Evidence map›Paper›PMID 39945308›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2025

Characterization of the Swi6/HP1 binding motif in its partner protein reveals the basis for the functional divergence of the HP1 family proteins in fission yeast.

Tomoyuki Oya, Mayo Tanaka, Aki Hayashi, Yuriko Yoshimura, Rinko Nakamura, Kyohei Arita, Yota Murakami, Jun-Ichi Nakayama

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Characterization of the Swi6/HP1 binding motif in its partner protein reveals the basis for the functional divergence of the HP1 family proteins in fission yeast.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    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.

Tomoyuki OyaDivision of Chromatin Regulation, National Institute for Basic Biology, Okazaki, Japan.
Mayo TanakaDivision of Chromatin Regulation, National Institute for Basic Biology, Okazaki, Japan.
Aki HayashiDivision of Chromatin Regulation, National Institute for Basic Biology, Okazaki, Japan.ORCID https://orcid.org/0000-0003-1953-1664
Yuriko YoshimuraDivision of Chromatin Regulation, National Institute for Basic Biology, Okazaki, Japan.
Rinko NakamuraDivision of Chromatin Regulation, National Institute for Basic Biology, Okazaki, Japan.
Kyohei AritaGraduate School of Medical Life Science, Yokohama City University, Yokohama, Kanagawa, Japan.ORCID https://orcid.org/0000-0002-9762-8405
Yota MurakamiLaboratory of Bioorganic Chemistry, Department of Chemistry, Faculty of Science, Hokkaido University, Sapporo, Japan.ORCID https://orcid.org/0000-0002-2023-1303
Jun-Ichi NakayamaDivision of Chromatin Regulation, National Institute for Basic Biology, Okazaki, Japan.ORCID https://orcid.org/0000-0002-5597-8239

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) 17H03713MEXT | Japan Society for the Promotion of Science (JSPS) 18H05532MEXT | Japan Society for the Promotion of Science (JSPS) 23114005MEXT | Japan Society for the Promotion of Science (JSPS) 24H02324MEXT | Japan Society for the Promotion of Science (JSPS) 26291072Mochida Memorial Foundation for Medical and Pharmaceutical ResearchOhsumi Frontier Science Foundation (OFSF)Takeda Science Foundation (TSF)Uehara Memorial Foundation (UMF)
6 · The paper itself

Abstract

The heterochromatin protein 1 (HP1) family recognizes lysine 9-methylated histone H3 (H3K9me) and recruits other transacting factors to establish higher order chromatin structures. In the fission yeast Schizosaccharomyces pombe (S. pombe), two HP1 family proteins, Swi6 and Chp2, play distinct roles in recruiting transacting factors: Swi6 primarily recruits Epe1, a Jumonji C domain-containing protein involved in histone H3K9 demethylation, whereas Chp2 recruits Mit1, a component of the Snf2/Hdac Repressive Complex. However, detailed mechanisms of how multiple HP1 family proteins and their respective interactors work cooperatively or exclusively to form higher order chromatin structures remain elusive. In this study, we investigated the interactions between Swi6 and Epe1. We found that Swi6 interacts with Epe1 through its chromoshadow domain, and identified a unique motif, named the FVI motif, in Epe1 involved in this interaction through detailed mapping of the region. Enhanced green fluorescent protein (EGFP) tethering assays showed that the FVI motif is sufficient to recruit ectopically expressed EGFP to heterochromatic regions, and mutational analyses revealed that conserved hydrophobic residues in this motif are essential for proper targeting. Structural simulations further supported the importance of these residues in Swi6 binding. Interestingly, Mit1 containing the Epe1 FVI motif was recruited to the heterochromatic regions by Swi6 but not by Chp2. Cells expressing mutant Mit1 maintained heterochromatic silencing even in chp2∆ cells, suggesting that Chp2 is not required for heterochromatin formation when Mit1 is recruited by Swi6. These findings highlight distinct HP1-binding motifs in interactors, contributing to functional divergence among HP1 family proteins.

Indexed as

Chromosomal Proteins, Non-HistoneSchizosaccharomycesSchizosaccharomyces pombe ProteinsAmino Acid MotifsChromobox Protein Homolog 5HeterochromatinNuclear ProteinsProtein BindingRepressor ProteinsCHP2 protein, S pombeChromobox Protein Homolog 5Chromosomal Proteins, Non-Histoneepe1 protein, S pombeHeterochromatinNuclear ProteinsRepressor ProteinsSchizosaccharomyces pombe ProteinsSwi6 protein, S pombechromodomainchromoshadow domainfission yeastheterochromatinheterochromatin protein 1histone methylation

Identifiers

PMID39945308
PMCPMC11833287

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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.