Warren F, Das A
Proc Natl Acad Sci U S A. 1984 Jun;81(12):3612-6. doi: 10.1073/pnas.81.12.3612.
Transcription antitermination by lambda N gene product is affected in a mutant Escherichia coli with altered ribosomal protein S10, caused by the nusE71 mutation. To study the role of translation in antitermination, we have fused the phage nutR locus, the site of action of N, with the lac regulatory region. We have monitored N action by measuring galactokinase, whose synthesis depends on suppression of terminators located between nutR and the galK cistron. We show that a deletion removing potential ribosome binding signals and AUG codons from the upstream region of nut site does not affect N action. Moreover, the lack of translation upstream of nutR does not overcome the antitermination defect caused by nusE mutation. When the upstream region is translated, however, N action is impaired if translation terminates 19 base pairs upstream of nutR . Termination of translation at further upstream sites, such as 23 or 97 base pairs upstream, does not interfere with N action. Our results suggest that the S10 ribosomal protein is required for N action without involving translation. These results also suggest that the nut site RNA itself plays an important role in the formation of a termination-resistant transcription complex.
由nusE71突变导致核糖体蛋白S10发生改变的突变型大肠杆菌中,λ N基因产物的转录抗终止作用受到影响。为了研究翻译在抗终止中的作用,我们将噬菌体nutR位点(N的作用位点)与lac调控区融合。我们通过测量半乳糖激酶来监测N的作用,半乳糖激酶的合成依赖于对位于nutR和galK顺反子之间的终止子的抑制。我们发现,从nut位点上游区域删除潜在的核糖体结合信号和AUG密码子并不影响N的作用。此外,nutR上游缺乏翻译并不能克服由nusE突变引起的抗终止缺陷。然而,当上游区域进行翻译时,如果翻译在nutR上游19个碱基对处终止,N的作用就会受损。在更上游的位点(如上游23或97个碱基对处)终止翻译不会干扰N的作用。我们的结果表明,S10核糖体蛋白对于N的作用是必需的,且不涉及翻译过程。这些结果还表明,nut位点RNA本身在形成抗终止转录复合物中起着重要作用。