Jianzhao Qi, Shijie Kang, Ming Zhang, Shen Qi, Yulai Li, Khassanov Vadim, Shuangtian Du, Minglei Li
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In contrast, the M13 genome was 52.10 Mbp, showed 2.34% heterozygosity, 13.89% repetitive sequences, and was assembled into 12 scaffolds. Collinearity analysis revealed extensive homologous regions between the M12 and M13 genomes. Phylogenetic analysis suggested that the divergence between M12 and M13 occurred approximately 4.575 million years ago (MYAs), while their divergence from <i>Auricularia subglabra</i> TFB-10046 SS5 occurred approximately 33.537 MYAs. Analyses of CYP450, carbohydrate-active enzymes (CAZymes), and gene family expansion/contraction revealed distinct genomic features between the two strains. SSR and LTR insertion time analyses revealed the genome dynamics of the two strains during their evolution. Analysis of secondary metabolite-associated biosynthetic gene clusters (BGCs) provides powerful clues to understand the origin of bioactive compounds in the <i>Auricularia</i> mushroom. 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引用次数: 0
摘要
黑木耳是一种常见的块状食用菌,具有相当的烹饪和药用价值。以柞水县为代表的秦岭地区是中国黑木耳的主产区。本研究选取秦岭地区2株野生黑木耳菌株M12和M13,对其驯化后的优良园艺性状进行了测序和鉴定。基于Illumina NovaSeq和PacBio Sequel II HiFi的测序装配结果显示,M12基因组大小为56.04 Mbp,杂合度为2.58%,重复序列为14.13%,采用HI-C技术锚定在12条染色体上。M13基因组为52.10 Mbp,杂合度为2.34%,重复序列为13.89%,共组装成12个支架。共线性分析显示M12和M13基因组之间存在广泛的同源区域。系统发育分析表明,M12与M13的分化发生在457.5万年前(MYAs),而与Auricularia subglabra TFB-10046 SS5的分化发生在33537万年前。CYP450、碳水化合物活性酶(CAZymes)和基因家族扩展/收缩的分析显示了两株菌株之间不同的基因组特征。SSR和LTR插入时间分析揭示了两个菌株在进化过程中的基因组动态。次生代谢物相关生物合成基因簇(BGCs)的分析为了解黑木耳中生物活性物质的来源提供了有力的线索。本研究首次对秦岭黑木耳属植物进行了基因组测序。这些结果不仅丰富了我们对黑木耳基因组的认识,而且为后续黑木耳的遗传育种、功能基因挖掘和药用成分开发提供了重要的基因组资源和理论依据。
Genomic Sequencing and Characterization of Two Auricularia Species from the Qinling Region: Insights into Evolutionary Dynamics and Secondary Metabolite Potential.
Auricularia mushrooms, common bulk edible fungi, have considerable culinary and medicinal value. The Qinling region, represented by Zhashui County, is the main production area of Auricularia mushrooms in China. In this study, two wild Auricularia strains, M12 and M13, selected from the Qinling region for their desirable horticultural traits after domestication, were sequenced and characterized. Sequencing assembly results based on Illumina NovaSeq and PacBio Sequel II HiFi showed that the M12 genome was 56.04 Mbp in size, with 2.58% heterozygosity and 14.13% repetitive sequences, and was anchored on 12 chromosomes using HI-C technology. In contrast, the M13 genome was 52.10 Mbp, showed 2.34% heterozygosity, 13.89% repetitive sequences, and was assembled into 12 scaffolds. Collinearity analysis revealed extensive homologous regions between the M12 and M13 genomes. Phylogenetic analysis suggested that the divergence between M12 and M13 occurred approximately 4.575 million years ago (MYAs), while their divergence from Auricularia subglabra TFB-10046 SS5 occurred approximately 33.537 MYAs. Analyses of CYP450, carbohydrate-active enzymes (CAZymes), and gene family expansion/contraction revealed distinct genomic features between the two strains. SSR and LTR insertion time analyses revealed the genome dynamics of the two strains during their evolution. Analysis of secondary metabolite-associated biosynthetic gene clusters (BGCs) provides powerful clues to understand the origin of bioactive compounds in the Auricularia mushroom. This work represents the first genome sequencing of the Auricularia species derived from the Qinling region. These results not only enriched our understanding of the Auricularia genome but also provided an important genomic resource and theoretical basis for the subsequent genetic breeding, functional gene mining, and development of medicinal components of Auricularia species.
期刊介绍:
Journal of Fungi (ISSN 2309-608X) is an international, peer-reviewed scientific open access journal that provides an advanced forum for studies related to pathogenic fungi, fungal biology, and all other aspects of fungal research. The journal publishes reviews, regular research papers, and communications in quarterly issues. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on paper length. Full experimental details must be provided so that the results can be reproduced.