Expression profiling and characterization of key RGA involved in lentil Fusarium wilt Race 5 resistance.

Autor: Nishmitha K; Division of Plant Pathology, ICAR-Indian Agricultural Research Institute, New Delhi, 110012, India., Singh R; Division of Genomic Resources, ICAR-National Bureau of Plant Genetic Resources, New Delhi, 110012, India., Akhtar J; Division of Plant Quarantine, ICAR-National Bureau of Plant Genetic Resources, New Delhi, 110012, India., Bashyal BM; Division of Plant Pathology, ICAR-Indian Agricultural Research Institute, New Delhi, 110012, India., Dubey SC; Indian Council of Agricultural Research, New Delhi, 110001, India., Tripathi A; Division of Plant Quarantine, ICAR-National Bureau of Plant Genetic Resources, New Delhi, 110012, India., Kamil D; Division of Plant Pathology, ICAR-Indian Agricultural Research Institute, New Delhi, 110012, India. deebakamil@gmail.com.
Jazyk: angličtina
Zdroj: World journal of microbiology & biotechnology [World J Microbiol Biotechnol] 2023 Sep 15; Vol. 39 (11), pp. 306. Date of Electronic Publication: 2023 Sep 15.
DOI: 10.1007/s11274-023-03748-4
Abstrakt: Fusarium wilt is a major threat to lentil production in India and worldwide. The presence of evolving virulent races has imposed the necessity of reliable management practices including breeding for resistance using unexplored germplasms. The magnitude of resistance by the plant is determined by rapid recognition of the pathogen and induction of defence genes. Resistance gene analogues have been key factors involved in the recognition and induction of defence response. In the present study, the expression of key RGA previously cloned was determined in three resistant accessions (L65, L83 and L90) and a susceptible accession (L27). The expression was assessed via qPCR at 24, 48 and 72 hpi against virulent race5 (CG-5). All the RGAs differentially transcribed in resistant and susceptible accession showed temporal variation. RGA Lc2, Lc8, Ln1 and Lo6 produced cDNA signals during early infection (24 hpi) predicting its involvement in recognition. LoRGA6 showed significant upregulation in L65 and L83 while downregulating in L27 and the full length of LoRGA6 loci was isolated by 5' and 3' RACE PCR. In-silico characterization revealed LoRGA6 loci code for 912 amino acids long polypeptide with a TIR motif at the N terminal and eight LRR motifs at the C terminal. The tertiary structure revealed a concave pocket-like structure at the LRR domain potentially involved in pathogen effectors interaction. The loci have ADP binding domain and ATPase activity. This has further paved the path for functional analysis of the loci by VIGS to understand the molecular mechanism of resistance.
(© 2023. The Author(s), under exclusive licence to Springer Nature B.V.)
Databáze: MEDLINE
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