DNA sequence evolution with neighbor-dependent mutation

被引:85
作者
Arndt, PF
Burge, CB
Hwa, T
机构
[1] Univ Calif San Diego, Dept Phys, La Jolla, CA 92093 USA
[2] MIT, Dept Biol, Cambridge, MA 02139 USA
关键词
DNA-sequence evolution; dinucleotide frequency; neighbor-dependent mutation; CpG-methylation-deamination;
D O I
10.1089/10665270360688039
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We introduce a model of DNA sequence evolution which can account for biases in mutation rates that depend on the identity of the neighboring bases. An analytic solution for this class of models is developed by adopting well-known methods of nonlinear dynamics. Results are presented for the CpG-methylation-deamination process, which dominates point substitutions in vertebrates. The dinucleotide frequencies generated by the model (using empirically obtained mutation rates) match the overall pattern observed in noncoding DNA. A web-based tool has been constructed to compute single- and dinucleotide frequencies for arbitrary neighbor-dependent mutation rates. Also provided is the backward procedure to infer the mutation rates using maximum likelihood analysis given the observed single- and dinucleotide frequencies. Reasonable estimates of the mutation rates can be obtained very efficiently, using generic noncoding DNA sequences as input, after masking out long homonucleotide subsequences. Our method is much more convenient and versatile to use than the traditional method of deducing mutation rates by counting mutation events in carefully chosen sequences. More generally, our approach provides a more realistic but still tractable description of noncoding genomic DNA and may be used as a null model for various sequence analysis applications.
引用
收藏
页码:313 / 322
页数:10
相关论文
共 21 条
[1]  
ARNDT PF, 2002, UNPUB
[2]   STRUCTURE AND VARIABILITY OF RECENTLY INSERTED ALU FAMILY MEMBERS [J].
BATZER, MA ;
KILROY, GE ;
RICHARD, PE ;
SHAIKH, TH ;
DESSELLE, TD ;
HOPPENS, CL ;
DEININGER, PL .
NUCLEIC ACIDS RESEARCH, 1990, 18 (23) :6793-6798
[3]   MEAN-FIELD (N,M)-CLUSTER APPROXIMATION FOR LATTICE MODELS [J].
BENAVRAHAM, D ;
KOHLER, J .
PHYSICAL REVIEW A, 1992, 45 (12) :8358-8370
[4]   MOLECULAR-BASIS OF BASE SUBSTITUTION HOTSPOTS IN ESCHERICHIA-COLI [J].
COULONDRE, C ;
MILLER, JH ;
FARABAUGH, PJ ;
GILBERT, W .
NATURE, 1978, 274 (5673) :775-780
[5]   Cytosine deamination plays a primary role in the evolution of mammalian isochores [J].
Fryxell, KJ ;
Zuckerkandl, E .
MOLECULAR BIOLOGY AND EVOLUTION, 2000, 17 (09) :1371-1383
[6]  
Gardiner C. W., 1997, HDB STOCHASTIC METHO
[7]   PATTERNS OF NUCLEOTIDE SUBSTITUTION IN PSEUDOGENES AND FUNCTIONAL GENES [J].
GOJOBORI, T ;
LI, WH ;
GRAUR, D .
JOURNAL OF MOLECULAR EVOLUTION, 1982, 18 (05) :360-369
[8]   DATING OF THE HUMAN APE SPLITTING BY A MOLECULAR CLOCK OF MITOCHONDRIAL-DNA [J].
HASEGAWA, M ;
KISHINO, H ;
YANO, TA .
JOURNAL OF MOLECULAR EVOLUTION, 1985, 22 (02) :160-174
[9]   WIDE VARIATIONS IN NEIGHBOR-DEPENDENT SUBSTITUTION RATES [J].
HESS, ST ;
BLAKE, JD ;
BLAKE, RD .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 236 (04) :1022-1033
[10]  
KARLIN S, 1995, TRENDS GENET, V11, P283