Journal
BMC PLANT BIOLOGY
Volume 15, Issue -, Pages -Publisher
BIOMED CENTRAL LTD
DOI: 10.1186/s12870-015-0514-5
Keywords
Lycopene; Lycopene beta-cyclase; beta-carotene; Provitamin A; RNA interference; Wheat
Categories
Funding
- International S & T Cooperation Key Projects of MoST [2009DFB30340]
- National Genetically Modified New Varieties of Major Projects of China [2013ZX08002004-007, 2014ZX08010004]
- National Natural Science Foundation of China [31071403, 31371614]
- Research Fund for the Doctoral Program of Higher Education of China [2012014211075]
- Open Research Fund of State Key Laboratory of Hybrid Rice in Wuhan University [KF201302]
Ask authors/readers for more resources
Background: Lycopene beta-cyclase (LCYB) is a key enzyme catalyzing the biosynthesis of beta-carotene, the main source of provitamin A. However, there is no documented research about this key cyclase gene's function and relationship with beta-carotene content in wheat. Therefore, the objectives of this study were to clone TaLCYB and characterize its function and relationship with beta-carotene biosynthesis in wheat grains. We also aimed to obtain more information about the endogenous carotenoid biosynthetic pathway and thus provide experimental support for carotenoid metabolic engineering in wheat. Results: In the present study, a lycopene beta-cyclase gene, designated TaLCYB, was cloned from the hexaploid wheat cultivar Chinese Spring. The cyclization activity of the encoded protein was demonstrated by heterologous complementation analysis. The TaLCYB gene was expressed differentially in different tissues of wheat. Although TaLCYB had a higher expression level in the later stages of grain development, the beta-carotene content still showed a decreasing tendency. The expression of TaLCYB in leaves was dramatically induced by strong light and the beta-carotene content variation corresponded with changes of TaLCYB expression. A post-transcriptional gene silencing strategy was used to down-regulate the expression of TaLCYB in transgenic wheat, resulting in a decrease in the content of beta-carotene and lutein, accompanied by the accumulation of lycopene to partly compensate for the total carotenoid content. In addition, changes in TaLCYB expression also affected the expression of several endogenous carotenogenic genes to varying degrees. Conclusion: Our results suggest that TaLCYB is a genuine lycopene cyclase gene and plays a crucial role in beta-carotene biosynthesis in wheat. Our attempt to silence it not only contributes to elucidating the mechanism of carotenoid accumulation in wheat but may also help in breeding wheat varieties with high provitamin A content through RNA interference (RNAi) to block specific carotenogenic genes in the wheat endosperm.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available