Ma Jian, Stiller Jiri, Zhao Qiang, Feng Qi, Cavanagh Colin, Wang Penghao, Gardiner Donald, Choulet Frédéric, Feuillet Catherine, Zheng You-Liang, Wei Yuming, Yan Guijun, Han Bin, Manners John M, Liu Chunji
CSIRO Agriculture Flagship, St Lucia, QLD, Australia; Triticeae Research Institute, Sichuan Agricultural University, Wenjiang, Chengdu, China.
CSIRO Agriculture Flagship, St Lucia, QLD, Australia.
PLoS One. 2014 Nov 18;9(11):e113309. doi: 10.1371/journal.pone.0113309. eCollection 2014.
Fusarium pathogens cause two major diseases in cereals, Fusarium crown rot (FCR) and head blight (FHB). A large-effect locus conferring resistance to FCR disease was previously located to chromosome arm 3BL (designated as Qcrs-3B) and several independent sets of near isogenic lines (NILs) have been developed for this locus. In this study, five sets of the NILs were used to examine transcriptional changes associated with the Qcrs-3B locus and to identify genes linked to the resistance locus as a step towards the isolation of the causative gene(s). Of the differentially expressed genes (DEGs) detected between the NILs, 12.7% was located on the single chromosome 3B. Of the expressed genes containing SNP (SNP-EGs) detected, 23.5% was mapped to this chromosome. Several of the DEGs and SNP-EGs are known to be involved in host-pathogen interactions, and a large number of the DEGs were among those detected for FHB in previous studies. Of the DEGs detected, 22 were mapped in the Qcrs-3B interval and they included eight which were detected in the resistant isolines only. The enrichment of DEG, and not necessarily those containing SNPs between the resistant and susceptible isolines, around the Qcrs-3B locus is suggestive of local regulation of this region by the resistance allele. Functions for 13 of these DEGs are known. Of the SNP-EGs, 28 were mapped in the Qcrs-3B interval and biological functions for 16 of them are known. These results provide insights into responses regulated by the 3BL locus and identify a tractable number of target genes for fine mapping and functional testing to identify the causative gene(s) at this QTL.
镰刀菌病原体在谷物中引发两种主要病害,即镰刀菌冠腐病(FCR)和赤霉病(FHB)。先前已将一个对FCR病害具有抗性的主效基因座定位到3B染色体臂(命名为Qcrs - 3B),并针对该基因座开发了几套独立的近等基因系(NILs)。在本研究中,使用了五套NILs来检测与Qcrs - 3B基因座相关的转录变化,并鉴定与抗性基因座连锁的基因,这是朝着分离致病基因迈出的一步。在NILs之间检测到的差异表达基因(DEGs)中,12.7%位于单条3B染色体上。在检测到的含有单核苷酸多态性的表达基因(SNP - EGs)中,23.5%定位到这条染色体上。已知一些DEGs和SNP - EGs参与宿主 - 病原体相互作用,并且大量的DEGs是先前研究中在FHB检测到的那些。在检测到的DEGs中,有22个定位在Qcrs - 3B区间,其中包括仅在抗性近等基因系中检测到的8个。Qcrs - 3B基因座周围DEG的富集,而不一定是抗性和感病近等基因系之间含有SNP的那些,表明抗性等位基因对该区域有局部调控作用。已知其中13个DEGs的功能。在SNP - EGs中,有28个定位在Qcrs - 3B区间,其中16个的生物学功能已知。这些结果为3B染色体臂基因座调控的反应提供了见解,并确定了数量可控的目标基因,用于精细定位和功能测试,以鉴定该QTL处的致病基因。