Squires C L, Greenblatt J, Li J, Condon C, Squires C L
Department of Biological Sciences, Columbia University, New York, NY 10027.
Proc Natl Acad Sci U S A. 1993 Feb 1;90(3):970-4. doi: 10.1073/pnas.90.3.970.
Using an in vitro transcription assay, we have successfully demonstrated read through of a Rho-dependent terminator by the ribosomal RNA antitermination system. The assay used a DNA template containing a promoter-antiterminator-terminator arrangement, RNA polymerase, termination factor Rho, antitermination factors NusA, NusB, NusE, and NusG, and a cellular extract depleted of NusB. Terminator read-through was highly efficient only in the presence of the extract and Nus factors, suggesting that an as yet uncharacterized cellular component is required for ribosomal antitermination. The NusB-depleted extract had no activity in the absence of NusB, confirming an absolute requirement for this protein in ribosomal RNA antitermination. The DNA template requirements were the same as those previously established in vivo; transcription of a wild-type boxA sequence is both necessary and sufficient to promote RNA polymerase modification into a terminator-resistant form.
通过体外转录试验,我们成功证明了核糖体RNA抗终止系统能够通读Rho依赖性终止子。该试验使用了一个包含启动子-抗终止子-终止子排列的DNA模板、RNA聚合酶、终止因子Rho、抗终止因子NusA、NusB、NusE和NusG,以及去除了NusB的细胞提取物。只有在提取物和Nus因子存在的情况下,终止子通读才非常高效,这表明核糖体抗终止需要一种尚未明确的细胞成分。在没有NusB的情况下,去除NusB的提取物没有活性,这证实了该蛋白质在核糖体RNA抗终止中是绝对必需的。DNA模板要求与先前在体内确定的要求相同;野生型boxA序列的转录对于促进RNA聚合酶修饰为抗终止形式既必要又充分。