Evidence map›Paper›PMID 22072070›Full record

ReviewHeredity2012

Making a long story short: noncoding RNAs and chromosome change.

J D Brown, S E Mitchell, R J O'Neill

Abstract readReview
In one paragraph

Review in Heredity, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Review
  2. Article
  3. A genome assembly of decaploidHorticulture research · 2024
    Article
  4. Article
  5. Highly Resolved Detection of Long Non-coding RNAs In Situ.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  6. Article
  7. Article
  8. Seq'ing identity and function in a repeat-derived noncoding RNA world.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2020
    Review
  9. A centromere satellite concomitant with extensive karyotypic diversity across the Peromyscus genus defies predictions of molecular drive.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2019
    Article
  10. Article
  11. Transposable elements: genome innovation, chromosome diversity, and centromere conflict.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2018
    Review
  12. Review
  13. Article
  14. Review
  15. The long non-coding RNAOncotarget · 2017
    Article
  16. Visualizing Long Noncoding RNAs on Chromatin.Methods in molecular biology (Clifton, N.J.) · 2016
    Article
  17. Satellite non-coding RNAs: the emerging players in cells, cellular pathways and cancer.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2015
    Review
  18. Article
  19. Article
  20. Charity begins at home: non-coding RNA functions in DNA repair.Nature reviews. Molecular cell biology · 2013
    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

3 authors.

J D BrownAllied Health Sciences Department, University of Connecticut, Storrs, CT, USA.
S E Mitchell
R J O'Neill

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As important as the events that influence selection for specific chromosome types in the derivation of novel karyotypes, are the events that initiate the changes in chromosome number and structure between species, and likewise polymorphisms, variants and disease states within species. Although once thought of as transcriptional 'noise', noncoding RNAs (ncRNAs) are now recognized as important mediators of epigenetic regulation and chromosome stability. Here we highlight recent work that illustrates the influence short and long ncRNAs have as participants in the function and stability of chromosome regions such as centromeres, telomeres, evolutionary breakpoints and fragile sites. We summarize recent evidence that ncRNAs can facilitate chromosome change and present mechanisms by which ncRNAs create DNA breaks. Finally, we present hypotheses on how they may create novel karyotypes and thus affect chromosome evolution.

Indexed as

AnimalsChromosomal InstabilityChromosome BreakpointsChromosome Fragile SitesChromosomesEvolution, MolecularHumansKaryotypeRNA, UntranslatedRNA, Untranslated

Identifiers

PMID22072070
PMCPMC3238116

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.