First published online March 22, 2002; 10.1104/pp.010886
Plant Physiol, May 2002, Vol. 129, pp. 201-210
Gibberellin Produced in the Cotyledon Is Required for Cell
Division during Tissue Reunion in the Cortex of Cut Cucumber and Tomato
Hypocotyls1
Masashi
Asahina,
Hiroaki
Iwai,
Akira
Kikuchi,
Shinjiro
Yamaguchi,
Yuji
Kamiya,
Hiroshi
Kamada, and
Shinobu
Satoh*
Institute of Biological Sciences, University of Tsukuba, Tsukuba,
Ibaraki, 305-8572, Japan (M.A., H.I., A.K., H.K., S.S.); and Plant
Science Center, The Institute of Physical and Chemical Research
(RIKEN), Wako, Saitama, 351-0198, Japan (S.Y., Y.K.)
Cucumber (Cucumis sativus) hypocotyls were
cut to one-half of their diameter transversely, and morphological and
histochemical analyses of the process of tissue reunion in the cortex
were performed. Cell division in the cortex commenced 3 d after
cutting, and the cortex was nearly fully united within 7 d.
4',6-Diamidino-2-phenylindole staining and 5-bromo-2'-deoxyuridine
labeling experiments indicate that nDNA synthesis occurred during this
process. In addition, specific accumulation of pectic substances was
observed in the cell wall of attached cells in the reunion region of
the cortex. Cell division during tissue reunion was strongly inhibited
when the cotyledon was removed. This inhibition was reversed by
applying gibberellin (GA, 10 4 M
GA3) to the apical tip of the cotyledon-less plant.
Supporting this observation, cell division in the cortex was inhibited
by treatment of the cotyledon with 10 4 M
uniconazole-P (an inhibitor of GA biosynthesis), and this inhibition was also reversed by simultaneous application of GA. In contrast to the
essential role of cotyledon, normal tissue reunion in cut hypocotyls
was still observed when the shoot apex was removed. The requirement of
GA for tissue reunion in cut hypocotyls was also evident in the
GA-deficient gib-1 mutant of tomato (Lycopersicon esculentum). Our results suggest that GA, possibly produced in cotyledons, is essential for cell division in reuniting cortex of cut hypocotyls.
1
This work was supported in part by a
Grant-in-Aid for the "Research for the Future" Program from the
Japan Society for the Promotion of Science (no.
JSPS-RFTF97L00601).
*
Corresponding author; e-mail pdp{at}sakura.cc.tsukuba.ac.jp; fax
81-298-53-4579.
© 2002 American Society of Plant Physiologists
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