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桦褐孔菌中桦木醇生物合成的独立进化

Independent evolution of betulin biosynthesis in Inonotus obliquus.

作者信息

Safronov Omid, Bal Güleycan Lutfullahoglu, Sipari Nina, Wilkens Maya, Safdari Pezhman, Smolander Olli-Pekka, Laine Pia K, Lihavainen Jenna, Silvan Niko, Rajaraman Sitaram, Paulin Lars G, Teeri Teemu H, Auvinen Petri, Sarjala Tytti, Overmyer Kirk, Richter Uwe, Salojärvi Jarkko

机构信息

Organismal and Evolutionary Biology Research Program, Faculty of Biological and Environmental Sciences, and Viikki Plant Science Centre, University of Helsinki, Helsinki, Finland.

Institute of Biotechnology, HiLIFE, University of Helsinki, Helsinki, Finland.

出版信息

Sci Rep. 2025 Jul 1;15(1):21319. doi: 10.1038/s41598-025-05414-1.

DOI:10.1038/s41598-025-05414-1
PMID:40594539
Abstract

Chaga mushroom (Inonotus obliquus) is a fungal species in the family Hymenochaetaceae (Basidiomycota) and the causative agent of white rot decay in Betula species. We assembled a high-quality 50.7 Mbp genome from PacBio sequencing and identified a lineage-specific whole genome duplication event approximately 1.3 million years ago, which has contributed to a major increase in biochemical diversity in the species through preferential retention of cytochrome P450 superfamily members. Secondary metabolism has further evolved through small-scale segmental duplications, such as tandem duplications within fungal biosynthetic gene clusters. Metabolomic fingerprinting confirmed increased complexity in terpene biosynthesis chemistry compared to related species that lacked the duplication event. This metabolic diversity may have arisen from co-evolution with the primary host species, which evolved high betulin content in its bark 4-8 million years ago.

摘要

桦褐孔菌(Inonotus obliquus)是锈革孔菌科(担子菌门)的一种真菌,也是桦木属物种白色腐朽的病原体。我们通过PacBio测序组装了一个高质量的5070万碱基对基因组,并鉴定出约130万年前发生的一次谱系特异性全基因组复制事件,该事件通过优先保留细胞色素P450超家族成员,极大地增加了该物种的生化多样性。次生代谢通过小规模的片段重复进一步进化,例如真菌生物合成基因簇内的串联重复。代谢组指纹图谱证实,与缺乏复制事件的相关物种相比,萜类生物合成化学的复杂性增加。这种代谢多样性可能源于与主要宿主物种的共同进化,该宿主物种在400万至800万年前其树皮中桦木醇含量较高。

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本文引用的文献

1
Therapeutic properties of (Chaga mushroom): A review.桦褐孔菌的治疗特性:综述
Mycology. 2023 Oct 20;15(2):144-161. doi: 10.1080/21501203.2023.2260408. eCollection 2024.
2
Multiple horizontal gene transfer events have shaped plant glycosyl hydrolase diversity and function.多次水平基因转移事件塑造了植物糖苷水解酶的多样性和功能。
New Phytol. 2024 Apr;242(2):809-824. doi: 10.1111/nph.19595. Epub 2024 Feb 28.
3
Plastome phylogenomics provide new perspective into the phylogeny and evolution of Betulaceae (Fagales).质体基因组系统发育学为桦木科(壳斗科)的系统发育和进化提供了新的视角。
BMC Plant Biol. 2022 Dec 24;22(1):611. doi: 10.1186/s12870-022-03991-1.
4
Genomic and Metabolomic Analyses of the Medicinal Fungus for Its Metabolite's Biosynthesis and Medicinal Application.药用真菌的基因组和代谢组分析及其代谢产物的生物合成与药用应用
J Fungi (Basel). 2022 Nov 25;8(12):1245. doi: 10.3390/jof8121245.
5
Genome sequencing of Inonotus obliquus reveals insights into candidate genes involved in secondary metabolite biosynthesis.桦褐孔菌基因组测序揭示了参与次生代谢物生物合成的候选基因。
BMC Genomics. 2022 Apr 20;23(1):314. doi: 10.1186/s12864-022-08511-x.
6
Whole genome sequencing of an edible and medicinal mushroom, Russula griseocarnosa, and its association with mycorrhizal characteristics.食用兼药用蘑菇灰肉红菇的全基因组测序及其与菌根特征的关联
Gene. 2022 Jan 15;808:145996. doi: 10.1016/j.gene.2021.145996. Epub 2021 Oct 8.
7
Transposable Elements Contribute to Genome Dynamics and Gene Expression Variation in the Fungal Plant Pathogen Verticillium dahliae.转座元件在真菌植物病原菌大丽轮枝菌的基因组动态和基因表达变异中发挥作用。
Genome Biol Evol. 2021 Jul 6;13(7). doi: 10.1093/gbe/evab135.
8
Gene family expansions and transcriptome signatures uncover fungal adaptations to wood decay.基因家族扩张和转录组特征揭示了真菌适应木材腐朽的机制。
Environ Microbiol. 2021 Oct;23(10):5716-5732. doi: 10.1111/1462-2920.15423. Epub 2021 Feb 15.
9
Improving the production of squalene-type triterpenoid 2,3;22,23-squalene dioxide by optimizing the expression of CYP505D13 in Saccharomyces cerevisiae.通过优化酿酒酵母中 CYP505D13 的表达来提高鲨烯型三萜 2,3;22,23-鲨烯二氧化物的产量。
J Biosci Bioeng. 2020 Sep;130(3):265-271. doi: 10.1016/j.jbiosc.2020.04.005. Epub 2020 May 15.
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Plant Biotechnol (Tokyo). 2018 Jun 25;35(2):131-139. doi: 10.5511/plantbiotechnology.18.0416a.