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Global DNA Methylation in the Chestnut Blight Fungus Cryphonectria parasitica and Genome-Wide Changes in DNA Methylation Accompanied with Sectorization

机译:板栗疫霉Cryphonectria parasitica中的全球DNA甲基化和DNA甲基化的基因组范围的变化与扇区化。

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摘要

Mutation in CpBck1, an ortholog of the cell wall integrity mitogen-activated protein kinase kinase kinase (MAPKKK) of Saccharomyces cerevisiae, in the chestnut blight fungus Cryphonectria parasitica resulted in a sporadic sectorization as culture proceeded. The progeny from the sectored area maintained the characteristics of the sector, showing a massive morphogenetic change, including robust mycelial growth without differentiation. Epigenetic changes were investigated as the genetic mechanism underlying this sectorization. Quantification of DNA methylation and whole-genome bisulfite sequencing revealed genome-wide DNA methylation of the wild-type at each nucleotide level and changes in DNA methylation of the sectored progeny. Compared to the wild-type, the sectored progeny exhibited marked genome-wide DNA hypomethylation but increased methylation sites. Expression analysis of two DNA methyltransferases, including two representative types of DNA methyltransferase (DNMTase), demonstrated that both were significantly down-regulated in the sectored progeny. However, functional analysis using mutant phenotypes of corresponding DNMTases demonstrated that a mutant of CpDmt1, an ortholog of RID of Neurospora crassa, resulted in the sectored phenotype but the CpDmt2 mutant did not, suggesting that the genetic basis of fungal sectorization is more complex. The present study revealed that a mutation in a signaling pathway component resulted in sectorization accompanied with changes in genome-wide DNA methylation, which suggests that this signal transduction pathway is important for epigenetic control of sectorization via regulation of genes involved in DNA methylation.
机译:CpBck1突变是板栗枯萎病菌寄生拟ry中的酿酒酵母细胞壁完整性有丝分裂原激活的蛋白激酶激酶激酶(MAPKKK)的直系同源基因,随着培养的进行,导致了零星的扇形化。来自扇形区的后代保持了扇形的特征,显示出巨大的形态发生变化,包括强劲的菌丝生长而没有分化。表观遗传的变化被作为这一部门的基础遗传机制进行了研究。 DNA甲基化和全基因组亚硫酸氢盐测序的定量揭示了在每个核苷酸水平上野生型的全基因组DNA甲基化和扇形后代的DNA甲基化变化。与野生型相比,扇形后代表现出明显的全基因组DNA低甲基化,但甲基化位点增加。对两种DNA甲基转移酶(包括两种代表性类型的DNA甲基转移酶(DNMTase))的表达分析表明,在扇形后代中两者均显着下调。但是,使用相应DNMTase的突变表型进行的功能分析表明,CspDmt1突变体(crus Neurospora crassa的RID的直系同源物)的突变体导致了扇形表型,但CpDmt2突变体却没有,这表明真菌扇形化的遗传基础更加复杂。本研究表明,信号通路成分的突变导致扇形化并伴随着全基因组DNA甲基化的变化,这表明该信号转导通路对于通过调控参与DNA甲基化的基因对扇形化进行表观遗传控制很重要。

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