Translational efficiency of bovine pyruvate carboxylase 5′ untranslated region messenger ribonucleic acid variants1

• Published in: Journal of animal science Vol. 86; no. 12; pp. 3401 - 3408
• Main Authors: Hazelton, S. R., Koser, S. L., Bidwell, C. A., Donkin, S. S.
• Format: Journal Article
• Language: English
• Published: Champaign Oxford University Press 01-12-2008
• Subjects: Cattle; Liver; Ribonucleic acid; Ribozymes; RNA; Zoology
• ISSN: 0021-8812; 1525-3163
• DOI: 10.2527/jas.2007-0798

The bovine pyruvate carboxylase (PC) gene is expressed as 6 alternatively spliced variants that share a common open reading frame but that differ within their 5' untranslated regions (UTR). The PC 5' UTR variants (A through F) contain 6 combinations of 5 exons and are 68, 253, 363, 89, 226, 178 bp in length, respectively. The objective of this experiment was to determine whether or not the bovine PC mRNA variants exhibit different translational efficiencies. Each bovine PC 5' UTR variant was linked to the firefly luciferase coding region, and the resulting constructs were transcribed and translated in a rabbit reticulocyte lysate assay. All constructs resulted in synthesis of luciferase protein. The abundance of luciferase protein synthesized from the UTR of bovine PC 5' D was greater (P < 0.05) than synthesis from either PC 5' UTR C or E, and the abilities of UTR D, A, B, and F to drive protein translation were similar. The disproportionate contribution to protein synthesis of the PC 5' D UTR compared with UTR variant C or E indicates a complexity of control for PC enzyme synthesis in the bovine that is dependent on the profile of PC variants. These observations are consistent with differences in PC variant expression that have been observed in vivo and indicate that when PC mRNA is elevated, the pattern of variants directs an increase in PC activity through augmented PC enzyme synthesis. [PUBLICATION ABSTRACT]