A new paradigm for transcription factor TFIIB functionality

Vladimir Gelev, Janice M. Zabolotny, Martin Lange, Makoto Hiromura, Sang Wook Yoo, Joseph S. Orlando, Anna Kushnir, Nobuo Horikoshi, Eric Paquet, Dimcho Bachvarov, Priscilla A. Schaffer, Anny Usheva

Research output: Contribution to journalArticlepeer-review

14 Scopus citations


Experimental and bioinformatic studies of transcription initiation by RNA polymerase II (RNAP2) have revealed a mechanism of RNAP2 transcription initiation less uniform across gene promoters than initially thought. However, the general transcription factor TFIIB is presumed to be universally required for RNAP2 transcription initiation. Based on bioinformatic analysis of data and effects of TFIIB knockdown in primary and transformed cell lines on cellular functionality and global gene expression, we report that TFIIB is dispensable for transcription of many human promoters, but is essential for herpes simplex virus-1 (HSV-1) gene transcription and replication. We report a novel cell cycle TFIIB regulation and localization of the acetylated TFIIB variant on the transcriptionally silent mitotic chromatids. Taken together, these results establish a new paradigm for TFIIB functionality in human gene expression, which when downregulated has potent anti-viral effects.

Original languageEnglish (US)
Article number3664
JournalScientific Reports
StatePublished - Jan 20 2014

ASJC Scopus subject areas

  • General


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