Blumenthal R M, Reeh S, Pedersen S
Proc Natl Acad Sci U S A. 1976 Jul;73(7):2285-8. doi: 10.1073/pnas.73.7.2285.
Transcriptional termination factor rho, the alpha subunit of RNA polymerase (RNA nucleotidyltransferase nucleosidetriphosphate: RNA nucleotidyltransferase, EC 2.7.7.6), and ribosomal protein S6 were resolved from whole-cell extracts of E. coli B/r by a high-resolution, two-dimensional polyacrylamide gel electrophoretic technique, and were identified through coelectrophoresis with the purified proteins. The regulation of rho, alpha, and S6 was studied, in steady-state cultures of E. coli B/r growing at rates ranging from 0.6 to 2.1 generations per hr, through the use of this gel technique and a double radioisotope labeling procedure. The regulatory patterns of rho and alpha are distinct from, but similar to, one another. Neither rho nor alpha shows the sharply increasing levels with increasing growth rate shown by the ribosomal proteins was exemplified by S6. The difference between the levels of rho and alpha, on the one hand, and S6, on the other, is most pronounced during rapid growth. The regulatory pattern of alpha is interesting, given the recent suggestion that the gene coding for alpha is contranscribed with genes coding for ribosomal proteins.
转录终止因子ρ、RNA聚合酶的α亚基(RNA核苷酸转移酶核苷三磷酸:RNA核苷酸转移酶,EC 2.7.7.6)和核糖体蛋白S6,通过高分辨率二维聚丙烯酰胺凝胶电泳技术从大肠杆菌B/r的全细胞提取物中分离出来,并通过与纯化蛋白共电泳进行鉴定。利用这种凝胶技术和双放射性同位素标记程序,在每小时生长速率为0.6至2.1代的大肠杆菌B/r稳态培养物中研究了ρ、α和S6的调控。ρ和α的调控模式彼此不同但又相似。ρ和α都没有表现出核糖体蛋白(如S6)随生长速率增加而急剧增加的水平。一方面,ρ和α的水平与另一方面S6的水平之间的差异在快速生长期间最为明显。鉴于最近有人提出编码α的基因与编码核糖体蛋白的基因共转录,α的调控模式很有趣。