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Alternative Splicing Regulation of Anthocyanin Biosynthesis in Camellia sinensis var. assamica Unveiled by PacBio Iso-Seq

机译:山茶花中红细胞素生物合成的替代剪接调节。 assamica由pacbio iso-seq推出

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摘要

Although the pathway and transcription factor regulation of anthocyanin biosynthesis in tea plants [ (L.) O. Ktze] are known, post-transcriptional regulation mechanisms involved in anthocyanin accumulation have not been comprehensively studied. We obtained the full-length transcriptome of a purple cultivar (‘Zijuan’) and a normal green cultivar (‘Yunkang 10#) of var. (Masters) showing different accumulation of anthocyanins and catechins through PacBio isoform sequencing (Iso-Seq). In total, 577,557 mapped full-length cDNAs were obtained, and 2,600 average-length gene isoforms were identified in both cultivars. After gene annotations and pathway predictions, we found that 98 key genes in anthocyanin biosynthesis pathways could have undergone alternative splicing (AS) events, and identified a total of 238 isoforms involved in anthocyanin biosynthesis. We verified expression of the , , , , , , , , , , , , , , , , , , , , genes and their AS transcripts using qRT-PCR. Correlation analysis of anthocyanin biosynthesis and gene expression results revealed that , , , , and are crucial AS transcripts for regulating anthocyanin biosynthesis in . Our results reveal post-transcriptional regulation of anthocyanin biosynthesis in tea plants, and provide more new insights into the regulation of secondary metabolism.
机译:虽然茶叶植物中花青素生物合成的途径和转录因子调节是已知的,但尚未全面研究参与花青素积累的转录后调节机制。我们获得了紫色品种的全长转录组('Zijuan')和var的正常绿色品种('yunkang 10#)。 (大师)显示通过PACBIO同种型测序(ISO-SEQ)的分类花青素和儿茶素的累积。总共可以获得577,557个映射全长CDNA,并在两个品种中鉴定了2,600个平均长度基因同种型。在基因注释和途径预测之后,我们发现花青素生物合成途径中的98个关键基因可能经历替代的剪接(AS)事件,并鉴定了参与花青素生物合成的238种同种型。使用QRT-PCR,我们验证了,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,血值,,,,血值,,,血值,,,血值,,,血值,,,血量量称为转录物。花青素生物合成和基因表达结果的相关分析显示,,,并且是调节花青素生物合成的转录物的关键。我们的结果揭示了茶叶植物中花青素生物合成的转录后调节,并为次生新陈代谢的调节提供了更新的洞察。

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