Evidence map›Paper›PMID 37437070›Full record

ArticlePloS one2023

Histone methyltransferase SUV39H1 regulates the Golgi complex via the nuclear envelope-spanning LINC complex.

Miyu Nishino, Hiromasa Imaizumi, Yuhki Yokoyama, Jun Katahira, Hiroshi Kimura, Nariaki Matsuura, Miki Matsumura

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Many faces of mammalian NSD methyltransferases.Cellular & molecular biology letters · 2026
    Review
  2. Review
  3. Review
  4. Reorganizing chromatin by cellular deformation.Current opinion in cell biology · 2024
    Review
  5. 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

7 authors at 4 institutions in 1 country.

Miyu NishinoGraduate School of Health Sciences, Ehime Prefectural University of Health Sciences, Ehime, Japan.
Hiromasa ImaizumiGraduate School of Medicine and Health Science, Osaka University, Osaka, Japan.ORCID 0000-0002-4901-1910
Yuhki YokoyamaGraduate School of Medicine and Health Science, Osaka University, Osaka, Japan.
Jun KatahiraLaboratories of Cellular Molecular Biology, Graduate School of Veterinary Sciences, Osaka Metropolitan University, Osaka, Japan.
Hiroshi KimuraInstitute of Innovative Research, Tokyo Institute of Technology, Yokohama, Japan.
Nariaki MatsuuraGraduate School of Medicine and Health Science, Osaka University, Osaka, Japan.
Miki MatsumuraGraduate School of Health Sciences, Ehime Prefectural University of Health Sciences, Ehime, Japan.ORCID 0000-0002-9492-7506
Osaka Health Science University · JPEhime Prefectural University of Health Science · JPOsaka Metropolitan University · JPTokyo Institute of Technology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell motility is related to the higher-order structure of chromatin. Stimuli that induce cell migration change chromatin organization; such stimuli include elevated histone H3 lysine 9 trimethylation (H3K9me3). We previously showed that depletion of histone H3 lysine 9 methyltransferase, SUV39H1, suppresses directional cell migration. However, the molecular mechanism underlying this association between chromatin and cell migration remains elusive. The Golgi apparatus is a cell organelle essential for cell motility. In this study, we show that loss of H3K9 methyltransferase SUV39H1 but not SETDB1 or SETDB2 causes dispersion of the Golgi apparatus throughout the cytoplasm. The Golgi dispersion triggered by SUV39H1 depletion is independent of transcription, centrosomes, and microtubule organization, but is suppressed by depletion of any of the following three proteins: LINC complex components SUN2, nesprin-2, or microtubule plus-end-directed kinesin-like protein KIF20A. In addition, SUN2 is closely localized to H3K9me3, and SUV39H1 affects the mobility of SUN2 in the nuclear envelope. Further, inhibition of cell motility caused by SUV39H1 depletion is restored by suppression of SUN2, nesprin-2, or KIF20A. In summary, these results show the functional association between chromatin organization and cell motility via the Golgi organization regulated by the LINC complex.

Indexed as

HistonesNuclear EnvelopeCentrosomeChromatinGolgi ApparatusHistone MethyltransferasesLysineChromatinHistone MethyltransferasesHistonesLysine

Identifiers

PMID37437070
PMCPMC10337926
OpenAlexW4384008882

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.