Sad3 and Sad4 are required for saponin biosynthesis and root development in oat

被引:108
作者
Mylona, Panagiota [1 ]
Owatworakit, Amorn [1 ]
Papadopoulou, Kalliopi [1 ]
Jenner, Helen [1 ]
Qin, Bo [1 ]
Findlay, Kim [1 ]
Hill, Lionel [1 ]
Qi, Xiaoquan [1 ]
Bakht, Saleha [1 ]
Melton, Rachel [1 ]
Osbourn, Anne [1 ]
机构
[1] John Innes Ctr Plant Sci Res, Norwich NR4 7UH, Norfolk, England
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1105/tpc.107.056531
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
Avenacins are antimicrobial triterpene glycosides that are produced by oat (Avena) roots. These compounds confer broad-spectrum resistance to soil pathogens. Avenacin A-1, the major avenacin produced by oats, is strongly UV fluorescent and accumulates in root epidermal cells. We previously defined nine loci required for avenacin synthesis, eight of which are clustered. Mutants affected at seven of these (including Saponin-deficient1 [Sad1], the gene for the first committed enzyme in the pathway) have normal root morphology but reduced root fluorescence. In this study, we focus on mutations at the other two loci, Sad3 (also within the gene cluster) and Sad4 (unlinked), which result in stunted root growth, membrane trafficking defects in the root epidermis, and root hair deficiency. While sad3 and sad4 mutants both accumulate the same intermediate, monodeglucosyl avenacin A-1, the effect on avenacin A-1 glucosylation in sad4 mutants is only partial. sad1/sad1 sad3/sad3 and sad1/sad1 sad4/sad4 double mutants have normal root morphology, implying that the accumulation of incompletely glucosylated avenacin A-1 disrupts membrane trafficking and causes degeneration of the epidermis, with consequential effects on root hair formation. Various lines of evidence indicate that these effects are dosage-dependent. The significance of these data for the evolution and maintenance of the avenacin gene cluster is discussed.
引用
收藏
页码:201 / 212
页数:12
相关论文
共 57 条
[1]   The role of root exudates in rhizosphere interations with plants and other organisms [J].
Bais, Harsh P. ;
Weir, Tiffany L. ;
Perry, Laura G. ;
Gilroy, Simon ;
Vivanco, Jorge M. .
ANNUAL REVIEW OF PLANT BIOLOGY, 2006, 57 :233-266
[2]   Alternate energy-dependent pathways for the vacuolar uptake of glucose and glutathione conjugates [J].
Bartholomew, DM ;
Van Dyk, DE ;
Lau, SMC ;
O'Keefe, DP ;
Rea, PA ;
Viitanen, PV .
PLANT PHYSIOLOGY, 2002, 130 (03) :1562-1572
[3]   The role of root exudates and allelochemicals in the rhizosphere [J].
Bertin, C ;
Yang, XH ;
Weston, LA .
PLANT AND SOIL, 2003, 256 (01) :67-83
[4]   A saponin-detoxifying enzyme mediates suppression of plant defences [J].
Bouarab, K ;
Melton, R ;
Peart, J ;
Baulcombe, D ;
Osbourn, A .
NATURE, 2002, 418 (6900) :889-892
[5]   Oxidative remodeling of chromoplast carotenoids:: Identification of the carotenoid dioxygenase CsCCD and CsZCD genes involved in crocus secondary metabolite biogenesis [J].
Bouvier, F ;
Suire, C ;
Mutterer, J ;
Camara, B .
PLANT CELL, 2003, 15 (01) :47-62
[6]   Glycosyltransferases: managers of small molecules [J].
Bowles, D ;
Isayenkova, J ;
Lim, EK ;
Poppenberger, B .
CURRENT OPINION IN PLANT BIOLOGY, 2005, 8 (03) :254-263
[7]   Glycosyltransferases of lipophilic small molecules [J].
Bowles, Dianna ;
Lim, Eng-Kiat ;
Poppenberger, Brigitte ;
Vaistij, Fabian E. .
ANNUAL REVIEW OF PLANT BIOLOGY, 2006, 57 :567-597
[8]   HOST-RANGE OF A PLANT-PATHOGENIC FUNGUS DETERMINED BY A SAPONIN DETOXIFYING ENZYME [J].
BOWYER, P ;
CLARKE, BR ;
LUNNESS, P ;
DANIELS, MJ ;
OSBOURN, AE .
SCIENCE, 1995, 267 (5196) :371-374
[9]  
Carter JP, 1999, APPL ENVIRON MICROB, V65, P3364
[10]   PATHOGENICITY OF TAKE-ALL FUNGUS TO OATS - ITS RELATIONSHIP TO THE CONCENTRATION AND DETOXIFICATION OF THE 4 AVENACINS [J].
CROMBIE, WML ;
CROMBIE, L ;
GREEN, JB ;
LUCAS, JA .
PHYTOCHEMISTRY, 1986, 25 (09) :2075-2083