A Proinsulin Gene Splice Variant with Increased Translation Efficiency Is Expressed in Human Pancreatic Islets

As glucose-induced insulin expression is mainly regulated at the translational level, and such regulation often involves the 5′-untranslated region (5′UTR), we examined the human proinsulin gene 5′UTR. RT-PCR and sequencing demonstrated that a proinsulin splice variant (SPV) generated from a cryptic...

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Bibliographic Details
Published in:Endocrinology (Philadelphia) 2002-07, Vol.143 (7), p.2541-2547
Main Authors: Shalev, Anath, Blair, Patrick J, Hoffmann, Steven C, Hirshberg, Boaz, Peculis, Brenda A, Harlan, David M
Format: Article
Language:English
Subjects:
5' Untranslated Regions
Alternative splicing
Efficiency
Gene expression
Glucose
In vivo methods and tests
Insulin
mRNA
Pancreas
Polymerase chain reaction
Preproinsulin
Protein folding
Real time
Reporter gene
rRNA
Transfection
Translation
Wheat germ
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Summary:As glucose-induced insulin expression is mainly regulated at the translational level, and such regulation often involves the 5′-untranslated region (5′UTR), we examined the human proinsulin gene 5′UTR. RT-PCR and sequencing demonstrated that a proinsulin splice variant (SPV) generated from a cryptic 5′-splice site and retaining the first 26 bp of intron 1 was present in human pancreatic islets from normal donors. The expression of this SPV was metabolically regulated, as shown by quantitative real-time RT-PCR, revealing a more than 10-fold increase in the SPV in isolated human islets incubated at 16.7 mm compared with 1.67 mm glucose. In vitro wheat-germ translation and in vivom transfection studies demonstrated that the altered 5′UTR of the SPV increased translation. The SPV yielded 4-fold more in vitro translated preproinsulin protein than the native proinsulin mRNA, and the SPV 5′UTR inserted upstream from a luciferase reporter gene resulted in a more than 6-fold higher luciferase activity, suggesting enhanced translation in vivo. Retention of the 26 bp changed the proposed secondary RNA structure of the SPV, which may facilitate ribosomal binding and explain the increase in translation efficiency. These results suggest a novel mechanism by which metabolic changes can modulate the expression of 5′UTR SPVs and thereby regulate translation efficiency.
ISSN:0013-7227
1945-7170
DOI:10.1210/endo.143.7.8920