Evidence map›Paper›PMID 30242288›Full record

ArticleNature communications2018

The chromatin remodeler RSF1 controls centromeric histone modifications to coordinate chromosome segregation.

Ho-Soo Lee, Zhonghui Lin, Sunyoung Chae, Young-Suk Yoo, Byung-Gyu Kim, Youngsoo Lee, Jared L Johnson, You-Sun Kim, Lewis C Cantley, Chang-Woo Lee and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. RSF1-Dependent PAR Turnover Promotes 53BP1 Liquid Condensate Formation at DNA Damage Sites.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  14. RSF1 in cancer: interactions and functions.Cancer cell international · 2021
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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

12 authors at 6 institutions in 3 countries.

Ho-Soo LeeDepartment of Biochemistry, Ajou University School of Medicine, Suwon, 16499, Korea.
Zhonghui LinDepartment of Pharmacology, University of Texas Southwestern Medical Center, 6001 Forest Park Road, Dallas, TX, 75930, USA.
Sunyoung ChaeInstitute of Medical Science, Ajou University School of Medicine, Suwon, 16499, Korea.
Young-Suk YooDepartment of Biochemistry, Ajou University School of Medicine, Suwon, 16499, Korea.
Byung-Gyu KimCenter for Genomic Integrity, Institute for Basic Science, UNIST, Ulsan, 44919, Korea.
Youngsoo LeeGenomic Instability Research Center, Ajou University School of Medicine, Suwon, 16499, Korea.ORCID http://orcid.org/0000-0003-4773-6464
Jared L JohnsonMeyer Cancer Center, Department of Medicine, Weill Cornell Medical College, New York, NY, 10065, USA.ORCID http://orcid.org/0000-0003-1802-6527
You-Sun KimDepartment of Biochemistry, Ajou University School of Medicine, Suwon, 16499, Korea.
Lewis C CantleyMeyer Cancer Center, Department of Medicine, Weill Cornell Medical College, New York, NY, 10065, USA.
Chang-Woo LeeDepartment of Molecular Biology, Sungkyunkwan University School of Medicine, Suwon, 16419, Korea.
Hongtao YuDepartment of Pharmacology, University of Texas Southwestern Medical Center, 6001 Forest Park Road, Dallas, TX, 75930, USA. hongtao.yu@utsouthwestern.edu.ORCID http://orcid.org/0000-0002-8861-049X
Hyeseong ChoDepartment of Biochemistry, Ajou University School of Medicine, Suwon, 16499, Korea. hscho@ajou.ac.kr.
Ajou University · KRCornell University · USFujian Business University · CNInstitute for Basic Science · KRSouthwestern Medical Center · USSungkyunkwan University · KR

Funding

Role of Phosphoinositides and Protein Kinases in the control of Cancer MetabolismR35CA197588 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI LEWIS C. CANTLEY · 2016 to 2026
$10.2M
National Research Foundation of Korea (NRF) 2011-0030043National Research Foundation of Korea (NRF) NRF-2017R1A2B3009256National Research Foundation of Korea (NRF) NRF-2017R1C1B2012037NCI NIH HHS R35 CA197588
6 · The paper itself

Abstract

Chromatin remodelers regulate the nucleosome barrier during transcription, DNA replication, and DNA repair. The chromatin remodeler RSF1 is enriched at mitotic centromeres, but the functional consequences of this enrichment are not completely understood. Shugoshin (Sgo1) protects centromeric cohesion during mitosis and requires BuB1-dependent histone H2A phosphorylation (H2A-pT120) for localization. Loss of Sgo1 at centromeres causes chromosome missegregation. Here, we show that RSF1 regulates Sgo1 localization to centromeres through coordinating a crosstalk between histone acetylation and phosphorylation. RSF1 interacts with and recruits HDAC1 to centromeres, where it counteracts TIP60-mediated acetylation of H2A at K118. This deacetylation is required for the accumulation of H2A-pT120 and Sgo1 deposition, as H2A-K118 acetylation suppresses H2A-T120 phosphorylation by Bub1. Centromeric tethering of HDAC1 prevents premature chromatid separation in RSF1 knockout cells. Our results indicate that RSF1 regulates the dynamics of H2A histone modifications at mitotic centromeres and contributes to the maintenance of chromosome stability.

Indexed as

Chromosome SegregationAcetylationCell Cycle ProteinsCentromereChromosomal InstabilityHeLa CellsHistone CodeHistone Deacetylase 1HumansLysine Acetyltransferase 5Nuclear ProteinsPhosphorylationTrans-ActivatorsCell Cycle ProteinsHDAC1 protein, humanHistone Deacetylase 1KAT5 protein, humanLysine Acetyltransferase 5Nuclear ProteinsRSF1 protein, humanSGO1 protein, humanTrans-Activators

Identifiers

PMID30242288
PMCPMC6155007
OpenAlexW2889819841

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.