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Mol. Cell. Biol., Jul 1996, 3291-3299, Vol 16, No. 7
KY Yankulov, M Pandes, S McCracken, D Bouchard and DL Bentley
We investigated the role of TFIIH in transcription by RNA polymerase II
(pol II) in vivo by microinjection of antibodies against this factor into
Xenopus oocytes. Five different antibodies directed against four subunits
of TFIIH were tested for effects on transcription of coinjected human
immunodeficiency virus type 2 and c-myc templates. Each of these antibodies
severely reduced the efficiency of elongation through human
immunodeficiency virus type 2 and c-myc terminator elements. In contrast,
an anti-TFIIB antibody did not inhibit elongation. Anti-TFIIH antibodies
also had a much smaller inhibitory effect on total transcription than did
anti-TFIIB or anti-pol II large subunit. Three inhibitors of TFIIH kinase
activity, H-7, H-8, and dichlororibofuranosylbenzimidazole (DRB), inhibited
elongation similarly to anti-TFIIH antibodies. These results strongly
suggest a role for TFIIH in the stimulation of transcriptional elongation
in vivo.
Copyright © 1996, American Society for Microbiology
TFIIH functions in regulating transcriptional elongation by RNA polymerase II in Xenopus oocytes
Amgen Institute, Toronto, Ontario, Canada.
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