Institute for Biology I, Unit of Plant Molecular Cell Biology, RWTH Aachen University, Aachen, Germany.
Plant Protection Institute, Centre for Agricultural Research, Hungarian Academy of Sciences, Budapest, Hungary.
mBio. 2019 Sep 24;10(5):e01692-19. doi: 10.1128/mBio.01692-19.
Due to their comparatively small genome size and short generation time, fungi are exquisite model systems to study eukaryotic genome evolution. Powdery mildew fungi present an exceptional case because of their strict host dependency (termed obligate biotrophy) and the atypical size of their genomes (>100 Mb). This size expansion is largely due to the pervasiveness of transposable elements on 70% of the genome and is associated with the loss of multiple conserved ascomycete genes required for a free-living lifestyle. To date, little is known about the mechanisms that drove these changes, and information on ancestral powdery mildew genomes is lacking. We report genome analysis of the early-diverged and exclusively sexually reproducing powdery mildew fungus , which we performed on the basis of a natural leaf epiphytic metapopulation sample. In contrast to other sequenced species of this taxonomic group, the assembled draft genome is surprisingly small (<30 Mb), has a higher content of conserved ascomycete genes, and is sparsely equipped with transposons (<10%), despite the conserved absence of a common defense mechanism involved in constraining repetitive elements. We speculate that transposable element spread might have been limited by this pathogen's unique reproduction strategy and host features and further hypothesize that the loss of conserved ascomycete genes may promote the evolutionary isolation and host niche specialization of powdery mildew fungi. Limitations associated with this evolutionary trajectory might have been in part counteracted by the evolution of plastic, transposon-rich genomes and/or the expansion of gene families encoding secreted virulence proteins. Powdery mildew fungi are widespread and agronomically relevant phytopathogens causing major yield losses. Their genomes have disproportionately large numbers of mobile genetic elements, and they have experienced a significant loss of highly conserved fungal genes. In order to learn more about the evolutionary history of this fungal group, we explored the genome of an Asian oak tree pathogen, , a species that diverged early during evolution from the remaining powdery mildew fungi. We found that the draft genome is comparatively compact, has a low number of protein-coding genes, and, despite the absence of a dedicated genome defense system, lacks the massive proliferation of repetitive sequences. Based on these findings, we infer an evolutionary trajectory that shaped the genomes of powdery mildew fungi.
由于真菌的基因组相对较小且世代时间短,因此它们是研究真核生物基因组进化的理想模式系统。白粉菌真菌是一个特殊的例子,因为它们严格的宿主依赖性(称为专性生物营养型)和不典型的基因组大小(> 100Mb)。这种大小的扩张在很大程度上是由于 70%的基因组上普遍存在转座元件,并且与多个保守的子囊菌基因的丧失有关,这些基因对于自由生活方式是必需的。迄今为止,对于驱动这些变化的机制知之甚少,并且缺乏有关原始白粉菌基因组的信息。我们报告了早期分化且仅通过有性繁殖的白粉菌真菌的基因组分析,我们是基于自然叶附生的复合种群样本进行的。与该分类群的其他已测序物种相比,组装的草案基因组出奇地小(<30Mb),具有更高含量的保守子囊菌基因,并且转座子的数量很少(<10%),尽管保守的缺失一种常见的防御机制涉及限制重复元件。我们推测,转座元件的传播可能受到该病原体独特的繁殖策略和宿主特征的限制,并且进一步假设保守的子囊菌基因的丧失可能促进白粉菌真菌的进化隔离和宿主生态位特化。与这种进化轨迹相关的限制可能部分被可塑的、富含转座子的基因组的进化和/或编码分泌毒力蛋白的基因家族的扩展所抵消。白粉菌真菌是广泛存在且具有农业重要性的植物病原体,会导致重大产量损失。它们的基因组中有不成比例数量的移动遗传元件,并且经历了高度保守真菌基因的大量丧失。为了更多地了解该真菌组的进化历史,我们探索了亚洲栎树病原体的基因组,该物种在进化过程中很早就与其余的白粉菌真菌分化。我们发现,草案基因组相对紧凑,具有较少的蛋白质编码基因,并且尽管缺乏专门的基因组防御系统,但缺乏重复序列的大量增殖。基于这些发现,我们推断出一种塑造白粉菌真菌基因组的进化轨迹。