首页> 外文OA文献 >Mapping of genomic DNA loop organization in a 500-kilobase region of the Drosophila X chromosome by the topoisomerase II-mediated DNA loop excision protocol.
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Mapping of genomic DNA loop organization in a 500-kilobase region of the Drosophila X chromosome by the topoisomerase II-mediated DNA loop excision protocol.

机译:通过拓扑异构酶II介导的DNA环切除方案在果蝇X染色体的500碱基对区域中绘制基因组DNA环组织。

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摘要

The recently developed procedure of chromosomal DNA loop excision by topoisomerase II-mediated DNA cleavage at matrix attachment sites (S. V. Razin, R. Hancock, O. Iarovaia, O. Westergaard, I. Gromova, and G. P. Georgiev, Cold Spring Harbor Symp. Quant. Biol. 58:25-35, 1993; I. I. Gromova, B. Thompsen, and S. V. Razin, Proc. Natl. Acad. Sci. USA 92:102-106, 1995) has been employed for mapping the DNA loop anchorage sites in a 500-kb region of the Drosophila melanogaster X chromosome. Eleven anchorage sites delimiting 10 DNA loops ranging in size from 20 to 90 kb were found within this region. Ten of these 11 anchorage sites colocalize with previously mapped scaffold attachment regions. However, a number of other scaffold attachment regions are found to be located in loop DNA.
机译:最近开发的通过拓扑异构酶II介导的DNA裂解在基质附着位点切割染色体DNA环的方法(SV Razin,R。Hancock,O。Iarovaia,O。Westergaard,I。Gromova和GP Georgiev,冷泉港的症状定量。参见,例如,J.Biol.58:25-35,1993; II Gromova,B.Thompsen和SV Razin,Proc.Natl.Acad.Sci.USA 92:102-106,1995)。果蝇X染色体的500kb区域。在该区域内发现了11个锚定位点,它们定界了10个DNA环,大小范围为20至90 kb。这11个锚固位点中有10个与先前映射的支架附着区域共定位。然而,发现许多其他支架附着区域位于环DNA中。

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