Suppr超能文献

人类个体的二维DNA指纹图谱

Two-dimensional DNA fingerprinting of human individuals.

作者信息

Uitterlinden A G, Slagboom P E, Knook D L, Vijg J

机构信息

Department of Molecular Biology, TNO Institute for Experimental Gerontology, Rijswijk, The Netherlands.

出版信息

Proc Natl Acad Sci U S A. 1989 Apr;86(8):2742-6. doi: 10.1073/pnas.86.8.2742.

Abstract

The limiting factor in the presently available techniques for the detection of DNA sequence variation in the human genome is the low resolution of Southern blot analysis. To increase the analytical power of this technique, we applied size fractionation of genomic DNA restriction fragments in conjunction with their sequence-dependent separation in denaturing gradient gels; the two-dimensional separation patterns obtained were subsequently transferred to nylon membranes. Hybridization analysis using minisatellite core sequences as probes resulted in two-dimensional genomic DNA fingerprints with a resolution of up to 625 separated spots per probe per human individual; by conventional Southern blot analysis, only 20-30 bands can be resolved. Using the two-dimensional DNA fingerprinting technique, we demonstrate in a small human pedigree the simultaneous transmission of 37 polymorphic fragments (out of 365 spots) for probe 33.15 and 105 polymorphic fragments (out of 625 spots) for probe 33.6. In addition, a mutation was detected in this pedigree by probe 33.6. We anticipate that this method will be of great use in studies aimed at (i) measuring human mutation frequencies, (ii) associating genetic variation with disease, (iii) analyzing genomic instability in relation to cancer and aging, and (iv) linkage analysis and mapping of disease genes.

摘要

目前用于检测人类基因组中DNA序列变异的现有技术的限制因素是Southern印迹分析分辨率较低。为了提高该技术的分析能力,我们将基因组DNA限制性片段的大小分级与它们在变性梯度凝胶中的序列依赖性分离相结合;随后将获得的二维分离模式转移到尼龙膜上。使用小卫星核心序列作为探针进行杂交分析,得到了二维基因组DNA指纹图谱,每个人类个体每个探针的分辨率高达625个分离斑点;通过传统的Southern印迹分析,只能分辨出20 - 30条带。使用二维DNA指纹技术,我们在一个小型人类家系中证明了探针33.15的37个多态性片段(共365个斑点)和探针33.6的105个多态性片段(共625个斑点)的同时传递。此外,通过探针33.6在这个家系中检测到了一个突变。我们预计该方法将在以下研究中发挥重要作用:(i)测量人类突变频率,(ii)将遗传变异与疾病关联起来,(iii)分析与癌症和衰老相关的基因组不稳定性,以及(iv)疾病基因的连锁分析和定位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80e8/286994/eff4334cef83/pnas00248-0232-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验