Saabale Parasappa R, Dubey Sunil C, Priyanka Kumari, Sharma Tilak R
1Division of Plant Pathology, Indian Agricultural Research Institute, New Delhi, 110 012 India.
2Present Address: Regional Research Centre, Indian Institute of Pulses Research, Dharwad, 580005 India.
3 Biotech. 2018 Feb;8(2):111. doi: 10.1007/s13205-018-1128-z. Epub 2018 Feb 5.
The present study reports the transcriptome analysis of resistance (WR315) and susceptible (JG62) genotypes of chickpea in response to f. sp. () race 4 using the method of suppression subtractive hybridization. Altogether, 162 chickpea-expressed sequence tags (ESTs) were identified from two libraries and analyzed to catalog eight functional categories. These ESTs could be assembled into 18 contigs and 144 singletons with 10 contigs and 68 singletons from compatible and 8 contigs and 70 singletons from incompatible interaction. The largest category consisted of ESTs which encode for proteins related to hypothetical proteins (22.8%), followed by energy and metabolism (20.3%)-related genes, defense and cell rescue-related genes (17.9%) and signal transduction-related genes (16%). Among them, 17.1 and 18.7% were defense-related genes in compatible and incompatible interaction, respectively. These ESTs mainly includes various putative genes related to oxidative burst, pathogenesis and secondary metabolism. Induction of putative superoxide dismutase, metallothionein, 4-coumarate-CoA ligase, heat shock proteins and cysteine proteases indicated oxidative burst after infection. The ESTs belonged to various functional categories which were directly and indirectly associated with defense signaling pathways. Quantitative and semi-quantitative polymerase chain reaction exhibited differential expression of candidate genes and detected higher levels in incompatible interaction compared to compatible interaction. The present study revealed partial molecular mechanism associated with the resistance in chickpea against , which is the key to design a strategy for incorporation of resistance via either biotechnological means or introgression of resistance genes.
本研究报告了采用抑制性消减杂交方法,对鹰嘴豆抗性(WR315)和敏感(JG62)基因型针对尖孢镰刀菌(Fusarium oxysporum f. sp. ciceris)4号生理小种的转录组分析。总共从两个文库中鉴定出162个鹰嘴豆表达序列标签(EST),并对其进行分析以归类为八个功能类别。这些EST可组装成18个重叠群和144个单拷贝序列,其中10个重叠群和68个单拷贝序列来自亲和互作,8个重叠群和70个单拷贝序列来自非亲和互作。最大的类别是编码与假定蛋白相关的EST(22.8%),其次是与能量和代谢相关的基因(20.3%)、防御和细胞拯救相关基因(17.9%)以及信号转导相关基因(16%)。其中,在亲和互作和非亲和互作中,防御相关基因分别占17.1%和18.7%。这些EST主要包括与氧化爆发、致病机制和次生代谢相关的各种假定基因。假定的超氧化物歧化酶、金属硫蛋白、4-香豆酸辅酶A连接酶、热休克蛋白和半胱氨酸蛋白酶的诱导表明感染后发生了氧化爆发。这些EST属于与防御信号通路直接或间接相关的各种功能类别。定量和半定量聚合酶链反应显示候选基因的差异表达,且与亲和互作相比,在非亲和互作中检测到更高水平。本研究揭示了鹰嘴豆对尖孢镰刀菌抗性相关的部分分子机制,这是通过生物技术手段或抗性基因渗入来设计抗性整合策略的关键。