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小卫星等位基因的变性梯度凝胶电泳分析

Denaturing gradient gel electrophoretic analysis of minisatellite alleles.

作者信息

Uitterlinden A G, Vijg J

机构信息

Genetic Diagnostics Department, Medscand Ingeny, Rijswijk, The Netherlands.

出版信息

Electrophoresis. 1991 Jan;12(1):12-6. doi: 10.1002/elps.1150120104.

Abstract

By two-dimensional DNA fingerprinting, an electrophoretic method which combines separation according to size with separation in a denaturing gradient, virtually all minisatellite sequences detected with a minisatellite core probe can be resolved (Uitterlinden et al., Proc. Natl. Acad. Sci. USA 1989, 86, 2742-2746). To investigate the electrophoretic behavior in denaturing gradient gels of allelic restriction fragments containing minisatellite sequences, we analyzed alleles of the two highly polymorphic minisatellite loci D7S22 and D2S44. The results obtained indicate that for these loci, depending on the restriction enzyme used to digest genomic DNA, alleles of different sizes migrate to regions of similar denaturant concentration, i.e. to isothermal positions in the denaturing gradient. Denaturing gradient gel electrophoresis also allows for the discrimination of restriction fragments which are the result of the presence of internal recognition sites in the minisatellite and, therefore, to distinguish between VNTR and restriction site polymorphisms.

摘要

通过二维DNA指纹图谱(一种将按大小分离与在变性梯度中分离相结合的电泳方法),实际上可以分辨出用小卫星核心探针检测到的所有小卫星序列(Uitterlinden等人,《美国国家科学院院刊》1989年,86卷,2742 - 2746页)。为了研究含有小卫星序列的等位基因限制性片段在变性梯度凝胶中的电泳行为,我们分析了两个高度多态性小卫星位点D7S22和D2S44的等位基因。所得结果表明,对于这些位点,根据用于消化基因组DNA的限制性酶的不同,不同大小的等位基因迁移到变性剂浓度相似的区域,即在变性梯度中的等温位置。变性梯度凝胶电泳还能够区分由于小卫星中存在内部识别位点而产生的限制性片段,从而区分VNTR和限制性位点多态性。

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