Evidence map›Paper›PMID 36396651›Full record

ArticleNature communications2022

H2A.Z deposition by SWR1C involves multiple ATP-dependent steps.

Jiayi Fan, Andrew T Moreno, Alexander S Baier, Joseph J Loparo, Craig L Peterson

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. 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
1.6field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Histone Variant H2A.Z Enhances Histone and Nucleosome Dynamics.Molecular & cellular proteomics : MCP · 2026
    Article
  3. Article
  4. Article
  5. DDM1 Maintains Heterochromatin by Regulating Histone Variants.International journal of molecular sciences · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Structure of the human TIP60 complex.Nature communications · 2024
    Article
  10. Article
  11. Article
  12. Identification of the main barriers to Ku accumulation in chromatin.bioRxiv : the preprint server for biology · 2024
    Article
  13. Review
  14. Review
  15. 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 2 institutions in 1 country.

Jiayi Fan *Program in Molecular Medicine, University of Massachusetts Chan Medical School, Worcester, MA, 01605, USA.
Andrew T Moreno *Department of Biological Chemistry and Molecular Pharmacology, Blavatnik Institute, Harvard Medical School, Boston, MA, 02115, USA.
Alexander S BaierProgram in Molecular Medicine, University of Massachusetts Chan Medical School, Worcester, MA, 01605, USA.ORCID 0000-0003-1647-9477
Joseph J LoparoDepartment of Biological Chemistry and Molecular Pharmacology, Blavatnik Institute, Harvard Medical School, Boston, MA, 02115, USA. Joseph_Loparo@hms.harvard.edu.ORCID 0000-0003-4941-4696
Craig L PetersonProgram in Molecular Medicine, University of Massachusetts Chan Medical School, Worcester, MA, 01605, USA. Craig.Peterson@umassmed.edu.ORCID 0000-0002-9448-555X
University of Massachusetts Chan Medical School · USHarvard University · US

Funding

Regulation of chromatin dynamicsR35GM122519 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Craig L Peterson · 2017 to 2026
$9.2M
Visualizing DNA break repair: single-molecule studies of non-homologous end joiningR01GM115487 · NIGMS · HARVARD MEDICAL SCHOOL · PI LOPARO, JOSEPH J. · 2015 to 2024
$3.1M
NIGMS NIH HHS R01 GM115487NIGMS NIH HHS R35 GM122519U.S. Department of Health & Human Services | National Institutes of Health (NIH) R35-GM122519U.S. Department of Health & Human Services | National Institutes of Health (NIH) RO1GM115487
6 · The paper itself

Abstract

Histone variant H2A.Z is a conserved feature of nucleosomes flanking protein-coding genes. Deposition of H2A.Z requires ATP-dependent replacement of nucleosomal H2A by a chromatin remodeler related to the multi-subunit enzyme, yeast SWR1C. How these enzymes use ATP to promote this nucleosome editing reaction remains unclear. Here we use single-molecule and ensemble methodologies to identify three ATP-dependent phases in the H2A.Z deposition reaction. Real-time analysis of single nucleosome remodeling events reveals an initial priming step that occurs after ATP addition that involves a combination of both transient DNA unwrapping from the nucleosome and histone octamer deformations. Priming is followed by rapid loss of histone H2A, which is subsequently released from the H2A.Z nucleosomal product. Surprisingly, rates of both priming and the release of the H2A/H2B dimer are sensitive to ATP concentration. This complex reaction pathway provides multiple opportunities to regulate timely and accurate deposition of H2A.Z at key genomic locations.

Indexed as

HistonesSaccharomyces cerevisiae ProteinsAdenosine TriphosphateChromatin Assembly and DisassemblyNucleosomesSaccharomyces cerevisiaeAdenosine TriphosphateHistonesNucleosomesSaccharomyces cerevisiae Proteins

Identifiers

PMID36396651
PMCPMC9672302
OpenAlexW4309235830

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.