Initiation by yeast RNA polymerase II at the adenoviral major late promoter in vitro

Neal F. Lue, Peter M. Flanagan, Katsunori Sugimoto, Roger D. Kornberg

Research output: Contribution to journalArticle

55 Citations (Scopus)

Abstract

Transcription of the yeast CYC1 promoter fused to a sequence lacking guanosine residues provided a rapid, sensitive assay of initiation by RNA polymerase II in yeast extracts. Initiation was enhanced by yeast and mammalian activator proteins. The adenoviral major late promoter fused to the G-minus sequence was transcribed in yeast extracts with an efficiency comparable to that observed in HeLa extracts, showing mat promoters as well as transcription factors are functionally interchangeable across species. Initiation occurred at different sites, approximately 30 and 63 to 69 base pairs downstream of the TATA element of the adenoviral promoter in HeLa and yeast extracts, respectively, distances characteristic of initiation in the two systems in vivo. A component of the transcription system and not the promoter sequence determines the distance to the initiation site.

Original languageEnglish (US)
Pages (from-to)661-664
Number of pages4
JournalScience
Volume246
Issue number4930
DOIs
StatePublished - Jan 1 1989
Externally publishedYes

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RNA Polymerase II
Yeasts
Guanosine
Base Pairing
Transcription Factors
In Vitro Techniques
Proteins

All Science Journal Classification (ASJC) codes

  • General

Cite this

Lue, Neal F. ; Flanagan, Peter M. ; Sugimoto, Katsunori ; Kornberg, Roger D. / Initiation by yeast RNA polymerase II at the adenoviral major late promoter in vitro. In: Science. 1989 ; Vol. 246, No. 4930. pp. 661-664.
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Initiation by yeast RNA polymerase II at the adenoviral major late promoter in vitro. / Lue, Neal F.; Flanagan, Peter M.; Sugimoto, Katsunori; Kornberg, Roger D.

In: Science, Vol. 246, No. 4930, 01.01.1989, p. 661-664.

Research output: Contribution to journalArticle

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