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Nucleic Acids Research, 1994, Vol. 22, No. 23 4932-4936
© 1994


MOLECULAR BIOLOGY

Role of a small RNA pol II subunit in TATA to transcription start site spacing

Elizabeth M. Furter-Graves, Benjamin D. Hall1 and Rolf Furter*

Institute for Cell Biology, Swiss Federal Insitute of Techonology ETH-Hönggerberg, CH-8093 Sürich, Switzeraland 1Department of Genetics, SK–50, University of Washington Seattle, WA 98195, USA

*To whom correpsondence should be addressed at: Department of Biochemistry and Molecular Biology, Lederfe Graduate Research Center, University of Massachusetrs, Amberst, MA 01003, USA

Received September 6, 1994. Revised October 17, 1994. Accepted October 17, 1994.

The yeast shi mutation affects the spacing between the TATA promoter element and transcription initiation sites; for the H2B and ADH1 genes, a series of start sites located –50 –80 bp downstream of TATA is used in addition to the wild-type initiation sites located at around 100 bp from TATA (1). Here, the yeast SHI wildtype gene has been isolated by complementation and shown to be identical to RPB9, the gene encoding a small subunit of RNA polymerase II. A point mutation in the shi gene, changing a cysteine residue in a putative zinc ribbon motif into a phenylalanine residue, was demonstrated to permit the observed usage of upstream initiation sites. Deletion of the non-essential SHI gene also results in usage of upstream initiation sites and causes conditional growth defects.


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