Mutant RNA polymerase of Escherichia coli terminates transcription in strains making defective rho factor.
Author(s) -
L Guarente,
Jon Beckwith
Publication year - 1978
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.75.1.294
Subject(s) - rna polymerase , transcription (linguistics) , microbiology and biotechnology , rna dependent rna polymerase , polymerase , biology , operon , rna polymerase i , sigma factor , termination factor , mutant , antitermination , rna polymerase ii , rna , genetics , dna , promoter , gene , gene expression , linguistics , philosophy
We have isolated a rifampicin-resistant mutant of Escherichia coli RNA polymerase that restores transcription termination in strains with a defective rho protein. In such strains, the mutant RNA polymerase terminates transcription at normally rho-dependent sites at the end of the trp operon, in bacteriophage lambda, and within the lac operon. In addition, a strain with this mutant RNA polymerase remains viable with an amber mutation in rho, whereas a strain with wild-type RNA polymerase does not. These results suggest that the mutant RNA polymerase can terminate transcription at normally rho-dependent sites in the absence of rho.
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