Insights into evolution of multicellular fungi from the assembled chromosomes of the mushroom Coprinopsis cinerea (Coprinus cinereus).

Published

Journal Article

The mushroom Coprinopsis cinerea is a classic experimental model for multicellular development in fungi because it grows on defined media, completes its life cycle in 2 weeks, produces some 10(8) synchronized meiocytes, and can be manipulated at all stages in development by mutation and transformation. The 37-megabase genome of C. cinerea was sequenced and assembled into 13 chromosomes. Meiotic recombination rates vary greatly along the chromosomes, and retrotransposons are absent in large regions of the genome with low levels of meiotic recombination. Single-copy genes with identifiable orthologs in other basidiomycetes are predominant in low-recombination regions of the chromosome. In contrast, paralogous multicopy genes are found in the highly recombining regions, including a large family of protein kinases (FunK1) unique to multicellular fungi. Analyses of P450 and hydrophobin gene families confirmed that local gene duplications drive the expansions of paralogous copies and the expansions occur in independent lineages of Agaricomycotina fungi. Gene-expression patterns from microarrays were used to dissect the transcriptional program of dikaryon formation (mating). Several members of the FunK1 kinase family are differentially regulated during sexual morphogenesis, and coordinate regulation of adjacent duplications is rare. The genomes of C. cinerea and Laccaria bicolor, a symbiotic basidiomycete, share extensive regions of synteny. The largest syntenic blocks occur in regions with low meiotic recombination rates, no transposable elements, and tight gene spacing, where orthologous single-copy genes are overrepresented. The chromosome assembly of C. cinerea is an essential resource in understanding the evolution of multicellularity in the fungi.

Full Text

Duke Authors

Cited Authors

  • Stajich, JE; Wilke, SK; Ahrén, D; Au, CH; Birren, BW; Borodovsky, M; Burns, C; Canbäck, B; Casselton, LA; Cheng, CK; Deng, J; Dietrich, FS; Fargo, DC; Farman, ML; Gathman, AC; Goldberg, J; Guigó, R; Hoegger, PJ; Hooker, JB; Huggins, A; James, TY; Kamada, T; Kilaru, S; Kodira, C; Kües, U; Kupfer, D; Kwan, HS; Lomsadze, A; Li, W; Lilly, WW; Ma, L-J; Mackey, AJ; Manning, G; Martin, F; Muraguchi, H; Natvig, DO; Palmerini, H; Ramesh, MA; Rehmeyer, CJ; Roe, BA; Shenoy, N; Stanke, M; Ter-Hovhannisyan, V; Tunlid, A; Velagapudi, R; Vision, TJ; Zeng, Q; Zolan, ME; Pukkila, PJ

Published Date

  • June 29, 2010

Published In

Volume / Issue

  • 107 / 26

Start / End Page

  • 11889 - 11894

PubMed ID

  • 20547848

Pubmed Central ID

  • 20547848

Electronic International Standard Serial Number (EISSN)

  • 1091-6490

Digital Object Identifier (DOI)

  • 10.1073/pnas.1003391107

Language

  • eng

Conference Location

  • United States