Rubinsztein D C, Amos W, Leggo J, Goodburn S, Jain S, Li S H, Margolis R L, Ross C A, Ferguson-Smith M A
East Anglian Regional Genetics Service, Molecular Genetics Laboratory, Addenbrooke's NHS Trust, Cambridge, UK.
Nat Genet. 1995 Jul;10(3):337-43. doi: 10.1038/ng0795-337.
Microsatellite DNA sequences are rapidly becoming the dominant source of nuclear genetic markers for a wide range of applications, from genome mapping to forensic testing to population studies. If misinterpretation is to be avoided, it is vital that we understand fully the way in which microsatellite sequences evolve. We have therefore compared allele length distributions for 42 microsatellites in humans with their homologues in a range of related primates. We find a highly significant trend for the loci to be longer in humans, showing that microsatellites can evolve directionally and at different rates in closely related species.
微卫星DNA序列正迅速成为广泛应用的核遗传标记的主要来源,这些应用涵盖从基因组图谱绘制到法医鉴定再到群体研究等多个领域。若要避免错误解读,全面了解微卫星序列的进化方式至关重要。因此,我们将人类42个微卫星的等位基因长度分布与其在一系列相关灵长类动物中的同源序列进行了比较。我们发现这些基因座在人类中显著更长,这表明微卫星在亲缘关系密切的物种中可定向且以不同速率进化。