Evidence map›Paper›PMID 26259146›Full record

ArticleNature communications2015

The chromatin remodeller RSF1 is essential for PLK1 deposition and function at mitotic kinetochores.

Ho-Soo Lee, Yong-Yea Park, Mi-Young Cho, Sunyoung Chae, Young-Suk Yoo, Myung-Hee Kwon, Chang-Woo Lee, Hyeseong Cho

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

24 citing papers in PubMed, 39 citations in OpenAlex.

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  7. Review
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  12. RSF1 in cancer: interactions and functions.Cancer cell international · 2021
    Review
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  20. Role of remodeling and spacing factor 1 in histone H2A ubiquitination-mediated gene silencing.Proceedings of the National Academy of Sciences of the United States of America · 2017
    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

8 authors at 2 institutions in 1 country.

Ho-Soo LeeDepartment of Biochemistry, Ajou University School of Medicine, Suwon 443-380, Korea.
Yong-Yea ParkDepartment of Biochemistry, Ajou University School of Medicine, Suwon 443-380, Korea.
Mi-Young ChoDepartment of Biochemistry, Ajou University School of Medicine, Suwon 443-380, Korea.
Sunyoung ChaeDepartment of Biochemistry, Ajou University School of Medicine, Suwon 443-380, Korea.
Young-Suk YooDepartment of Biochemistry, Ajou University School of Medicine, Suwon 443-380, Korea.
Myung-Hee KwonDepartment of Biomedical Sciences, Graduate School of Ajou University, Suwon 443-380, Korea.
Chang-Woo LeeDepartment of Molecular Cell Biology, Sungkyunkwan University School of Medicine, Suwon 440-746, Korea.
Hyeseong ChoDepartment of Biochemistry, Ajou University School of Medicine, Suwon 443-380, Korea.
Ajou University · KRSungkyunkwan University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulation of PLK1 at kinetochores is essential for chromosome alignment and segregation; however, the mechanism underlying PLK1 recruitment to kinetochores remains unresolved. The chromatin remodeller RSF1 tightly associates with centromere proteins, but its mitotic function is unknown. Here we show that RSF1 localizes at mitotic kinetochores and directly binds PLK1. RSF1 depletion disrupts localization of PLK1 at kinetochores; the C-terminal fragment of RSF1, which can bind PLK1, is sufficient to restore PLK1 localization. Moreover, CDK1 phosphorylates RSF1 at Ser1375, and this phosphorylation is necessary for PLK1 recruitment. Subsequently, PLK1 phosphorylates RSF1 at Ser1359, stabilizing PLK1 deposition. Importantly, RSF1 depletion mimicks the chromosome misalignment phenotype resulting from PLK1 knockdown; these defects are rescued by RSF1 S1375D or RSF1 S1359D but not RSF1 S1375A, showing a functional link between phosphorylation of RSF1 and chromosome alignment. Together, these data show that RSF1 is an essential centromeric component that recruits PLK1 to kinetochores and plays a crucial role in faithful cell division.

Indexed as

MitosisAmino Acid SequenceCDC2 Protein KinaseCell Cycle ProteinsCyclin-Dependent KinasesGene Knockout TechniquesHeLa CellsHumansKinetochoresMolecular Sequence DataNuclear ProteinsPhosphorylationPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsTrans-ActivatorsCDC2 Protein KinaseCDK1 protein, humanCell Cycle ProteinsCyclin-Dependent KinasesNuclear ProteinsPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsRSF1 protein, humanTrans-Activators

Identifiers

PMID26259146
PMCPMC4918322
OpenAlexW2247714798

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.