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• W2084301939 abstract "MeCP2 is a methyl-CpG binding protein that can repress transcription of nearby genes. In humans, mutations in the MECP2 gene are the major cause of Rett syndrome. By searching expressed sequence tag (EST) databases we have found a novel MeCP2 splice isoform (MeCP2alpha) which encodes a distinct N-terminus. We demonstrate that the MeCP2alpha mRNA splice variant is more abundant than the previously annotated MeCP2 mRNA (MeCP2beta) in mouse tissues and human brain. Furthermore, MeCP2beta mRNA has an upstream open reading frame that inhibits its translation. As a result of these differences, >90% of MeCP2 in mouse brain is MeCP2alpha. Both protein isoforms are nuclear and colocalize with densely methylated heterochromatic foci in mouse cells. The presence of a previously unknown MeCP2 isoform has implications for the genetic screening of Rett syndrome patients and for studies of the functional significance of MeCP2." @default.
• W2084301939 created "2016-06-24" @default.
• W2084301939 creator A5058084937 @default.
• W2084301939 date "2004-03-08" @default.
• W2084301939 modified "2023-10-18" @default.
• W2084301939 title "The major form of MeCP2 has a novel N-terminus generated by alternative splicing" @default.
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• W2084301939 doi "https://doi.org/10.1093/nar/gkh349" @default.
• W2084301939 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/390342" @default.
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• W2084301939 hasPublicationYear "2004" @default.
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