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In silico structural-functional characterization of three differentially expressed resistance gene analogs identified in Dalbergia sissoo against dieback disease reveals their role in immune response regulation
by
Ul Haq, Imran
, Nasir, Bukhtawer
, Ijaz, Siddra
, Ali, Hayssam M.
, Kaur, Sukhwinder
, Razzaq, Hafiza Arooj
in
Binding sites
/ Biology
/ Dalbergia sissoo
/ Defensive behavior
/ Dieback
/ Disease
/ Disease resistance
/ Economic importance
/ Genes
/ Genomes
/ Genomics
/ Germplasm
/ Homology
/ homology modeling
/ Immune response
/ Immune system
/ Kinases
/ leucine-rich repeats
/ Localization
/ nucleotide-binding site
/ Pathogens
/ Plant immunity
/ Plant Science
/ Population decline
/ protein fingerprints
/ Proteins
/ Signal transduction
/ Structural analysis
/ Structure-function relationships
/ Transcriptomes
/ Transthyretin
2023
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In silico structural-functional characterization of three differentially expressed resistance gene analogs identified in Dalbergia sissoo against dieback disease reveals their role in immune response regulation
by
Ul Haq, Imran
, Nasir, Bukhtawer
, Ijaz, Siddra
, Ali, Hayssam M.
, Kaur, Sukhwinder
, Razzaq, Hafiza Arooj
in
Binding sites
/ Biology
/ Dalbergia sissoo
/ Defensive behavior
/ Dieback
/ Disease
/ Disease resistance
/ Economic importance
/ Genes
/ Genomes
/ Genomics
/ Germplasm
/ Homology
/ homology modeling
/ Immune response
/ Immune system
/ Kinases
/ leucine-rich repeats
/ Localization
/ nucleotide-binding site
/ Pathogens
/ Plant immunity
/ Plant Science
/ Population decline
/ protein fingerprints
/ Proteins
/ Signal transduction
/ Structural analysis
/ Structure-function relationships
/ Transcriptomes
/ Transthyretin
2023
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In silico structural-functional characterization of three differentially expressed resistance gene analogs identified in Dalbergia sissoo against dieback disease reveals their role in immune response regulation
by
Ul Haq, Imran
, Nasir, Bukhtawer
, Ijaz, Siddra
, Ali, Hayssam M.
, Kaur, Sukhwinder
, Razzaq, Hafiza Arooj
in
Binding sites
/ Biology
/ Dalbergia sissoo
/ Defensive behavior
/ Dieback
/ Disease
/ Disease resistance
/ Economic importance
/ Genes
/ Genomes
/ Genomics
/ Germplasm
/ Homology
/ homology modeling
/ Immune response
/ Immune system
/ Kinases
/ leucine-rich repeats
/ Localization
/ nucleotide-binding site
/ Pathogens
/ Plant immunity
/ Plant Science
/ Population decline
/ protein fingerprints
/ Proteins
/ Signal transduction
/ Structural analysis
/ Structure-function relationships
/ Transcriptomes
/ Transthyretin
2023
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In silico structural-functional characterization of three differentially expressed resistance gene analogs identified in Dalbergia sissoo against dieback disease reveals their role in immune response regulation
Journal Article
In silico structural-functional characterization of three differentially expressed resistance gene analogs identified in Dalbergia sissoo against dieback disease reveals their role in immune response regulation
2023
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Overview
Plant immunity includes enemy recognition, signal transduction, and defensive response against pathogens. We experimented to identify the genes that contribute resistance against dieback disease to Dalbergia sissoo , an economically important timber tree. In this study, we investigated the role of three differentially expressed genes identified in the dieback-induced transcriptome in Dalbergia sissoo. The transcriptome was probed using DOP-rtPCR analysis. The identified RGAs were characterized in silico as the contributors of disease resistance that switch on under dieback stress. Their predicted fingerprints revealed involvement in stress response. Ds-DbRCaG-02-Rga.a, Ds-DbRCaG-04-Rga.b, and Ds-DbRCaG-06-Rga.c showed structural homology with the Transthyretin-52 domain, EAL associated YkuI_C domain, and Src homology-3 domain respectively, which are the attributes of signaling proteins possessing a role in regulating immune responses in plants. Based on in-silico structural and functional characterization, they were predicted to have a role in immune response regulation in D. sissoo.
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