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BHLH IRIDOID SYNTHESIS 3 is a member of a bHLH gene cluster regulating terpenoid indole alkaloid biosynthesis in Catharanthus roseus

机译:BHLH IRIDOID合成3是在Catharanthus Roseus中调节Terpenoid Indole生物合成的BHLH基因簇的成员

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Basic helix-loop-helix (bHLH) transcription factors (TFs) are key regulators of plant specialized metabolites, including terpenoid indole alkaloids (TIAs) in Catharanthus roseus. Two previously characterized subgroup-IVa bHLH TFs, BIS1 (bHLH Iridoid Synthesis 1) and BIS2 regulate iridoid biosynthesis in the TIA pathway. We reanalyzed the recently updated C. roseus genome sequence and discovered that BIS1 and BIS2 are clustered on the same genomic scaffold with a previously uncharacterized bHLH gene, designated as BIS3. Only a few bHLH gene clusters have been studied to date. Comparative analysis of 49 genome sequences from different plant lineages revealed the presence of analogous bHLH clusters in core angiosperms, including the medicinal plants Calotropis gigantea (giant milkweed) and Gelsemium sempervirens (yellow jessamine), but not in the analyzed basal angiosperm and lower plants. Similar to the iridoid pathway genes, BIS3 is highly expressed in roots and induced by methyl jasmonate. BIS3 activates the promoters of iridoid branch genes, geraniol synthase (GES), geraniol 10-hydroxylase (G10H), 8-hydroxygeraniol oxidoreductase (8HGO), iridoid synthase (IS), 7-deoxyloganetic acid glucosyl transferase (7-DLGT), and 7-deoxyloganic acid hydroxylase (7DLH), but not iridoid oxidase (IO). Transactivation of the promoters was abolished when BIS3 is converted to a dominant repressor by fusing with the ERF-associated amphiphilic repression (EAR) sequence. In addition, BIS3 acts synergistically with BIS1 and BIS2 to activate the G10H promoter in tobacco cells. Mutation of the known bHLH TF binding motif, G-box (CACGTG) in the G10H promoter significantly reduced but did not abolish the transactivation by BIS3. Promoter deletion analysis of G10H suggests that the sequences adjacent to the G-box are also involved in the regulation by BIS3. Overexpression of BIS3 in C. roseus flower petals significantly upregulated the expression of iridoid biosynthetic genes and increased loganic acid accumulation. BIS2 expression was significantly induced by BIS3 although BIS3 did not directly activate the BIS2 promoter. Our results advance our understanding of the regulation of plant specialized metabolites by bHLH TF clusters.? 2021 The Authors. Plant Direct published by American Society of Plant Biologists, Society for Experimental Biology and John Wiley & Sons Ltd.
机译:基本螺旋环 - 螺旋(BHLH)转录因子(TFS)是植物专门的代谢物的关键调节因子,包括丘安斯丘斯山脉的萜类吲哚生物碱(TIAS)。两种以前表征的亚组-IVA-IVA BHLH TFS,BIS1(BHLH IRIDOID合成1)和BIS2调节TIA途径中的虹膜生物合成。我们重新评估了最近更新的C.罗斯基因组序列,并发现BIS1和BIS2与以前没有特征的BHLH基因在同一基因组支架上聚集在相同的基因组支架上,所述BHLH基因被指定为双层3。迄今为止仅研究了几个BHLH基因集群。来自不同植物谱系的49个基因组序列的对比分析表明,核心植物植物中类似的BHLH簇存在,包括药用植物Calotropis Gigantea(巨乳)和凝聚术(黄杰胺),但不在分析的基础高管培养物和下植物中。类似于虹膜途径基因,BIS3在根中高度表达并被哌酸甲酯诱导。 BIS3激活Iridoid分支基因的启动子,Geraniol合酶(GES),Geraniol 10-羟化酶(G10H),8-羟基甲醇氧化还原酶(8HGO),虹膜合酶(IS),7-脱氧糖酸葡萄糖酰转移酶(7-DLGT)和7-脱氧糖酸羟化酶(7DLH),但不是虹膜氧化酶(IO)。当通过用ERF相关的两亲粘度(耳)序列将BIS3转化为显性阻遏物时,减少了启动子的转移。此外,BIS3用BIS1和BIS2协同作用,以在烟草细胞中激活G10H启动子。在G10h启动子中,已知的BHLH TF结合基序的突变显着降低,但未减少BIS3的反式激活。 G10h的启动子缺失分析表明,G箱附近的序列也参与了BIS3的调节。 C.玫瑰花花瓣中BIS3的过度表达显着上调了虹膜生物合成基因的表达和增加的逻酸积累。双BIS3显着诱导BIS2表达,尽管BIS3没有直接激活双层启动子。我们的成果通过BHLH TF集群提高了对植物专业代谢物调节的理解。 2021作者。植物直接发表美国植物生物学家,实验生物学学会和约翰瓦里和儿子有限公司

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