Comparative transcriptome analysis of Gastrodia elata (Orchidaceae) in response to fungus symbiosis to identify gastrodin biosynthesis-related genes

被引:50
作者
Tsai, Chi-Chu [1 ,2 ]
Wu, Keh-Ming [3 ]
Chiang, Tzen-Yuh [4 ]
Huang, Chun-Yen [1 ]
Chou, Chang-Hung [5 ]
Li, Shu-Ju [1 ]
Chiang, Yu-Chung [6 ,7 ]
机构
[1] Kaohsiung Dist Agr Improvement Stn, Crop Improvement Div, Pingtung 900, Taiwan
[2] Natl Pingtung Univ Sci & Technol, Grad Inst Biotechnol, Pingtung 912, Taiwan
[3] Welgene Biotech Co Ltd, Taipei 115, Taiwan
[4] Cheng Kung Univ, Dept Life Sci, Tainan 701, Taiwan
[5] China Med Univ, Res Ctr Biodivers, Taichung 404, Taiwan
[6] Natl Sun Yat Sen Univ, Dept Biol Sci, Kaohsiung 804, Taiwan
[7] Kaohsiung Med Univ, Dept Biomed Sci & Environm Biol, Kaohsiung 807, Taiwan
关键词
Gastrodin; Deep sequencing; Gene regulation; Monooxygenase; Glycosyltransferase; MESSENGER-RNA DECAY; AROMATIC-COMPOUNDS; DRUG DISCOVERY; SEQ DATA; EXPRESSION; GLYCOSYLTRANSFERASES; METABOLISM; QUANTIFICATION; IDENTIFICATION; CONSTITUENTS;
D O I
10.1186/s12864-016-2508-6
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Gastrodia elata Blume (Orchidaceae) is an important Chinese medicine with several functional components. In the life cycle of G. elata, the orchid develops a symbiotic relationship with two compatible mycorrhizal fungi Mycena spp. and Armillaria mellea during seed germination to form vegetative propagation corm and vegetative growth to develop tubers, respectively. Gastrodin (p-hydroxymethylphenol-beta-D-glucoside) is the most important functional component in G. elata, and gastrodin significantly increases from vegetative propagation corms to tubers. To address the gene regulation mechanism in gastrodin biosynthesis in G. elata, a comparative analysis of de novo transcriptome sequencing among the vegetative propagation corms and tubers of G. elata and A. mellea was conducted using deep sequencing. Results: Transcriptome comparison between the vegetative propagation corms and juvenile tubers of G. elata revealed 703 differentially expressed unigenes, of which 298 and 405 unigenes were, respectively up-regulated (fold-change >= 2, q-value < 0.05, the trimmed mean of M-values (TMM)-normalized fragments per kilobase of transcript per Million mapped reads (FPKM) > 10) and down-regulated (fold-change <= 0.5, q-value < 0.05, TMM-normalized FPKM > 10) in juvenile tubers. After Gene Ontology (GO) annotation and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis, 112 up-regulated unigenes with KEGG Ortholog identifiers (KOids) or enzyme commission (EC) numbers were assigned to 159 isogroups involved in seventy-eight different pathways, and 132 down-regulated unigenes with KOids or EC numbers were assigned to 168 isogroups, involved in eighty different pathways. The analysis of the isogroup genes from all pathways revealed that the two unigenes TRINITY_DN54282_c0_g1 (putative monooxygenases) and TRINITY_DN50323_c0_g1 (putative glycosyltransferases) might participate in hydroxylation and glucosylation in the gastrodin biosynthetic pathway. Conclusions: The gene expression of the two unique unigenes encoding monooxygenase and glycosyltransferase significantly increases from vegetative propagation corms to tubers, and the molecular basis of gastrodin biosynthesis in the tubers of G. elata is proposed.
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页数:16
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