Evidence map›Paper›PMID 25132173›Full record

ArticleMolecular cell2014

NuA4 initiates dynamic histone H4 acetylation to promote high-fidelity sister chromatid recombination at postreplication gaps.

Nealia C M House, Jiahui H Yang, Stephen C Walsh, Jonathan M Moy, Catherine H Freudenreich

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
7.0field-weighted citation impact, top 4% 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

40 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Homologous recombination within repetitive DNA.Current opinion in genetics & development · 2021
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Structure-forming repeats and their impact on genome stability.Current opinion in genetics & development · 2021
    Review
  16. Review
  17. Review
  18. Genetic Assays to Study Repeat Fragility in Saccharomyces cerevisiae.Methods in molecular biology (Clifton, N.J.) · 2020
    Article
  19. Distinct roles foreLife · 2019
    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.

Nealia C M HouseDepartment of Biology, Tufts University, Medford, MA 02155, USA.
Jiahui H YangDepartment of Biology, Tufts University, Medford, MA 02155, USA.
Stephen C WalshDepartment of Biology, Tufts University, Medford, MA 02155, USA.
Jonathan M MoyDepartment of Biology, Tufts University, Medford, MA 02155, USA.
Catherine H FreudenreichDepartment of Biology, Tufts University, Medford, MA 02155, USA; Program in Genetics, Sackler School of Graduate Biomedical Sciences, Tufts University, Boston, MA 02111, USA. Electronic address: catherine.freudenreich@tufts.edu.
Tufts University · US

Funding

Mutations Arising During DNA RepairP01GM105473 · NIGMS · BRANDEIS UNIVERSITY · PI LOVETT, SUSAN THOMAS · 2014 to 2018
$8.6M
Stability &Fragility of Trinucleotide Repeats in YeastR01GM063066 · NIGMS · TUFTS UNIVERSITY MEDFORD · PI FREUDENREICH, CATHERINE H · 2001 to 2010
$2.4M
NIGMS NIH HHS P01 GM105473NIGMS NIH HHS P01GM105473NIGMS NIH HHS R01 GM063066NIGMS NIH HHS R01GM063066
6 · The paper itself

Abstract

CAG/CTG trinucleotide repeats are unstable, fragile sequences that strongly position nucleosomes, but little is known about chromatin modifications required to prevent genomic instability at these or other structure-forming sequences. We discovered that regulated histone H4 acetylation is required to maintain CAG repeat stability and promote gap-induced sister chromatid recombination. CAG expansions in the absence of H4 HATs NuA4 and Hat1 and HDACs Sir2, Hos2, and Hst1 depended on Rad52, Rad57, and Rad5 and were therefore arising through homology-mediated postreplication repair (PRR) events. H4K12 and H4K16 acetylation were required to prevent Rad5-dependent CAG repeat expansions, and H4K16 acetylation was enriched at CAG repeats during S phase. Genetic experiments placed the RSC chromatin remodeler in the same PRR pathway, and Rsc2 recruitment was coincident with H4K16 acetylation. Here we have utilized a repetitive DNA sequence that induces endogenous DNA damage to identify histone modifications that regulate recombination efficiency and fidelity during postreplication gap repair.

Indexed as

Sister Chromatid ExchangeAcetylationChromatin Assembly and DisassemblyChromosomes, FungalDNA DamageDNA RepairDNA ReplicationGenome, FungalGenomic InstabilityHistone AcetyltransferasesHistone DeacetylasesHistonesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTrinucleotide RepeatsHistone AcetyltransferasesHistone DeacetylasesHistonesNuA4 protein, S cerevisiaeSaccharomyces cerevisiae Proteins

Identifiers

PMID25132173
PMCPMC4169719
OpenAlexW2050357231

What OpenQuestion holds

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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.