Simmler M C, Johnsson C, Petit C, Rouyer F, Vergnaud G, Weissenbach J
EMBO J. 1987 Apr;6(4):963-9. doi: 10.1002/j.1460-2075.1987.tb04846.x.
Two pseudoautosomal loci DXYS15 and DXYS17 from the pairing region of the human sex chromosomes display a high variability with at least eight alleles each. The structural elements responsible for the polymorphisms have been isolated and sequenced. In both cases the variations result from DNA rearrangements occurring in tandemly repeated sequences (minisatellites) of 21-29 nucleotides for DXYS15 and 28-33 nucleotides for DXYS17. At reduced stringency, the DXYS15 minisatellite detects other hypervariable sequences located in other parts of the genome and hence represents a new family of minisatellites. In contrast to most other known hypervariable families, the DXYS15 hypervariable sequence displays a very high AT content.
来自人类性染色体配对区域的两个拟常染色体基因座DXYS15和DXYS17各显示出至少八个等位基因的高度变异性。负责多态性的结构元件已被分离并测序。在这两种情况下,变异都是由串联重复序列(微卫星)中的DNA重排导致的,DXYS15的串联重复序列为21 - 29个核苷酸,DXYS17的为28 - 33个核苷酸。在较低严谨性条件下,DXYS15微卫星可检测到位于基因组其他部位的其他高变序列,因此代表了一个新的微卫星家族。与大多数其他已知的高变家族不同,DXYS15高变序列显示出非常高的AT含量。