Brassica orthologs from BANYULS belong to a small multigene family, which is involved in procyanidin accumulation in the seed

被引:35
作者
Auger, Bathilde [1 ]
Baron, Cecile [1 ]
Lucas, Marie-Odile [1 ]
Vautrin, Sonia [2 ]
Berges, Helene [2 ]
Chalhoub, Boulos [3 ]
Fautrel, Alain [4 ]
Renard, Michel [1 ]
Nesi, Nathalie [1 ]
机构
[1] Univ Rennes 1, UMR Ameliorat Plantes & Biotechnol Vegetales 118, INRA, F-35653 Le Rheu, France
[2] INRA, Ctr Natl Ressources Genom Vegetale, F-31326 Castanet Tolosan, France
[3] Univ Evry, CNRS, INRA, UMR Unite Rech Genom Vegetale 1165, F-91057 Evry, France
[4] Univ Rennes 1, INSERM, IFR Biogenouest Plate Forme Histopathol 140, U620, F-35043 Rennes, France
关键词
Anthocyanidin reductase; BANYULS genes; Brassica; Flavonoid metabolism; Seed coat-specific promoter; ANTHOCYANIDIN REDUCTASE GENE; ARABIDOPSIS-THALIANA; PROANTHOCYANIDIN BIOSYNTHESIS; FLAVONOID BIOSYNTHESIS; NAPUS; COLOR; RAPESEED; MARKERS; IDENTIFICATION; PIGMENTATION;
D O I
10.1007/s00425-009-1017-0
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
As part of a research programme focused on flavonoid biosynthesis in the seed coat of Brassica napus L. (oilseed rape), orthologs of the BANYULS gene that encoded anthocyanidin reductase were cloned in B. napus as well as in the related species Brassica rapa and Brassica oleracea. B. napus genome contained four functional copies of BAN, two originating from each diploid progenitor. Amino acid sequences were highly conserved between the Brassicaceae including B. napus, B. rapa, B. oleracea as well as the model plant Arabidopsis thaliana. Along the 200 bp in 5' of the ATG codon, Bna.BAN promoters (ProBna.BAN) were conserved with AtANR promoter and contained putative cis-acting elements. In addition, transgenic Arabidopsis and oilseed rape plants carrying the first 230 bp of ProBna.BAN fused to the UidA reporter gene were generated. In the two Brassicaceae backgrounds, ProBna.BAN activity was restricted to the seed coat. In B. napus seed, ProBna.BAN was activated in procyanidin-accumulating cells, namely the innermost layer of the inner integument and the micropyle-chalaza area. At the transcriptional level, the four Bna.BAN genes were expressed in the seed. Laser microdissection assays of the seed integuments showed that Bna.BAN expression was restricted to the inner integument, which was consistent with the activation profile of ProBna.BAN. Finally, Bna.BAN genes were mapped onto oilseed rape genetic maps and potential co-localisations with seed colour quantitative trait loci are discussed.
引用
收藏
页码:1167 / 1183
页数:17
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