Deciphering the role of alternative splicing as modulators of defense response in the MYMIVVigna mungo pathosystem

Author:

Laskar Parbej1,Hazra Anjan2ORCID,Pal Amita3ORCID,Kundu Anirban1ORCID

Affiliation:

1. Plant Genomics and Bioinformatics Laboratory Ramakrishna Mission Vivekananda Centenary College Kolkata India

2. Agricultural and Ecological Research Unit Indian Statistical Institute Kolkata India

3. Division of Plant Biology Bose Institute Kolkata India

Abstract

AbstractAlternative splicing (AS) is a crucial regulatory mechanism that impacts transcriptome and proteome complexity under stressful situations. Although its role in abiotic stresses is somewhat understood, our understanding of the mechanistic regulation of pre‐messenger RNA splicing in plant‐pathogen interaction is meager. To comprehend this unexplored immune reprogramming mechanism, transcriptome profiles of Mungbean Yellow Mosaic India Virus (MYMIV)‐resistant and susceptible Vigna mungo genotypes were analyzed for AS genes that may underlie the resistance mechanism. Results revealed a repertoire of AS‐isoforms accumulated during pathogenic infestation, with intron retention being the most common AS mechanism. Identification of 688 differential alternatively spliced (DAS) genes in the resistant host elucidates its robust antiviral response, whereas 322 DAS genes were identified in the susceptible host. Enrichment analyses confirmed DAS transcripts pertaining to stress, signaling, and immune system pathways have undergone maximal perturbations. Additionally, a strong regulation of the splicing factors has been observed both at the transcriptional and post‐transcriptional levels. qPCR validation of candidate DAS transcripts with induced expression upon MYMIV infection demonstrated a competent immune response in the resistant background. The AS‐impacted genes resulted either in partial/complete loss of functional domains or altered sensitivity to micro‐RNA‐mediated gene silencing. A complex regulatory module, miR7517‐ATAF2, has been identified in an aberrantly spliced ATAF2 isoform that exposes an intronic miR7517 binding site, thereby suppressing the negative regulator to enhance the defense reaction. The present study establishes AS as a noncanonical immune reprogramming mechanism that operates in parallel, thereby offering an alternative strategy for developing yellow mosaic‐resistant V. mungo cultivars.

Publisher

Wiley

Subject

Cell Biology,Plant Science,Genetics,General Medicine,Physiology

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