Liu K, Hanna M M
Department of Botany and Microbiology, University of Oklahoma, Norman 73019 USA.
J Mol Biol. 1995 Apr 7;247(4):547-58. doi: 10.1006/jmbi.1994.0161.
We have examined the interaction between NusA and the nascent RNA in Escherichia coli transcription complexes on four different templates. Photocrosslinking CTP and UTP analogs were incorporated internally and at the 3' end of the RNA. Identical templates with and without boxA sequences were compared. We found that NusA did not contact the ten nucleotides nearest to the 3' end of the RNA in complexes containing RNA up to 20 nucleotides long. Longer RNA did crosslink to NusA with all four templates examined, however. We reported that RNA 80 nucleotides long from the bacteriophage T7 A1 promoter substituted in two RNA stem-loops with photocrosslinking UMP analogs did not crosslink to NusA, even though interaction between NusA and the transcription complex were demonstrated. Here, we report that when this same RNA is substituted at CMP residues, it does crosslink to NusA. Templates containing the E. coli ribosomal RNA promoter rrnG P2, with and without a boxA sequence downstream, were compared. Long RNAs from both crosslinked to NusA, and thus boxA RNA sequences are not required for interaction with NusA. NusA did not interact with the free RNA containing boxA once released from the transcription complex, nor did it interact with RNA in a binary complex containing only RNA polymerase and RNA, without the DNA template.
我们研究了在四种不同模板上的大肠杆菌转录复合物中NusA与新生RNA之间的相互作用。光交联CTP和UTP类似物被掺入到RNA内部和3'末端。比较了有无boxA序列的相同模板。我们发现,在含有长度达20个核苷酸的RNA的复合物中,NusA不与最靠近RNA 3'末端的十个核苷酸接触。然而,在所检测的所有四种模板中,更长的RNA确实与NusA发生了交联。我们曾报道,来自噬菌体T7 A1启动子的80个核苷酸长的RNA在两个RNA茎环中被光交联UMP类似物取代后,即使已证明NusA与转录复合物之间存在相互作用,该RNA也未与NusA交联。在此,我们报道,当该相同RNA在CMP残基处被取代时,它确实与NusA交联。比较了含有大肠杆菌核糖体RNA启动子rrnG P2且下游有无boxA序列的模板。来自两者的长RNA均与NusA交联,因此与NusA相互作用不需要boxA RNA序列。一旦从转录复合物中释放出来,NusA不与含有boxA的游离RNA相互作用,在仅含有RNA聚合酶和RNA而无DNA模板的二元复合物中,NusA也不与RNA相互作用。