Nucleic Acids Research, Vol 27, Issue 5 1289-1295, Copyright © 1999 by Oxford University Press
K Duvel, CM Egli and GH Braus
The yeast TRP4 mRNA 3' end formation element is a bidirectional element
which functions in both orien-tations in an artificial in vivo test system.
In this study, the role of 3' end formation was analysed in the context of
the entire TRP4 gene. The 3' untranslated region (3'UTR) of TRP4 was
altered and changes were analysed for their influence on TRP4 gene
expression. The 3'UTR in reverse orientation was fully functional and did
not affect TRP4 gene expression. Exchanging the TRP4 3'UTR by the
bidirectional ARO4 or the unidirectional GCN4 3' end formation element
allowed efficient gene expression. Deletion of the entire TRP4 3'UTR
resulted in 70% reduction of TRP4 mRNA and 50% reduced specific Trp4 enzyme
activity in comparison to wild-type. A single point mutation within the
TRP4 3'UTR caused the same effect on gene expression. This point mutation
did not only affect the efficiency of 3' end formation, but also produced
new poly(A) sites which were situated upstream of the wild-type poly(A)
sites. Therefore this sequence motif in the TRP4 3'UTR acts simultaneously
as both an efficiency and positioning element.
ARTICLES
A single point mutation in the yeast TRP4 gene affects efficiency of mRNA 3' end processing and alters selection of the poly(A) site
Institute of Microbiology and Genetics, Georg-August-University, Grisebachstrasse 8, D-37077 Gottingen, Germany.
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