Sequence specificity in CpG mutation hotspots
- 4 November 1996
- journal article
- Published by Wiley in FEBS Letters
- Vol. 396 (2-3) , 119-122
- https://doi.org/10.1016/0014-5793(96)01075-7
Abstract
CpG dinucleotides are efficiently methylated in vertebrate genomes except in the CpG islands having a high C+G content. Methylated CpGs are the single most mutated dinucleotide. Sequences surrounding disease causing CpG mutation sites were analyzed from locus-specific mutation databases. Both tetra- and heptanucleotide analyses indicated clear overall sequence preference for having pyrimidines 5' and purines 3' to the mutated 5-methylcytosine. The most mutated tetranucleotides are TCGA and TCGG, the former being also a frequent restriction and modification site. The results will help in elucidating the still controversial mutation mechanism of CpG doublets.Keywords
This publication has 13 references indexed in Scilit:
- Somatic point mutations in the p53 gene of human tumors and cell lines: updated compilationNucleic Acids Research, 1996
- The haemophilia A mutation search test and resource site, home page of the factor VIII mutation database: HAMSTeRSNucleic Acids Research, 1996
- BTKbase, mutation database for X-linked agammaglobulinemia (XLA)Nucleic Acids Research, 1996
- PAH Mutation Analysis Consortium Database: a database for disease- producing and other allelic variation at the human PAH locusNucleic Acids Research, 1996
- BTKbase: a database of XLA-causing mutationsImmunology Today, 1995
- CpNpG methylation in mammalian cellsNature Genetics, 1995
- Periodicity of eight nucleotides in purine distribution around human genomic CpG dinucleotidesSomatic Cell and Molecular Genetics, 1995
- Methylation, mutation and cancerBioEssays, 1992
- A comprehensive set of sequence analysis programs for the VAXNucleic Acids Research, 1984
- Molecular basis of base substitution hotspots in Escherichia coliNature, 1978