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首页> 外文期刊>Frontiers in Plant Science >Insights into the Sesquiterpenoid Pathway by Metabolic Profiling and De novo Transcriptome Assembly of Stem-Chicory ( Cichorium intybus Cultigroup “Catalogna”)
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Insights into the Sesquiterpenoid Pathway by Metabolic Profiling and De novo Transcriptome Assembly of Stem-Chicory ( Cichorium intybus Cultigroup “Catalogna”)

机译:通过代谢分析和<斜视> de novoh-/斜体>转录组合组装的茎 - 菊苣(<斜景>浅色intybus cultigroup“Catalogna”)的洞察

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Stem-chicory of the “Catalogna” group is a vegetable consumed for bitter-flavored stems. Type and levels of bitter sesquiterpene lactones (STLs) participate in conferring bitterness in vegetables. The content of lactucin—and lactucopocrin-like STLs was higher in “Molfettese” than “Galatina” landrace stalks, regardless of the cultivation sites, consistently with bitterness scores and gustative differences. The “Galatina” transcriptome assembly resulted in 58,872 unigenes, 77% of which were annotated, paving the way to molecular investigation of the STL pathway. Comparative transcriptome analysis allowed the identification of 69,352 SNPs and of 1640 differentially expressed genes that maintained the pattern independently of the site. Enrichment analyses revealed that 4 out of 29 unigenes were up-regulated in “Molfettese” vs “Galatina” within the sesquiterpenoid pathway. The expression of two germacrene A - synthase ( GAS ) and one - oxidase ( GAO ) genes of the costunolide branch correlated positively with the contents of lactucin-like molecules, supporting that STL biosynthesis regulation occurs at the transcriptional level. Finally, 46 genes encoding transcription factors ( TFs ) maintained a differential expression pattern between the two varieties regardless of the growth site; correlation analyses among TFs, GAS, GAO gene expressions and STLs contents suggest that one MYB and one bHLH may act in the pathway.
机译:“Catalogna”组的Stem-Chicory是用于苦味茎的蔬菜。苦味倍二萜烯内酯(STL)的类型和水平参与促进蔬菜的苦味。无论培养位点,霉菌蛋白 - 和霉菌泌体样STL的含量高于“Galatina”的Landrace Stalks,与培养位点一致,符合苦味评分和呼气差异。 “加利提纳”转录组组件导致58,872个unigenes,其中77%被注释,铺平了STL途径的分子调查。比较转录组分析允许鉴定69,352个SNP和1640个差异表达基因,其独立于现场维持该模式。富集分析表明,在筛窦内的“Molfettese”与“Galatina”中有29个unigenes中的4个中有4个。肋糖苷分枝的两个生长酮A合酶(气体)和单氧化酶(GaO)基因的表达与乳酸状分子的含量正相关,支持在转录水平下发生STL生物合成调节。最后,编码转录因子(TFS)的46个基因在两种品种之间保持差异表达模式,无论生长位点如何; TFS,Gas,GaO基因表达和STLS内容中的相关分析表明,一个MYB和一个BHLH可以在途径中起作用。

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