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The Involvement of Hydrogen Peroxide in the Differentiation of
Secondary Walls in Cotton Fibers1
Tamara S. Potikha,
Cheryl C. Collins,
Douglas I. Johnson,
Deborah
P. Delmer, and
Alex Levine*
Department of Plant Sciences, Hebrew University of Jerusalem,
Jerusalem, Givat-Ram 91904, Israel (T.S.P., A.L.); Department of
Microbiology and Molecular Genetics, University of Vermont, 202 Stafford Hall, Burlington, Vermont 05405 (C.C.C., D.I.J.); and Section
of Plant Biology, University of California, One Shields Avenue, Davis,
California 95616-8537 (D.P.D.)
H2O2 is a
widespread molecule in many biological systems. It is created
enzymatically in living cells during various oxidation reactions and by
leakage of electrons from the electron transport chains. Depending on
the concentration H2O2 can induce cell
protective responses, programmed cell death, or necrosis. Here we
provide evidence that H2O2 may function as a
developmental signal in the differentiation of secondary walls in
cotton (Gossypium hirsutum) fibers. Three lines of
evidence support this conclusion: (a) the period of
H2O2 generation coincided with the onset of
secondary wall deposition, (b) inhibition of
H2O2 production or scavenging the available
H2O2 from the system prevented the wall
differentiation process, and (c) exogenous addition of
H2O2 prematurely promoted secondary wall
formation in young fibers. Furthermore, we provide support for the
concept that H2O2 generation could be mediated by the expression of the small GTPase Rac, the accumulation of which
was shown previously to be strongly induced during the onset of
secondary wall differentiation. In support of Rac's role in the
activation of NADPH oxidase and the generation of reactive oxygen
species, we transformed soybean (Glycine max) and
Arabidopsis cells with mutated Rac genes. Transformation with a
dominantly activated cotton Rac13 gene resulted in
constitutively higher levels of H2O2, whereas
transformation with the antisense and especially with dominant-negative
Rac constructs decreased the levels of H2O2.
1
This work was supported by grants from the
U.S.-Israel Binational Agricultural Research and Development Fund and
the Israel Academy of Sciences and by a fellowship to T.S.P. from the
Giladi Foundation.
*
Corresponding author; e-mail alexl{at}leonardo.ls.huji.ac.il; fax
972-2-658-4425.
Plant Physiol. (1999) 119: 849-858
Copyright Clearance Center: 0032-0889/99/119//10
© 1999 American Society of Plant Physiologists
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