Dolatabadian Aria, Amas Junrey C, Thomas William J W, Sayari Mohammad, Al-Mamun Hawlader Abdullah, Edwards David, Batley Jacqueline
School of Biological Sciences, The University of Western Australia, Perth, WA 6009, Australia.
Department of Plant Science, University of Manitoba, Winnipeg, MB R3T 2N2, Canada.
Genes (Basel). 2025 Jul 22;16(8):849. doi: 10.3390/genes16080849.
This study identifies and classifies resistance gene analogues (RGAs) in the genomes of , and using the RGAugury pipeline. RGAs were categorised into four main classes: receptor-like kinases (RLKs), receptor-like proteins (RLPs), nucleotide-binding leucine-rich repeat (NLR) proteins and transmembrane-coiled-coil (TM-CC) genes. A total of 4499 candidate RGAs were detected, with species-specific proportions. RLKs were the most abundant across all genomes, followed by TM-CCs and RLPs. The sub-classification of RLKs and RLPs identified LRR-RLKs, LRR-RLPs, LysM-RLKs, and LysM-RLPs. Atypical NLRs were more frequent than typical ones in all species. Atypical NLRs were more frequent than typical ones in all species. We explored the relationship between chromosome size and RGA count using regression analysis. In and , larger chromosomes generally harboured more RGAs, while displayed the opposite trend. Exceptions were observed in all species, where some larger chromosomes contained fewer RGAs in and , or more RGAs in . The distribution and density of RGAs across chromosomes were examined. RGA distribution was skewed towards chromosomal ends, with patterns differing across RGA types. Sequence hierarchical pairwise similarity analysis revealed distinct gene clusters, suggesting evolutionary relationships. The study also identified homologous genes among RGAs and non-RGAs in each species, providing insights into disease resistance mechanisms. Finally, RLKs and RLPs were co-localised with reported disease resistance loci in indicating significant associations. Phylogenetic analysis of cloned RGAs and QTL-mapped RLKs and RLPs identified distinct clusters, enhancing our understanding of their evolutionary trajectories. These findings provide a comprehensive view of RGA diversity and genomics in these Brassicaceae species, providing valuable insights for future research in plant disease resistance and crop improvement.
本研究使用RGAugury流程在、和的基因组中鉴定并分类抗性基因类似物(RGA)。RGA被分为四个主要类别:类受体激酶(RLK)、类受体蛋白(RLP)、核苷酸结合富含亮氨酸重复序列(NLR)蛋白和跨膜卷曲螺旋(TM-CC)基因。共检测到4499个候选RGA,具有物种特异性比例。RLK在所有基因组中最为丰富,其次是TM-CC和RLP。RLK和RLP的亚分类鉴定出富含亮氨酸重复序列的类受体激酶(LRR-RLK)、富含亮氨酸重复序列的类受体蛋白(LRR-RLP)、溶菌酶M类受体激酶(LysM-RLK)和溶菌酶M类受体蛋白(LysM-RLP)。在所有物种中,非典型NLR比典型NLR更常见。我们使用回归分析探索了染色体大小与RGA数量之间的关系。在和中,较大的染色体通常含有更多的RGA,而呈现相反的趋势。在所有物种中都观察到了例外情况,在和中一些较大的染色体含有较少的RGA,或者在中含有较多的RGA。研究了RGA在染色体上的分布和密度。RGA分布偏向染色体末端,不同RGA类型的模式不同。序列层次成对相似性分析揭示了不同的基因簇,表明了进化关系。该研究还在每个物种的RGA和非RGA中鉴定出同源基因,为抗病机制提供了见解。最后,RLK和RLP与中报道的抗病基因座共定位,表明存在显著关联。对克隆的RGA以及数量性状位点定位的RLK和RLP进行系统发育分析,确定了不同的簇,加深了我们对其进化轨迹的理解。这些发现提供了这些十字花科物种中RGA多样性和基因组学的全面视图,为未来植物抗病性研究和作物改良提供了有价值的见解。