TY - JOUR
T1 - Mechanism of action of DRB. III. Effect on specific in vitro initiation of transcription
AU - Zandomeni, Ruben
AU - Bunick, David
AU - Ackerman, Steven
AU - Mittleman, Barbara
AU - Weinmann, Roberto
AU - Chambon, P.
N1 - Funding Information:
We thank Judith Owen and Dr Nigel Fraser for plasmid p69 containing the adenovirus major late and EIV promoters, Dr R. Roberts and T. Gingeras for the M-13 adenovirus major late promoter recombinants, and Dr M. Concino for the labeled undecanucleotide. This research was supported by grants CA-10815 and CA-21124 from the National Cancer Institute and AI-13231 from the National Institute of Allergy and Infectious Diseases. D. B. was supported by 5T-32CA-07922 and S. A. by 2T-32-CA09171, U.S. Public Health Service Training grants.
PY - 1983/7/5
Y1 - 1983/7/5
N2 - 5,6-Dichloro-1-β-d-ribofuranosylbenzimidazole, an adenosine analogue, has been used previously as an inhibitor of heterogeneous nuclear and messenger RNA synthesis. In an in vitro transcriptional system, we have detected inhibition of synthesis of full-length runoff RNAs at concentrations at which in vivo mRNA synthesis is inhibited. By hybridization of RNA synthesized in vitro to single-stranded DNA and gel analysis, we were able to reduce the background of the transcription reaction, detect DRB-induced inhibition of full-length runoff RNAs and DRB-insensitive transcription of short RNAs. To establish further the effect of DRB on initiation of transcription, preincubation experiments with template, whole cell extract and two initial nucleotides of the transcript were performed. Elongation was then measured as discrete-sized RNAs transcribed from the truncated template after addition of the other triphosphates (one of them labeled), in the presence or absence of DRB. An effect on initiation but not on elongation or termination was detected. Fingerprint analysis of these runoff RNAs indicates that the labeling of U in the presence of DRB is uniform throughout the molecule. A model to explain a novel interpretation of the action of DRB is presented.
AB - 5,6-Dichloro-1-β-d-ribofuranosylbenzimidazole, an adenosine analogue, has been used previously as an inhibitor of heterogeneous nuclear and messenger RNA synthesis. In an in vitro transcriptional system, we have detected inhibition of synthesis of full-length runoff RNAs at concentrations at which in vivo mRNA synthesis is inhibited. By hybridization of RNA synthesized in vitro to single-stranded DNA and gel analysis, we were able to reduce the background of the transcription reaction, detect DRB-induced inhibition of full-length runoff RNAs and DRB-insensitive transcription of short RNAs. To establish further the effect of DRB on initiation of transcription, preincubation experiments with template, whole cell extract and two initial nucleotides of the transcript were performed. Elongation was then measured as discrete-sized RNAs transcribed from the truncated template after addition of the other triphosphates (one of them labeled), in the presence or absence of DRB. An effect on initiation but not on elongation or termination was detected. Fingerprint analysis of these runoff RNAs indicates that the labeling of U in the presence of DRB is uniform throughout the molecule. A model to explain a novel interpretation of the action of DRB is presented.
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U2 - 10.1016/S0022-2836(83)80098-9
DO - 10.1016/S0022-2836(83)80098-9
M3 - Article
C2 - 6876157
AN - SCOPUS:0021095472
SN - 0022-2836
VL - 167
SP - 561
EP - 574
JO - Journal of Molecular Biology
JF - Journal of Molecular Biology
IS - 3
ER -