Guarente L, Nye J S, Hochschild A, Ptashne M
Proc Natl Acad Sci U S A. 1982 Apr;79(7):2236-9. doi: 10.1073/pnas.79.7.2236.
The lambda phage repressor is both a positive and a negative regulator of gene transcription. We describe a mutant lambda phage repressor that has specifically lost its activator function. The mutant binds to the lambda phage operator sites and represses the lambda phage promoters PR and PL. However, it fails to stimulate transcription from the promoter PRM. The mutation lies in that portion of repressor--namely, the amino-terminal domain--that has been shown [Sauer, R. T., Pabo, C. O., Meyer, B. J., Ptashne, M. & Backman, K. C. (1979) Nature (London) 279, 396-400] to mediate stimulation of PRM. We suggest that the mutation has altered that region of repressor which, in the wild-type, contacts RNA polymerase to activate transcription from PRM.
λ噬菌体阻遏物既是基因转录的正调控因子,也是负调控因子。我们描述了一种突变型λ噬菌体阻遏物,它特异性地丧失了激活功能。该突变体与λ噬菌体操纵位点结合,并抑制λ噬菌体启动子PR和PL。然而,它无法刺激PRM启动子的转录。突变位于阻遏物的特定部分,即氨基末端结构域,该结构域已被证明[索尔,R.T.,帕博,C.O.,迈耶,B.J.,普塔什内,M.和巴克曼,K.C.(1979年)《自然》(伦敦)279卷,396 - 400页]介导对PRM的刺激。我们认为该突变改变了阻遏物的那个区域,在野生型中,该区域与RNA聚合酶接触以激活PRM的转录。