Evidence map›Paper›PMID 42549674›Full record

ReviewNucleus (Austin, Tex.)2026

More than SAM: mechanisms of action of the Polycomb group protein polyhomeotic.

Nanu Pal, Tim M Gemeinhardt, Rowan D H Barrett, Nicole J Francis

Abstract readReview
In one paragraph

Review in Nucleus (Austin, Tex.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Nanu PalMontreal Clinical Research Institute (IRCM), Montreal, QC, Canada.
Tim M GemeinhardtMontreal Clinical Research Institute (IRCM), Montreal, QC, Canada.ORCID 0000-0003-0241-1009
Rowan D H BarrettDepartment of Biology, McGill University, Montreal, QC, Canada.ORCID 0000-0003-3044-2531
Nicole J FrancisMontreal Clinical Research Institute (IRCM), Montreal, QC, Canada.ORCID 0000-0002-1810-2959

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Polycomb Group (PcG) system controls developmental transitions and cell states across species. Two main PcG complexes, Polycomb Repressive Complexes 1 and 2 (PRC1, PRC2), regulate transcription and form epigenetic memory through chromatin. Polyhomeotic (Ph) is an essential PRC1 subunit that has received relatively little attention, perhaps because it is not implicated in either depositing or recognizing histone post-translational modifications (PTMs). Instead, Ph regulates chromatin architecture through its hallmark polymerizing sterile alpha motif (SAM). Here we review the biochemistry and function of Ph and mammalian polyhomeotic-like proteins (PHCs). We describe the role of SAM polymerization and evidence for essential polymerization-independent SAM functions. The evolutionary origins of Ph and possible co-evolution of disordered and ordered regions to maintain but modify Ph function are considered. Finally, we draw parallels between SAM function in animals and a recently discovered polymerization activity in a plant PcG protein that may reflect convergent evolution.

Indexed as

DNA-Binding ProteinsPolycomb-Group ProteinsAnimalsChromatinHumansPolymerizationChromatinDNA-Binding ProteinsPolycomb-Group ProteinsChromatincondensateepigeneticsevolutiongene regulationhead-to-tail polymerizationintrinsically disordered regionphase separationPolycomb

Identifiers

PMID42549674
PMCPMC13449738

What OpenQuestion holds

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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.