Hart C M, Roberts J W
Section of Biochemistry, Molecular and Cell Biology, Cornell University, Ithaca, NY 14853.
J Mol Biol. 1994 Apr 1;237(3):255-65. doi: 10.1006/jmbi.1994.1229.
In order to determine how much of the natural sequence is required for function of the lambda tR1 rho-dependent terminator, and to determine the minimum length required, we made two deletion series of a tR1 derivative that contains mostly foreign DNA, encoding C-rich RNA, substituted for the natural upstream sequences of tR1. We find the minimum transcript length to be 85 to 90 nucleotides, although an additional 10 to 25 nucleotides provide more efficient termination. Sequences as close as ten nucleotides to the release sites could be replaced without destroying termination, although termination efficiency was reduced by substitution of these proximal regions with DNA encoding the cytidine-rich RNA that is active at upstream sites. These results suggest that sequences proximal and distal to release sites have different functions and optimal structures for rho activation. We also show that two potential stem-loop structures in the tR1 region are not essential for terminator function, or for pausing at the release region. The results are consistent with the model that any pause site downstream of DNA encoding unstructured C-rich RNA is a potential rho-dependent terminator.
为了确定λtR1 ρ依赖性终止子发挥功能所需的天然序列长度,并确定其所需的最小长度,我们构建了两个缺失系列,它们来源于一个tR1衍生物,该衍生物大部分包含外源DNA,编码富含C的RNA,替代了tR1的天然上游序列。我们发现最小转录本长度为85至90个核苷酸,不过额外的10至25个核苷酸能实现更高效的终止。距离释放位点近至十个核苷酸的序列可以被替换而不破坏终止,尽管用编码在上游位点有活性的富含胞嘧啶RNA的DNA替换这些近端区域会降低终止效率。这些结果表明,释放位点近端和远端的序列对于ρ激活具有不同的功能和最佳结构。我们还表明,tR1区域中的两个潜在茎环结构对于终止子功能或在释放区域的暂停并非必不可少。这些结果与以下模型一致:编码无结构富含C的RNA的DNA下游的任何暂停位点都是潜在的ρ依赖性终止子。