Literature DB >> 20405910

Unique physical properties and interactions of the domains of methylated DNA binding protein 2.

Rajarshi P Ghosh1, Tatiana Nikitina, Rachel A Horowitz-Scherer, Lila M Gierasch, Vladimir N Uversky, Kristopher Hite, Jeffrey C Hansen, Christopher L Woodcock.   

Abstract

Methylated DNA binding protein 2 (MeCP2) is a methyl CpG binding protein whose key role is the recognition of epigenetic information encoded in DNA methylation patterns. Mutation or misregulation of MeCP2 function leads to Rett syndrome as well as a variety of other autism spectrum disorders. Here, we have analyzed in detail the properties of six individually expressed human MeCP2 domains spanning the entire protein with emphasis on their interactions with each other, with DNA, and with nucleosomal arrays. Each domain contributes uniquely to the structure and function of the full-length protein. MeCP2 is approximately 60% unstructured, with nine interspersed alpha-molecular recognition features (alpha-MoRFs), which are polypeptide segments predicted to acquire secondary structure upon forming complexes with binding partners. Large increases in secondary structure content are induced in some of the isolated MeCP2 domains and in the full-length protein by binding to DNA. Interactions between some MeCP2 domains in cis and trans seen in our assays likely contribute to the structure and function of the intact protein. We also show that MeCP2 has two functional halves. The N-terminal portion contains the methylated DNA binding domain (MBD) and two highly disordered flanking domains that modulate MBD-mediated DNA binding. One of these flanking domains is also capable of autonomous DNA binding. In contrast, the C-terminal portion of the protein that harbors at least two independent DNA binding domains and a chromatin-specific binding domain is largely responsible for mediating nucleosomal array compaction and oligomerization. These findings led to new mechanistic and biochemical insights regarding the conformational modulations of this intrinsically disordered protein, and its context-dependent in vivo roles.

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Year:  2010        PMID: 20405910      PMCID: PMC2872689          DOI: 10.1021/bi9019753

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  78 in total

1.  Analysis of molecular recognition features (MoRFs).

Authors:  Amrita Mohan; Christopher J Oldfield; Predrag Radivojac; Vladimir Vacic; Marc S Cortese; A Keith Dunker; Vladimir N Uversky
Journal:  J Mol Biol       Date:  2006-08-04       Impact factor: 5.469

2.  Multiple modes of interaction between the methylated DNA binding protein MeCP2 and chromatin.

Authors:  Tatiana Nikitina; Xi Shi; Rajarshi P Ghosh; Rachel A Horowitz-Scherer; Jeffrey C Hansen; Christopher L Woodcock
Journal:  Mol Cell Biol       Date:  2006-11-13       Impact factor: 4.272

Review 3.  MeCP2 in Rett syndrome: transcriptional repressor or chromatin architectural protein?

Authors:  Lisa Helbling Chadwick; Paul A Wade
Journal:  Curr Opin Genet Dev       Date:  2007-02-20       Impact factor: 5.578

Review 4.  Rett syndrome: a Rosetta stone for understanding the molecular pathogenesis of autism.

Authors:  Janine M LaSalle; Amber Hogart; Karen N Thatcher
Journal:  Int Rev Neurobiol       Date:  2005       Impact factor: 3.230

Review 5.  Methods for the detection and analysis of protein-protein interactions.

Authors:  Tord Berggård; Sara Linse; Peter James
Journal:  Proteomics       Date:  2007-08       Impact factor: 3.984

Review 6.  MeCP2 dysfunction in Rett syndrome and related disorders.

Authors:  Paolo Moretti; Huda Y Zoghbi
Journal:  Curr Opin Genet Dev       Date:  2006-05-02       Impact factor: 5.578

7.  Intrinsic disorder and autonomous domain function in the multifunctional nuclear protein, MeCP2.

Authors:  Valerie H Adams; Steven J McBryant; Paul A Wade; Christopher L Woodcock; Jeffrey C Hansen
Journal:  J Biol Chem       Date:  2007-03-19       Impact factor: 5.157

8.  Composition Profiler: a tool for discovery and visualization of amino acid composition differences.

Authors:  Vladimir Vacic; Vladimir N Uversky; A Keith Dunker; Stefano Lonardi
Journal:  BMC Bioinformatics       Date:  2007-06-19       Impact factor: 3.169

9.  Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation.

