Haploid embryogenesis
A switch to haploid embryogenesis is controlled by the activity of histone deacetylases (HDACs). Blocking HDAC activity with HDAC inhibitors (HDACi), e.g., trichostatin A (TSA), in Brassica napus, B. rapa, Arabidopsis thaliana , and Capsicum annuum male gametophytes leads to a large increase in the proportion of cells that undergo embryogenic growth. In B. napus , treatment with one specific HDACi (SAHA) improves the conversion (i.e., germination) of these embryos into seedlings. Existing methods of culturing microspores of angiosperm plants following stress to produce haploid embryos, haploid plants, and double haploid plants can be improved by adding HDACi to the culture medium. Advantageously, species hitherto recalcitrant to haploid embryogenesis via microspore culture are rendered useful when using HDACi. Haploid and double haploid plants are of industrial application in the plant breeding programmes.
1. A method of producing a haploid plant embryo comprising culturing or growing haploid plant material in the presence of a histone deacetylase inhibitor (HDACi) chosen from phenylbutyric acid or a salt thereof, butyric acid or a salt thereof, and isobutyric acid or a salt thereof.
2. The method of claim 1 , wherein the HDACi is chosen from potassium butyrate, sodium butyrate, sodium n-butyrate, ammonium butyrate, and lithium butyrate.
3. The method of claim 1 , further comprising converting the haploid plant embryo into a seedling.
4. The method of claim 3 , further comprising growing the seedling into a haploid plant.
5. A method of producing a double haploid plant comprising
culturing or growing haploid plant material in the presence of a HDACi, stimulating or allowing a spontaneous chromosome doubling, and
growing the double haploid plant material into a seedling, plantlet, or plant,
wherein the HDACi is chosen from phenylbutyric acid or a salt thereof, butyric acid or a salt thereof, and isobutyric acid or a salt thereof.
6. The method of claim 5 , wherein the HDACi is a salt chosen from potassium butyrate, sodium butyrate, sodium n-butyrate, ammonium butyrate, and lithium butyrate.
7. The method of claim 5 , wherein the haploid plant material is cultured or grown in the presence of the HDACi for a period of time sufficient to allow a spontaneous chromosome doubling.
8. The method of claim 5 , wherein the haploid plant material is cultured or grown in the presence of the HDACi for a period of time sufficient to induce haploid embryo formation.
9. The method of claim 5 , wherein the haploid plant material is cultured or grown in the presence of the HDACi for between 1 hour and 20 hours.
10. The method of claim 9 , wherein the haploid plant material is cultured or grown in the presence of the HDACi for between 2 hours and 20 hours.
11. The method of claim 5 , wherein following exposure to the HDACi, the haploid plant material is transferred to a growth medium free of the HDACi.
12. The method of claim 5 , wherein the chromosome doubling is stimulated by exposing the haploid plant material to a chromosome doubling agent.
13. The method of claim 5 , wherein the haploid plant material is subjected to physical stress before culturing with the HDACi.
14. The method of claim 13 , wherein the physical stress is chosen from one or more of temperature, osmotic stress, and starvation.
15. The method of claim 5 , wherein the haploid plant material is an immature male gametophyte or a microspore.
16. The method of claim 5 , wherein the plant is a species or variety of Brassica or Capsicum.
17. The method of claim 5 , wherein compared to a haploid plant material cultured without the HDACi, the equivalent HDACi cultured plant material generates at least 10% more haploid embryos, haploid seedlings, or double haploid seedlings.