Evidence map›Paper›PMID 24561252›Full record

ArticleCell reports2014

RNA-DNA differences are generated in human cells within seconds after RNA exits polymerase II.

Isabel X Wang, Leighton J Core, Hojoong Kwak, Lauren Brady, Alan Bruzel, Lee McDaniel, Allison L Richards, Ming Wu, Christopher Grunseich, John T Lis and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

43 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
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  6. Article
  7. Article
  8. Genomic Landscapes of Noncoding RNAs RegulatingMolecular and cellular biology · 2021
    Article
  9. Article
  10. Article
  11. Review
  12. Transcriptional frameshifts contribute to protein allergenicity.The Journal of clinical investigation · 2020
    Article
  13. RNA abasic sites in yeast and human cells.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

11 authors at 5 institutions in 1 country.

Isabel X WangLife Sciences Institute, University of Michigan, Ann Arbor, MI 48109, USA.
Leighton J CoreDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, USA.
Hojoong KwakDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA.
Lauren BradyCell and Molecular Biology Graduate Program, University of Pennsylvania, Philadelphia, PA 19104, USA.
Alan BruzelLife Sciences Institute, University of Michigan, Ann Arbor, MI 48109, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA.
Lee McDanielDepartment of Genetics, University of Pennsylvania, Philadelphia, PA 19104, USA.
Allison L RichardsHuman Genetics Graduate Program, University of Michigan, Ann Arbor, MI 48109, USA.
Ming WuHoward Hughes Medical Institute, Chevy Chase, MD 20815, USA.
Christopher GrunseichNeurogenetics Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
John T LisDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, USA. Electronic address: johnlis@cornell.edu.
Vivian G CheungLife Sciences Institute, University of Michigan, Ann Arbor, MI 48109, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA; Departments of Pediatrics and Genetics, University of Michigan, Ann Arbor, MI 48109, USA. Electronic address: vgcheung@umich.edu.
University of Michigan–Ann Arbor · USCornell University · USUniversity of Pennsylvania · USHoward Hughes Medical Institute · USNational Institutes of Health · US

Funding

Studies of Hereditary Neurological Disease: Disease MechanismsZIANS003038 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI FISCHBECK, KENNETH · 2009 to 2023
$19.5M
University of Michigan Training Program in Genomic ScienceT32HG000040 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Sebastian Zoellner · 1995 to 2026
$16.4M
COORDINATE GENE REGULATION IN ANIMAL CELLSR01GM025232 · NIGMS · CORNELL UNIVERSITY ITHACA · PI LIS, JOHN T · 1985 to 2020
$8.4M
COORDINATE GENE REGULATION IN ANIMAL CELLSR37GM025232 · NIGMS · CORNELL UNIVERSITY ITHACA · PI LIS, JOHN THOMAS · 1995 to 2004
$2.5M
Genetics of individual variation in response to radiation exposureR01ES015733 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI CHEUNG, VIVIAN G · 2007 to 2011
$2.3M
Regulatory Variants of Widely-Expressed Genes and Their Role in Disease SusceptibR21MH087384 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI CHEUNG, VIVIAN G · 2009 to 2010
$1.3M
Howard Hughes Medical InstituteNHGRI NIH HHS T32 HG000040NIEHS NIH HHS ES015733NIEHS NIH HHS R01 ES015733NIGMS NIH HHS GM25232NIGMS NIH HHS R01 GM025232NIGMS NIH HHS R37 GM025232NIMH NIH HHS MH087384NIMH NIH HHS R21 MH087384
6 · The paper itself

Abstract

RNA sequences are expected to be identical to their corresponding DNA sequences. Here, we found all 12 types of RNA-DNA sequence differences (RDDs) in nascent RNA. Our results show that RDDs begin to occur in RNA chains ~55 nt from the RNA polymerase II (Pol II) active site. These RDDs occur so soon after transcription that they are incompatible with known deaminase-mediated RNA-editing mechanisms. Moreover, the 55 nt delay in appearance indicates that they do not arise during RNA synthesis by Pol II or as a direct consequence of modified base incorporation. Preliminary data suggest that RDD and R-loop formations may be coupled. These findings identify sequence substitution as an early step in cotranscriptional RNA processing.

Indexed as

Catalytic DomainCell Culture TechniquesDNAGene ExpressionHumansRNARNA Polymerase IITranscription, GeneticDNARNARNA Polymerase II

Identifiers

PMID24561252
PMCPMC4918108
OpenAlexW1982641924

What OpenQuestion holds

Textmetadata
LicenceTDM
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.