Evidence map›Paper›PMID 23788651›Full record

ArticleGenome research2013

DNA damage induces targeted, genome-wide variation of poly(A) sites in budding yeast.

Joel H Graber, Fathima I Nazeer, Pei-chun Yeh, Jason N Kuehner, Sneha Borikar, Derick Hoskinson, Claire L Moore

Abstract read
In one paragraph

Article in Genome research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
–field-weighted citation impact
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

36 citing papers in PubMed.

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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

7 authors.

Joel H GraberCenter for Genome Dynamics, The Jackson Laboratory, Bar Harbor, Maine 04609, USA;
Fathima I Nazeer
Pei-chun Yeh
Jason N Kuehner
Sneha Borikar
Derick Hoskinson
Claire L Moore

Funding

UNC and PERLEGEN, IncP50GM076468 · NIGMS · JACKSON LABORATORY · PI GRABER, JOEL H · 2006 to 2015
$31.0M
Training in Education and Critical Research SkillsK12GM074869 · NIGMS · TUFTS UNIVERSITY BOSTON · PI MOORE, CLAIRE L · 2006 to 2017
$8.5M
Molecular mechanism of mRNA 3'-end formation in yeastR01GM041752 · NIGMS · TUFTS UNIVERSITY BOSTON · PI MOORE, CLAIRE L · 1989 to 2010
$4.0M
Integrated Studies of 3'-UTR Mediated Gene RegulationR01GM072706 · NIGMS · JACKSON LABORATORY · PI GRABER, JOEL H · 2006 to 2009
$986k
NIGMS NIH HHS GM041752NIGMS NIH HHS GM072706NIGMS NIH HHS K12 GM074869NIGMS NIH HHS P50 GM076468NIGMS NIH HHS R01 GM041752NIGMS NIH HHS R01 GM072706
6 · The paper itself

Abstract

Systemic response to DNA damage and other stresses is a complex process that includes changes in the regulation and activity of nearly all stages of gene expression. One gene regulatory mechanism used by eukaryotes is selection among alternative transcript isoforms that differ in polyadenylation [poly(A)] sites, resulting in changes either to the coding sequence or to portions of the 3' UTR that govern translation, stability, and localization. To determine the extent to which this means of regulation is used in response to DNA damage, we conducted a global analysis of poly(A) site usage in Saccharomyces cerevisiae after exposure to the UV mimetic, 4-nitroquinoline 1-oxide (4NQO). Two thousand thirty-one genes were found to have significant variation in poly(A) site distributions following 4NQO treatment, with a strong bias toward loss of short transcripts, including many with poly(A) sites located within the protein coding sequence (CDS). We further explored one possible mechanism that could contribute to the widespread differences in mRNA isoforms. The change in poly(A) site profile was associated with an inhibition of cleavage and polyadenylation in cell extract and a decrease in the levels of several key subunits in the mRNA 3'-end processing complex. Sequence analysis identified differences in the cis-acting elements that flank putatively suppressed and enhanced poly(A) sites, suggesting a mechanism that could discriminate between variable and constitutive poly(A) sites. Our analysis indicates that variation in mRNA length is an important part of the regulatory response to DNA damage.

Indexed as

DNA DamageGenome, Fungal3' Untranslated Regions5' Untranslated RegionsCyclic N-OxidesExpressed Sequence TagsGene Expression Regulation, FungalGenes, FungalOpen Reading FramesPolyadenylationRNA, FungalRNA IsoformsRNA, MessengerSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSequence Analysis, RNA3' Untranslated Regions4-nitropyridine 1-oxide5' Untranslated RegionsCyclic N-OxidesRNA, FungalRNA IsoformsRNA, MessengerSaccharomyces cerevisiae Proteins

Identifiers

PMID23788651
PMCPMC3787265

What OpenQuestion holds

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LicenceCC BY-NC
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.