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Biology subjects

Murch, S. J.

Publications and source records attributed to Murch, S. J..

3 recordsLinked to original sources

Auxin is metabolized through kynurenine in Hypericum perforatum L.

Recent studies have demonstrated the presence of kynurenine (KYN) and kynurenic acid (KYNA) in several plant species, but the metabolic function of these metabolites remains undefined. We hypothesized that KYN and KYNA are metabolites of auxin and play a role in plant morphogenesis. To test our hypothesis, we developed a plant tissue-culture-based bioassay using Hypericum perforatum (St. Johns wort; SJW), a model system for auxin and indoleamine metabolism and pharmacological inhibitors (PF-04859989, RO-61-8048, and KMO inhibitor II, JM6) of human kynurenine pathways enzymes. SJW is an interesting model system because explants root in the absence of plant growth regulators but supplementation of the culture media with 10 M IAA induces a callus response without de novo root organogenesis. Supplementation of the culture media with 10 M KYN increased root number and internodal length relative to basal media. We used a previously validated high-resolution mass spectrometry analytical method to quantify KYN, KYNA, and 3-hydroxyanthranilic acid (3-HAA). KYN, KYNA and 3-HAA were quantified in roots and shoots of SJW grown on basal media. Supplementation of the culture media with 10 M KYN increased the concentration of KYN, KYNA and 3-HAA in roots and shoots. Treatment with 10 M IAA increased KYN and 3-HAA concentration in shoots. Three pharmaceutical candidates that are kynurenine pathway inhibitors in humans were taken up into the tissues from the culture media and increased KYN content as compared to basal control. Together, these data propose a role for KYN in IAA metabolism, shoot and root organogenesis. HighlightsO_LIKynurenine metabolites are detected and accumulate in H. perforatum tissue culture C_LIO_LIIAA redirects metabolism towards accumulation of KYN and 3-HAA in shoots C_LIO_LIExogenous KYN promotes KYNA accumulation C_LIO_LIPharmacological inhibition alters kynurenine pathway metabolite profiles in a tissue-specific manner C_LIO_LIKynurenine and IAA differentially regulate root development C_LI

plant biology↗

Sex-Specific Ethylene Responses and Convergent Plasticity: Multi-Omic Insights into Cannabis Sexual Plasticity

Cannabis sativa L. exhibits remarkable sexual plasticity: both XX and XY individuals can undergo complete phenotypic sex reversal in response to ethylene modulation. While this phenomenon is well documented, the molecular mechanisms remain underexplored. Here, we present the first multi-omic study of hormonally induced sex change in both XX and XY Cannabis plants, integrating transcriptomic profiling, ethylene pathway metabolite quantification, and whole-genome sequencing across three genetically distinct genotypes. Treatments with silver thiosulfate (STS) and ethephon induced >80% phenotypic conversion, but transcriptomic responses diverged sharply between chromosomal sexes. We profiled 47 ethylene-related genes (ERGs) and identified 14 high-confidence candidates--including CsACS1, CsACO5, CsERF1, and CsMTN--with sex-specific, time-dependent expression patterns that support a two-phase model of plasticity: early transcriptional reprogramming followed by stabilization of new floral identities. Several candidate ERGs were in non-recombining regions of the X chromosome or absent from the Y, while most showed low nucleotide diversity, suggesting functional constraint. These findings provide a high-resolution view of ethylene-responsive sex plasticity and demonstrate that convergent floral phenotypes arise from distinct regulatory programs in XX and XY plants. Our work advances the molecular understanding of sexual plasticity in dioecious species and identifies candidate genes for the development of sex-stable cultivars in Cannabis and other crops.

developmental biology↗

Prenatal glyphosate exposure disrupts the gut-brain axis across several generations in mice.

Glyphosate, a widely used herbicide in North America, has become prevalent in the food supply, raising concerns about potential health impacts. In this exploratory study, male and female F0 mice were exposed to glyphosate through drinking water during mating and gestation. We investigated whether prenatal exposure at dietary-relevant levels (0.01 mg/kg/day, Average American Diet, [AAD]) or the U.S. EPAs acceptable daily intake (1.75 mg/kg/day, [EPA upper limit]) altered gut, metabolic, and behavioral outcomes across two generations in mice with or without genetic susceptibility to colitis (Muc2+/- and Muc2-/-, respectively). Healthy (Muc2+/-) offspring of glyphosate-exposed mice exhibited colonic goblet cell depletion, reduced mucin-2 expression, and pro-inflammatory cytokine profiles in both F1 and F2 generations. These healthy (Muc2+/-) offspring also developed metabolic dysfunction, including impaired glucose tolerance, insulin resistance, and reduced GLP-1 in serum. Behavioral deficits were also observed in healthy (Muc+/-) mice including reduced locomotion and working memory, and these changes were associated with altered microbiome composition and gut-brain mediators. These findings suggest that prenatal glyphosate exposure, even below regulatory thresholds, may disrupt multiple physiological systems across generations, highlighting the need for further research and regulatory consideration.

pharmacology and toxicology↗