Evidence map›Paper›PMID 32623337›Full record

ArticleiScience2020

Interaction of RSC Chromatin Remodeling Complex with Nucleosomes Is Modulated by H3 K14 Acetylation and H2B SUMOylation In Vivo.

Neha Jain, Davide Tamborrini, Brian Evans, Shereen Chaudhry, Bryan J Wilkins, Heinz Neumann

Open access · goldAbstract read
In one paragraph

Article in iScience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. SMARCD1 and Its Functional Relevance in SWI/SNF and Cancer.International journal of molecular sciences · 2026
    Review
  2. Review
  3. Article
  4. Article
  5. Histone modification inComputational and structural biotechnology journal · 2023
    Review
  6. Article
  7. Review
  8. Histone sumoylation and chromatin dynamics.Nucleic acids research · 2021
    Review
  9. 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

6 authors at 2 institutions in 2 countries.

Neha JainDepartment of Structural Biochemistry, Max-Planck-Institute of Molecular Physiology, Otto-Hahn-Strasse 11, 44227 Dortmund, Germany.
Davide TamborriniDepartment of Structural Biochemistry, Max-Planck-Institute of Molecular Physiology, Otto-Hahn-Strasse 11, 44227 Dortmund, Germany.
Brian EvansDepartment of Chemistry and Biochemistry, Manhattan College, 4513 Manhattan College Parkway, Bronx, NY 10471, USA.
Shereen ChaudhryDepartment of Chemistry and Biochemistry, Manhattan College, 4513 Manhattan College Parkway, Bronx, NY 10471, USA.
Bryan J WilkinsDepartment of Chemistry and Biochemistry, Manhattan College, 4513 Manhattan College Parkway, Bronx, NY 10471, USA. Electronic address: bwilkins01@manhattan.edu.
Heinz NeumannDepartment of Structural Biochemistry, Max-Planck-Institute of Molecular Physiology, Otto-Hahn-Strasse 11, 44227 Dortmund, Germany; Department of Chemical Engineering and Biotechnology, University of Applied Sciences Darmstadt, Stephanstrasse 7, 64295 Darmstadt, Germany. Electronic address: heinz.neumann@mpi-dortmund.mpg.de.
Manhattan University · USMax Planck Institute of Molecular Physiology · DE

Funding

The spatiotemporal mapping of the RSC and SWI/SNF chromatin remodeler complexes on the nucleosome in living cells.R15GM124600 · NIGMS · MANHATTAN COLLEGE · PI WILKINS, BRYAN JASON · 2017 to 2017
$368k
NIGMS NIH HHS R15 GM124600
6 · The paper itself

Abstract

Chromatin remodeling complexes are multi-subunit nucleosome translocases that reorganize chromatin in the context of DNA replication, repair, and transcription. To understand how these complexes find their target sites on chromatin, we use genetically encoded photo-cross-linker amino acids to map the footprint of Sth1, the catalytic subunit of the RSC complex, on nucleosomes in living yeast. We find that H3 K14 acetylation induces the interaction of the Sth1 bromodomain with the H3 tail and mediates the interaction of RSC with neighboring nucleosomes rather than recruiting it to chromatin. RSC preferentially resides on H2B SUMOylated nucleosomes in vivo and shows a moderately enhanced affinity due to this modification in vitro. Furthermore, RSC is not ejected from chromatin in mitosis, but changes its mode of nucleosome binding. Our in vivo analyses show that RSC recruitment to specific chromatin targets involves multiple histone modifications likely in combination with histone variants and transcription factors.

Indexed as

Biological SciencesMolecular BiologyMolecular Interaction

Identifiers

PMID32623337
PMCPMC7334588
OpenAlexW3036441421

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.