Evidence map›Paper›PMID 31430649›Full record

ReviewCurrent opinion in neurobiology2019

Genomic insights into MeCP2 function: A role for the maintenance of chromatin architecture.

Daniel R Connolly, Zhaolan Zhou

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in neurobiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

27 citing papers in PubMed, 36 citations in OpenAlex.

  1. Protective role of mirtazapine in adult female Mecp2Journal of neurodevelopmental disorders · 2020
    Trial
  2. Article
  3. Review
  4. Article
  5. A novel heterozygous pathogenic variation in theTranslational pediatrics · 2026
    Article
  6. Article
  7. Epigenetic Signatures of Social Defeat Stress Varying Duration.International journal of molecular sciences · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. RettDb: the Rett syndrome omics database to navigate the Rett syndrome genomic landscape.Database : the journal of biological databases and curation · 2024
    Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. 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

2 authors at 1 institution in 1 country.

Daniel R ConnollyDepartment of Genetics, Epigenetics Institute, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA; Medical Scientist Training Program, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Zhaolan ZhouDepartment of Genetics, Epigenetics Institute, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA. Electronic address: zhaolan@pennmedicine.upenn.edu.
University of Pennsylvania · US

Funding

Understanding the Pathogenic Mechanisms of Rett SyndromeR01NS081054 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI Zhaolan Zhou · 2013 to 2026
$5.6M
Pathogenic Studies of CDKL5 DisorderR01NS102731 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI ZHOU, ZHAOLAN · 2018 to 2022
$2.7M
Understanding the Epigenetic Mechanisms Underlying Stress-related Neuropsychiatric DisordersR01MH111719 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI ZHOU, ZHAOLAN · 2018 to 2021
$2.2M
NIMH NIH HHS R01 MH111719NINDS NIH HHS R01 NS081054NINDS NIH HHS R01 NS102731
6 · The paper itself

Abstract

Methyl-CpG binding protein 2 (MeCP2) plays fundamental roles in the nervous system, as both gain-of-function and loss-of-function of MECP2 are associated with severe neurological conditions. Understanding the molecular function of MeCP2 will not only provide insights into the pathogenesis of MeCP2-related disorders, but will also shed light on the epigenetic regulation of neuronal function. In the past few years, a number of studies have provided mechanistic evidence that MeCP2 recruits co-repressor complexes to particular sequences of methylated DNA. Additionally, innovative design and high-throughput sequencing technologies have provided opportunities to study the effects of MeCP2 on the neuronal transcriptome at an unprecedented level of detail, demonstrating that MeCP2 modulates gene expression in a context-specific manner. These findings have raised new questions and challenged current models of MeCP2 function. In this review, we describe several recent developments, highlight future challenges, and articulate a model by which MeCP2 functions as an organizer of chromatin architecture to modulate global gene expression in the nervous system.

Indexed as

ChromatinRett SyndromeDNA MethylationEpigenesis, GeneticGenomeGenomicsMethyl-CpG-Binding Protein 2ChromatinMethyl-CpG-Binding Protein 2

Identifiers

PMID31430649
PMCPMC6889049
OpenAlexW2967938001

What OpenQuestion holds

Textmetadata
LicenceTDM
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.