Please use this identifier to cite or link to this item: http://223.31.159.10:8080/jspui/handle/123456789/1164
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dc.contributor.authorPrasad, Ashish-
dc.contributor.authorHari‑Gowthem, Gunaseelen-
dc.contributor.authorMuthamilarasan, Mehanathan-
dc.contributor.authorHussain, Zakir-
dc.contributor.authorYadav, Pawan Kumar-
dc.contributor.authorTripathi, Sandhya-
dc.contributor.authorPrasad, Manoj-
dc.date.accessioned2021-02-12T07:09:23Z-
dc.date.available2021-02-12T07:09:23Z-
dc.date.issued2021-
dc.identifier.citationTheoretical and Applied Genetics, 134(5): 1463-1474en_US
dc.identifier.issn0040-5752-
dc.identifier.otherhttps://doi.org/10.1007/s00122-021-03783-5-
dc.identifier.urihttps://link.springer.com/article/10.1007/s00122-021-03783-5-
dc.identifier.urihttp://223.31.159.10:8080/jspui/handle/123456789/1164-
dc.descriptionAccepted date: 22 January 2021en_US
dc.description.abstractAutophagy is a highly conserved catabolic process regulating cellular homeostasis and adaptation to different biotic and abiotic stress. Several autophagy-related proteins (ATGs) are reported to be involved in autophagic processes, and considering their importance in regulating growth and stress adaptation, these proteins have been identified and characterized in several plant species. However, there is no information available on the role of autophagy-related proteins regulating the tolerance of tomato to tomato leaf curl disease (ToLCD). Given this, the present genome-wide study identified thirty ATG-encoding genes (SlATG) in tomato, followed by their functional characterization. Expression profiling of the SlATG genes in contrasting tomato cultivars subjected to virus infection showed a 4.5-fold upregulation of SlATG18f in the tolerant cultivar. Further, virus-induced gene silencing of SlATG18f in the tolerant cultivar conferred disease susceptibility, which suggested the role of this gene in Tomato leaf curl New Delhi virus tolerance. Comparison of the gene sequence of both tolerant and susceptible cultivars along with the 5′ upstream regions identified an SNP (A/T) at -2916 upstream of the start codon. A cleaved amplified polymorphic sequence (CAPS) marker was developed targeting this region, which showed a significant association with the tolerance characteristics in the tomato germplasm (R2 = 0.1787). Altogether, the study identified a potential gene that could be used to develop ToLCNDV tolerant tomato cultivars using transgene-based or marker-assisted breeding-based approaches.en_US
dc.description.sponsorshipThe authors’ work in the area of plant–virus interaction is supported by the NIPGR Core grant and the Department of Biotechnology, Govt. of India, India (Project File No. BT/PR7024/PBD/16/1015/2012). The research fellowships awarded to A.P. by the Council of Scientific and Industrial Research, Govt. of India and G.H-G. by the Department of Biotechnology, Govt. of India are acknowledged. The authors thank Dr. Swarup K Parida, Scientist, NIPGR, New Delhi, India, for critically reading the manuscript. The authors are also thankful to DBT-eLibrary Consortium (DeLCON) for providing access to e-resources.en_US
dc.language.isoen_USen_US
dc.publisherSpringer Nature Publishing AGen_US
dc.subjectTomato leaf curl New Delhi virusen_US
dc.subjectSlATG18fen_US
dc.titleMolecular characterization of SlATG18f in response to Tomato leaf curl New Delhi virus infection in tomato and development of a CAPS marker for leaf curl disease toleranceen_US
dc.typeArticleen_US
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