Two differentially regulated Arabidopsis genes define a new branch of the DFR superfamily

被引:24
作者
Ostergaard, L
Lauvergeat, V
Næsted, H
Mattsson, O
Mundy, J
机构
[1] Univ Copenhagen, Dept Plant Physiol, Inst Mol Biol, DK-1353 Copenhagen K, Denmark
[2] UMR CNRS UPS 5546, F-31326 Castanet Tolosan, France
关键词
abscisic acid; Arabidopsis thaliana; AtCRL; DFR superfamily; differential regulation; vascular tissue;
D O I
10.1016/S0168-9452(00)00407-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Two tandem genes were identified on Arabidopsis chromosome II (AtCRL1 and AtCRL2) encoding proteins with homology to members of the dihydroflavunol-4-reductase (DFR) superfamily. The encoded CRL1 and CRL2 proteins share 87% mutual amino acid sequence identity whereas their promoter regions are highly divergent, suggesting differential regulation of the CRL genes, Phylogenetic analysis placed CRL1 and CRL2 in a separate branch of the DFR superfamily. Northern blotting showed strong AtCRL1 induction by abscisic acid (ABA), drought, and heat shock, and high expression level in seeds: thus resembling the expression pattern of late embryogenic abundant ABA-responsive genes. Differential expression of the two genes during plant development was confirmed in plants expressing transcriptional fusions between the two promoters and the Escherichia coli P-glucuronidase reporter gene. This showed that, whereas high expression of AtCRL1 in mature seeds declines during subsequent vegetative growth, transcriptional activity from the AtCRL2 promoter increases during vegetative growth. Expression of both genes is restricted to vascular tissue. Based upon their homology to proteins involved in lignin synthesis, we propose that ArCRL2 is involved in generating conducting tissue late in development, while AtCRL1 is involved in vascular tissue differentiation and/or synthesis in the germinating embryos. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:463 / 472
页数:10
相关论文
共 30 条
[1]   Role of Arabidopsis MYC and MYB homologs in drought- and abscisic acid-regulated gene expression [J].
Abe, H ;
YamaguchiShinozaki, K ;
Urao, T ;
Iwasaki, T ;
Hosokawa, D ;
Shinozaki, K .
PLANT CELL, 1997, 9 (10) :1859-1868
[2]   FLAVONOID SYNTHESIS IN PETUNIA-HYBRIDA - PARTIAL CHARACTERIZATION OF DIHYDROFLAVONOL-4-REDUCTASE GENES [J].
BELD, M ;
MARTIN, C ;
HUITS, H ;
STUITJE, AR ;
GERATS, AGM .
PLANT MOLECULAR BIOLOGY, 1989, 13 (05) :491-502
[3]   Strategies for engineering water-stress tolerance in plants [J].
Bohnert, HJ ;
Jensen, RG .
TRENDS IN BIOTECHNOLOGY, 1996, 14 (03) :89-97
[4]   Interactions among enzymes of the Arabidopsis flavonoid biosynthetic pathway [J].
Burbulis, IE ;
Winkel-Shirley, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (22) :12929-12934
[5]   GENETIC AND DEVELOPMENTAL CONTROL OF ANTHOCYANIN BIOSYNTHESIS [J].
DOONER, HK ;
ROBBINS, TP ;
JORGENSEN, RA .
ANNUAL REVIEW OF GENETICS, 1991, 25 :173-199
[6]  
Felsenstein J., 1989, CLADISTICS, V5, P164, DOI DOI 10.1111/J.1096-0031.1989.TB00562.X
[7]   PURIFICATION AND CHARACTERIZATION OF CINNAMOYL-COENZYME A-NADP OXIDOREDUCTASE IN EUCALYPTUS-GUNNII [J].
GOFFNER, D ;
CAMPBELL, MM ;
CAMPARGUE, C ;
CLASTRE, M ;
BORDERIES, G ;
BOUDET, A ;
BOUDET, AM .
PLANT PHYSIOLOGY, 1994, 106 (02) :625-632
[8]   A novel aromatic alcohol dehydrogenase in higher plants: molecular cloning and expression [J].
Goffner, D ;
Van Doorsselaere, J ;
Yahiaoui, N ;
Samaj, J ;
Grima-Pettenati, J ;
Boudet, AM .
PLANT MOLECULAR BIOLOGY, 1998, 36 (05) :755-765
[9]   CLONING OF CDNA CODING FOR DIHYDROFLAVONOL-4-REDUCTASE (DFR) AND CHARACTERIZATION OF DFR EXPRESSION IN THE COROLLAS OF GERBERA-HYBRIDA VAR REGINA (COMPOSITAE) [J].
HELARIUTTA, Y ;
ELOMAA, P ;
KOTILAINEN, M ;
SEPPANEN, P ;
TEERI, TH .
PLANT MOLECULAR BIOLOGY, 1993, 22 (02) :183-193
[10]   Genomic organization of the genes encoding dihydroflavonol 4-reductase for flower pigmentation in the Japanese and common morning glories [J].
Inagaki, Y ;
Johzuka-Hisatomi, Y ;
Mori, T ;
Takahashi, S ;
Hayakawa, Y ;
Peyachoknagul, S ;
Ozeki, Y ;
Iida, S .
GENE, 1999, 226 (02) :181-188