Kwiatkowska Dorota
Department of Biophysics and Cell Biology, University of Silesia, Jagiellońska 28, 40-032 Katowice, Poland.
J Exp Bot. 2008;59(2):187-201. doi: 10.1093/jxb/erm290. Epub 2008 Feb 5.
The shoot apical meristem generates stem, leaves, and lateral shoot meristems during the entire shoot ontogeny. Vegetative leaves are generated by the meristem in the vegetative developmental phase, while in the reproductive phase either bracts subtending lateral flower primordia (or paraclades), or perianth and strictly reproductive organs are formed. Meristem growth is fully characterized by the principal growth rates, directions, volumetric, and areal growth rates. Growth modelling or sequential in vivo methods of meristem observation complemented by growth quantification allow the above growth variables to be estimated. Indirectly, growth is assessed by cell division rates and other cell cycle parameters. Temporal and spatial changes of growth and geometry take place at the meristem during the transition from the vegetative to the reproductive phase. During the vegetative phase, meristem growth is generally indeterminate. In the reproductive phase it is almost always determinate, but the extent of determinacy depends on the inflorescence architecture. In the vegetative phase the central meristem zone is the slowest growing region. The transition from the vegetative to the reproductive phase is accompanied by an increase in mitotic activity in this zone. The more determinate is the meristem growth, the stronger is this mitotic activation. However, regardless of the extent of the activation, in angiosperms the tunica/corpus structure of the meristem is preserved and therefore the mitotic activity of germ line cells remains relatively low. In the case of the thoroughly studied model angiosperm plant Arabidopsis thaliana, it is important to recognize that the flower primordium develops in the axil of a rudimentary bract. Another important feature of growth of the inflorescence shoot apical meristem is the heterogeneity of the peripheral zone. Finally, the role of mechanical factors in growth and functioning of the meristem needs further investigation.
在整个地上部个体发育过程中,茎尖分生组织产生茎、叶和侧枝分生组织。营养叶由营养发育阶段的分生组织产生,而在生殖阶段,要么形成侧花原基(或侧枝)下方的苞片,要么形成花被和严格意义上的生殖器官。分生组织的生长完全由主要生长速率、方向、体积和面积生长速率来表征。生长建模或体内连续观察分生组织的方法,辅以生长定量分析,能够估算上述生长变量。间接而言,生长通过细胞分裂速率和其他细胞周期参数来评估。在从营养阶段向生殖阶段转变的过程中,分生组织的生长和几何形状会发生时空变化。在营养阶段,分生组织的生长通常是无限的。在生殖阶段,它几乎总是有限的,但有限的程度取决于花序结构。在营养阶段,中央分生组织区是生长最慢的区域。从营养阶段向生殖阶段的转变伴随着该区域有丝分裂活性的增加。分生组织生长的确定性越高,这种有丝分裂激活就越强。然而,无论激活程度如何,在被子植物中,分生组织的原套/原体结构得以保留,因此生殖细胞系的有丝分裂活性仍然相对较低。就经过充分研究的模式被子植物拟南芥而言,重要的是要认识到花原基在退化苞片的叶腋处发育。花序茎尖分生组织生长的另一个重要特征是外周区的异质性。最后,机械因素在分生组织生长和功能中的作用需要进一步研究。