Literature DB >> 9838042

Methylation of CpG dinucleotides in the lacI gene of the Big Blue transgenic mouse.

Y H You1, A Halangoda, V Buettner, K Hill, S Sommer, G Pfeifer.   

Abstract

Cytosine residues at CpG dinucleotides can be methylated by endogenous methyltransferases in mammalian cells. The resulting 5-methylcytosine base may undergo spontaneous deamination to form thymine causing G/C to A/T transition mutations. Methylated CpGs also can form preferential targets for environmental mutagens and carcinogens. The Big Blue(R) transgenic mouse has been used to investigate tissue and organ specificity of mutations and to deduce mutational mechanisms in a mammal in vivo. The transgenic mouse contains approximately 40 concatenated lambda-like shuttle vectors, each of which contains one copy of an Escherichia coli lacI gene as a mutational target. lacI mutations in lambda transgenic mice are characterized by a high frequency of spontaneous mutations targeted to CpG dinucleotides suggesting an important contribution from methylation-mediated events. To study the methylation status of CpGs in the lacI gene, we have mapped the distribution of 5-methylcytosines along the DNA-binding domain and flanking sequences of the lacI gene of transgenic mice. We analyzed genomic DNA from various tissues including thymus, liver, testis, and DNA derived from two thymic lymphomas. The mouse genomic DNAs and methylated and unmethylated control DNAs were chemically cleaved, then the positions of 5-methylcytosines were mapped by ligation-mediated PCR which can be used to distinguish methylated from unmethylated cytosines. Our data show that most CpG dinucleotides in the DNA binding domain of the lacI gene are methylated to a high extent (>98%) in all tissues tested; only a few sites are partially (70-90%) methylated. We conclude that tissue-specific methylation is unlikely to contribute significantly to tissue-specific mutational patterns, and that the occurrence of common mutation sites at specific CpGs in the lacI gene is not related to selective methylation of only these sequences. The data confirm previous suggestions that the high frequency of CpG mutations in lacI transgenes is related to the presence of 5-methylcytosine bases. Copyright 1998 Elsevier Science B.V.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9838042     DOI: 10.1016/s1383-5718(98)00147-8

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  9 in total

1.  Evidence for mutation showers.

Authors:  Jicheng Wang; Kelly D Gonzalez; William A Scaringe; Kimberly Tsai; Ning Liu; Dongqing Gu; Wenyan Li; Kathleen A Hill; Steve S Sommer
Journal:  Proc Natl Acad Sci U S A       Date:  2007-05-07       Impact factor: 11.205

2.  Epigenetic regulation of genetic integrity is reprogrammed during cloning.

Authors:  Patricia Murphey; Yukiko Yamazaki; C Alex McMahan; Christi A Walter; Ryuzo Yanagimachi; John R McCarrey
Journal:  Proc Natl Acad Sci U S A       Date:  2009-03-02       Impact factor: 11.205

3.  Through a glass, darkly: reflections of mutation from lacI transgenic mice.

Authors:  G R Stuart; B W Glickman
Journal:  Genetics       Date:  2000-07       Impact factor: 4.562

4.  Mutation frequency and specificity with age in liver, bladder and brain of lacI transgenic mice.

Authors:  G R Stuart; Y Oda; J G de Boer; B W Glickman
Journal:  Genetics       Date:  2000-03       Impact factor: 4.562

5.  Spontaneous hepatocellular carcinoma is reduced in transgenic mice overexpressing human O6- methylguanine-DNA methyltransferase.

Authors:  Z Q Zhou; D Manguino; K Kewitt; G W Intano; C A McMahan; D C Herbert; M Hanes; R Reddick; Y Ikeno; C A Walter
Journal:  Proc Natl Acad Sci U S A       Date:  2001-10-16       Impact factor: 11.205

6.  Rev1 promotes replication through UV lesions in conjunction with DNA polymerases η, ι, and κ but not DNA polymerase ζ.

Authors:  Jung-Hoon Yoon; Jeseong Park; Juan Conde; Maki Wakamiya; Louise Prakash; Satya Prakash
Journal:  Genes Dev       Date:  2015-12-15       Impact factor: 11.361

7.  Transitions at CpG dinucleotides, geographic clustering of TP53 mutations and food availability patterns in colorectal cancer.

Authors:  Fabio Verginelli; Faraz Bishehsari; Francesco Napolitano; Mahboobeh Mahdavinia; Alessandro Cama; Reza Malekzadeh; Gennaro Miele; Giancarlo Raiconi; Roberto Tagliaferri; Renato Mariani-Costantini
Journal:  PLoS One       Date:  2009-08-31       Impact factor: 3.240

8.  A human cancer-associated truncation of MBD4 causes dominant negative impairment of DNA repair in colon cancer cells.

Authors:  S A Bader; M Walker; D J Harrison
Journal:  Br J Cancer       Date:  2007-02-06       Impact factor: 7.640

9.  Comparative genomic study reveals a transition from TA richness in invertebrates to GC richness in vertebrates at CpG flanking sites: an indication for context-dependent mutagenicity of methylated CpG sites.

Authors:  Yong Wang; Frederick C C Leung
Journal:  Genomics Proteomics Bioinformatics       Date:  2008-12       Impact factor: 7.691

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.