| Literature DB >> 34270033 |
Ana María Castillo1, Isabel Valero-Rubira2, Sandra Allué2, María Asunción Costar2, María Pilar Vallés2.
Abstract
The use of doubled haploid (DH) plants in plant breeding programmes is the fastest route to release new varieties (4-6 years), allowing for a rapid response to end-user needs. Microspore embryogenesis is one of the most efficient methods for DH plant production in bread wheat. In this process, microspores triggered by a stress treatment or by application of bioactive compounds are reprogrammed to follow an embryogenic pathway that leads to the production of haploid or DH plants. In this chapter, we describe a protocol for anther culture of bread wheat. This protocol is based on an osmotic and starvation treatment of the anthers followed by the application of a microtubule disrupting agent. Anthers are cultured in an ovary pre-conditioned medium with mature ovaries from cv. Caramba. This protocol has been applied to a wide range of genotypes and F1s from bread and spelt wheat.Entities:
Keywords: Anther culture; Bread wheat; Colchicine; Doubled haploid; Microspore embryogenesis
Year: 2021 PMID: 34270033 DOI: 10.1007/978-1-0716-1315-3_11
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745