Pannekoek H, Brammar W J, Pouwels P H
Medical Biological Laboratory TNO, Rijswijk, The Netherlands.
Mol Gen Genet. 1975;136(3):199-214. doi: 10.1007/BF00334015.
RNA transcribed in vitro from DNA of a tryptophan (trp) transducing strain of bacteriophage phi80 which contains the trp regulatory elements consists of a polycistronic messenger transcribed from the structural genes, and possibly the regulatory region, and a separate RNA species (called trp regRNA) which is transcribed from the regulatory region. This conclusion is based on hybridization experiments with trp RNA synthesized in vitro and the separate DNA strands of trp transducing strains of lambda with and without the trp regulatory elements. The length of trp regRNA determined by filtration on Sephadex G-200 is 110-180 nucleotides. From the amount and the length of trp regRNA we have calculated that 8-20 copies of trp regRNA are synthesized per copy of polycistronic trp mRNA. We conclude that during transcription of the trp operon RNA polymerase frequently is rejected at a specific site ahead of the first structural gene, trpE. The termination factor Rho is not involved in this process. A different protein fraction, which specifically stimulates the synthesis of trp enzymes in an in vitro protein-synthesizing system (Pouwels and Van Rotterdam, 1975), was found to antagonize the abortive synthesis of trp mRNA. A model is proposed for the control of transcription of the trp genes, which operates through a mechanism of punctuation of RNA synthesis at a specific site on the DNA template and anti-termination of RNA synthesis by means of a positive control factor.
从含有色氨酸(trp)调控元件的噬菌体phi80的色氨酸(trp)转导菌株的DNA体外转录的RNA,由从结构基因以及可能从调控区转录而来的多顺反子信使RNA,和一种从调控区转录而来的单独RNA种类(称为trp regRNA)组成。这一结论是基于对体外合成的trp RNA与带有和不带有trp调控元件的λtrp转导菌株的单链DNA进行杂交实验得出的。通过在Sephadex G - 200上过滤测定的trp regRNA长度为110 - 180个核苷酸。根据trp regRNA的量和长度,我们计算出每拷贝多顺反子trp mRNA合成8 - 20拷贝的trp regRNA。我们得出结论,在trp操纵子转录过程中,RNA聚合酶经常在第一个结构基因trpE之前的特定位点被终止。终止因子Rho不参与这一过程。发现一种在体外蛋白质合成系统中能特异性刺激trp酶合成的不同蛋白质组分(Pouwels和Van Rotterdam,1975)可拮抗trp mRNA的流产合成。提出了一个trp基因转录调控模型,该模型通过DNA模板上特定位点的RNA合成标点机制和借助正调控因子的RNA合成抗终止机制来运作。