies in Saccharomyces cerevisiae vary from transcript to transcript by approximately two orders of magnitude. Many of the poorly translated transcripts were found to respond to the appropriate external stimulus by recruiting ribosomes. Unexpectedly, a high frequency of these transcripts showed the appearance of altered 5' leaders that coincide with increased ribosome loading.

resultsOf the detectable transcripts in S. cerevisiae, 8% were found to be underloaded with ribosomes. Gene ontology categories of responses to stress or external stimuli were overrepresented in this population of transcripts. Seventeen poorly loaded transcripts involved in responses to pheromone, nitrogen starvation, and osmotic stress were selected for detailed study and were found to respond to the appropriate environmental signal with increased ribosome loading. Twelve of these regulated transcripts exhibited structural changes in their 5' transcript leaders in response to the environmental signal. In many of these the coding region remained intact, whereas regulated shortening of the 5' end truncated the open reading frame in others. Colinearity between the gene and transcript sequences eliminated regulated splicing as a mechanism for these alterations in structure.

conclusionFrequent occurrence of coordinated changes in transcript structure and translation efficiency, in at least three different gene regulatory networks, suggests a widespread phenomenon. It is likely that many of these altered 5' leaders arose from changes in promoter usage. We speculate that production of translationally silenced transcripts may be one mechanism for allowing low-level transcription activity necessary for maintaining an open chromatin structure while not allowing inappropriate protein production.

Indexed as

Gene Silencing5' Untranslated RegionsAquaporinsDeoxyribonucleases, Type II Site-SpecificDown-RegulationGenes, FungalGenes, Mating Type, FungalMutationNitrogenOsmosisPheromonesProtein BiosynthesisRibosomesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTranscription, Genetic5' Untranslated RegionsAquaporinsAQY1 protein, S cerevisiaeDeoxyribonucleases, Type II Site-SpecificNitrogenPheromonesSaccharomyces cerevisiae ProteinsSCEI protein, S cerevisiae

Identifiers

PMID16420678
PMCPMC1414110
OpenAlexW1836542508

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.