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人类基因组中稀有切割限制内切酶位点过多。

Overabundance of rare-cutting restriction endonuclease sites in the human genome.

作者信息

Smith D I, Golembieski W, Gilbert J D, Kizyma L, Miller O J

出版信息

Nucleic Acids Res. 1987 Feb 11;15(3):1173-84. doi: 10.1093/nar/15.3.1173.

Abstract

A human chromosome 3-specific cosmid library was constructed from a somatic cell hybrid containing human chromosome 3 as its only human component. This library was screened to identify 230 human recombinants which contained an average insert size of 37 kilobases. DNA prepared from 54 of these cosmids, representing 2000 kilobases of human DNA, was then tested for restriction endonuclease sites for EcoRI, HindIII, KpnI, XhoI, and DraI, as well as those of the rare-cutting restriction endonucleases NotI, SfiI, NruI, MluI, SacII, and BssHII. Sites for the latter enzymes were much more abundant than would be expected from theoretical calculations, reflecting non-random clustering of these sites. This has important implications for the use of these enzymes in the construction of physical maps of chromosomes. Some individual cosmids contained large numbers of rare sites, offering an alternative means of physically mapping chromosomes based upon identifying clusters of rare restriction sites. These clusters appear to be spaced an average of 1000 kb apart.

摘要

从一个仅含人类3号染色体作为其唯一人类成分的体细胞杂种构建了一个人类3号染色体特异性黏粒文库。筛选该文库以鉴定出230个平均插入片段大小为37千碱基的人类重组体。然后对从其中54个黏粒制备的DNA(代表2000千碱基的人类DNA)进行了EcoRI、HindIII、KpnI、XhoI和DraI等限制性内切酶位点的检测,以及稀有切割限制性内切酶NotI、SfiI、NruI、MluI、SacII和BssHII的位点检测。后一类酶的位点比理论计算预期的要丰富得多,这反映了这些位点的非随机聚类。这对于在构建染色体物理图谱中使用这些酶具有重要意义。一些单个黏粒含有大量稀有位点,这为基于鉴定稀有限制性位点簇来进行染色体物理图谱构建提供了一种替代方法。这些簇似乎平均相隔1000 kb。

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A rapid method to identify cosmids containing rare restriction sites.
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