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Hormone regulation of development in plant cells
Authors:Terry L. Shininger
Affiliation:(1) Department of Biology, University of Utah, 84112 Salt Lake City, Utah
Abstract:Summary Hormonal stimulation of dedifferentiation and redifferentiation can be studied in explanted, cultured plant tissues. Some of the questions about development which one would like to answer with such a system revolve around the role of quiescence in the stabilization of the differentiated state, the role of replication in the stimulation of redifferentiation and the means by which cells are brought out of the quiescent state. Such a system also offers the potential for revealing the level(s) at which plant hormones operate in the stimulation of replication and differentiation since the responses to hormones can be achieved in vitro. The pea-root cortical parenchyma system has been utilized as a model system in the study of cytokinin plus auxin stimulation of redevelopment of mature, quiescent root cells. The first detected response of the root parenchyma to excision and culture with both of these hormones is an enhanced rate of RNA synthesis between 9 and 12 hr after the initiation of culture. DNA synthesis is stimulated 36 to 39 hr after RNA synthesis (after 48 hr in culture). During this 48-hr period various cytological changes have been observed which are compatible with renewed nucleic acid synthesis, but cytological changes have not been observed prior to the onset of hormone-stimulated RNA synthesis. The first mitoses and cytokineses occur after 60 and 72 hr, respectively. Terminally differentiated tracheary elements are first formed in these cultures after 120 to 168 hr when both the cytokinin and auxin are present at adequate levels. Studies employing inhibitors suggest that tracheary element differentiation is dependent upon the DNA replication that normally accompanies cell replication. Temperature probes of the period between the initiation of cultures and the appearance of the terminally differentiated tracheary elements have been initiated and, in conjunction with previous studies employing inhibitors and analogues, may allow one to distinguish between a variety of potential models of hormone-stimulated redifferentiation. Presented in the Opening Symposium on Nutritional Factors and Differentiation at the 28th Annual Meeting of the Tissue Culture Association, New Orleans, Louisiana, June 6–9, 1977. Supported in part by grants from the National Science Foundation (GB 36948) and the Public Health Service (RR 07092).
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