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Stevenson, P.

Publications and source records attributed to Stevenson, P..

3 recordsLinked to original sources

Pollen sterols are highly diverse but phylogenetically conserved

Sterols regulate cell membrane fluidity and are precursors for hormone and secondary metabolite production in plants, but plant sterols also have a critical role as nutrients in herbivores. Here we describe the distribution of 78 different sterols from pollen of 295 UK wildflower taxa and use this data to develop an evolutionary rationale for the diversity of sterols in pollen compared to vegetative tissues. The sterolome was a function of plant lineage and conserved in groups as high as subfamily. Insect herbivores are auxotrophic for sterols, and notably bees can not modify them therefore rely on dietary sources, primarily pollen, to meet their metabolic needs. Most pollen in the present study contained high proportions of {Delta}5 sterols including {beta}-sitosterol, 24-methylenecholesterol and isofucosterol, which are important sterols for bees. The sterols recorded in honey bees occurred in the pollen of only 68% of plant taxa, however, none matched these proportions exactly suggesting they must forage pollen from multiple plant taxa to satisfy their sterol requirements. We conclude that there is evidence for pollen sterol composition being the result of diverse driving forces including plant lineage and pollinator nutritional requirements.

biochemistry↗

Loss of Ezh2 in the medial ganglionic eminence alters interneuron fate, cell morphology and gene expression profiles

Enhancer of zeste homolog 2 (Ezh2) is responsible for trimethylation of histone 3 at lysine 27 (H3K27me3), resulting in gene repression. Here, we explore the role of Ezh2 in forebrain GABAergic interneuron development. Loss of Ezh2 increases somatostatin-expressing (SST+) and decreases parvalbumin-expressing (PV+) interneurons in multiple brain regions. We also observe fewer MGE-derived interneurons in the first postnatal week, indicating reduced interneuron production. Intrinsic electrophysiological properties in SST+ and PV+ interneurons are normal, but PV+ interneurons display increased axonal complexity in Ezh2 mutant mice. Single cell multiome analysis revealed differential gene expression patterns in the embryonic MGE that are predictive of these cell fate changes. Lastly, CUT&Tag analysis revealed differential H3K27me3 levels at specific genomic loci, with some genes displaying a relative increase in H3K27me3 indicating they may be resistant to epigenetic modifications. Thus, loss of Ezh2 in the MGE alters interneuron fate, morphology, and gene expression and regulation.

neuroscience↗

Dynamic perineuronal net expression during learned maternal behavior is cortical hemisphere-specific and dependent on methyl-CpG-binding protein 2

Cortical neuronal circuits along the sensorimotor pathways are shaped by experience during critical periods of heightened plasticity in early postnatal development. After closure of critical periods, measured histologically by the formation and maintenance of extracellular matrix structures called perineuronal nets (PNNs), the adult mouse brain exhibits restricted plasticity and maturity. Mature PNNs are typically considered to be stable structures that restrict synaptic plasticity on cortical parvalbumin+ GABAergic neurons. Changes in environment (i.e. novel behavioral training) or social contexts (i.e. motherhood) are known to elicit synaptic plasticity in relevant neural circuitry. However, little is known about concomitant changes in the PNNs surrounding the cortical parvalbumin+ GABAergic neurons. Here, we show novel changes in PNN density in the primary somatosensory cortex (SS1) of adult female mice after maternal experience, using systematic microscopy analysis of a whole brain region. On average, PNNs were increased in the right barrel field and decreased in the left forelimb regions. Individual mice had left hemisphere dominance in PNN density. Using adult female mice deficient in methyl-CpG-binding protein 2 (MECP2), an epigenetic regulator involved in regulating experience-dependent plasticity, we found that MECP2 is critical for this precise and dynamic expression of PNN. Adult naive Mecp2-heterozygous females (Het) had increased PNN density in specific subregions in both hemispheres before maternal experience. The laterality in PNN expression seen in naive Het was lost after maternal experience, suggesting possible intact mechanisms for plasticity. Together, our results identify subregion and hemisphere-specific alterations in PNN expression in adult females, suggesting extracellular matrix plasticity as a possible neurobiological mechanism for adult behaviors in rodents.

neuroscience↗