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Volume 272, Number 52, Issue of December 26, 1997
pp. 33319-33326
(Received for publication, April 7, 1997, and in revised form, September 10, 1997)
From the Laboratoire de Biochimie et Physiologie Moléculaire
des Plantes, CNRS (Unité de Recherche 2133), Institut National de
la Recherche Agronomique et École Nationale Supérieure
d'Agronomie, F-34060 Montpellier cédex 1, France
Two pathways have been implicated in the
regulation of maize ferritin synthesis in response to iron. One of them
involves the plant hormone abscisic acid (ABA) and controls the
expression of ZmFer2 gene(s). Another pathway,
ABA-independent, has been characterized in a de-rooted maize plantlet
system and involves an oxidative step. The ZmFer1 maize
ferritin gene is not regulated by ABA, and it is shown in this paper
that the corresponding mRNA accumulates in de-rooted maize
plantlets and BMS (Black Mexican Sweet) maize cell suspension cultures
in response to iron via the oxidative pathway described previously. To
investigate ZmFer1 gene regulation further, the BMS cell
system has been used to develop a transient expression assay using a
ZmFer1-
Inhibition of the Iron-induced ZmFer1 Maize
Ferritin Gene Expression by Antioxidants and Serine/Threonine
Phosphatase Inhibitors
-glucuronidase fusion. Both iron induction and
antioxidant inhibition of ZmFer1 gene expression were
observed in this system. Using Northern blot analysis and transient
expression experiments, it was shown that both okadaic acid and
calyculin A, two serine/ threonine phosphatase inhibitors,
specifically inhibit ZmFer1 gene expression. These data
indicate that an okadaic acid-sensitive protein phosphatase activity is
involved in the regulation of the ZmFer1 ferritin gene in
maize cells, and this activity is required for iron-induced expression
of this gene.
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