Microsatellite mutations in the germline: implications for evolutionary inference

被引:513
作者
Ellegren, H [1 ]
机构
[1] Uppsala Univ, Evolutionary Biol Ctr, Dept Evolutionary Biol, SE-75236 Uppsala, Sweden
关键词
D O I
10.1016/S0168-9525(00)02139-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Microsatellite DNA sequences mutate at rates several orders of magnitude higher than that of the bulk of DNA. Such high rates mean that spontaneous mutations that form new-length variants can realistically be seen in pedigree analysis. Data on observed mutation events from various organisms are now accumulating, allowing inferences on DNA sequence evolution to be made through an unusually direct approach. Here I discuss and integrate microsatellite mutation data in an evolutionary context. A striking feature of the mutation process is that it seems highly heterogeneous, with distinct differences between species, repeat types, loci and alleles. Age and sex also affect the mutation rate. Within genomes at equilibrium, the microsatellite-length distribution is a delicate balance between biased mutation processes and point mutations acting towards the decay of repetitive DNA. Indeed, simple repeats do not evolve simply.
引用
收藏
页码:551 / 558
页数:8
相关论文
共 66 条
[1]   Microsatellites show mutational bias and heterozygote instability [J].
Amos, W ;
Sawcer, SJ ;
Feakes, RW ;
Rubinsztein, DC .
NATURE GENETICS, 1996, 13 (04) :390-391
[2]   Microsatellite conservation, polymorphism, and GC content in shrews of the genus Sorex (Insectivora, Mammalia) [J].
Balloux, F ;
Ecoffey, E ;
Fumagalli, L ;
Goudet, J ;
Wyttenbach, A ;
Hausser, J .
MOLECULAR BIOLOGY AND EVOLUTION, 1998, 15 (04) :473-475
[3]   The length distribution of perfect dimer repetitive DNA is consistent with its evolution by an unbiased single-step mutation process [J].
Bell, GI ;
Jurka, J .
JOURNAL OF MOLECULAR EVOLUTION, 1997, 44 (04) :414-421
[4]  
BICHARA M, 1995, GENETICS, V140, P897
[5]   Mutation rate in human microsatellites:: Influence of the structure and length of the tandem repeat [J].
Brinkmann, B ;
Klintschar, M ;
Neuhuber, F ;
Hühne, J ;
Rolf, B .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (06) :1408-1415
[6]   Cis-acting modifiers of expanded CAG CTG triplet repeat expandability:: associations with flanking GC content and proximity to CpG islands [J].
Brock, GJR ;
Anderson, NH ;
Monckton, DG .
HUMAN MOLECULAR GENETICS, 1999, 8 (06) :1061-1067
[7]   Microsatellite evolution: polarity of substitutions within repeats and neutrality of flanking sequences [J].
Brohede, J ;
Ellegren, H .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1999, 266 (1421) :825-833
[8]   MICROSATELLITES AND THEIR APPLICATION TO POPULATION GENETIC-STUDIES [J].
BRUFORD, MW ;
WAYNE, RK .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1993, 3 (06) :939-943
[9]   TRIPLET REPEAT MUTATIONS IN HUMAN-DISEASE [J].
CASKEY, CT ;
PIZZUTI, A ;
FU, YH ;
FENWICK, RG ;
NELSON, DL .
SCIENCE, 1992, 256 (5058) :784-789
[10]   Relative mutation rates at di-, tri-, and tetranucleotide microsatellite loci [J].
Chakraborty, R ;
Kimmel, M ;
Stivers, DN ;
Davison, LJ ;
Deka, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (03) :1041-1046