Evidence map›Paper›PMID 31522911›Full record

ReviewDNA repair2019

Actin' between phase separated domains for heterochromatin repair.

Chetan C Rawal, Christopher P Caridi, Irene Chiolo

Abstract readReview
In one paragraph

Review in DNA repair, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Myosin in chromosome organisation and gene expression.Biochemical Society transactions · 2023
    Review
  7. Article
  8. Review
  9. Multi-scale dynamics of heterochromatin repair.Current opinion in genetics & development · 2021
    Review
  10. Review
  11. Review
  12. Article
  13. Complex Chromatin Motions for DNA Repair.Frontiers in genetics · 2020
    Review
  14. Arp2/3 and Unc45 maintain heterochromatin stability inExperimental biology and medicine (Maywood, N.J.) · 2019
    Article
  15. 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.

Chetan C RawalUniversity of Southern California, Molecular and Computational Biology Department, Los Angeles, CA, 90089, USA.
Christopher P CaridiUniversity of Southern California, Molecular and Computational Biology Department, Los Angeles, CA, 90089, USA.
Irene ChioloUniversity of Southern California, Molecular and Computational Biology Department, Los Angeles, CA, 90089, USA. Electronic address: chiolo@usc.edu.

Funding

Roles of nuclear architecture and phase separation in heterochromatin repair dynamicsR01GM117376 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHIOLO, IRENE E · 2015 to 2023
$3.3M
NIGMS NIH HHS R01 GM117376
6 · The paper itself

Abstract

DNA double-strand breaks (DSBs) are particularly challenging to repair in pericentromeric heterochromatin because of the increased risk of aberrant recombination in highly repetitive sequences. Recent studies have identified specialized mechanisms enabling 'safe' homologous recombination (HR) repair in heterochromatin. These include striking nuclear actin filaments (F-actin) and myosins that drive the directed motion of repair sites to the nuclear periphery for 'safe' repair. Here, we summarize our current understanding of the mechanisms involved, and propose how they might operate in the context of a phase-separated environment.

Indexed as

DNA Breaks, Double-StrandedRecombinational DNA RepairActinsAnimalsCell NucleusDNAEukaryotaHeterochromatinHumansActinsDNAHeterochromatinDSB repairHeterochromatinHomologous recombinationNuclear actin filamentsPhase separation

Identifiers

PMID31522911
PMCPMC6764897

What OpenQuestion holds

Textmetadata
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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.