Syme Robert A, Martin Anke, Wyatt Nathan A, Lawrence Julie A, Muria-Gonzalez Mariano J, Friesen Timothy L, Ellwood Simon R
Centre for Crop and Disease Management, Department of Environment and Agriculture, Curtin University, Bentley, WA, Australia.
Centre for Crop Health, University of Southern Queensland, Toowoomba, QLD, Australia.
Front Genet. 2018 Apr 18;9:130. doi: 10.3389/fgene.2018.00130. eCollection 2018.
, f. (PTT) and f. (PTM) cause significant diseases in barley, but little is known about the large-scale genomic differences that may distinguish the two forms. Comprehensive genome assemblies were constructed from long DNA reads, optical and genetic maps. As repeat masking in fungal genomes influences the final gene annotations, an accurate and reproducible pipeline was developed to ensure comparability between isolates. The genomes of the two forms are highly collinear, each composed of 12 chromosomes. Genome evolution in is characterized by genome fissuring through the insertion and expansion of transposable elements (TEs), a process that isolates blocks of genic sequence. The phenomenon is particularly pronounced in PTT, which has a larger, more repetitive genome than PTM and more recent transposon activity measured by the frequency and size of genome fissures. PTT has a longer cultivated host association and, notably, a greater range of host-pathogen genetic interactions compared to other spp., a property which associates better with genome size than pathogen lifestyle. The two forms possess similar complements of TE families with Tc1/Mariner and LINE-like Tad-1 elements more abundant in PTT. Tad-1 was only detectable as vestigial fragments in PTM and, within the forms, differences in genome sizes and the presence and absence of several TE families indicated recent lineage invasions. Gene differences between forms are mainly associated with gene-sparse regions near or within TE-rich regions, with many genes possessing characteristics of fungal effectors. Instances of gene interruption by transposons resulting in pseudogenization were detected in PTT. In addition, both forms have a large complement of secondary metabolite gene clusters indicating significant capacity to produce an array of different molecules. This study provides genomic resources for functional genetics to help dissect factors underlying the host-pathogen interactions.
大麦中的禾谷镰刀菌(Fusarium graminearum)的两种形态,即禾谷镰刀菌(PTT)和禾谷镰刀菌(PTM)会引发严重病害,但对于可能区分这两种形态的大规模基因组差异却知之甚少。利用长DNA reads、光学图谱和遗传图谱构建了全面的基因组组装。由于真菌基因组中的重复序列掩盖会影响最终的基因注释,因此开发了一种准确且可重复的流程以确保分离株之间的可比性。这两种形态的基因组高度共线,均由12条染色体组成。禾谷镰刀菌的基因组进化特征是通过转座元件(TEs)的插入和扩展导致基因组断裂,这一过程会隔离基因序列块。这种现象在PTT中尤为明显,其基因组比PTM更大、更具重复性,并且通过基因组断裂的频率和大小衡量的转座子活性更新。与其他禾谷镰刀菌物种相比,PTT与栽培宿主的关联时间更长,值得注意的是,其宿主 - 病原体遗传相互作用的范围更广,这种特性与基因组大小的关联比病原体生活方式更好。这两种形态拥有相似的TE家族互补性,其中Tc1/Mariner和类似LINE的Tad - 1元件在PTT中更为丰富。Tad - 1在PTM中仅能检测到残余片段,并且在这两种形态中,基因组大小的差异以及几个TE家族的有无表明了近期谱系入侵。两种形态之间的基因差异主要与富含TE区域附近或内部的基因稀疏区域相关,许多基因具有真菌效应子的特征。在PTT中检测到转座子导致基因中断并产生假基因的情况。此外,两种形态都有大量的次生代谢物基因簇,表明它们有显著能力产生一系列不同的分子。本研究为功能遗传学提供了基因组资源,以帮助剖析宿主 - 病原体相互作用的潜在因素。