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Hildreth, S. B.

Publications and source records attributed to Hildreth, S. B..

3 recordsLinked to original sources

Crosstalk between Flavonoids and the Plant Circadian Clock

Flavonoids are a well-known class of specialized metabolites that play key roles in plant development, reproduction, and survival. Flavonoids are also of considerable interest from the perspective of human health, both as phytonutrients and pharmaceuticals. RNA-Seq analysis of an Arabidopsis null allele for chalcone synthase (CHS), which catalyzes the first step in flavonoid biosynthesis, has uncovered evidence that these compounds influence the expression of circadian clock genes in plants. Analysis of promoter-luciferase constructs showed that the transcriptional activity of genes encoding two components of the central clock, CCA1 and TOC1, across the day/night cycle is altered in CHS-deficient seedlings. The effect of flavonoids on circadian function was furthermore reflected in photosynthetic activity, with chlorophyll cycling abolished in the mutant line. Analysis of a mutant lacking flavonoid 3-hydroxylase (F3H) activity, and thus able to synthesize mono- but not di-hydroxylated B-ring flavonoids, suggests that the latter are at least partially responsible, as further supported by the effects of quercetin on CCA1 promoter activity in wild-type seedlings. Collectively, these experiments point to a previously-unknown connection between flavonoids and circadian cycling in plants and open the way to better understanding of the molecular basis of flavonoid action.

plant biology

Comparative metabolomics of fruits and leaves in a hyperdiverse lineage suggests fruits are a key incubator of phytochemical diversification

Interactions between plants and leaf herbivores have long been implicated as the major driver of plant secondary metabolite diversity. However, other plant-animal interactions, such as those between fruits and frugivores, may also be involved in phytochemical diversification. Using 12 species of Piper, we conducted untargeted metabolomics and molecular networking with extracts of fruits and leaves. We evaluated organ-specific secondary metabolite composition and compared multiple dimensions of phytochemical diversity across organs, including richness, structural complexity, and variability across samples at multiple scales within and across species. Plant organ identity significantly influenced secondary metabolite composition, both independent of and in interaction with species identity. Leaves and fruit shared a majority of compounds, but fruits contained more unique compounds and had higher total estimated chemical richness. While organ-level chemical richness and structural complexity varied substantially across species, fruit diversity exceeded leaf diversity in more species than the reverse. Furthermore, the variance in chemical composition across samples was higher for fruits than leaves. By documenting a broad pattern of high phytochemical diversity in fruits relative to leaves, this study lays groundwork for incorporating fruit into a comprehensive and integrative understanding of the ecological and evolutionary factors shaping secondary metabolite composition at the whole-plant level.

plant biology

Catechol-Containing Compounds are a Broad Class of Amyloid Inhibitors: I. Redox State is a Key Determinant of the Activities of the Inhibitory Activities

Mechanisms of amyloid inhibition remains poorly understood, in part because most protein targets of amyloid assembly are partially unfolded or intrinsically disordered, which hinders detailed structural characterization of protein-inhibitor complexes and structural-based mechanistic elucidation. Herein we employed a small molecule screening approach to identify inhibitors against three prototype amyloidogenic proteins: amylin, A{beta} and tau. One remarkable class of inhibitors identified was catechol-containing compounds and redox-related quinones/anthraquinones. Further mechanistic studies determined that the redox state of the broad class of catechol-containing compounds is a key determinant of the amyloid inhibitor activities.

biochemistry