These genomes vary in size from 18 844 nucleotides (nt) in Hanseniaspora uvarum to 109 103 nt in Moniliophthora perniciosa. There is no apparent correlation of genome size and gene content: size differences can be attributed to the size of introns and intergenic regions and the presence of integrated plasmids. Of the two major types of mitochondrial introns, type I is the norm in fungal mitochondrial genomes, while type II are usually present only in plant mitochondrial genomes (Lang et al., 2007). Trametes cingulata (Bakshi et al., 1970)

HIF inhibitor is a heterothallic dikaryon originally isolated from rotting Shorea robusta lumber. We present the sequence of the T. cingulata mitochondrial genome and compare it with the mitochondrial genomes of five basidiomycete species. Trametes is a representative genus of the polypore clade in the subphylum Agaricomycotina (Ko & Jung, 1999; Hibbett et al., 2007). The available mitochondrial

genomes of Basidiomycota at NCBI are represented by four species of Agaricomycotina including Pleurotus ostreatus (Wang et al., 2008), M. perniciosa (Formighieri et al., 2008), Schizophyllum commune and Cryptococcus neoformans var. grubii. The Ustilaginomycotina Atezolizumab clinical trial is a sister clade of the Agaricomycotina and we have selected Ustilago maydis as a representative for this group. Trametes cingulata was obtained from the American Type Culture Collection (http://www.atcc.org accession number ) and maintained and grown on 2% malt extract agar plates at room temperature. DNA was isolated from hyphae essentially as described by Raeder & Broda (1985). Hyphae were

collected by filtration or centrifugation, Abiraterone ic50 washed with 20 mM EDTA, pH 8.0, and freeze-dried for 24–48 h. Samples were crushed at room temperature in a mortar and resuspended in extraction buffer (200 mM Tris-Cl, pH 8.5, 250 mM NaCl, 25 mM EDTA, 0.5% SDS) using about 2 mL per 0.1 g of dried tissue. Phenol (∼0.7 vol.) was added to the slurry, which was then mixed for 2 min. Following the addition of ∼0.3 vol. chloroform, mixing and centrifugation at 10 000 g for 1 h, the aqueous layer was transferred to a new tube and 1/20 vol. of 20 mg mL−1 RNAse A was added and incubated 37 °C for 20 min. The RNAse was extracted with 1 vol. chloroform and the tube was centrifuged at 10 000 g for 10 min. DNA was precipitated from the aqueous layer by the slow addition of isopropanol (∼1 vol.). The precipitated mass of DNA was sequentially washed with 50% isopropanol and 70% ethanol, dried briefly and resuspended in TE buffer (10 mM Tris-Cl pH 7.5, 1 mM EDTA). This preparation included genomic and mtDNA. DNA was sequenced using a GLS FLX sequencer (http://www.454.com) and assembled using a gs de novo assembler (version 1.1.03). The final mitochondrial genome assembly was performed using bioinformatic procedures developed at the Computational Genetics Laboratory at the Minnesota Supercomputing Institute. The raw end reads of the assembled contigs were compared using blast (Altschul et al.