首页> 美国卫生研究院文献>Scientific Reports >Transcriptome-derived investigation of biosynthesis of quinolizidine alkaloids in narrow-leafed lupin (Lupinus angustifolius L.) highlights candidate genes linked to iucundus locus
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Transcriptome-derived investigation of biosynthesis of quinolizidine alkaloids in narrow-leafed lupin (Lupinus angustifolius L.) highlights candidate genes linked to iucundus locus

机译:转录组研究在阔叶羽扇豆羽扇豆(Lupinus angustifolius L.)中喹诺唑烷生物碱的生物合成过程突出显示了与iucundus基因座相关的候选基因

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摘要

Unravelling the biosynthetic pathway of quinolizidine alkaloids (QAs), regarded as antinutritional compounds of narrow-leafed lupin (NLL) seeds, is fundamental to best exploit NLL as food or feed. We investigated 12 candidate genes connected to QA biosynthesis, selecting them by transcriptomic and genomic approaches, from the landscape of genes differentially expressed in leaves of the high- and low-alkaloid NLL accessions. Linkage analysis enabled the assessment of the location of the candidate genes in relation to iucundus, a major locus of unknown identity, that confers reduced QA content in seeds. The key finding was the identification of APETALA2/ethylene response transcription factor, RAP2-7, cosegregating with the iucundus locus and located within a region with highly significant QTLs that affect QA composition. We additionally identified a 4-hydroxy-tetrahydrodipicolinate synthase (DHDPS) gene involved in L-lysine biosynthesis as being closely linked to iucundus. The distributed location of other remaining candidates (including previously known QA genes) across different linkage groups, also indirectly supports the transcription factor as a possible regulator of lupin alkaloid biosynthesis. Our findings provide crucial insight into QA biosynthesis in NLL. Additionally, we evaluated and selected appropriate reference genes for qRT-PCRs to analyse the expression levels of QA genes in NLL.
机译:揭示被认为是窄叶羽扇豆(NLL)种子的抗营养化合物的喹喔啉生物碱(QAs)的生物合成途径,是最佳利用NLL作为食物或饲料的基础。我们研究了与QA生物合成相关的12个候选基因,并通过转录组学和基因组方法从高,低生物碱NLL品种叶片中差异表达的基因格局中选择了它们。连锁分析可以评估候选基因与iucundus有关,后者是身份不明的主要基因座,可降低种子中的QA含量。关键发现是鉴定APETALA2 /乙烯反应转录因子RAP2-7,其与iucundus基因座共分离,并位于影响QA组成的QTL高度重要的区域内。我们还确定了参与L-赖氨酸生物合成的4-羟基-四氢二吡啶甲酸合酶(DHDPS)基因与iucundus密切相关。其他剩余候选物(包括先前已知的QA基因)在不同连接基团之间的分布位置也间接支持了转录因子作为羽扇豆生物碱生物合成的可能调节剂。我们的发现为NLL中的QA生物合成提供了至关重要的见解。此外,我们评估并选择了适合qRT-PCR的参考基因,以分析NLL中QA基因的表达水平。

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