Authors:  Xinsheng Nan; Jianghui Hou; Alan Maclean; Jamal Nasir; Maria Jose Lafuente; Xinhua Shu; Skirmantas Kriaucionis; Adrian Bird
Journal:  Proc Natl Acad Sci U S A       Date:  2007-02-12       Impact factor: 11.205

10.  DisProt: the Database of Disordered Proteins.

Authors:  Megan Sickmeier; Justin A Hamilton; Tanguy LeGall; Vladimir Vacic; Marc S Cortese; Agnes Tantos; Beata Szabo; Peter Tompa; Jake Chen; Vladimir N Uversky; Zoran Obradovic; A Keith Dunker
Journal:  Nucleic Acids Res       Date:  2006-12-01       Impact factor: 16.971

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  55 in total

1.  Kaiso uses all three zinc fingers and adjacent sequence motifs for high affinity binding to sequence-specific and methyl-CpG DNA targets.

Authors:  Bethany A Buck-Koehntop; Maria A Martinez-Yamout; H Jane Dyson; Peter E Wright
Journal:  FEBS Lett       Date:  2012-01-30       Impact factor: 4.124

Review 2.  Binding of the Rett syndrome protein, MeCP2, to methylated and unmethylated DNA and chromatin.

Authors:  Jeffrey C Hansen; Rajarshi P Ghosh; Christopher L Woodcock
Journal:  IUBMB Life       Date:  2010-10       Impact factor: 3.885

3.  MeCP2 binds cooperatively to its substrate and competes with histone H1 for chromatin binding sites.

Authors:  Rajarshi P Ghosh; Rachel A Horowitz-Scherer; Tatiana Nikitina; Luda S Shlyakhtenko; Christopher L Woodcock
Journal:  Mol Cell Biol       Date:  2010-08-02       Impact factor: 4.272

Review 4.  Post-translational modifications of the intrinsically disordered terminal domains of histone H1: effects on secondary structure and chromatin dynamics.

Authors:  A Roque; I Ponte; P Suau
Journal:  Chromosoma       Date:  2016-04-21       Impact factor: 4.316

5.  Functional conservation of MBD proteins: MeCP2 and Drosophila MBD proteins alter sleep.

Authors:  T Gupta; H R Morgan; J A Bailey; S J Certel
Journal:  Genes Brain Behav       Date:  2016-09-06       Impact factor: 3.449

6.  An intrinsically disordered region of methyl-CpG binding domain protein 2 (MBD2) recruits the histone deacetylase core of the NuRD complex.

Authors:  Megha A Desai; Heather D Webb; Leander M Sinanan; J Neel Scarsdale; Ninad M Walavalkar; Gordon D Ginder; David C Williams
Journal:  Nucleic Acids Res       Date:  2015-03-09       Impact factor: 16.971

Review 7.  Rett syndrome and MeCP2.

Authors:  Vichithra R B Liyanage; Mojgan Rastegar
Journal:  Neuromolecular Med       Date:  2014-03-11       Impact factor: 3.843

8.  Coil-to-helix transitions in intrinsically disordered methyl CpG binding protein 2 and its isolated domains.

Authors:  Kristopher C Hite; Anna A Kalashnikova; Jeffrey C Hansen
Journal:  Protein Sci       Date:  2012-03-09       Impact factor: 6.725

Review 9.  Disease mutations in disordered regions--exception to the rule?

Authors:  Vladimir Vacic; Lilia M Iakoucheva
Journal:  Mol Biosyst       Date:  2011-11-14

Review 10.  Rett syndrome: a complex disorder with simple roots.

Authors:  Matthew J Lyst; Adrian Bird
Journal:  Nat Rev Genet       Date:  2015-03-03       Impact factor: 53.242

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