Pangeneric analyses reveal the divergent genome evolution and ecologies between morels and truffles in the Morchellaceae.

IF 7.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Current Biology Pub Date : 2025-09-08 Epub Date: 2025-08-05 DOI:10.1016/j.cub.2025.07.037
Gregory Bonito, Shingo Miyauchi, Richard D Hayes, Hao Tan, Alan Kuo, Aaron Robinson, Xinxin Wang, Jud Van Wyk, Annegret Kohler, Laure Fauchery, Elodie Drula, Gian Maria Niccolò Benucci, Emmanuelle Morin, Martin Ryberg, Faheema Kalsoom Khan, Melissa Cravero, Reid Longley, Kerrie Barry, Alicia Clum, Kecia Duffy, Anna Lipzen, Kurt LaButti, Robert Riley, Vasanth Singan, Andrei Steindorff, Jie Wang, Tom Bruns, Sundy Maurice, Philippe Clowez, Saskia Bindschedler, Pilar Junier, Patrick Chain, Igor V Grigoriev, Francis M Martin
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引用次数: 0

Abstract

Morels are iconic macrofungi known for their culinary value and spring emergence. Molecular phylogenetic studies have hitherto failed to elucidate the evolution of the ecological lifestyles of true and false morels, impeding their capacity to resolve longstanding debates regarding the extent of their saprotrophy and the potential for biotrophic associations with plants. In this study, we examined the evolutionary history and molecular innovations of Morchellaceae by generating high-quality genomes from species encompassing all the major clades within this family. We used conserved single-copy orthologs to infer the evolutionary history of true and false morels and related truffles. The genome size, transposable element content, and polysaccharide-degrading enzyme gene content are consistent with an ectomycorrhizal lifestyle for the Morchellaceae truffles Leucangium carthusianum and Kalapuya brunnea, whereas the other clades, including all true morels (Morchella spp.), exhibited genomic signatures of saprotrophic habits characterized by a highly conserved set of genes encoding plant biomass-related degrading enzymes. Morchellaceae species were found to be predominantly heterothallic, with either the MAT1-1 or MAT1-2 loci; however, the occurrence of colocalized mating-type idiomorphs, indicative of homothallism, was observed in M. rufobrunnea, M. peruviana, L. carthusianum, and the outgroup taxon Gyromitra esculenta. This study revealed a wealth of largely undiscovered genomic traits, including saprotrophic potential within Morchellaceae and a lack of biotrophic markers, and contributes to our understanding of the intricate evolutionary trajectories of the modes of nutrition in soil fungi.

泛属分析揭示了羊肚菌科与松露的基因组进化和生态差异。
羊肚菌是标志性的大型真菌,以其烹饪价值和春季出现而闻名。分子系统发育研究迄今未能阐明真假羊肚菌的生态生活方式的演变,阻碍了他们解决长期以来关于其腐坏程度和与植物生物营养关联的潜力的争论。在这项研究中,我们通过从包含该家族所有主要分支的物种中生成高质量的基因组来研究羊肚菌科的进化史和分子创新。我们使用保守的单拷贝同源来推断真假摩尔菌和相关松露的进化史。羊肚菌科松露Leucangium carthusianum和Kalapuya brunnea的基因组大小、转座因子含量和多糖降解酶基因含量与外生菌根生活方式一致,而其他分支,包括所有真正的羊肚菌(羊肚菌属),表现出腐坏营养习惯的基因组特征,其特征是一组高度保守的编码植物生物量相关降解酶的基因。羊肚菌科物种以异thalic为主,具有MAT1-1或MAT1-2位点;然而,在M. rufobrunnea、M. peruviana、L. carthusianum和外群分类群Gyromitra esculenta中发现了同体性的共定位交配型自形。这项研究揭示了大量未被发现的基因组特征,包括羊肚菌科的腐坏营养潜力和缺乏生物营养标记,并有助于我们理解土壤真菌营养模式的复杂进化轨迹。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current Biology
Current Biology 生物-生化与分子生物学
CiteScore
11.80
自引率
2.20%
发文量
869
审稿时长
46 days
期刊介绍: Current Biology is a comprehensive journal that showcases original research in various disciplines of biology. It provides a platform for scientists to disseminate their groundbreaking findings and promotes interdisciplinary communication. The journal publishes articles of general interest, encompassing diverse fields of biology. Moreover, it offers accessible editorial pieces that are specifically designed to enlighten non-specialist readers.
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