AN ARABIDOPSIS MYB HOMOLOG IS INDUCED BY DEHYDRATION STRESS AND ITS GENE-PRODUCT BINDS TO THE CONSERVED MYB RECOGNITION SEQUENCE
Citation
T. Urao et al., AN ARABIDOPSIS MYB HOMOLOG IS INDUCED BY DEHYDRATION STRESS AND ITS GENE-PRODUCT BINDS TO THE CONSERVED MYB RECOGNITION SEQUENCE, The Plant cell, 5(11), 1993, pp. 1529-1539
Categorie Soggetti
Biology,"Plant Sciences
SICI code
1040-4651(1993)5:11<1529:AAMHII>2.0.ZU;2-K
Abstract
An Arabidopsis cDNA (Atmyb2) that contains a sequence that encodes a t
ranscription factor, which is a homolog of MYB, was cloned from a cDNA
library prepared from dehydrated Arabidopsis rosette plants. A gene (
Atmyb2) corresponding to the Atmyb2 cDNA was also cloned and its nucle
otide sequence was determined. RNA gel blot analysis showed that the A
tmyb2 mRNA was induced by dehydration and disappeared upon rehydration
. The Atmyb2 mRNA also accumulated upon salt stress and with the onset
of treatment with abscisic acid. A beta-glucuronidase reporter gene d
riven by the Atmyb2 promoter was induced by dehydration and salt stres
s in transgenic Arabidopsis plants. These observations indicate that A
tmyb2 is responsive to dehydration at the transcriptional level. The p
utative protein (ATMYB2) encoded by Atmyb2 has 274 amino acids, a mole
cular mass of 32 kD, and a putative DNA binding domain that shows cons
iderable homology to plant MYB-related proteins, such as maize C1. A f
usion protein that included ATMYB2 was expressed in Escherichia coli,
and it bound specifically to oligonucleotides that contained a consens
us MYB recognition sequence (TAACTG), such as is found in the simian v
irus 40 enhancer and the maize bronze-1 promoter. Binding was sequence
specific, as indicated by a gel mobility shift experiment. These resu
lts suggest that a MYB-related transcription factor is involved in the
regulation of genes that are responsive to water stress in Arabidopsi
s.