MeCP2 recognizes cytosine methylated tri-nucleotide and di-nucleotide sequences to tune transcription in the mammalian brain.
Mutations in the gene encoding the methyl-CG binding protein MeCP2 cause several neurological disorders including Rett syndrome. The di-nucleotide methyl-CG (mCG) is the classical MeCP2 DNA recognition sequence, but additional methylated sequence targets have been reported. Here we show by in vitro...
Saved in:
| Main Authors: | Sabine Lagger, John C Connelly, Gabriele Schweikert, Shaun Webb, Jim Selfridge, Bernard H Ramsahoye, Miao Yu, Chuan He, Guido Sanguinetti, Lawrence C Sowers, Malcolm D Walkinshaw, Adrian Bird |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Public Library of Science (PLoS)
2017-05-01
|
| Series: | PLoS Genetics |
| Online Access: | https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1006793&type=printable |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Genetic modifiers of MeCP2 function in Drosophila.
by: Holly N Cukier, et al.
Published: (2008-09-01) -
Identification of a guanine nucleotide exchange factor for Arf3, the yeast orthologue of mammalian Arf6.
by: Alison K Gillingham, et al.
Published: (2007-09-01) -
MeCP2 dependent heterochromatin reorganization during neural differentiation of a novel Mecp2-deficient embryonic stem cell reporter line.
by: Bianca Bertulat, et al.
Published: (2012-01-01) -
NUCLEOTIDES IN NUTRITION OF CHILDREN
by: T.G. Reshetova, et al.
Published: (2010-11-01) -
Orphan CpG islands identify numerous conserved promoters in the mammalian genome.
by: Robert S Illingworth, et al.
Published: (2010-09-01)