Evidence map›Paper›PMID 38812048›Full record

ReviewBiology direct2024

Lysine-specific methyltransferase Set7/9 in stemness, differentiation, and development.

Alexandra Daks, Sergey Parfenyev, Oleg Shuvalov, Olga Fedorova, Alexander Nazarov, Gerry Melino, Nickolai A Barlev

Abstract readReview
In one paragraph

Review in Biology direct, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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.

Alexandra DaksInstitute of Cytology, Russian Academy of Sciences, St Petersburg, Russian Federation, 194064. alexandra.daks@gmail.com.
Sergey ParfenyevInstitute of Cytology, Russian Academy of Sciences, St Petersburg, Russian Federation, 194064.
Oleg ShuvalovInstitute of Cytology, Russian Academy of Sciences, St Petersburg, Russian Federation, 194064.
Olga FedorovaInstitute of Cytology, Russian Academy of Sciences, St Petersburg, Russian Federation, 194064.
Alexander NazarovInstitute of Cytology, Russian Academy of Sciences, St Petersburg, Russian Federation, 194064.
Gerry MelinoDepartment of Experimental Medicine, TOR, University of Rome Tor Vergata, 00133, Rome, Italy.
Nickolai A BarlevInstitute of Cytology, Russian Academy of Sciences, St Petersburg, Russian Federation, 194064. nikolai.barlev@nu.edu.kz.

Funding

Russian Science Foundation 19-75-10059
6 · The paper itself

Abstract

The enzymes performing protein post-translational modifications (PTMs) form a critical post-translational regulatory circuitry that orchestrates literally all cellular processes in the organism. In particular, the balance between cellular stemness and differentiation is crucial for the development of multicellular organisms. Importantly, the fine-tuning of this balance on the genetic level is largely mediated by specific PTMs of histones including lysine methylation. Lysine methylation is carried out by special enzymes (lysine methyltransferases) that transfer the methyl group from S-adenosyl-L-methionine to the lysine residues of protein substrates. Set7/9 is one of the exemplary protein methyltransferases that however, has not been fully studied yet. It was originally discovered as histone H3 lysine 4-specific methyltransferase, which later was shown to methylate a number of non-histone proteins that are crucial regulators of stemness and differentiation, including p53, pRb, YAP, DNMT1, SOX2, FOXO3, and others. In this review we summarize the information available to date on the role of Set7/9 in cellular differentiation and tissue development during embryogenesis and in adult organisms. Finally, we highlight and discuss the role of Set7/9 in pathological processes associated with aberrant cellular differentiation and self-renewal, including the formation of cancer stem cells.

Indexed as

Cell DifferentiationHistone-Lysine N-MethyltransferaseAnimalsHumansMethylationProtein Processing, Post-TranslationalStem CellsHistone-Lysine N-MethyltransferaseSETD7 protein, humanCancer stem cellsDevelopmentDifferentiationEmbryogenesisHistone modificationsiPSCp53Set7/9 methyltransferaseStem cellsStemness

Identifiers

PMID38812048
PMCPMC11137904

What OpenQuestion holds

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LicenceCC BY
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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.