Evidence map›Paper›PMID 25768301›Full record

ArticlePLoS genetics2015

NatB domain-containing CRA-1 antagonizes hydrolase ACER-1 linking acetyl-CoA metabolism to the initiation of recombination during C. elegans meiosis.

Jinmin Gao, Hyun-Min Kim, Andrew E Elia, Stephen J Elledge, Monica P Colaiácovo

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

23 citing papers in PubMed, 38 citations in OpenAlex.

  1. T2T genomes ofGenome research · 2026
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  14. Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  15. Review
  16. Meiosis.WormBook : the online review of C. elegans biology · 2017
    Review
  17. Regulation of Crossover Frequency and Distribution during Meiotic Recombination.Cold Spring Harbor symposia on quantitative biology · 2017
    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

5 authors at 1 institution in 1 country.

Jinmin GaoDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.
Hyun-Min KimDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.
Andrew E EliaDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.
Stephen J ElledgeDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.
Monica P ColaiácovoDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.
Harvard University · US

Funding

Dana Farber/Harvard Cancer Consortium Career Development Program in Clinical OncologyK12CA087723 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI David Tsai Ting · 2002 to 2026
$17.9M
Synaptonemal Complex Assembly and Function in MeiosisR01GM072551 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI Monica P Colaiacovo · 2005 to 2026
$7.5M
GENETICS OF CELL CYCLE &DNA DAMAGE REGULATION IN YEASTR01GM044664 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI ELLEDGE, STEPHEN J · 1990 to 2016
$2.0M
Howard Hughes Medical InstituteNCI NIH HHS K12 CA087723NIGMS NIH HHS R01 GM044664NIGMS NIH HHS R01 GM072551NIGMS NIH HHS R01GM072551NIGMS NIH HHS R01GM44664
6 · The paper itself

Abstract

The formation of DNA double-strand breaks (DSBs) must take place during meiosis to ensure the formation of crossovers, which are required for accurate chromosome segregation, therefore avoiding aneuploidy. However, DSB formation must be tightly regulated to maintain genomic integrity. How this regulation operates in the context of different chromatin architectures and accessibility, and how it is linked to metabolic pathways, is not understood. We show here that global histone acetylation levels undergo changes throughout meiotic progression. Moreover, perturbations to global histone acetylation levels are accompanied by changes in the frequency of DSB formation in C. elegans. We provide evidence that the regulation of histone acetylation requires CRA-1, a NatB domain-containing protein homologous to human NAA25, which controls the levels of acetyl-Coenzyme A (acetyl-CoA) by antagonizing ACER-1, a previously unknown and conserved acetyl-CoA hydrolase. CRA-1 is in turn negatively regulated by XND-1, an AT-hook containing protein. We propose that this newly defined protein network links acetyl-CoA metabolism to meiotic DSB formation via modulation of global histone acetylation.

Indexed as

Recombination, GeneticAcetylationAcetyl-CoA HydrolaseAcetyl Coenzyme AAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsDNA Breaks, Double-StrandedHistonesX ChromosomeACER-1 protein, C elegansAcetyl-CoA HydrolaseAcetyl Coenzyme ACaenorhabditis elegans ProteinsCRA-1 protein, C elegansHistones

Identifiers

PMID25768301
PMCPMC4359108
OpenAlexW2086878180

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.