Abstract
Glutelin is a major seed storage protein, accounting for 60-80 % of the total endosperm protein content in rice. To test whether we could augment the expression of an introduced recombinant protein in rice by suppressing the glutelin gene, we generated transgenic glutelin RNAi (glu RNAi) rice seeds. RNA gel blot analyses confirmed that the endogenous glutelin gene was severely suppressed in these transgenic rice lines. RT-PCR analysis further revealed that all the members of glutelin multigene family were downregulated. Transgenic glu RNAi rice seeds expressing a recombinant red fluorescent protein (RFP) showed stronger fluorescence than seeds transformed with the RFP gene only. Western blot analysis further revealed that the relative accumulation of RFP in glu RNAi seeds was twofold higher than that in the RFP-only transgenic seeds. These results suggest that RNAi targeting of an endogenous storage protein could be of great utility in obtaining higher transgene expression in genetically engineered rice and other plant lines.
| Original language | English |
|---|---|
| Pages (from-to) | 347-353 |
| Number of pages | 7 |
| Journal | Plant Biotechnology Reports |
| Volume | 6 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - Oct 2012 |
Bibliographical note
Funding Information:Acknowledgments We thank Dr. Tom Okita and Dr. Ju-Kon Kim for kindly providing the anti-AGPase antibody and pMJ202 vector, respectively. We also thank Dr. Tanaka-Katsube for technical assistance and helpful discussions. This work was supported by National Academy of Agricultural Science, Rural Development Administration (PJ006680 to Y.-M. Kim), Korea.
Keywords
- Glutelin
- RFP
- RNAi
- Rice
- Seed storage protein
- Transgenic crop
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