Nucleic Acids Research, Vol 24, Issue 22 4577-4583, Copyright © 1996 by Oxford University Press
R Kiyama and M Oishi
Transcription of poly(dA) x poly(dT)-containing sequences was investigated
in vitro using plasmids carrying a (dA)34 x (dT)34 tract in the coding
region of the lacZ gene. The efficiency of transcription of the (dT)34
sequence on the transcribing strand by Escherichia coli RNA polymerase was
substantially lower (approximately 60%) than that of the (dA)34 sequence or
of the control lacZ gene. Analysis of the transcription process of the
(dT)34 sequence by T3 RNA polymerase showed that the transcription was
frequently arrested or terminated at the middle as well as immediately
proximal of the (dA)34 x (dT)34 tract, and it occurred more prominently
following accumulation of transcription products. This inhibition was
strongly enhanced by the addition of the oligonucleotide (dT)34 or poly(U)
to the reaction mixture, while (dA)34 and the duplex (dA)34 x (dT)34
suppressed the inhibition. A similar transcriptional inhibition was also
observed in transcription mediated by T7 RNA polymerase and eukaryotic RNA
polymerase II. We also demonstrated RNA x DNA complex formation of the
(dA)34 x (dT)34 tract with poly(U), but not with poly(A). These findings
strongly suggest that poly(dT)-containing template sequences interact and
form a complex with its transcription products, possibly an RNA x DNA
triplex, which blocks further transcription. This would explain the
instability of the plasmids transcribing mRNAs with poly(U) but not poly(A)
tracts and the underrepresentation of poly(U) but not poly(A) tracts in
mRNAs.
ARTICLES
In vitro transcription of a poly(dA) x poly(dT)-containing sequence is inhibited by interaction between the template and its transcripts
Institute of Molecular and Cellular Biosciences, The University of Tokyo, Bunkyo-ku, Japan. kiyamar@hgc.ims.u-tokyo.ac.jp
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