Biology subjects

Tharayil, N.

Publications and source records attributed to Tharayil, N..

5 recordsLinked to original sources

bioRxiv2025

Integrated multi-omics analysis reveals divergent molecular responses in Palmer amaranth (Amaranthus palmeri) biotypes susceptible and resistant to glyphosate

Environmental stress triggers coordinated changes across genetic, transcriptomic, proteomic, and metabolomic levels in plants, yet the extent of synchronization across these omic layers remains underexplored. We captured transcriptomic, proteomic and metabolomic perturbation of glyphosate-resistant (GR) and glyphosate-susceptible (GS) Palmer amaranth (Amaranthus palmeri) biotypes 24 hours after herbicide treatment, quantifying 30,371 transcripts, 5,606 proteins, and 220 metabolites. Glyphosate perturbed threefold more transcripts and proteins in GS than in GR and caused the accumulation of shikimate intermediates in both biotypes. In GS, glyphosate severely disrupted primary metabolism, including photosynthesis and carbon fixation, leading to a collapse of energy production and impairment of phenylpropanoid and terpenoid biosynthesis, compromising defense and detoxification. In contrast, GR maintained cellular homeostasis, with minimal perturbation in carbon metabolism and upregulation of detoxifying pathways, indicating metabolic rerouting. Integrated multi-omics analysis captured stress responses hidden from single-omic analysis, including elevated glutathione metabolism, perturbation of the phenylpropanoid pathway and elevated raffinose family oligosaccharide metabolism in GR, and perturbation of taurine-hypotaurine metabolism in GS. Transcript and protein changes were broadly correlated, but GS exhibited signs of translational inhibition under glyphosate stress, indicating reduced protein synthesis. These findings reveal pervasive perturbation of glyphosate beyond the shikimate pathway within 24 hours after exposure, and underscore the importance of multi-omics integration to elucidate complex stress responses in plants.

plant biology↗

bioRxiv2025

Temporal analysis of physiological phenotypes identifies novel metabolic and genetic underpinnings of senescence in maize

Leaf senescence induces extensive metabolome reprogramming to optimize nutrient recycling, enhance resilience to abiotic and biotic stress, and improve productivity. However, the characterization of these metabolic shifts and the identification of key metabolites and pathways remains limited. We generated a temporal map of physiological and metabolic diversity in genetically diverse maize inbred lines varying for the staygreen trait. Combinatorial analysis of physiological and metabolic changes revealed substantial metabolic perturbations and identified 84 leaf metabolites associated with senescence. Non-staygreen inbred lines exhibited higher accumulation of primary metabolites including sugar alcohols such as mannitol and erythritol, and amino acids such as phenylalanine and arginine. In contrast, the staygreen inbred lines showed higher abundance of secondary metabolites, primarily phenylpropanoids, including caffeic acid, chlorogenic acid, and eriodictyol. Linking metabolome to the genome identified 56 novel candidate genes expressed in adult maize leaf that regulate metabolic flux during senescence. Reverse genetic analysis validated the role of naringenin chalcone and eriodictyol in both maize and Arabidopsis, demonstrating a conserved function of these phenylpropanoids in leaf senescence across monocots and dicots. Our study provides valuable insights into the coordinated physiological and metabolic changes driving leaf senescence and identifies novel genes underlying this complex developmental process.

plant biology↗

bioRxiv2022

Metabolite profiles across populations of Palmer amaranth (Amaranthus palmeri) highlight the specificity and inducibility of phytochemical response to glyphosate stress.

Modifications of the phytochemical profile form a vital component of physiological stress adaptation in plants. However, the specificity and uniqueness of phytochemical changes with respect to the identity of stressors is less known. Here, we investigated the commonality and specificity of metabolic perturbations induced by a specific stressor - glyphosate, and a general stressor - drought, across multiple glyphosate-resistant (GR) and -susceptible (GS) biotypes of a dominant agricultural weed, Amaranthus palmeri. In the absence of stress, the native metabolite profile of GS- and GR-biotypes was similar, and amplification of the EPSPS gene in GR-biotypes did not translate to a higher abundance of downstream metabolites. Further, glyphosate treatment initially inhibited the shikimate pathway in both GS- and GR-biotypes, from which the GR-biotypes recovered, indicating inducibility in the functionalization of the EPSPS enzyme. The accumulation of phenylpropanoids produced downstream of the shikimate pathway, was higher in GR-biotypes than GS-biotypes, with a preferential accumulation of compounds with higher antioxidant potential. However, this increase was not observed in response to drought treatment, where the metabolic perturbations were pervasive but limited in magnitude compared to glyphosate stress. Overall, while native phytochemistry of A. palmeri was similar irrespective of the level of glyphosate susceptibility, the specific stressor, glyphosate, imparted metabolic perturbations that were localized but higher in magnitude, while the specificity of phytochemical response to the general stressor, drought, was minimal. Taken together, these results suggest that, at the metabolic level, the glyphosate resistance mechanism in A. palmeri is partly induced and specific to herbicide stress. SIGNIFICANCE STATEMENTUnderstanding changes in physiology, especially those related to secondary metabolites with adaptogenic functions, is imperative to decipher the basis of stress adaptation in plants. This study provides critical information on native and stress-induced phytochemical differences between multiple glyphosate-resistant and -susceptible weed biotypes, thus, shedding light on the metabolome-level orchestration of gene amplification-mediated glyphosate resistance mechanism in an economically devastating weed, Palmer amaranth (Amaranthus palmeri).

