Evidence map›Paper›PMID 33979575›Full record

ArticleMolecular cell2021

Methylation of histone H3 at lysine 37 by Set1 and Set2 prevents spurious DNA replication.

Helena Santos-Rosa, Gonzalo Millán-Zambrano, Namshik Han, Tommaso Leonardi, Marie Klimontova, Simona Nasiscionyte, Luca Pandolfini, Kostantinos Tzelepis, Till Bartke, Tony Kouzarides

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2021. 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
1.5field-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

17 citing papers in PubMed, 25 citations in OpenAlex.

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  10. The protein methylation network in yeast: A landmark in completeness for a eukaryotic post-translational modification.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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

10 authors at 3 institutions in 4 countries.

Helena Santos-RosaThe Gurdon Institute and Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK. Electronic address: hsrs2@gurdon.cam.ac.uk.
Gonzalo Millán-ZambranoThe Gurdon Institute and Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK; Centro Andaluz de Biología Molecular y Medicina Regenerativa (CABIMER), 41092 Sevilla, Spain.
Namshik HanThe Gurdon Institute and Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK; Milner Therapeutics Institute, University of Cambridge, Cambridge CB2 0AW, UK.
Tommaso LeonardiThe Gurdon Institute and Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK; Center for Genomic Science Istituto Italiano di Tecnologia (IIT), 20139 Milano, Italy.
Marie KlimontovaThe Gurdon Institute and Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK.
Simona NasiscionyteInstitute of Functional Epigenetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Luca PandolfiniThe Gurdon Institute and Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK; Istituto Italiano di Tecnologia (IIT), Center for Human Technologies (CHT), 16152 Genova, Italy.
Kostantinos TzelepisThe Gurdon Institute and Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK; Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge CB10 1SA, UK.
Till BartkeInstitute of Functional Epigenetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Tony KouzaridesThe Gurdon Institute and Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK. Electronic address: t.kouzarides@gurdon.cam.ac.uk.
Wellcome/Cancer Research UK Gurdon Institute · GBHelmholtz Zentrum München · DEUniversity of Cambridge · GB

Funding

Cancer Research UK 17001Cancer Research UK 27321Cancer Research UK A18061Cancer Research UK C6946/A24843Cancer Research UK RG72100Cancer Research UK RG96894European Research Council 309952Wellcome Trust 210926Wellcome Trust 210926/Z/18/ZWellcome Trust RG94424Wellcome Trust WT203144
6 · The paper itself

Abstract

DNA replication initiates at genomic locations known as origins of replication, which, in S. cerevisiae, share a common DNA consensus motif. Despite being virtually nucleosome-free, origins of replication are greatly influenced by the surrounding chromatin state. Here, we show that histone H3 lysine 37 mono-methylation (H3K37me1) is catalyzed by Set1p and Set2p and that it regulates replication origin licensing. H3K37me1 is uniformly distributed throughout most of the genome, but it is scarce at replication origins, where it increases according to the timing of their firing. We find that H3K37me1 hinders Mcm2 interaction with chromatin, maintaining low levels of MCM outside of conventional replication origins. Lack of H3K37me1 results in defective DNA replication from canonical origins while promoting replication events at inefficient and non-canonical sites. Collectively, our results indicate that H3K37me1 ensures correct execution of the DNA replication program by protecting the genome from inappropriate origin licensing and spurious DNA replication.

Indexed as

DNA ReplicationDNA, FungalHistone-Lysine N-MethyltransferaseHistonesMethylationMethyltransferasesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsDNA, FungalHistone-Lysine N-MethyltransferaseHistonesMCM2 protein, S cerevisiaeMethyltransferasesSaccharomyces cerevisiae ProteinsSET1 protein, S cerevisiaeSet2 protein, S cerevisiaeH3K37methylationHistone modificationsMCMOrigin licensingReplication originsSet1Set2

Identifiers

PMID33979575
PMCPMC7612968
OpenAlexW3161317282

What OpenQuestion holds

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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.