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Peer-reviewedCC BYDiscover Plants

Genome wide identification and in silico mRNA expression profiling of the WRKY transcription factor gene family in Salvia hispanica

  1. 1Department of Integrated and Advanced Technology, School of Engineering and Sciences, Sir Padampat Singhania University

Abstract

This study presents the first comprehensive in silico genome-wide identification, characterization, and mRNA expression profiling of the WRKY transcription factor (TF) gene family in Salvia hispanica L. (chia), a nutritious crop of the family Lamiaceae. A total of 35 CsWRKY genes were identified from the chia reference genome and classified into 7 phylogenetic groups (I, IIa–IIe, III) based on WRKY domain number and zinc-finger motif type. Mean protein length, molecular weight and isoelectric point were 332.8 aa, 37,499 Da and 7.62, respectively, and protein length was almost perfectly correlated with molecular weight (r = 0.9995). Subcellular-localization prediction indicated predominantly nuclear and cytoplasmic distribution. Gene-structure analysis revealed 2–7 exons, and MEME identified 15 conserved motifs including the invariant WRKYGQK heptapeptide. Segmental duplication predominated and has evolved under purifying selection. Promoter analysis detected 20 cis-acting regulatory element classes, and a maximum-likelihood phylogeny grouped CsWRKYs with orthologs from Arabidopsis thaliana, Oryza sativa, Glycine max, Medicago truncatula and Physcomitrella patens. In silico expression profiling used only verified, publicly available S. hispanica RNA-Seq datasets and was therefore restricted to tissue-specific and developmental patterns; because no abiotic-stress RNA-Seq dataset is currently available for chia, no stress-responsive expression analysis was performed. Homology models were built and docked with in silico predictions identifying CsWRKY3 as the strongest binder. These in silico predictions provide a preliminary genomic framework that requires future experimental validation and may guide the study of WRKY-mediated processes in chia.

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BibTeX
@article{tiwari2026genome,
  title = {{Genome wide identification and in silico mRNA expression profiling of the WRKY transcription factor gene family in Salvia hispanica}},
  author = {Shivani Tiwari},
  journal = {Discover Plants},
  year = {2026},
  month = oct,
  doi = {10.1007/s44372-026-00972-8},
  url = {https://doi.org/10.1007/s44372-026-00972-8},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Genome wide identification and in silico mRNA expression profiling of the WRKY transcription factor gene family in Salvia hispanica
AU  - Shivani Tiwari
PY  - 2026
DA  - 2026/10/25
JO  - Discover Plants
DO  - 10.1007/s44372-026-00972-8
UR  - https://doi.org/10.1007/s44372-026-00972-8
AB  - This study presents the first comprehensive in silico genome-wide identification, characterization, and mRNA expression profiling of the WRKY transcription factor (TF) gene family in Salvia hispanica L. (chia), a nutritious crop of the family Lamiaceae. A total of 35 CsWRKY genes were identified from the chia reference genome and classified into 7 phylogenetic groups (I, IIa–IIe, III) based on WRKY domain number and zinc-finger motif type. Mean protein length, molecular weight and isoelectric point were 332.8 aa, 37,499 Da and 7.62, respectively, and protein length was almost perfectly correlated with molecular weight (r = 0.9995). Subcellular-localization prediction indicated predominantly nuclear and cytoplasmic distribution. Gene-structure analysis revealed 2–7 exons, and MEME identified 15 conserved motifs including the invariant WRKYGQK heptapeptide. Segmental duplication predominated and has evolved under purifying selection. Promoter analysis detected 20 cis-acting regulatory element classes, and a maximum-likelihood phylogeny grouped CsWRKYs with orthologs from Arabidopsis thaliana, Oryza sativa, Glycine max, Medicago truncatula and Physcomitrella patens. In silico expression profiling used only verified, publicly available S. hispanica RNA-Seq datasets and was therefore restricted to tissue-specific and developmental patterns; because no abiotic-stress RNA-Seq dataset is currently available for chia, no stress-responsive expression analysis was performed. Homology models were built and docked with in silico predictions identifying CsWRKY3 as the strongest binder. These in silico predictions provide a preliminary genomic framework that requires future experimental validation and may guide the study of WRKY-mediated processes in chia.
SN  - 3005-1207
ER  -