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High-Throughput Sequencing and De Novo Assembly of Red and Green Forms of the Perilla frutescens var. crispa Transcriptome

机译:紫苏红色和绿色形式的高通量测序和从头组装。脆皮转录组

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摘要

Perilla frutescens var. crispa (Labiatae) has two chemo-varietal forms, i.e. red and green forms of perilla, that differ in the production of anthocyanins. To facilitate molecular biological and biochemical studies in perilla-specialized metabolism we used Illumina RNA-sequencing technology in our comprehensive comparison of the transcriptome map of the leaves of red and green forms of perilla. Sequencing generated over 1.2 billion short reads with an average length of 101 nt. De novo transcriptome assembly yielded 47,788 and 47,840 unigenes in the red and green forms of perilla plants, respectively. Comparison of the assembled unigenes and existing perilla cDNA sequences showed highly reliable alignment. All unigenes were annotated with gene ontology (GO) and Enzyme Commission numbers and entered into the Kyoto Encyclopedia of Genes and Genomes. We identified 68 differentially expressed genes (DEGs) in red and green forms of perilla. GO enrichment analysis of the DEGs showed that genes involved in the anthocyanin metabolic process were enriched. Differential expression analysis revealed that the transcript level of anthocyanin biosynthetic unigenes encoding flavonoid 3’-hydroxylase, dihydroflavonol 4-reductase, and anthocyanidin synthase was significantly higher in red perilla, while the transcript level of unigenes encoding limonene synthase was significantly higher in green perilla. Our data serve as a basis for future research on perilla bio-engineering and provide a shortcut for the characterization of new functional genes in P. frutescens.
机译:紫苏frutescens var。 crispa(Labiatae)具有两种化学变体形式,即紫苏的红色和绿色形式,其花色苷的产生有所不同。为了促进紫苏专门代谢中的分子生物学和生化研究,我们在对紫苏和绿紫苏叶的转录组图谱进行全面比较时使用了Illumina RNA测序技术。测序产生了超过12亿个短读,平均长度为101 nt。从头转录组装配产生的紫苏植物的红色和绿色形式分别产生47,788和47,840单基因。组装的单基因和现有的紫苏cDNA序列的比较显示高度可靠的比对。所有的单基因都用基因本体论(GO)和酶委员会编号进行注释,并进入《京都基因与基因组百科全书》。我们确定了紫苏红色和绿色形式的68个差异表达基因(DEG)。对DEG的GO富集分析表明,参与花色苷代谢过程的基因被富集。差异表达分析表明,红色紫苏中编码类黄酮3′-羟化酶,二氢黄酮醇4-还原酶和花色素苷合酶的花色苷生物合成单基因的转录水平显着高于绿色紫苏中编码柠檬烯合酶的单基因的转录水平显着更高。我们的数据为紫苏生物工程的未来研究奠定了基础,并为表征欧洲假单胞菌中的新功能基因提供了捷径。

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