TY - JOUR
T1 - Analysis of gene network regulating yeast multidrug resistance by artificial activation of transcription factors
T2 - Involvement of Pdr3 in salt tolerance
AU - Onda, Miyuki
AU - Ota, Kazuhisa
AU - Chiba, Tomoko
AU - Sakaki, Yoshiyuki
AU - Ito, Takashi
N1 - Funding Information:
We are grateful to S. Kuhara and K. Tashiro (Kyushu University) for their valuable advices on DNA microarray technology. We also thank S. Harashima (Osaka University) for CgHIS3 marker. This work was partly supported by research grants from Ministry of Education, Culture, Sports, Science and Technology, Japan.
PY - 2004/5/12
Y1 - 2004/5/12
N2 - We established a strategy to constitutively activate Zn2Cys 6-type protein by fusing its DNA-binding domain with the VP16 trans-activation domain. To explore gene network regulating yeast multidrug resistance, the strategy was applied to Pdr1, Pdr3 and Yrr1, known to regulate multidrug resistance, as well as three uncharacterized Yrr1-related transcription factors. DNA microarray analysis revealed that all of the six mutants induce typical drug transporter genes including SNQ2 and YOR1, suggesting redundancy in regulation. On the other hand, each displays a unique spectrum of targets, which is coincident with the phylogenetic tree of the transcription factors and presumably reflects their functional specification. Indeed, careful analysis of target genes specific to each transcription factor led us to reveal an unexpected role for Pdr3 in salt tolerance. The strategy would thus contribute not only to identify target genes but to reveal redundancy and specificity in complex gene regulatory networks.
AB - We established a strategy to constitutively activate Zn2Cys 6-type protein by fusing its DNA-binding domain with the VP16 trans-activation domain. To explore gene network regulating yeast multidrug resistance, the strategy was applied to Pdr1, Pdr3 and Yrr1, known to regulate multidrug resistance, as well as three uncharacterized Yrr1-related transcription factors. DNA microarray analysis revealed that all of the six mutants induce typical drug transporter genes including SNQ2 and YOR1, suggesting redundancy in regulation. On the other hand, each displays a unique spectrum of targets, which is coincident with the phylogenetic tree of the transcription factors and presumably reflects their functional specification. Indeed, careful analysis of target genes specific to each transcription factor led us to reveal an unexpected role for Pdr3 in salt tolerance. The strategy would thus contribute not only to identify target genes but to reveal redundancy and specificity in complex gene regulatory networks.
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U2 - 10.1016/j.gene.2004.02.003
DO - 10.1016/j.gene.2004.02.003
M3 - Article
C2 - 15145054
AN - SCOPUS:2442495304
SN - 0378-1119
VL - 332
SP - 51
EP - 59
JO - Gene
JF - Gene
IS - 1-2
ER -