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A Chemical-Induced, Seed-Soaking Activation Procedure for Regulated Gene Expression in Rice

Inducible gene expression has emerged as a powerful tool for plant functional genomics. The estrogen receptor-based, chemical-inducible system XVE has been used in many plant species, but the limited systemic movement of inducer β-estradiol in transgenic rice plants has prohibited a wide use of the...

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Detalles Bibliográficos
Autores principales: Chen, Zaijie, Cheng, Qianqian, Hu, Chanquan, Guo, Xinrui, Chen, Ziqiang, Lin, Yan, Hu, Taijiao, Bellizzi, Maria, Lu, Guodong, Wang, Guo-Liang, Wang, Zonghua, Chen, Songbiao, Wang, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566991/
https://www.ncbi.nlm.nih.gov/pubmed/28871269
http://dx.doi.org/10.3389/fpls.2017.01447
Descripción
Sumario:Inducible gene expression has emerged as a powerful tool for plant functional genomics. The estrogen receptor-based, chemical-inducible system XVE has been used in many plant species, but the limited systemic movement of inducer β-estradiol in transgenic rice plants has prohibited a wide use of the XVE system in this important food crop. Here, we constructed an improved chemical-regulated, site-specific recombination system by employing the XVE transactivator in combination with a Cre/loxP-FRT system, and optimized a seed-soaking procedure for XVE induction in rice. By using a gus gene and an hpRNAi cassette targeted for OsPDS as reporters, we demonstrated that soaking transgenic seeds with estradiol solution could induce highly efficient site-specific recombination in germinating embryos, resulting in constitutive and high-level expression of target gene or RNAi cassette in intact rice plants from induced seeds. The strategy reported here thereby provides a useful gene activation approach for effectively regulating gene expression in rice.