Abstract
Formation of the shoot apical meristem (SAM) has been extensively investigated in zygotic embryos of flowering plants, where it follows a prolonged and dynamic developmental pattern underlined by precise temporal and spatial changes in gene expression. Studies conducted on the plant model system Arabidopsis have revealed that SAM formation is controlled by a genetic network and involves the participation of several regulatory genes expressed at different stages of development. As a general rule apical meristem development in vivo occurs very early; at the globular stage of development in flowering plants and in club-stage embryos of conifers. Once formed, meristems of zygotic embryos are stable structures that become reactivated at the onset of germination. Shoot apical meristem formation during in vitro embryogenesis is demarked by structural events similar to those described for zygotic embryos, although differences can be observed during the late phases of development, where cellular differentiation and formation of intercellular spaces disrupt the architecture of SAMs produced in culture. These events, which denote the “unstable” nature of SAMs of somatic embryos, often result in poor conversion frequency and reduced plant regeneration. By using Picea glauca (Moench) Voss (white spruce) somatic embryos and microspore-derived embryos of Brassica napus L. (canola) as model systems, this review provides methods for improving SAM formation through manipulations of the culture medium which alter the cellular redox status. Meristem marker genes from Arabidopsis, such as WUSCHEL (which is required for the acquisition of stem fate identity), represent a valuable tool for estimating the quality of SAM produced by microspore-derived embryos of canola. In spruce, the identification of two novel meristem marker genes, HBK1 and PgAGO, will allow similar studies in conifers.
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