Evidence map›Paper›PMID 38321951›Full record

ArticleNucleic acids research2024

Extending MeCP2 interactome: canonical nucleosomal histones interact with MeCP2.

David Ortega-Alarcon, Rafael Claveria-Gimeno, Sonia Vega, Ladan Kalani, Olga C Jorge-Torres, Manel Esteller, Juan Ausio, Olga Abian, Adrian Velazquez-Campoy

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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
10.5field-weighted citation impact, top 1% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. MECP2Science China. Life sciences · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. MeCP2 is a naturally supercharged protein with cell membrane transduction capabilities.Protein science : a publication of the Protein Society · 2024
    Article
  13. Epigenetics in rare neurological diseases.Frontiers in cell and developmental biology · 2024
    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

9 authors at 4 institutions in 2 countries.

David Ortega-AlarconInstitute of Biocomputation and Physics of Complex Systems (BIFI), Joint Unit GBsC-CSIC-BIFI, Universidad de Zaragoza, 50018 Zaragoza, Spain.
Rafael Claveria-GimenoCertest Biotec S.L., 50840 Zaragoza, Spain.
Sonia VegaInstitute of Biocomputation and Physics of Complex Systems (BIFI), Joint Unit GBsC-CSIC-BIFI, Universidad de Zaragoza, 50018 Zaragoza, Spain.
Ladan KalaniDepartment of Biochemistry and Microbiology, University of Victoria, Victoria, BCV8W 2Y2, Canada.ORCID 0000-0002-0892-3745
Olga C Jorge-TorresJosep Carreras Leukaemia Research Institute (IJC), 08916 Badalona, Barcelona, Spain.
Manel EstellerJosep Carreras Leukaemia Research Institute (IJC), 08916 Badalona, Barcelona, Spain.ORCID 0000-0003-4490-6093
Juan AusioDepartment of Biochemistry and Microbiology, University of Victoria, Victoria, BCV8W 2Y2, Canada.
Olga AbianInstitute of Biocomputation and Physics of Complex Systems (BIFI), Joint Unit GBsC-CSIC-BIFI, Universidad de Zaragoza, 50018 Zaragoza, Spain.
Adrian Velazquez-CampoyInstitute of Biocomputation and Physics of Complex Systems (BIFI), Joint Unit GBsC-CSIC-BIFI, Universidad de Zaragoza, 50018 Zaragoza, Spain.ORCID 0000-0001-5702-4538
Universidad de Zaragoza · ESUniversity of Victoria · CAInstitució Catalana de Recerca i Estudis Avançats · ESJosep Carreras Leukaemia Research Institute · ES

Funding

Autonomous Community of AragónCentro de Investigación Biomédica en Red en Enfermedades Hepáticas y DigestivasERDF A way of Making Europe PID2021-127296OB-I00Fondo de Investigaciones Sanitarias from Instituto de Salud Carlos III and European Union ERDF/ESFGobierno de Aragón E45_23RMinisterio de Ciencia e InnovaciónMinisterio de Economía y Competitividad BFU2016-78232-PSpanish Ministry of Science and Innovation PRTR-C17.I1
6 · The paper itself

Abstract

MeCP2 is a general regulator of transcription involved in the repression/activation of genes depending on the local epigenetic context. It acts as a chromatin regulator and binds with exquisite specificity to gene promoters. The set of epigenetic marks recognized by MeCP2 has been already established (mainly, cytosine modifications in CpG and CpA), as well as many of the constituents of its interactome. We unveil a new set of interactions for MeCP2 with the four canonical nucleosomal histones. MeCP2 interacts with high affinity with H2A, H2B, H3 and H4. In addition, Rett syndrome associated mutations in MeCP2 and histone epigenetic marks modulate these interactions. Given the abundance and the structural/functional relevance of histones and their involvement in epigenetic regulation, this new set of interactions and its modulating elements provide a new addition to the 'alphabet' for this epigenetic reader.

Indexed as

Epigenesis, GeneticHistonesMethyl-CpG-Binding Protein 2NucleosomesAnimalsHumansMutationProtein BindingRett SyndromeHistonesMECP2 protein, humanMethyl-CpG-Binding Protein 2Nucleosomes

Identifiers

PMID38321951
PMCPMC11039998
OpenAlexW4391592373

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.