Somatic Embryogenesis and Agrobacterium-Mediated Gene Transfer Procedures in Chilean Temperate Japonica Rice Varieties for Precision Breeding

Author:

Barrera Marion12ORCID,Olmedo Blanca2ORCID,Zúñiga Carolina2,Cepeda Mario2ORCID,Olivares Felipe2ORCID,Vergara Ricardo2ORCID,Cordero-Lara Karla3,Prieto Humberto2ORCID

Affiliation:

1. Natural Sciences, Mathematics, and Environment Faculty, Metropolitan Technological University, Santiago 8330526, Chile

2. Biotechnology Laboratory, La Platina Research Station, INIA-Chile, Santiago 8831314, Chile

3. Rice Breeding Program, Quilamapu Research Station, INIA-Chile, Chillán 3780000, Chile

Abstract

Rice (Oryza sativa) varieties are generated through breeding programs focused on local requirements. In Chile, the southernmost rice producer, rice productivity relies on the use and generation of temperate japonica germplasms, which need to be adapted to the intensifying effects of climate change. Advanced biotechnological tools can contribute to these breeding programs; new technologies associated with precision breeding, including gene editing, rely on procedures such as regeneration and gene transfer. In this study, the local rice varieties Platino, Cuarzo, Esmeralda, and Zafiro were evaluated for somatic embryogenesis potential using a process that involved the combined use of auxins and cytokinins. An auxin-based (2,4-D) general medium (2N6) allowed for the induction of embryogenic masses in all the genotypes. After induction, masses required culturing either in N6R (kinetin; Platino) or N6RN (BAP, kinetin, IBA, and 2,4-D; Cuarzo, Esmeralda, and Zafiro) to yield whole plants using regeneration medium (N6F, no hormone). The sprouting rates indicated Platino as the most responsive genotype; for this reason, this variety was evaluated for gene transfer. Fifteen-day-old embryo masses were assayed for Agrobacterium-mediated transformation using the bacterial strain EHA105 harboring pFLC-Myb/HPT/GFP, a modified T-DNA vector harboring a geminivirus-derived replicon. The vector included the green fluorescent protein reporter gene, allowing for continuous traceability. Reporter mRNA was produced as early as 3 d after agroinfiltration, and stable expression of the protein was observed along the complete process. These achievements enable further biotechnological steps in these and other genotypes from our breeding program.

Funder

National Institute of Agriculture-Chile

Publisher

MDPI AG

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