Role of mRNA Secondary Structure in Translational Repression of the Maize Transcriptional ActivatorLc ,
- 1 March 2001
- journal article
- Published by Oxford University Press (OUP) in Plant Physiology
- Vol. 125 (3), 1380-1387
- https://doi.org/10.1104/pp.125.3.1380
Abstract
Lc, a member of the maize (Zea mays) R/B gene family, encodes a basic helix-loop-helix transcriptional activator of the anthocyanin biosynthetic pathway. It was previously shown that translation of the Lc mRNA is repressed by a 38-codon upstream open reading frame (uORF) in the 5' leader. In this study, we report that a potential hairpin structure near the 5'end of the Lc mRNA also represses downstream translation in the rabbit reticulocyte in vitro translation system and in transient transformation assays. Base pairing of the hairpin is important for repression because its destabilization increases translation of the uORF and the downstream ORF. However, translation of the uORF is not required for the hairpin-mediated repression. Instead, the uORF and the 5'-proximal hairpin mediate two independent levels of repression. Although the uORF represses downstream translation due to inefficient reinitiation of ribosomes that translate uORF, the hairpin inhibits ribosome loading at the 5' end of the mRNA.Keywords
This publication has 22 references indexed in Scilit:
- Inefficient Reinitiation Is Responsible for Upstream Open Reading Frame–Mediated Translational Repression of the Maize R GenePlant Cell, 1998
- Features in the 5′ non-coding sequences of rabbit α and β-globin mRNAs that affect translational efficiencyJournal of Molecular Biology, 1994
- Molecular homology among members of the R gene family in maizeThe Plant Journal, 1993
- [35] Transient expression analysis in plants using firefly luciferase reporter genePublished by Elsevier ,1992
- A Regulatory Gene as a Novel Visible Marker for Maize TransformationScience, 1990
- Lc, a member of the maize R gene family responsible for tissue-specific anthocyanin production, encodes a protein similar to transcriptional activators and contains the myc-homology region.Proceedings of the National Academy of Sciences, 1989
- Regulation of anthocyanin biosynthetic genes introduced into intact maize tissues by microprojectilesProceedings of the National Academy of Sciences, 1989
- Introns increase gene expression in cultured maize cells.Genes & Development, 1987
- A nonchromatographic assay for expression of the chloramphenicol acetyltransferase gene in eucaryotic cellsAnalytical Biochemistry, 1986
- Improved Estimation of Secondary Structure in Ribonucleic AcidsNature New Biology, 1973