Location: Sunflower and Plant Biology Research2013 Annual Report
1a. Objectives (from AD-416):
The objective of the project is to develop an efficient protocol for doubled haploid production in sunflower that can be adopted by seed companies with modest laboratory facilities and personnel with some training in tissue culture techniques.
1b. Approach (from AD-416):
Two approaches will be undertaken simultaneously by the postdoctoral affiliate, both approaches having precedents in other crops. (1) Anther culture: C. C. Jan initiated work on anther culture in the 1980s, but put it aside when other projects became higher priority. Dr. Jan envisions that the postdoctoral affiliate would develop a protocol for extraction of anthers from sunflower florets at an optimum stage of development and determining optimum tissue culture media and environmental conditions for induction of embryos, germination to plantlets, chromosome doubling, confirmation of haploid production, and growth to a mature, homozygous plant. (2) Foreign pollen: Under the direction Lili Qi and Brent Hulke, the postdoctoral affiliate will explore the potential for sunflower haploid production by fertilization of sunflower ovules with foreign pollen (as is done with wheat by fertilization by corn pollen, in which the ovule is fertilized, but the corn chromosomes are eventually eliminated, leaving a haploid wheat embryo that can be doubled). The postdoctoral affiliate will identify potential sources of foreign pollen from the family Compositae, but outside of the genus Helianthus, and test them for their ability to induce haploid production in sunflower. Special attention will be given to foreign pollen sources that are easy to grow, maintain, and have prolific pollen production. Optimum tissue culture conditions for growth of fertilized embryos to mature plants will be determined.
3. Progress Report:
Eight inbred lines and 18 wild species were used as donor materials for an anther culture approach. Anthers with light yellow-white color were dissected and cultured on callus and embryoid inducing media, which have proven successful for inducting embryos. Various concentrations and combinations of cytokinin and auxin were tested for shoot regeneration, including BAP (0.5-1.0 mg/l), NAA (0-0.5 mg/l) and kinetin (0-0.5 mg/l). Additionally, activated charcoal was added to the medium for testing. The same inbred lines and wild species were also used for microspore culture. Immature buds or inflorescences were surface sterilized with bleach and rinsed with sterilized dH2O, and then a 0.3 M mannitol solution was used to release the microspores. The ground mannitol slurry was filtered in sequence through a size 60 steel mesh, 80 µm nylon filter, and 30 µm nylon filter, respectively. After centrifugation, the pellets were combined and re-suspended in a 0.3 M mannitol solution. A 1.0 M maltose solution was used for microspore isolation. The isolated microspores were then mixed with a liquid culture medium and kept in an incubator without light at 32 oC for 3 days and then move to another incubator without light at 24 oC for 4 to 6 weeks. Various basic media and plant growth regulators of different concentrations and combinations were evaluated. Embryo inducer, 2-HNA, (2-hydroxynicotinic acid) was also incorporated in the culture medium during the experiment. Meanwhile, 0.5 g/l activated charcoal was also added to the culture medium to examine its effect on microspore culture. As a result, MS medium with 0.5 mg/l 2, 4-D and 0.5 mg/l BAP and 0.5g/l activated charcoal worked better for line RHA274 than other medium and other plant materials. Some embryo-like structures were observed. The approach of irradiated pollen haploid induction was recently added to the project. The plan is to use nmsHA89, nmsP21, and cmsHA89 as female parents, and to use selected USDA maintainer and restorer lines as the pollinators.