Wolff R K, Nakamura Y, White R
Department of Cellular, Viral, and Molecular Biology, University of Utah, Salt Lake City 84132.
Genomics. 1988 Nov;3(4):347-51. doi: 10.1016/0888-7543(88)90126-7.
Variable-number tandem-repeat (VNTR) DNA markers are contributing new power to human genetic studies because their hypervariable nature allows individualization at the DNA level. The practical value of VNTR markers has been well established for genetic linkage mapping, forensic biology, paternity testing, and monitoring of bone marrow transplants. A popular hypothesis attributes generation of variability at VNTR loci to unequal exchange between homologous chromosomes at meiosis. Contrary to the prediction of this hypothesis, we report here the finding that a newly generated VNTR allele is parental for closely spaced flanking markers; the new allele was generated by loss of one repeat unit, without exchange of flanking DNA sequences. These results are consistent with sister chromatid exchange and polymerase slippage or deletion, as well as with some models for gene conversion.
可变数目串联重复(VNTR)DNA标记正在为人类遗传学研究增添新的力量,因为其高度可变的特性能够在DNA水平上实现个体化识别。VNTR标记在基因连锁图谱构建、法医生物学、亲子鉴定以及骨髓移植监测等方面的实用价值已得到充分证实。一种流行的假说是,VNTR位点的变异性产生是由于减数分裂时同源染色体之间的不等交换。与该假说的预测相反,我们在此报告一项发现:一个新产生的VNTR等位基因对于紧密相邻的侧翼标记而言是亲本型的;这个新等位基因是通过一个重复单元的缺失产生的,而侧翼DNA序列并未发生交换。这些结果与姐妹染色单体交换、聚合酶滑动或缺失以及一些基因转换模型是一致的。