Evidence map›Paper›PMID 21031501›Full record

ReviewIUBMB life2010

Binding of the Rett syndrome protein, MeCP2, to methylated and unmethylated DNA and chromatin.

Jeffrey C Hansen, Rajarshi P Ghosh, Christopher L Woodcock

Open access · bronzeAbstract readReview
In one paragraph

Review in IUBMB life, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.2field-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

50 citing papers in PubMed, 104 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. RettDb: the Rett syndrome omics database to navigate the Rett syndrome genomic landscape.Database : the journal of biological databases and curation · 2024
    Article
  6. Article
  7. Epigenetics in rare neurological diseases.Frontiers in cell and developmental biology · 2024
    Review
  8. Article
  9. Article
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  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
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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

3 authors at 2 institutions in 1 country.

Jeffrey C HansenDepartment of Biochemistry and Molecular Biology, Colorado State University, Fort Collins, CO 80523, USA. jeffrey.c.hansen@colostate.edu
Rajarshi P Ghosh
Christopher L Woodcock
University of Massachusetts Amherst · USIn-Q-Tel · US

Funding

MeCP2 Structure and FunctionR01GM066834 · NIGMS · COLORADO STATE UNIVERSITY-FORT COLLINS · PI HANSEN, JEFFREY C · 2003 to 2011
$2.4M
Role of MeCP2 as a Chromatin Architectural ProteinR01GM070897 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI WOODCOCK, CHRISTOPHER L. · 2004 to 2007
$1.0M
NIGMS NIH HHS GM066834NIGMS NIH HHS GM070897NIGMS NIH HHS R01 GM066834NIGMS NIH HHS R01 GM070897
6 · The paper itself

Abstract

Methylated CpG Binding Protein 2 (MeCP2) is a nuclear protein named for its ability to selectively recognize methylated DNA. Much attention has been focused on understanding MeCP2 structure and function in the context of its role in Rett syndrome, a severe neurodevelopmental disorder that afflicts one in 10,000-15,000 girls. Early studies suggested a connection between DNA methylation, MeCP2, and establishment of a repressive chromatin structure at specific gene promoters. However, it is now recognized that MeCP2 can both activate and repress specific genes depending on the context. Likewise, in the cell, MeCP2 is bound to unmethylated DNA and chromatin in addition to methylated DNA. Thus, to understand the molecular basis of MeCP2 functionality, it is necessary to unravel the complex interrelationships between MeCP2 binding to unmethylated and methylated regions of the genome. MeCP2 is unusual and interesting in that it is an intrinsically disordered protein, that is, much of its primary sequence fails to fold into secondary structure and yet is functional. The unique structure of MeCP2 is the subject of the first section of this article. We then discuss recent investigations of the in vitro binding of MeCP2 to unmethylated and methylated DNA, and the potential ramifications of this work for in vivo function. We close by focusing on mechanistic studies indicating that the binding of MeCP2 to chromatin results in compaction into local (secondary) and global (tertiary) higher order structures. MeCP2 also competes with histone H1 for nucleosomal binding sites. The recent finding that MeCP2 is found at near stoichiometric levels with nucleosomes in neuronal cells underscores the multiple modes of engagement of MeCP2 with the genome, which include the cooperative tracking of methylation density.

Indexed as

Binding SitesChromatinDNADNA MethylationFemaleGenome, HumanHistonesHumansMethyl-CpG-Binding Protein 2NucleosomesPromoter Regions, GeneticProtein BindingProtein Structure, SecondaryRett SyndromeChromatinDNAHistonesMethyl-CpG-Binding Protein 2Nucleosomes

Identifiers

PMID21031501
PMCPMC3096928
OpenAlexW2102289595

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.