Department of Plant Pathology and Microbiology, University of California, Riverside, CA 92521, USA.
Proc Natl Acad Sci U S A. 2010 Jun 29;107(26):11889-94. doi: 10.1073/pnas.1003391107. Epub 2010 Jun 14.
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.
双孢蘑菇 Coprinopsis cinerea 是真菌中多细胞发育的经典实验模型,因为它在定义的培养基上生长,在 2 周内完成其生命周期,产生约 10(8)个同步的减数分裂细胞,并且可以在发育的所有阶段通过突变和转化进行操作。C. cinerea 的 3700 万碱基对基因组被测序并组装成 13 条染色体。减数分裂重组率沿染色体变化很大,并且在减数分裂重组率低的基因组的大区域中没有反转录转座子。在染色体的低重组区域,具有可识别的同源物的单拷贝基因是主要的。相比之下,在高度重组区域中发现了等位基因的多拷贝基因,包括独特于多细胞真菌的一大类蛋白激酶(FunK1)家族。对 P450 和疏水性蛋白基因家族的分析证实了局部基因重复驱动了等位基因拷贝的扩张,并且扩张发生在 Agaricomycotina 真菌的独立谱系中。来自微阵列的基因表达谱分析用于剖析双核体形成(交配)的转录程序。FunK1 激酶家族的几个成员在有性形态发生过程中受到差异调控,并且相邻重复的协调调控很少见。C. cinerea 和共生担子菌 Laccaria bicolor 的基因组共享广泛的同线性区域。最大的同线性块出现在减数分裂重组率低、没有转座元件和紧密基因间隔的区域,其中同源单拷贝基因的比例过高。C. cinerea 的染色体组装是理解真菌中多细胞性进化的重要资源。