Literature DB >> 8914970

Sequence specificity in CpG mutation hotspots.

J Ollila1, I Lappalainen, M Vihinen.   

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.

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Year:  1996        PMID: 8914970     DOI: 10.1016/0014-5793(96)01075-7

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  22 in total

1.  KinMutBase, a database of human disease-causing protein kinase mutations.

Authors:  K A Stenberg; P T Riikonen; M Vihinen
Journal:  Nucleic Acids Res       Date:  2000-01-01       Impact factor: 16.971

2.  Analysis of the COL1A1 and COL1A2 genes by PCR amplification and scanning by conformation-sensitive gel electrophoresis identifies only COL1A1 mutations in 15 patients with osteogenesis imperfecta type I: identification of common sequences of null-allele mutations.

Authors:  J Körkkö; L Ala-Kokko; A De Paepe; L Nuytinck; J Earley; D J Prockop
Journal:  Am J Hum Genet       Date:  1998-01       Impact factor: 11.025

3.  BTKbase, mutation database for X-linked agammaglobulinemia (XLA).

Authors:  M Vihinen; O Brandau; L J Brandén; S P Kwan; I Lappalainen; T Lester; J G Noordzij; H D Ochs; J Ollila; S M Pienaar; P Riikonen; B K Saha; C I Smith
Journal:  Nucleic Acids Res       Date:  1998-01-01       Impact factor: 16.971

4.  Neighboring-nucleotide effects on the rates of germ-line single-base-pair substitution in human genes.

Authors:  M Krawczak; E V Ball; D N Cooper
Journal:  Am J Hum Genet       Date:  1998-08       Impact factor: 11.025

5.  Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia.

Authors:  Alexandre Bolze; Nizar Mahlaoui; Minji Byun; Bridget Turner; Nikolaus Trede; Steven R Ellis; Avinash Abhyankar; Yuval Itan; Etienne Patin; Samuel Brebner; Paul Sackstein; Anne Puel; Capucine Picard; Laurent Abel; Lluis Quintana-Murci; Saul N Faust; Anthony P Williams; Richard Baretto; Michael Duddridge; Usha Kini; Andrew J Pollard; Catherine Gaud; Pierre Frange; Daniel Orbach; Jean-Francois Emile; Jean-Louis Stephan; Ricardo Sorensen; Alessandro Plebani; Lennart Hammarstrom; Mary Ellen Conley; Licia Selleri; Jean-Laurent Casanova
Journal:  Science       Date:  2013-04-11       Impact factor: 47.728

6.  Spectrum of disease-causing mutations in protein secondary structures.

Authors:  Sofia Khan; Mauno Vihinen
Journal:  BMC Struct Biol       Date:  2007-08-29

7.  Mutation scanning by meltMADGE: validations using BRCA1 and LDLR, and demonstration of the potential to identify severe, moderate, silent, rare, and paucimorphic mutations in the general population.

Authors:  Khalid K Alharbi; Mohammed A Aldahmesh; Emmanuel Spanakis; Lema Haddad; Roslyn A Whittall; Xiao-he Chen; Hamid Rassoulian; Matt J Smith; Julie Sillibourne; Nicola J Ball; Nikki J Graham; Patricia J Briggs; Iain A Simpson; David I W Phillips; Deborah A Lawlor; Shu Ye; Stephen E Humphries; Cyrus Cooper; George Davey Smith; Shah Ebrahim; Diana M Eccles; Ian N M Day
Journal:  Genome Res       Date:  2005-07       Impact factor: 9.043

8.  GC content increased at CpG flanking positions of fish genes compared with sea squirt orthologs as a mechanism for reducing impact of DNA methylation.

Authors:  Yong Wang; Frederick C C Leung
Journal:  PLoS One       Date:  2008-11-13       Impact factor: 3.240

9.  Prediction of disease-related mutations affecting protein localization.

Authors:  Kirsti Laurila; Mauno Vihinen
Journal:  BMC Genomics       Date:  2009-03-23       Impact factor: 3.969

10.  Prognostic implications of troponin T variations in inherited cardiomyopathies using systems biology.

Authors:  Rameen Shakur; Juan Pablo Ochoa; Alan J Robinson; Abhishek Niroula; Aneesh Chandran; Taufiq Rahman; Mauno Vihinen; Lorenzo Monserrat
Journal:  NPJ Genom Med       Date:  2021-06-14       Impact factor: 8.617

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