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全面鉴定茶树(Camellia sinensis)次生代谢途径相关的全长转录本和可变剪接。

Comprehensive identification of the full-length transcripts and alternative splicing related to the secondary metabolism pathways in the tea plant (Camellia sinensis).

机构信息

Tea Research Institute, Guizhou Academy of Agricultural Science, Guiyang, 550006, Guizhou, China.

College of tea science, Guizhou University, Guiyang, 550025, Guizhou, China.

出版信息

Sci Rep. 2019 Feb 25;9(1):2709. doi: 10.1038/s41598-019-39286-z.

DOI:10.1038/s41598-019-39286-z
PMID:30804390
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6389920/
Abstract

Flavonoids, theanine and caffeine are the main secondary metabolites of the tea plant (Camellia sinensis), which account for the tea's unique flavor quality and health benefits. The biosynthesis pathways of these metabolites have been extensively studied at the transcriptional level, but the regulatory mechanisms are still unclear. In this study, to explore the transcriptome diversity and complexity of tea plant, PacBio Iso-Seq and RNA-seq analysis were combined to obtain full-length transcripts and to profile the changes in gene expression during the leaf development. A total of 1,388,066 reads of insert (ROI) were generated with an average length of 1,762 bp, and more than 54% (755,716) of the ROIs were full-length non-chimeric (FLNC) reads. The Benchmarking Universal Single-Copy Orthologue (BUSCO) completeness was 92.7%. A total of 93,883 non-redundant transcripts were obtained, and 87,395 (93.1%) were new alternatively spliced isoforms. Meanwhile, 7,650 differential expression transcripts (DETs) were identified. A total of 28,980 alternative splicing (AS) events were predicted, including 1,297 differential AS (DAS) events. The transcript isoforms of the key genes involved in the flavonoid, theanine and caffeine biosynthesis pathways were characterized. Additionally, 5,777 fusion transcripts and 9,052 long non-coding RNAs (lncRNAs) were also predicted. Our results revealed that AS potentially plays a crucial role in the regulation of the secondary metabolism of the tea plant. These findings enhanced our understanding of the complexity of the secondary metabolic regulation of tea plants and provided a basis for the subsequent exploration of the regulatory mechanisms of flavonoid, theanine and caffeine biosynthesis in tea plants.

摘要

类黄酮、茶氨酸和咖啡因是茶树(Camellia sinensis)的主要次生代谢产物,它们构成了茶叶独特的风味品质和健康益处。这些代谢产物的生物合成途径已在转录水平上进行了广泛研究,但调控机制仍不清楚。在这项研究中,为了探索茶树的转录组多样性和复杂性,我们结合 PacBio Iso-Seq 和 RNA-seq 分析,获得全长转录本,并分析叶片发育过程中基因表达的变化。总共生成了 1,388,066 个插入片段(ROI)的reads,平均长度为 1,762bp,超过 54%(755,716)的 ROI 是全长非嵌合(FLNC)reads。基准通用单拷贝同源物(BUSCO)的完整性为 92.7%。总共获得了 93,883 个非冗余转录本,其中 87,395(93.1%)是新的可变剪接异构体。同时,鉴定了 7,650 个差异表达转录本(DET)。共预测了 28,980 个可变剪接(AS)事件,包括 1,297 个差异 AS(DAS)事件。鉴定了参与类黄酮、茶氨酸和咖啡因生物合成途径的关键基因的转录本异构体。此外,还预测了 5,777 个融合转录本和 9,052 个长非编码 RNA(lncRNA)。我们的结果表明,AS 可能在茶树次生代谢调控中发挥关键作用。这些发现增强了我们对茶树次生代谢调控复杂性的理解,为后续探索茶树类黄酮、茶氨酸和咖啡因生物合成的调控机制提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d1/6389920/c03fbc11a079/41598_2019_39286_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d1/6389920/5b9320b546bd/41598_2019_39286_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d1/6389920/3c12256fa8c8/41598_2019_39286_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d1/6389920/be14f80e34f3/41598_2019_39286_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d1/6389920/4db970642a42/41598_2019_39286_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d1/6389920/63379b3e073a/41598_2019_39286_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d1/6389920/5f2904c8d836/41598_2019_39286_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d1/6389920/2f4f72d260cc/41598_2019_39286_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d1/6389920/c03fbc11a079/41598_2019_39286_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d1/6389920/5b9320b546bd/41598_2019_39286_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d1/6389920/3c12256fa8c8/41598_2019_39286_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d1/6389920/be14f80e34f3/41598_2019_39286_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d1/6389920/4db970642a42/41598_2019_39286_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d1/6389920/63379b3e073a/41598_2019_39286_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d1/6389920/5f2904c8d836/41598_2019_39286_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d1/6389920/2f4f72d260cc/41598_2019_39286_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d1/6389920/c03fbc11a079/41598_2019_39286_Fig8_HTML.jpg

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