Evidence map›Paper›PMID 24882724›Full record

ReviewSeminars in cell & developmental biology2014

Post-transcriptional RNA regulons affecting cell cycle and proliferation.

Jeff G Blackinton, Jack D Keene

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in cell & developmental biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

74 citing papers in PubMed, 99 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Biomolecular NMR assignments · 2024
    Article
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  7. Article
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  15. Cancer cells hijack RNA processing to rewrite the message.Biochemical Society transactions · 2022
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

14 more citing papers are in PubMed but not listed here.

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

2 authors at 2 institutions in 1 country.

Jeff G BlackintonDepartment of Molecular Genetics & Microbiology, Duke University Medical Center, Box 3020, Durham, NC 27710, USA.
Jack D KeeneDepartment of Molecular Genetics & Microbiology, Duke University Medical Center, Box 3020, Durham, NC 27710, USA. Electronic address: keene001@mc.duke.edu.
Duke Medical Center · USDuke University Hospital · US

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI JOHN N. NORTON · 1985 to 2026
$174.8M
ROLE OF P53 IN THE CELLULAR RESPONSE TO DNA DAMAGER01ES005777 · NIEHS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI KASTAN, MICHAEL B · 1992 to 2017
$2.3M
RNA Dynamics of Transient Macromolecular Complexes in Cancer CellsR01CA157268 · NCI · DUKE UNIVERSITY · PI KEENE, JACK D · 2011 to 2015
$1.7M
NCI NIH HHS P30 CA014236NCI NIH HHS R01 CA157268NCI NIH HHS R01CA157268NIEHS NIH HHS R01 ES005777NIEHS NIH HHS R01ES005777
6 · The paper itself

Abstract

The cellular growth cycle is initiated and maintained by punctual, yet agile, regulatory events involving modifications of cell cycle proteins as well as coordinated gene expression to support cyclic checkpoint decisions. Recent evidence indicates that post-transcriptional partitioning of messenger RNA subsets by RNA-binding proteins help physically localize, temporally coordinate, and efficiently translate cell cycle proteins. This dynamic organization of mRNAs encoding cell cycle components contributes to the overall economy of the cell cycle consistent with the post-transcriptional RNA regulon model of gene expression. This review examines several recent studies demonstrating the coordination of mRNA subsets encoding cell cycle proteins during nuclear export and subsequent coupling to protein synthesis, and discusses evidence for mRNA coordination of p53 targets and the DNA damage response pathway. We consider how these observations may connect to upstream and downstream post-transcriptional coordination and coupling of splicing, export, localization, and translation. Published examples from yeast, nematode, insect, and mammalian systems are discussed, and we consider genetic evidence supporting the conclusion that dysregulation of RNA regulons may promote pathogenic states of growth such as carcinogenesis.

Indexed as

Cell CycleCell ProliferationActive Transport, Cell NucleusAnimalsDNA DamageGene ExpressionHumansRegulonRNA InterferenceRNA, MessengerRNA TransportRNA, MessengerCancerDNA damagep53Posttranscriptional regulationRNA-binding proteinsTranslational control

Identifiers

PMID24882724
PMCPMC4163074
OpenAlexW2059924918

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.