In the "1KFG: Deep Sequencing of Ecologically-relevant Dikarya" project (CSP1974), we aim to sequence additional sampling of genomic diversity within keystone lineages of plant-interacting fungi and saprophytic fungi that are of special ecological importance for understanding terrestrial ecosystems. In addition, comparative genome analysis with saprotrophic, mycorrhizal and pathogenic fungi will provide new insights into the specific and conserved adaptations associated with each fungal lifestyle.
Within the framework of CSP1974, we are sequencing phylogenetically and morphologically diverse species of Morchellaceae. These fungi include economically important edible morels (Morchella), putatively toxic false-morels (Verpa), and the edible hypogeous truffle genera Leucangium and Kalapuya (1–3). The ecology of these taxa is still poorly understood. Some Morchella species are suspected to be mycorrhizal symbionts (4), others grow as endophytes within plant roots (5,6), some farm bacteria (7), but the majority of species (including the cultivated species of morels) are considered to be general saprotrophs (8,9). The Morchellaceae lineage is hypothesized to have originated and radiated in the Northern Hemisphere, later dispersing into Southern hemisphere regions (10). Genomic data generated by this project will be used to better identify genomic features underlying the distinct ecology, diversity, and morphology of Morchellaceae fungi.
Here we present the genome of Morchella angusticeps, a black morel within the Elata clade that is common across North America, east of the Rocky Mountains (11). M. angusticeps is characterized by a network of irregularly-shaped ridges and pits. This species tends to fruit singly or scattered over a wide area under various hardwoods but only in unburned habitats (11).
Researchers who wish to publish analyses using data from unpublished CSP genomes are respectfully required to contact the PI and JGI to avoid potential conflicts on data use and coordinate other publications with the CSP master paper(s).
References
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- Trappe, M. J., Trappe, J. & Bonito, G. Kalapuya brunnea gen. & sp. nov. and its relationship to the other sequestrate genera in Morchellaceae. Mycologia 102, 1058–1065 (2010).
- Buscot, F. Mycorrhizal succession and morel biology. Mycorrhizas in ecosystems 220–224 (1992).
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- Baynes, M., Newcombe, G., Dixon, L., Castlebury, L. & O’Donnell, K. A novel plant–fungal mutualism associated with fire. Fungal Biol. 116, 133–144 (2012).
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- Benucci, G. M. N., Longley, R., Zhang, P., Zhao, Q., Bonito, G. & Yu, F. Microbial communities associated with the black morel Morchella sextelata cultivated in greenhouses. PeerJ 7, e7744 (2019).
- Hobbie, E. A., Rice, S. F., Weber, N. S. & Smith, J. E. Isotopic evidence indicates saprotrophy in post-fire Morchella in Oregon and Alaska. Mycologia 108, 638–645 (2016).
- O’Donnell, K., Rooney, A. P., Mills, G. L., Kuo, M., Weber, N. S. & Rehner, S. A. Phylogeny and historical biogeography of true morels (Morchella) reveals an early Cretaceous origin and high continental endemism and provincialism in the Holarctic. Fungal Genet. Biol. 48, 252–265 (2011).
- Kuo, M., Dewsbury, D. R., O'Donnell, K., Carter, M. C., Rehner, S. A., Moore, J. D., Moncalvo, J., Canfield, S. A., Stephenson, S. L., Methven, A. S., & Volk, T. J. Taxonomic revision of true morels (Morchella) in Canada and the United States, Mycologia, 104:5, 1159-1177 (2012)