plant biology↗

bioRxiv2022

Common and lifestyle-specific traits of mycorrhiza-associated metabolite alterations in plant roots reflects strategies of root-mycorrhizal interactions

Convergent patterns in morphological and genetic traits of mycorrhizas have been well-documented and reflect common selection forces that define mycorrhizas. However, generalizable patterns of mycorrhiza-associated chemical alterations, which are immediately linked to plant and fungal strategies for successful symbiosis, have yet to be emerged. Comparing root metabolomes of phylogenetically-diverse plants inoculated by mycorrhizal fungi across two major lifestyles (arbuscular- vs. ecto-mycorrhizas), our study uncovers metabolite changes unique to each mycorrhizal lifestyle and those common across plant-mycorrhizal combinations irrespective of lifestyles. Arbuscular and ecto- mycorrhizal colonized roots accumulated different sets of carbohydrates, indicating unique carbon partitioning strategies: particularly, arbuscular mycorrhizal roots accumulated cyclic polyols inaccessible for symbionts, suggesting tighter regulation of plants in carbon partitioning. Mycorrhizas also altered specialized metabolism, featuring frequent increases of flavan-3-ols and decreases of flavanols irrespective of mycorrhizal lifestyles, suggesting tactical reconfiguration of specialized metabolites to facilitate/contain symbiosis. Our data show for the first time, to our knowledge, that part of the root metabolite alterations by mycorrhizas were relatively common across plant-mycorrhizal systems, highlighting their potentially critical regulatory and evolutionary role for successful symbiosis. This commonality appears robust to phylogenetic diversity of host plants and thus may be widespread in land plants. Our findings offer future research venues to elucidate the finer roles of these common traits of mycorrhiza-associated metabolite alterations and thus help to eventually develop a comprehensive understanding of this omnipresent plant-fungus partnership.

ecology↗

bioRxiv2020

Genetic Architecture of Maize Rind Strength Revealed by the Analysis of Divergently Selected Populations

Stalk lodging, breakage of the stalk at or below the ear, causes substantial yield losses in maize. The strength of the stalk rind, commonly measured as rind penetrometer resistance (RPR), is an important contributor to stalk lodging resistance. To enhance RPR genetic architecture, we conducted selection mapping on populations developed by 15 cycles of divergent selection for high (C15-H) and low (C15-L) RPR. We also performed time-course transcriptome and metabolic analyses on developing stalks of high (Hrpr1) and low (Lrpr1) RPR inbred lines derived from the C15-H and C15-L populations, respectively. Divergent selection significantly altered allele frequencies at 3,656 and 3,412 single nucleotide polymorphisms (SNP) in the C15-H and C15-L populations, respectively. While the majority of the SNPs under selection were unique, 110 SNPs were common in both populations indicating the fixation of alleles with alternative effects. Remarkably, preferential selection on the genomic regions associated with lignin and polysaccharide biosynthesis genes was observed in C15-H and C15-L populations, respectively. This observation was supported by higher lignification and lower extractability of cell wall-bound sugars in Hrpr1 compared to Lrpr1. Tricin, a monolignol important for incorporation of lignin in grass cell walls, emerged as a key determinant of the different cell wall properties of Hrpr1 and Lrpr1. Integration of selection mapping with transcriptomics and previous genetic studies on RPR identified 40 novel candidate genes including ZmMYB31, ZmNAC25, ZmMADS1, two PAL paralogues, two lichenases, ZmEXPA2, ZmIAA41, and Caleosin. Enhanced mechanistic and genetic understanding of RPR provides a foundation for improved stalk lodging resistance.

genetics↗