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腺病毒4型(E亚组)DNA的限制酶切图谱分析及分子克隆

Restriction mapping and molecular cloning of adenovirus type 4 (subgroup E) DNA.

作者信息

Kitchingman G R

出版信息

Gene. 1982 Dec;20(2):205-10. doi: 10.1016/0378-1119(82)90039-7.

Abstract

The locations of thirty restriction endonuclease cleavage sites were determined on the genome of adenovirus type 4 (Ad4), the sole member of the subgroup E adenovirions. The restriction endonucleases Bg/II, EcoRI, HindIII, HpaI, KpnI, SalI, and XbaI cut Ad4 DNA 10, 3, 2, 3, 5, 5 and 3 times, respectively. Orientation of the linear Ad4 map with respect to left and right molecular ends was accomplished by taking advantage of the limited sequence homology between Ad2 and Ad4. Ten non-overlapping fragments of Ad4 DNA representing 98% of the genome, map units 1.6 to 99.6, have been cloned into the plasmid vector pKC7.

摘要

在腺病毒4型(Ad4)的基因组上确定了30个限制性内切酶切割位点的位置,Ad4是E亚组腺病毒粒子的唯一成员。限制性内切酶Bg/II、EcoRI、HindIII、HpaI、KpnI、SalI和XbaI分别切割Ad4 DNA 10次、3次、2次、3次、5次、5次和3次。利用Ad2和Ad4之间有限的序列同源性,完成了线性Ad4图谱相对于左右分子末端的定向。代表基因组98%(图谱单位1.6至99.6)的10个不重叠的Ad4 DNA片段已被克隆到质粒载体pKC7中。

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