Monitoring individual development of isolated wheat zygotes: a novel approach to study early embryogenesis

Summary

A culture method has been established by which development of isolated wheat (Triticum aestivum L.) zygotes can be monitored individually until formation of multicellular structures. As was shown recently, these isolated zygotes have a high capacity to form differentiated embryos and normal plants, and thus constitute a suitable object to study early embryogenesis. After being isolated within 6 h after pollination (hap), zygotes were immobilized in an agarose droplet directly on a microscopic chamber slide, which allows for both subsequent development through co-culture with feeder aggregates, as well as detailed observation and photographic documentation of individiual behavior. Shortly after fertilization, the wheat zygote, like the unfertilized egg cell, is characterized by one conspicuous nucleolus. Typically, a second and a third nucleolus appeared between 5 and 8.5 hap. Between 7 and 15 hap, we observed nucleolar vacuolation indicating enhanced ribosomal activity. Continuous cell expansion with slight cell elongation was detected until around 15 hap, followed by a period of transitory reduction in cell volume which roughly corresponded with mitosis. Mitotic prophase of a zygote could easily be detected by the disappearance of all nucleoli within a few minutes. The division plane was generally established perpendicular to the formerly established cell elongation axis. At cytokinesis, which was completed by 19 hap in 90% of the individuals observed, 2 or 3 nucleoli were detected again per daughter cell. The first cell division, including the establishment of a cleavage furrow with intercellular spaces, was completed in all cases within 23 hap. Since this result is in accordance with what is known from earlier studies based upon fixed material, and since the zygotes subsequently continue embryogenesis, in vitro development is assumed to be analogous to that in planta. This experimental system constitutes a valuable experimental tool for further detailed research, both at the cellular and at the molecular level.