In silico mining of WRKY TFs through Solanum melongena L. and Solanum incanum L. transcriptomes and identification of SiWRKY53 as a source of resistance to bacterial wilt

WRKY蛋白质结构域 青枯菌 生物 龙葵 青枯病 系统发育树 蜜环菊 转录组 表达序列标记 遗传学 植物 生物信息学 基因 基因表达 细菌
作者
Pallavi Mishra,Ajay Tripathi,Sarvesh Pratap Kashyap,Mohd Aamir,Kavindra Nath Tiwari,Vinay Kumar Singh,S. K. Tiwari
出处
期刊:Plant Gene [Elsevier BV]
卷期号:26: 100278-100278 被引量:19
标识
DOI:10.1016/j.plgene.2021.100278
摘要

Eggplant growth and yield is highly disrupted due to attack by microbial pathogens including bacteria, viruses and fungi. Among these, Ralstonia solanacearum , a soil-borne gram negative bacterium threatens the eggplant productivity on large-scale. While its management is difficult, it could be controlled if the wild species offering candidate resistant genes are known. Since WRKY transcription factors (TFs) are among the major class of regulatory genes playing crucial roles in plant survival during stress conditions challenged due to heat, cold, drought, salinity and pathogens, we utilized the de novo transcriptome sequence of Solanum melongena and S. incanum (available at the TSA database of NCBI with primary accessions GAYR00000000 and GAYS00000000) for mining and characterization of WRKY TFs. As per our findings, 32 and 34 putative WRKY TFs in S. melongena and S. incanum , respectively were identified, which were annotated as WRKY 1 to WRKY 75, and were classified into groups I, IIA-IIE, and III following the fundamental classification of WRKY TFs in eukaryotes. Phylogenetic analysis of all the SmWRKY and SiWRKY showed significant correlation with this classification system. Further, quantitative RT-PCR expression profiling of selected WRKY genes was carried out at different time intervals in eggplant infected by R. solanacearum cultures. Expression analysis revealed the drastic up-regulation of group III SiWRKY53 during 7th day (12.6 folds) and 10th day (27.1 folds) of infection, confirming it as an ideal target gene for enhanced tolerance to bacterial wilt and molecular breeding for development of resistant eggplant cultivars. • Transcriptome-wide identification and characterization of WRKY TFs done using the RNA-seq of S. melongena and S. incanum . • 32 SmWRKY and 34 SiWRKY identified and arranged into separate groups following the standard WRKY classification system. • qRT-PCR analysis of WRKYs in response to R. solanacearum to study disease intensity in cultivated and wild eggplant species. • Results revealed the highest up-regulation of SiWRKY53 on 7 th and 10 th day of the bacterial treatment.
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