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

机译:人类基因组中罕见的限制性内切核酸酶位点过多。

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摘要

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.
机译:从含有人染色体3作为其唯一人类成分的体细胞杂种构建人染色体3特异性粘粒文库。筛选该文库以鉴定230个人重组体,其平均插入片段大小为37kb。然后测试了由54个代表2000 DNA碱基的粘粒制备的DNA的EcoRI,HindIII,KpnI,XhoI和DraI的限制性核酸内切酶位点,以及稀切的限制性核酸内切酶NotI,SfiI和NruI的限制性内切酶位点。 ,MluI,SacII和BssHII。后一种酶的位点比理论计算所预期的要丰富得多,这反映了这些位点的非随机聚集。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。一些单独的粘粒包含大量的稀有位点,提供了基于鉴定稀有限制性位点簇的物理映射染色体的替代方法。这些簇似乎平均间隔为1000 kb。

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