Evidence map›Paper›PMID 25232834›Full record

ArticlePLoS genetics2014

A genetic assay for transcription errors reveals multilayer control of RNA polymerase II fidelity.

Jordan D Irvin, Maria L Kireeva, Deanna R Gotte, Brenda K Shafer, Ingold Huang, Mikhail Kashlev, Jeffrey N Strathern

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

20 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Review
  3. Structural basis of transcription: RNA polymerase II substrate binding and metal coordination using a free-electron laser.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Transcription fidelity and its roles in the cell.Current opinion in microbiology · 2018
    Review
  15. AGenetics · 2017
    Article
  16. Article
  17. RNA polymerase II senses obstruction in the DNA minor groove via a conserved sensor motif.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  18. Article
  19. Article
  20. Review
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 at 2 institutions in 1 country.

Jordan D IrvinNCI Center for Cancer Research, Frederick, Maryland, United States of America; U.S. Army Medical Research and Materiel Command, Fort Detrick, Maryland, United States of America.
Maria L KireevaNCI Center for Cancer Research, Frederick, Maryland, United States of America.
Deanna R GotteNCI Center for Cancer Research, Frederick, Maryland, United States of America.
Brenda K ShaferNCI Center for Cancer Research, Frederick, Maryland, United States of America.
Ingold HuangNCI Center for Cancer Research, Frederick, Maryland, United States of America.
Mikhail KashlevNCI Center for Cancer Research, Frederick, Maryland, United States of America.
Jeffrey N StrathernNCI Center for Cancer Research, Frederick, Maryland, United States of America.
Center for Cancer Research · USUnited States Army Medical Research and Development Command · US

Funding

Fidelity of TranscriptionZIABC010992 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI STRATHERN, JEFFREY · 2009 to 2016
$5.5M
Intramural NIH HHS
6 · The paper itself

Abstract

We developed a highly sensitive assay to detect transcription errors in vivo. The assay is based on suppression of a missense mutation in the active site tyrosine in the Cre recombinase. Because Cre acts as tetramer, background from translation errors are negligible. Functional Cre resulting from rare transcription errors that restore the tyrosine codon can be detected by Cre-dependent rearrangement of reporter genes. Hence, transient transcription errors are captured as stable genetic changes. We used this Cre-based reporter to screen for mutations of Saccharomyces cerevisiae RPB1 (RPO21) that increase the level of misincorporation during transcription. The mutations are in three domains of Rpb1, the trigger loop, the bridge helix, and in sites involved in binding to TFIIS. Biochemical characterization demonstrates that these variants have elevated misincorporation, and/or ability to extend mispaired bases, or defects in TFIIS mediated editing.

Indexed as

Amino Acid SequenceCatalytic DomainCodonGene Expression Regulation, FungalGenes, ReporterMolecular Sequence DataMutationRNA Polymerase IISaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTranscription, GeneticCodonRNA Polymerase IISaccharomyces cerevisiae Proteins

Identifiers

PMID25232834
PMCPMC4168980
OpenAlexW1995964501

What OpenQuestion holds

Textmetadata
LicenceCC0
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.