Abstract
In higher plants, cytokinesis is achieved by cell plate formation, which is responsible for the assembly of the new plasma membrane and new wall matrix. In somatic cell types, this process initiates with the generation of an immature cell plate between separating groups of anaphase chromosomes, and proceeds by centrifugal growth of the cell plate. This cytokinetic process contrasts with those in animal, fungal, and most alga cells, where cleavage of parental cytoplasm starts from the cell cortex with inward furrowing of the plasma membrane (Pickett-Heaps 1975; Gunning 1982; Glotzer 2001; Guertin et al. 2002). The outward cleavage characterizing higher plant cytokinesis ensures partitioning of daughter nuclei irrespective of parental cell volume and selected division plane, and thus is thought to contribute to the ability of higher plants to flexibly set the plane of cell division, and thereby generate variable cell arrangements. Much information about the structure and function of the apparatus responsible for this higher plant-specific cytokinesis, namely the phragmoplast, has been accumulated through studies using stamen hair cells of Tradescantia and endosperm cells of Haemanthus (Gunning 1982; Bajer et al. 1987).
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Asada, T., Yasuhara, H. (2004). Cell Plate Formation: Knowledge from Studies Using Tobacco BY-2 Cells. In: Nagata, T., Hasezawa, S., Inzé, D. (eds) Tobacco BY-2 Cells. Biotechnology in Agriculture and Forestry, vol 53. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-10572-6_9
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DOI: https://doi.org/10.1007/978-3-662-10572-6_9
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