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JBC, Vol. 250, Issue 8, 2866-2871, Apr, 1975
E. Domingo, C. Escarmis and R. C. Warner
The effect of the sigma subunit of RNA polymerase on the rate and asymmetry
of the in vitro transcription of Escherichia coli and Azotobacter
vinelandii phage DNAs has been studied with purified E. coli and A.
vinelandii RNA polymerases and hybrid enzymes containing the core subunits
of one enzyme and sigma from the other. The effect of sigma on the rate of
transcription is characteristic of the template and not of the enzyme and
depends on ionic strength. The rate of transcription of A. vinelandii phage
A21 DNA is decreased by sigma at high ionic strength, but shows the more
characteristic stimulation at KCl concentrations below 0.05 M. In contrast,
the stimulation by sigma of T4 DNA transcription increased with an increase
in the KCl concentrations. All combinations of core and sigma subunits
behaved similarly with respect to stimulation or inhibition by sigma and
with respect to asymmetric transcription of S13 replicative form (RF)DNA.
However, the heterologous, but not the homologous combinations of core and
sigma transcribed A21 symmetrically. S13 RF DNA in the superhelical, but
not in the relaxed configuration, is transcribed asymmetrically by the A.
vinelandii core enzyme. A role for the core subunits in specific site
recognition is indicated by this observation.
Transcription of bacteriophage deoxyribonucleic acid. Comparison of Escherichia coli and Azotobacter vinelandii sigma subunits
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