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Differences in cytokinin control on cellular dynamics of zucchini cotyledons cultivated in two experimental systems
Author(s) -
StoynovaBakalova E.,
Petrov P.,
Gigova L.,
Ivanova N.
Publication year - 2011
Publication title -
plant biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.871
H-Index - 87
eISSN - 1438-8677
pISSN - 1435-8603
DOI - 10.1111/j.1438-8677.2009.00315.x
Subject(s) - cotyledon , cytokinin , biology , palisade cell , cell division , mitosis , botany , germination , microbiology and biotechnology , cell , auxin , biochemistry , gene
The effect of endogenous cytokinins on the pattern of palisade cell division post‐germination does not depend on the conditions of cotyledon development – in planta (attached to seedlings) or in vitro (isolated from dry zucchini seeds and cultured on water). In cotyledons originating from 4‐day‐old seedlings (experimental system 1), exogenous cytokinin temporarily (in the first 2 day of cultivation) enhanced post‐mitotic cell enlargement of palisade cells, mainly due to enhanced water uptake and use of cell storage compounds, all of which lead to cotyledon senescence. Cytokinin is not able to resume the completed palisade cell division on day 5. As a result, the number of cells and the final areas of treated and control cotyledons are quite similar. By contrast, the effects of cytokinin on cotyledons isolated from dry seeds (experimental system 2) are better expressed, promoting an increase in number of palisade cells accompanied by additional cotyledon area enlargement. However, the prolonged post‐mitotic cell expansion in control cotyledons compensates for the reduced speed of cell growth and division activity and decreases differences in final cotyledon area between treatments. The results define cell division as the primary target of cytokinin stimulation in cotyledon tissues competent for division, and determine the temporal patterns of palisade cell cycling related to cotyledon age. This knowledge permits a better choice of experimental system to study effects on cell proliferation and cell growth, as well as cell enlargement and senescence‐related events using physiologically homogeneous material.