Evidence map›Paper›PMID 38647066›Full record

ArticleNucleic acids research2024

Extensive long-range polycomb interactions and weak compartmentalization are hallmarks of human neuronal 3D genome.

Ilya A Pletenev, Maria Bazarevich, Diana R Zagirova, Anna D Kononkova, Alexander V Cherkasov, Olga I Efimova, Eugenia A Tiukacheva, Kirill V Morozov, Kirill A Ulianov, Dmitriy Komkov and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. International journal of molecular sciences · 2025
    Review
  7. Histone bivalency in CNS development.Genes & development · 2025
    Review
  8. Epigenetics and the timing of neuronal differentiation.Current opinion in neurobiology · 2024
    Review
  9. Review
  10. Review
  11. 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

17 authors at 5 institutions in 2 countries.

Ilya A PletenevCenter for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, Moscow 121205, Russia.
Maria BazarevichCenter for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, Moscow 121205, Russia.
Diana R ZagirovaCenter for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, Moscow 121205, Russia.
Anna D KononkovaCenter for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, Moscow 121205, Russia.
Alexander V CherkasovCenter for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, Moscow 121205, Russia.
Olga I EfimovaVladimir Zelman Center for Neurobiology and Brain Rehabilitation, Skolkovo Institute of Science and Technology, Moscow 121205, Russia.
Eugenia A TiukachevaDepartment of Biological and Medical Physics, Moscow Institute of Physics and Technology, Moscow 141700, Russia.
Kirill V MorozovCenter for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, Moscow 121205, Russia.
Kirill A UlianovCenter for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, Moscow 121205, Russia.
Dmitriy KomkovCenter for Precision Genome Editing and Genetic Technologies for Biomedicine, Institute of Gene Biology, Russian Academy of Sciences, Moscow 119334, Russia.
Anna V TvorogovaCenter for Precision Genome Editing and Genetic Technologies for Biomedicine, Institute of Gene Biology, Russian Academy of Sciences, Moscow 119334, Russia.
Vera E GolimbetLaboratory of Clinical Genetics, Mental Health Research Center, Moscow 115522, Russia.
Nikolay V KondratyevLaboratory of Clinical Genetics, Mental Health Research Center, Moscow 115522, Russia.
Sergey V RazinDepartment of Molecular Biology, Faculty of Biology, M.V. Lomonosov Moscow State University, Moscow 119991, Russia.
Philipp KhaitovichVladimir Zelman Center for Neurobiology and Brain Rehabilitation, Skolkovo Institute of Science and Technology, Moscow 121205, Russia.
Sergey V UlianovDepartment of Molecular Biology, Faculty of Biology, M.V. Lomonosov Moscow State University, Moscow 119991, Russia.ORCID 0000-0002-6187-310X
Ekaterina E KhrameevaCenter for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, Moscow 121205, Russia.ORCID 0000-0001-6188-9139
Skolkovo Institute of Science and Technology · RUInstitute of Gene Biology · RULomonosov Moscow State University · RUMental Health Research Center of Russian Academy of Medical Sciences · RUCentre National de la Recherche Scientifique · FR

Funding

Russian Science Foundation 21-74-10102
6 · The paper itself

Abstract

Chromatin architecture regulates gene expression and shapes cellular identity, particularly in neuronal cells. Specifically, polycomb group (PcG) proteins enable establishment and maintenance of neuronal cell type by reorganizing chromatin into repressive domains that limit the expression of fate-determining genes and sustain distinct gene expression patterns in neurons. Here, we map the 3D genome architecture in neuronal and non-neuronal cells isolated from the Wernicke's area of four human brains and comprehensively analyze neuron-specific aspects of chromatin organization. We find that genome segregation into active and inactive compartments is greatly reduced in neurons compared to other brain cells. Furthermore, neuronal Hi-C maps reveal strong long-range interactions, forming a specific network of PcG-mediated contacts in neurons that is nearly absent in other brain cells. These interacting loci contain developmental transcription factors with repressed expression in neurons and other mature brain cells. But only in neurons, they are rich in bivalent promoters occupied by H3K4me3 histone modification together with H3K27me3, which points to a possible functional role of PcG contacts in neurons. Importantly, other layers of chromatin organization also exhibit a distinct structure in neurons, characterized by an increase in short-range interactions and a decrease in long-range ones.

Indexed as

ChromatinGenome, HumanPolycomb-Group ProteinsBrainHistonesHumansNeuronsPromoter Regions, GeneticChromatinHistonesPolycomb-Group Proteins

Identifiers

PMID38647066
PMCPMC11194087
OpenAlexW4395010433

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.