ABSTRACT
Umbilicaria muehlenbergii strain KoLRILF000956 is amenable to Agrobacterium tumefaciens-mediated transformation (ATMT), making it the only known genetically tractable lichen-forming fungus to date. We report another advancement in lichen genetics, a draft genome assembly for U. muehlenbergii with a size of 34,812,353 bp and a GC content of 47.12%, consisting of seven scaffolds.
GENOME ANNOUNCEMENT
Over 19% of all known fungal species (approximately 14,000 species) participate in a symbiotic relationship with green algae, cyanobacteria, or both to form lichen. Among them, nearly 98% belong to the phylum Ascomycota. The lichens produce useful metabolites with properties of pharmaceutical interest such as anti-HIV, antitumor, antimicrobial, anti-inflammatory, and antioxidant activities. However, unlike other well-studied ascomycetous fungi, including model fungi (1–3) and phytopathogenic fungi (4–7), lichen-forming fungi had no well-established transformation system. Recently, the first successful transformation of a lichen fungus, Umbilicaria muehlenbergii, via Agrobacterium tumefaciens has been reported (8).
U. muehlenbergii belongs to the family Umbilicariaceae. The genera in this family are distributed in a wide range of climates, including artic, boreal, austral, temperate, and montane regions (9). Umbilicaria spp. contain polysaccharides that showed anti-HIV and antitumor activities (10–12). As U. muehlenbergii is dimorphic, it can be grown rapidly in culture in the yeast form, while most other lichen-forming fungi grow extremely slowly in axenic culture (13, 14). This is advantageous in studying lichen biology. Moreover, the recently developed transformation system offers a possibility for systematic gene functional studies. Here, we present the genome sequence of U. muehlenbergii, which is anticipated to go hand-in-hand with the aforementioned technological progress to elucidate the genetic blueprint of this fungus.
Umbilicaria muehlenbergii strain KoLRILF000956 was isolated from a rock at Mt. Tulaopoding, Jilin Province, China, in 2012. DNA was extracted from the fungus grown in axenic culture using a DNeasy minikit (Qiagen, Valencia, CA), according to the manufacturer's instructions. The genomic DNA was sequenced at Macrogen, Inc., Seoul, South Korea, by an Illumina HiSeq2000 system using a whole-genome shotgun strategy. The total length of the assembled genome of U. muehlenbergii KoLRILF000956 was 34,812,353 bp, with a GC content of 47.12%, representing 663-fold coverage. The genome was assembled into seven scaffolds (≥1,000 bp) using the ALLPATHS-LG assembler (15) and SSPACE version 2.0 (16). Subsequent gene prediction analysis using MAKER (17) yielded a total of 8,294 protein-coding genes. Using the three previously developed gene family pipelines (18–20), we predicted 299 transcription factor genes, 67 cytochrome P450 genes, and 1,488 genes encoding secretory proteins. In addition, 20 putative polyketide synthase genes, containing ketoacyl synthase, acyltransferase, and acyl carrier domains, were predicted by domain search (21).
Since a transformation system has now been developed for U. muehlenbergii, the draft genome of U. muehlenbergii is a valuable resource for identifying the genes for symbiosis and production of secondary metabolites in lichen, and it also provide a platform to facilitate comparative genomics with other lichen-forming fungi. Moreover, further analysis of the genome will provide insights for functional, biological, and chemical analyses in lichen.
Nucleotide sequence accession numbers.The draft genome sequence of U. muehlenbergii KoLRILF000956 has been deposited at GenBank under the accession number JFDN00000000. The version described in this article is version JFDN01000000. The scaffold sequences were also deposited at GenBank under accession numbers from KK106981 to KK106987 (seven scaffolds).
ACKNOWLEDGMENTS
This work was supported by grants from the Korea National Research Resource Center Program through the National Research Foundation of Korea (2012M3A9B8021726), the National Research Foundation of Korea grant funded by the Ministry of Education (2011-0019465), the Korean government (2008-0061897, 2013-003196, 2013R1A1A2013062, and 2013R1A1A2060561), and the Next-Generation BioGreen21 Program of Rural Development Administration in Korea (PJ00821201).
FOOTNOTES
- Received 3 April 2014.
- Accepted 9 April 2014.
- Published 24 April 2014.
- Copyright © 2014 Park et al.
This is an open-access article distributed under the terms of the Creative Commons Attribution 3.0 Unported license.
