Minisatellite origins in yeast and humans

被引:34
作者
Haber, JE
Louis, EJ [1 ]
机构
[1] John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
[2] Brandeis Univ, Rosenstiel Basic Med Sci Res Ctr, Waltham, MA 02254 USA
[3] Brandeis Univ, Dept Biol, Waltham, MA 02254 USA
基金
英国惠康基金;
关键词
D O I
10.1006/geno.1997.5153
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Variable numbers of tandem repeats are valuable markers in genetic studies. The arrays of interest are simple microsatellites, containing repetitions of 1-5 nucleotides, and minisatellites, with multiple iterations of approximately 10 to 100 bp. Microsatellite origins can be explained by replication errors in regions fortuitously containing two or more adjacent short repeats. Microsatellite variation arises by replication errors lan the absence of mismatch correction (a. Parsons et al., 1993, Cell 75: 1227-1236; M. Strand et ab., 1993, Nature 365: 274-276). Variation in the size of minisatellites is thought to involve homologous recombination processes, including gene conversions (J. Buard and G. Vergnaud, 1994, EMBO J. 13: 3203-3210; A. J. Jeffreys et al., 1994, Nature Genet. 6: 136-145) and possibly unequal exchanges among repeats. However, the origins of minisatellites are less obvious. The probability of finding a direct tandem repeat of minisatellite size by chance alone is very low [<4(-(10 to 100))]. Here me report the finding of short direct repeats of 5 to PO bp flanking many yeast and human minisatellites that may be involved in their origins through replication slippage or unequal crossings over. (C) 1998 Academic Press.
引用
收藏
页码:132 / 135
页数:4
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