Tröster H, Kissel W, Trendelenburg M F, Hofmann A
Institute of Experimental Pathology, German Cancer Research Center, Heidelberg, Federal Republic of Germany.
Mol Gen Genet. 1989 Jun;217(2-3):533-5. doi: 10.1007/BF02464928.
Eight representative recombinant background clones of lambda EMBL3 were analysed using KpnI, BamHI, SalI, EcoRI and HindIII digestion. We found that lambda EMBL3 carries its own left arm in the BamHI cloning site. In the way, recombinant molecules were found to be generated which can grow on Escherichia coli strain NM539. In all cases analysed, the left arm DNA was inserted in a head to tail orientation. Seven clones carried a restored BamHI site at the cos site-BamHI site connection. In the region where the inserted left arm and the right arm were ligated, BamHI cloning produces a large palindromic sequence consisting of two polylinkers. This BamHI site was incompletely cleaved in all cases analysed. We assume that a part of the lambda DNA molecule in this region shows a cruciform structure prohibiting recognition or cleavage of this site by restriction endonuclease BamHI.
使用KpnI、BamHI、SalI、EcoRI和HindIII酶切分析了8个具有代表性的λEMBL3重组背景克隆。我们发现λEMBL3在BamHI克隆位点携带自身的左臂。通过这种方式,发现产生了可在大肠杆菌菌株NM539上生长的重组分子。在所有分析的情况中,左臂DNA以头对尾的方向插入。7个克隆在粘性末端位点 - BamHI位点连接处带有恢复的BamHI位点。在插入的左臂和右臂连接的区域,BamHI克隆产生了一个由两个多克隆位点组成的大回文序列。在所有分析的情况中,这个BamHI位点均未被完全切割。我们推测该区域中λDNA分子的一部分呈现十字形结构,从而阻止限制性内切酶BamHI识别或切割该位点。