Evidence map›Paper›PMID 21865163›Full record

ArticleThe Journal of biological chemistry2011

Genetic and genomic analyses of RNA polymerase II-pausing factor in regulation of mammalian transcription and cell growth.

Jianlong Sun, Haihui Pan, Chengwei Lei, Bin Yuan, Sreejith J Nair, Craig April, Balaji Parameswaran, Brandy Klotzle, Jian-Bing Fan, Jianhua Ruan and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Negative elongation factor is essential for endometrial function.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  7. Article
  8. Article
  9. RNA polymerase II pausing as a context-dependent reader of the genome.Biochemistry and cell biology = Biochimie et biologie cellulaire · 2016
    Review
  10. Collective Properties of a Transcription Initiation Model Under Varying Environment.Journal of computational biology : a journal of computational molecular cell biology · 2016
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. The Mediator complex and transcription elongation.Biochimica et biophysica acta · 2013
    Review
  19. 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 3 institutions in 1 country.

Jianlong SunDepartment of Molecular Medicine/Institute of Biotechnology, University of Texas Health Science Center at San Antonio, San Antonio, Texas 78245, USA.
Haihui Pan
Chengwei Lei
Bin Yuan
Sreejith J Nair
Craig April
Balaji Parameswaran
Brandy Klotzle
Jian-Bing Fan
Jianhua Ruan
Rong Li
The University of Texas Health Science Center at San Antonio · USIllumina (United States) · USThe University of Texas at San Antonio · US

Funding

Computational Discovery and Analysis of Community Structures in Biology NetworksSC3GM086305 · NIGMS · UNIVERSITY OF TEXAS SAN ANTONIO · PI RUAN, JIANHUA · 2009 to 2012
$555k
NIGMS NIH HHS SC3 GM086305NIGMS NIH HHS SC3GM086305
6 · The paper itself

Abstract

Many mammalian genes are occupied by paused RNA polymerase II (pol II) in the promoter-proximal region on both sides of the transcription start site. However, the impact of pol II pausing on gene expression and cell biology is not fully understood. In this study, we used a Cre-Lox system to conditionally knock out the b subunit of mouse negative elongation factor (Nelf-b), a key pol II-pausing factor, in mouse embryonic fibroblasts. We found that Nelf-b was associated with the promoter-proximal region of the majority of expressed genes, yet genetic ablation of Nelf-b only affected the steady-state mRNA levels of a small percentage of the Nelf-b-associated genes. Interestingly, Nelf-b deletion also increased levels of transcription start site upstream transcripts at multiple negative elongation factor-associated genes. The direct target genes of Nelf-b were highly enriched with those involved in the control of cell growth and cell death. Correspondingly, Nelf-b knock-out mouse embryonic fibroblasts exhibited slower progression from quiescence to proliferation, as well as in a cycling cell population. Furthermore, Nelf-b deletion also resulted in increased apoptosis. Thus, the genetic and genomic studies provide new physiological and molecular insight into Nelf-mediated pol II pausing.

Indexed as

Cell ProliferationAnimalsApoptosisCell LineEmbryo, MammalianFibroblastsGene DeletionGenomeMiceNuclear ProteinsRNA-Binding ProteinsRNA, MessengerRNA Polymerase IICobra1 protein, mouseNuclear ProteinsRNA-Binding ProteinsRNA, MessengerRNA Polymerase II

Identifiers

PMID21865163
PMCPMC3196092
OpenAlexW1965029037

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.