Identification of a flavonol 7-O-rhamnosyltransferase gene determining flavonoid pattern in Arabidopsis by transcriptome coexpression analysis and reverse genetics

被引:218
作者
Yonekura-Sakakibara, Keiko
Tohge, Takayuki
Niida, Rie
Saito, Kazuki
机构
[1] RIKEN, Plant Sci Ctr, Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[2] Chiba Univ, Grad Sch Pharmaceut Sci, Inage Ku, Chiba 2638522, Japan
关键词
D O I
10.1074/jbc.M611498200
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
Glycosylation plays a major role in the remarkable chemical diversity of flavonoids in plants including Arabidopsis thaliana. The wide diversity encoded by the large family-1 glycosyltransferase ( UGT) gene family makes it difficult to determine the biochemical function of each gene solely from its primary sequence. Here we used transcriptome coexpression analysis combined with a reverse genetics approach to identify a gene that is prominent in determining the flavonoid composition of Arabidopsis. Using transcriptome coexpression analysis accessible on the ATTED-II public data base, the expression pattern of a UGT gene, UGT89C1, was found to be highly correlated with known flavonoid biosynthetic genes. No C-7 rhamnosylated flavonols were detected in either of two T-DNA ugt89c1 mutants. This specific metabolite deficiency in the mutants was complemented by stable transformation with the genomic fragment containing intact UGT89C1. Glutathione S-transferasefused recombinant UGT89C1 protein converted kaempferol 3-O-glucoside to kaempferol 3-O-glucoside-7-O-rhamnoside and recognized 3-O-glycosylated flavonols and UDP-rhamnose as substrates, but not flavonol aglycones, 3-O-glycosylated anthocyanins or other UDP-sugars. These results show that UGT89C1 is a flavonol 7-O-rhamnosyltransferase. The abundance of UGT89C1 transcripts in floral buds was consistent with the flavonoid accumulation of C-7 rhamnosylated flavonols in Arabidopsis organs. Our present study demonstrates that the integration of transcriptome coexpression analysis with a reverse genetic approach is a versatile tool for understanding a multigene family of a metabolic pathway in Arabidopsis.
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收藏
页码:14932 / 14941
页数:10
相关论文
共 47 条
  • [1] [Anonymous], 1989, Molecular Cloning
  • [2] THE SYNTHESIS AND CHARACTERIZATION OF URIDINE 5'-(BETA-L-RHAMNOPYRANOSYL DIPHOSPHATE) AND ITS ROLE IN THE ENZYMATIC-SYNTHESIS OF RUTIN
    BARBER, GA
    BEHRMAN, EJ
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1991, 288 (01) : 239 - 242
  • [3] A gene expression map of the Arabidopsis root
    Birnbaum, K
    Shasha, DE
    Wang, JY
    Jung, JW
    Lambert, GM
    Galbraith, DW
    Benfey, PN
    [J]. SCIENCE, 2003, 302 (5652) : 1956 - 1960
  • [4] Bowles D, 2002, BIOCHEM SOC T, V30, P301, DOI 10.1042/BST0300301
  • [5] Glycosyltransferases of lipophilic small molecules
    Bowles, Dianna
    Lim, Eng-Kiat
    Poppenberger, Brigitte
    Vaistij, Fabian E.
    [J]. ANNUAL REVIEW OF PLANT BIOLOGY, 2006, 57 : 567 - 597
  • [6] ISOLATION AND CHARACTERIZATION OF A CDNA CLONE CORRESPONDING TO THE RT LOCUS OF PETUNIA-HYBRIDA
    BRUGLIERA, F
    HOLTON, TA
    STEVENSON, TW
    FARCY, E
    LU, CY
    CORNISH, EC
    [J]. PLANT JOURNAL, 1994, 5 (01) : 81 - 92
  • [7] Floral dip:: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana
    Clough, SJ
    Bent, AF
    [J]. PLANT JOURNAL, 1998, 16 (06) : 735 - 743
  • [8] NASCArrays: a repository for microarray data generated by NASC's transcriptomics service
    Craigon, DJ
    James, N
    Okyere, J
    Higgins, J
    Jotham, J
    May, S
    [J]. NUCLEIC ACIDS RESEARCH, 2004, 32 : D575 - D577
  • [9] The secondary metabolism of Arabidopsis thaliana:: growing like a weed
    D'Auria, JC
    Gershenzon, J
    [J]. CURRENT OPINION IN PLANT BIOLOGY, 2005, 8 (03) : 308 - 316
  • [10] Davies K. M., 2006, Flavonoids: chemistry, biochemistry and applications, P143