Abstract

The nucleosome is generally found to be a strong barrier to transcript elongation by RNA polymerase II (pol II) in vitro. The elongation factors TFIIF and TFIIS have been shown to cooperate in maintaining pol II in the catalytically competent state on pure DNA templates. We now show that although TFIIF or TFIIS alone is modestly stimulatory for nucleosome traversal, both factors together increase transcription through nucleosomes in a synergistic manner. We also studied the effect of TFIIF and TFIIS on transcription of nucleosomes containing a Sin mutant histone. The Sin point mutations reduce critical histone-DNA contacts near the center of the nucleosome. Significantly, we found that nucleosomes with a Sin mutant histone are traversed to the same extent and at nearly the same rate as equivalent pure DNA templates if both TFIIS and TFIIF are present. Thus, the nucleosome is not necessarily an insurmountable barrier to transcript elongation by pol II. If unfolding of template DNA from the nucleosome surface is facilitated and the tendency of pol II to retreat from barriers is countered, transcription of nucleosomal templates can be rapid and efficient.

Highlights

  • Point, it is essential to develop in vitro systems that duplicate these processes

  • We have recently shown that nucleosomes containing Sin mutant histones do provide a significantly lower barrier to nucleosome traversal by polymerase II (pol II) [21]

  • We tested whether the elongation factors TFIIS and TFIIF could significantly improve transcript elongation by pol II through the 603R nucleosome

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Summary

Introduction

Point, it is essential to develop in vitro systems that duplicate these processes. Progress toward this goal has been somewhat limited because even single nucleosomes have generally proven to be strong barriers to transcribing pol II in vitro [11, 13,14,15,16,17]. Results with nucleosomes containing Sin mutant or tailless histones do demonstrate directly that targeted unfolding of DNA from the octamer surface has the potential to play a major role in effective transcript elongation in vivo.

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