CpG/CpNpG motifs in the coding region are preferred sites for mutagenesis in the breast cancer susceptibility genes

被引:4
作者
Cheung, Lydia W. T.
Lee, Yiu Fai
Ng, Tuen Wai
Ching, Wai Ki
Khoo, Ui Soon
Ng, Michael K. P.
Wong, Alice S. T. [1 ]
机构
[1] Univ Hong Kong, Sch Biol Sci, Hong Kong, Hong Kong, Peoples R China
[2] Univ Hong Kong, Dept Math, Hong Kong, Hong Kong, Peoples R China
[3] Univ Hong Kong, Dept Pathol, Hong Kong, Hong Kong, Peoples R China
[4] Hong Kong Baptist Univ, Dept Math, Hong Kong, Hong Kong, Peoples R China
来源
FEBS LETTERS | 2007年 / 581卷 / 24期
关键词
breast cancer susceptibility gene; BRCA1; BRCA2; gene mutation;
D O I
10.1016/j.febslet.2007.08.061
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The range of BRCA1/BRCA2 gene mutations is diverse and the mechanism accounting for this heterogeneity is obscure. To gain insight into the endogenous mutational mechanisms involved, we evaluated the association of specific sequences (i.e. CpG/CpNpG motifs, homonucleotides, short repeats) and mutations within the genes. We classified 1337 published mutations in BRCA1 (1765 BRCA2 mutations) for each specific sequence, and employed computer simulation combined with mathematical calculations to estimate the true underlying tendency of mutation occurrence. Interestingly, we found no mutational bias to homonucleotides and repeats in deletions/insertions and substitutions but striking bias to CpG/CpNpG in substitutions in both genes. This suggests that methylation-dependent DNA alterations would be a major mechanism for mutagenesis, (c) 2007 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:4668 / 4674
页数:7
相关论文
共 32 条
  • [21] MUTATIONS OF THE APC (ADENOMATOUS POLYPOSIS-COLI) GENE
    NAGASE, H
    NAKAMURA, Y
    [J]. HUMAN MUTATION, 1993, 2 (06) : 425 - 434
  • [22] Sequence specificity in CpG mutation hotspots
    Ollila, J
    Lappalainen, I
    Vihinen, M
    [J]. FEBS LETTERS, 1996, 396 (2-3) : 119 - 122
  • [23] REDSTON MS, 1994, CANCER RES, V54, P3025
  • [24] MODEL FOR THE PARTICIPATION OF QUASI-PALINDROMIC DNA-SEQUENCES IN FRAMESHIFT MUTATION
    RIPLEY, LS
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (13): : 4128 - 4132
  • [25] Rodenhiser D, 1996, ONCOGENE, V12, P2623
  • [26] Homonucleotide tracts, short repeats and CpG/CpNpG motifs are frequent sites for heterogeneous mutations in the Neurofibromatosis type 1 (NF1) tumour-suppressor gene
    Rodenhiser, DI
    Andrews, JD
    Mancini, DN
    Jung, JH
    Singh, SM
    [J]. MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1997, 373 (02) : 185 - 195
  • [27] Meiotic microdeletion breakpoints in the BRCA1 gene are significantly associated with symmetric DNA-sequence elements
    Schmucker, B
    Krawczak, M
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (06) : 1454 - 1456
  • [28] STRAND BIAS IN MUTATION INVOLVING 5-METHYLCYTOSINE DEAMINATION IN THE HUMAN HPRT GENE
    SKANDALIS, A
    FORD, BN
    GLICKMAN, BW
    [J]. MUTATION RESEARCH, 1994, 314 (01): : 21 - 26
  • [29] Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1
    Smith, TM
    Lee, MK
    Szabo, CI
    Jerome, N
    McEuen, M
    Taylor, M
    Hood, L
    King, MC
    [J]. GENOME RESEARCH, 1996, 6 (11) : 1029 - 1049
  • [30] Occurrence and consequences of coding sequence insertions and deletions in mammalian genomes
    Taylor, MS
    Ponting, CP
    Copley, RR
    [J]. GENOME RESEARCH, 2004, 14 (04) : 555 - 566