Morita Yasumasa, Hoshino Atsushi, Kikuchi Yasumasa, Okuhara Hiroaki, Ono Eiichiro, Tanaka Yoshikazu, Fukui Yuko, Saito Norio, Nitasaka Eiji, Noguchi Hiroshi, Iida Shigeru
National Institute for Basic Biology, Okazaki 444-8585, Japan.
Plant J. 2005 May;42(3):353-63. doi: 10.1111/j.1365-313X.2005.02383.x.
Bright blue or red flowers in the Japanese morning glory (Ipomoea nil) contain anthocyanidin 3-O-sophoroside derivatives, whereas the reddish-brown or purplish-gray petals in its dusky mutants accumulate anthocyanidin 3-O-glucoside derivatives. The Dusky gene was found to encode a novel glucosyltransferase, UDP-glucose:anthocyanidin 3-O-glucoside-2''-O-glucosyltransferase (3GGT), which mediates the glucosylation of anthocyanidin 3-O-glucosides to yield anthocyanidin 3-O-sophorosides. Ipomoea nil carries one copy of the 3GGT gene that contains no intron and produces 1.6-kbp transcripts mainly in the petals and tubes of flower buds at around 24 h before flower opening. The gene products of both In3GGT in I. nil and Ip3GGT in the common morning glory (Ipomoea purpurea) comprise 459 amino acids and showed a close relationship to the petunia UDP-rhamnose:anthocyanidin 3-O-glucoside-6''-O-rhamnosyltransferase (3RT), which controls the addition of a rhamnose molecule to anthocyanidin 3-O-glucosides for conversion into anthocyanidin 3-O-rutinosides. All of the 30 dusky mutants tested were found to carry the 4-bp insertion mutations GGAT or CGAT at an identical position near the 3' end of the gene, and the insertions caused frameshift mutations. The expected 3GGT enzymatic activities were found in the crude extracts of Escherichia coli, in which the 3GGT cDNA of I. nil or I. purpurea was expressed, while no such activity was detected in the extracts expressed with the dusky mutant cDNAs containing 4-bp insertions. Moreover, the introduced Ip3GGT cDNA efficiently produced 3GGT that converted cyanidin 3-O-glucoside into cyanidin 3-O-sophoroside in transgenic petunia plants.
日本牵牛(裂叶牵牛)的亮蓝色或红色花朵含有花青素3 - O - 槐糖苷衍生物,而其暗色突变体中红棕色或紫灰色花瓣则积累花青素3 - O - 葡萄糖苷衍生物。已发现暗色基因编码一种新型糖基转移酶,即尿苷二磷酸葡萄糖:花青素3 - O - 葡萄糖苷 - 2'' - O - 葡萄糖基转移酶(3GGT),它介导花青素3 - O - 葡萄糖苷的糖基化反应以生成花青素3 - O - 槐糖苷。裂叶牵牛携带一个3GGT基因拷贝,该基因不含内含子,主要在开花前约24小时的花芽花瓣和花管中产生1.6千碱基的转录本。裂叶牵牛中的In3GGT和圆叶牵牛(矮牵牛)中的Ip3GGT的基因产物均由459个氨基酸组成,并且与矮牵牛尿苷二磷酸鼠李糖:花青素3 - O - 葡萄糖苷 - 6'' - O - 鼠李糖基转移酶(3RT)关系密切,后者控制将一个鼠李糖分子添加到花青素3 - O - 葡萄糖苷上以转化为花青素3 - O - 芸香糖苷。在所测试的30个暗色突变体中,均发现在该基因3'端附近的同一位置携带4碱基插入突变GGAT或CGAT,这些插入导致了移码突变。在表达裂叶牵牛或圆叶牵牛3GGT cDNA的大肠杆菌粗提物中发现了预期的3GGT酶活性,而在用含有4碱基插入的暗色突变体cDNA表达的提取物中未检测到这种活性。此外,导入的Ip3GGT cDNA在转基因矮牵牛植株中高效产生了将花青素3 - O - 葡萄糖苷转化为花青素3 - O - 槐糖苷的3GGT。