Luk K C, Szybalski W
Gene. 1982 Mar;17(3):247-58. doi: 10.1016/0378-1119(82)90140-8.
For cloning, assaying the function and sequencing terminators, we have constructed the pD12 plasmid, in which the late promotor p'R of phage lambda controls the expression of the galK gene of the pK03 plasmid of McKenney et al. (1981). The lambda tL3 terminator region was cloned in this plasmid between the promoter and the galK gene, and found to be 90-94% effective in preventing galactokinase expression in both rho+ and rho- hosts. Is is also active in vitro, both in the presence or absence of the rho factor. The termination point is located at 4320 bp to the left of the SL startpoint of the PL-RNA, just downstream of gene exo. We have sequenced 356 bp of the hitherto uncharted lambda DNA to the right of the TaqI cut, which in turn is 110 bp to the right of the b522 deletion at 63.9% lambda. The tL3 terminator has several features common to other rho-independent termination sequences, including an 81% G+C-rich region of 2X8-bp symmetry ("stem") with a 5-bp intervening "loop", partially overlapping and followed by a sequence transcribed into the pyrimidine-rich CCUUUCU-OH 3' terminus of the RNA. The termination point that follows the last U was determined by the S1 mapping technique.
为了进行克隆、功能测定和终止子测序,我们构建了pD12质粒,其中噬菌体λ的晚期启动子p'R控制着McKenney等人(1981年)pK03质粒的galK基因的表达。λ tL3终止子区域被克隆到该质粒的启动子和galK基因之间,发现在rho+和rho-宿主中,它在阻止半乳糖激酶表达方面的效率为90%-94%。它在体外也有活性,无论有无rho因子。终止点位于PL-RNA的SL起始点左侧4320 bp处,恰好在exo基因的下游。我们对TaqI切割位点右侧迄今未绘制图谱的356 bp λ DNA进行了测序,TaqI切割位点又在λ 63.9%处b522缺失位点右侧110 bp处。tL3终止子具有其他不依赖rho的终止序列共有的几个特征,包括一个81%富含G+C的区域,具有2×8 bp对称性(“茎”),中间有一个5 bp的“环”,部分重叠,后面跟着一个转录成富含嘧啶的CCUUUCU-OH 3' RNA末端的序列。最后一个U之后的终止点是通过S1作图技术确定的。