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基于串联重复序列可变数目(VNTR)和限制性酶切位点多态性的复杂DNA多态性鉴定。

Identification of complex DNA polymorphisms based on variable number of tandem repeats (VNTR) and restriction site polymorphism.

作者信息

Waye J S, Fourney R M

机构信息

Central Forensic Laboratory, Royal Canadian Mounted Police, Ottawa, Ontario.

出版信息

Hum Genet. 1990 Feb;84(3):223-7. doi: 10.1007/BF00200563.

Abstract

Restriction fragment length polymorphisms (RFLPs) of genomic DNA are generally attributable to base changes that create or abolish restriction endonuclease sites or to nucleotide sequence insertions or deletions that alter the distance separating two restriction sites. Minisatellite or variable number of tandem repeats (VNTR) markers are prominent examples of the latter type of polymorphism. In this report, we describe complex DNA polymorphisms that are due both to the presence of VNTRs as well as to altered restriction endonuclease sites. A strategy for identifying such polymorphisms and resolving their component allelic fragments is demonstrated.

摘要

基因组DNA的限制性片段长度多态性(RFLP)通常归因于产生或消除限制性内切酶位点的碱基变化,或归因于改变两个限制性位点之间距离的核苷酸序列插入或缺失。微卫星或可变数目串联重复序列(VNTR)标记是后一种多态性类型的突出例子。在本报告中,我们描述了复杂的DNA多态性,其既归因于VNTR的存在,也归因于限制性内切酶位点的改变。展示了一种识别此类多态性并解析其组成等位基因片段的策略。

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