Mittasch Juliane, Strack Dieter, Milkowski Carsten
Department of Secondary Metabolism, Leibniz Institute of Plant Biochemistry, Weinberg 3, 06120, Halle (Saale), Germany.
Planta. 2007 Jan;225(2):515-22. doi: 10.1007/s00425-006-0360-7. Epub 2006 Aug 15.
This study describes a systematic screen for secondary product UDP-glycosyltransferases (UGTs; EC 2.4.1) involved in seed development of oilseed rape (Brassica napus) and was aimed at identifying genes related to UGT84A9 encoding UDP-glucose:sinapate glucosyltransferase (EC 2.4.1.120), a proven target for molecular breeding approaches to reduce the content of anti-nutritive sinapate esters. By RT-PCR with primers recognizing the conserved signature motif of UGTs, 13 distinct ESTs could be generated from seed RNA. Sequence analysis allowed to assign the isolated ESTs to groups B, D, E, and L of the UGT family. In an alternative approach, two open reading frames related to UGT84A9 were cloned from the B. napus genome and designated as UGT84A10 and UGT84A11, respectively. Functional expression of UGT84A10 revealed that the encoded enzyme catalyzes the formation of 1-O-acylglucosides (beta-acetal esters) with several hydroxycinnamates whereas, in our hands, the recombinant UGT84A11 did not display this enzymatic activity. Semi-quantitative RT-PCR confirmed that the majority of potential UGTs specified by the isolated ESTs is differentially expressed. A pronounced transcriptional up-regulation during seed development was evident for UGT84A9 and one EST (BnGT3) clustering in group E of UGTs. UGT84A10 was highly induced in flowers and expressed to a moderate level in late seed maturation indicating a possible involvement in seed-specific sinapate ester biosynthesis.
本研究描述了对参与油菜籽(甘蓝型油菜)种子发育的次生产物UDP-糖基转移酶(UGTs;EC 2.4.1)进行的系统筛选,旨在鉴定与UGT84A9相关的基因,UGT84A9编码UDP-葡萄糖:芥子酸葡萄糖基转移酶(EC 2.4.1.120),这是分子育种方法中降低抗营养性芥子酸酯含量的一个已证实的靶点。通过使用识别UGTs保守特征基序的引物进行RT-PCR,可从种子RNA中产生13个不同的EST。序列分析允许将分离的EST分配到UGT家族的B、D、E和L组。在另一种方法中,从甘蓝型油菜基因组中克隆了两个与UGT84A9相关的开放阅读框,分别命名为UGT84A10和UGT84A11。UGT84A10的功能表达表明,编码的酶催化与几种羟基肉桂酸形成1-O-酰基葡萄糖苷(β-缩醛酯),而在我们的实验中,重组UGT84A11没有显示出这种酶活性。半定量RT-PCR证实,由分离的EST指定的大多数潜在UGTs存在差异表达。UGT84A9和一个聚类在UGTs E组的EST(BnGT3)在种子发育过程中明显转录上调。UGT84A10在花中高度诱导,并在种子成熟后期中等水平表达,表明其可能参与种子特异性芥子酸酯的生物合成。