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THE PLANT CELL, Vol 1, Issue 10 969-976, Copyright © 1989 by American Society of Plant Biologists
Abscisic Acid-Responsive Sequences from the Em Gene of Wheat
W. R. Marcotte Jr, S. H. Russell and R. S. Quatrano
Molecular Biology, Central Research and Development, Experimental Station, E.I. du Pont de Nemours and Co., Inc., Wilmington, Delaware 19880-0402
We demonstrate that a chimeric gene containing the [beta]-glucuronidase
(GUS) reporter gene linked to a 646-base pair 5[prime] fragment (-554 to
+92) from the abscisic acid (ABA)-regulated Em gene from wheat is correctly
expressed in transgenic tobacco. We observe high activity only in embryos
of mature seeds, and immature seeds cultured on ABA show enhanced
expression. Using a rice transient assay, we identify a 260-base pair
fragment (-168 to +92) that accounts for the ABA-specific 15-fold to
20-fold increase in GUS expression. A 50-base pair sequence (-152 to -103)
fused 5[prime] in either orientation to a truncated cauliflower mosaic
virus promoter (35S) increases GUS activity threefold in the presence of
ABA. Insertion of the Em 5[prime]-untranslated region (+6 to +86) between
the 35S promoter and the ATG of GUS results in a 10-fold increase in GUS
activity in the absence of ABA. These results suggest the following two
functional fragments of the Em 5[prime] region: an ABA response element
from -152 to -103 and an element between +6 and +86 that quantitatively
increases the ABA response.
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