Koczyk Grzegorz, Dawidziuk Adam, Popiel Delfina
Department of Biometrics and Bioinformatics
Department of Pathogen Genetics and Plant Resistance and Institute of Plant Genetics, Polish Academy of Sciences, Poznan, Poland.
Genome Biol Evol. 2015 Nov 3;7(11):3132-54. doi: 10.1093/gbe/evv204.
In recent years, the influx of newly sequenced fungal genomes has enabled sampling of secondary metabolite biosynthesis on an unprecedented scale. However, explanations of extant diversity which take into account both large-scale phylogeny reconstructions and knowledge gained from multiple genome projects are still lacking. We analyzed the evolutionary sources of genetic diversity in aromatic polyketide biosynthesis in over 100 model fungal genomes. By reconciling the history of over 400 nonreducing polyketide synthases (NR-PKSs) with corresponding species history, we demonstrate that extant fungal NR-PKSs are clades of distant siblings, originating from a burst of duplications in early Pezizomycotina and thinned by extensive losses. The capability of higher fungi to biosynthesize the simplest precursor molecule (orsellinic acid) is highlighted as an ancestral trait underlying biosynthesis of aromatic compounds. This base activity was modified during early evolution of filamentous fungi, toward divergent reaction schemes associated with biosynthesis of, for example, aflatoxins and fusarubins (C4-C9 cyclization) or various anthraquinone derivatives (C6-C11 cyclization). The functional plasticity is further shown to have been supplemented by modularization of domain architecture into discrete pieces (conserved splice junctions within product template domain), as well as tight linkage of key accessory enzyme families and divergence in employed transcriptional factors. Although the majority of discord between species and gene history is explained by ancient duplications, this landscape has been altered by more recent duplications, as well as multiple horizontal gene transfers. The 25 detected transfers include previously undescribed events leading to emergence of, for example, fusarubin biosynthesis in Fusarium genus. Both the underlying data and the results of present analysis (including alternative scenarios revealed by sampling multiple reconciliation optima) are maintained as a freely available web-based resource: http://cropnet.pl/metasites/sekmet/nrpks_2014.
近年来,新测序的真菌基因组大量涌入,使得次生代谢产物生物合成的采样规模达到了前所未有的程度。然而,目前仍缺乏能够兼顾大规模系统发育重建以及从多个基因组计划中获取的知识来解释现存多样性的研究。我们分析了100多个模式真菌基因组中芳香族聚酮化合物生物合成过程中遗传多样性的进化来源。通过将400多种非还原型聚酮合酶(NR-PKSs)的历史与相应物种的历史进行比对,我们证明现存的真菌NR-PKSs是远亲分支,起源于早期粪壳菌纲的一次复制爆发,并因大量丢失而减少。高等真菌生物合成最简单前体分子(苔色酸)的能力被突出显示为芳香族化合物生物合成的一个祖先特征。这种基本活性在丝状真菌的早期进化过程中发生了改变,朝着与例如黄曲霉毒素和镰孢菌素(C4-C9环化)或各种蒽醌衍生物(C6-C11环化)生物合成相关的不同反应方案发展。功能可塑性还进一步表现为结构域架构模块化成分离的片段(产物模板结构域内保守的剪接连接),以及关键辅助酶家族的紧密联系和所采用转录因子的差异。尽管物种与基因历史之间的大多数不一致可以用古代复制来解释,但这种情况已因近期的复制以及多次水平基因转移而发生了改变。检测到的25次转移包括一些此前未描述的事件,例如导致镰刀菌属中镰孢菌素生物合成的出现。基础数据以及当前分析的结果(包括通过对多个比对最优解进行采样揭示的替代情况)均作为一个免费的基于网络的资源予以保留:http://cropnet.pl/metasites/sekmet/nrpks_2014 。