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J Biol Chem, Vol. 273, Issue 32, 20109-20113, August 7, 1998
From the Departments of The mammalian Kv1.4 voltage-gated
potassium channel mRNA contains an unusually long (1.2 kilobases)
5'-untranslated region (UTR) and includes 18 AUG codons upstream of the
authentic site of translation initiation. Computer-predicted secondary
structures of this region reveal complex stem-loop structures that
would serve as barriers to 5'
Translation Initiation of a Cardiac Voltage-gated Potassium
Channel by Internal Ribosome Entry
,
,
Physiology and Biophysics and
§ Microbiology and Molecular Genetics, College of Medicine,
University of California, Irvine, California 92697
3' ribosomal scanning. These features suggested that translation initiation in Kv1.4 might occur
by the mechanism of internal ribosome entry, a mode of initiation employed by a variety of RNA viruses but only a limited number of
vertebrate genes. To test this possibility we introduced the 5'-UTR of
mouse Kv1.4 mRNA into the intercistronic region of a bicistronic vector containing two tandem reporter genes,
chloramphenicol acetyltransferase and luciferase. The control construct
translated only the upstream chloramphenicol cistron in transiently
transfected mammalian cells. In contrast, the construct containing the
mKv1.4 UTR efficiently translated the luciferase cistron as
well, demonstrating the presence of an internal ribosome entry segment.
Progressive 5'
3' deletions localized the activity to a 3'-proximal
200-nucleotide fragment. Suppression of cap-dependent
translation by extracts from poliovirus-infected HeLa cells in an
in vitro translation assay eliminated translation of the
upstream cistron while allowing translation of the downstream cistron.
Our results indicate that the 5'-untranslated region of
mKv1.4 contains a functional internal ribosome entry
segment that may contribute to unusual and physiologically important
modes of translation regulation for this and other potassium channel
genes.
Copyright © 1998 by The American Society for Biochemistry and Molecular Biology, Inc.
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