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Antimitotic and hormone effects on green double haploid plant production through anther culture of Mediterranean japonica rice
Authors:Isidre Hooghvorst  " target="_blank">Eduardo Ramos-Fuentes  " target="_blank">Camilo López-Cristofannini  " target="_blank">Mirari Ortega  " target="_blank">Raimon Vidal  " target="_blank">Xavier Serrat  " target="_blank">Salvador Nogués
Institution:1.Departament de Biologia Evolutiva, Ecologia i Ciencies Ambientals, Secció de Fisiologia Vegetal,Universitat de Barcelona,Barcelona,Spain;2.Rocalba S.A.,Girona,Spain;3.Càmara Arrossera del Montsià i Secció de Crèdit SCCL,Amposta,Spain
Abstract:Rice double haploid (DH) plants are produced mainly through anther culture. In order to improve the anther culture protocol, microspores of two japonica rice genotypes (NRVC980385 and H28) were subjected to three growth regulator combinations and four colchicine treatments on induction medium. In addition, a post anther culture procedure using colchicine or oryzalin was tested to induce double haploid plantlets from haploid plantlets. A cold pre-treatment of microspores for 9 days at 10 °C increased callus induction 50-fold in the NRCV980385 genotype. For both genotypes, 2 mg L?1 2,4-D and 1 mg L?1 kinetin on colchicine-free induction medium gave the best culture responses. The culturability of both genotypes changed on colchicine-supplemented induction media. A high genotype dependency was recorded for callus induction, callus regenerating green plantlets and regeneration of green double haploid plantlets. Colchicine at 300 mg L?1 for 48 h enhanced callus induction 100-fold in H28. Colchicine-supplemented media clearly improved green double haploid plantlet regeneration. We showed that the post-anther culture treatment of haploid plantlets at 500 mg L?1 of colchicine permitted fertile double haploid plantlets to be generated. Finally, an enhanced medium-throughput flow cytometry protocol for rice was tested to analyse all the plantlets from anther and post anther culture.
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