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De Novo Transcriptome Assembly in Shiraia bambusicola to Investigate Putative Genes Involved in the Biosynthesis of Hypocrellin A

机译:孟加拉国Shiraia bambusicola的De Novo转录组大会研究涉及hypocrellin A的生物合成的推定基因

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摘要

Shiraia bambusicola is a species of the monotypic genus Shiraia in the phylum Ascomycota. In China, it is known for its pharmacological properties that are used to treat rheumatic arthritis, sciatica, pertussis, tracheitis and so forth. Its major medicinal active metabolite is hypocrellin A, which exhibits excellent antiviral and antitumor properties. However, the genes involved in the hypocrellin A anabolic pathways were still unknown due to the lack of genomic information for this species. To investigate putative genes that are involved in the biosynthesis of hypocrellin A and determine the pathway, we performed transcriptome sequencing for Shiraia bambusicola S4201-W and the mutant S4201-D1 for the first time. S4201-W has excellent hypocrellin A production, while the mutant S4201-D1 does not. Then, we obtained 38,056,034 and 39,086,896 clean reads from S4201-W and S4201-D1, respectively. In all, 17,923 unigenes were de novo assembled, and the N50 length was 1970 bp. Based on the negative binomial distribution test, 716 unigenes were found to be upregulated, and 188 genes were downregulated in S4201-D1, compared with S4201-W. We have found seven unigenes involved in the biosynthesis of hypocrellin A and proposed a putative hypocrellin A biosynthetic pathway. These data will provide a valuable resource and theoretical basis for future molecular studies of hypocrellin A, help identify the genes involved in the biosynthesis of hypocrellin A and help facilitate functional studies for enhancing hypocrellin A production.
机译:Shimia bambusicola是子囊门中的一个单型Shiraia属。在中国,以治疗风湿性关节炎,坐骨神经痛,百日咳,气管炎等的药理学特性而闻名。它的主要药用活性代谢产物是hypercrellin A,它具有出色的抗病毒和抗肿瘤特性。然而,由于缺乏该物种的基因组信息,涉及hypercrellin A合成代谢途径的基因仍是未知的。为了调查参与hypercrellin A的生物合成的推定基因并确定该途径,我们首次进行了Shimia bambusicola S4201-W和突变体S4201-D1的转录组测序。 S4201-W具有极好的降乳素A产生,而突变体S4201-D1没有。然后,我们分别从S4201-W和S4201-D1获得了38,056,034和39,086,896干净读取。总共重新组装了17,923个单基因,N50长度为1970 bp。根据负二项分布测试,与S4201-W相比,S4201-D1中有716个单基因被上调,而188个基因被下调。我们发现了七个参与hypercrellin A生物合成的单基因,并提出了一个假定的hypercrellin A生物合成途径。这些数据将为未来的果胶蛋白A分子研究提供有价值的资源和理论基础,有助于鉴定参与果胶蛋白A生物合成的基因,并有助于促进功能研究以增强果胶蛋白A的产生。

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