Biology subjects

McConnell, E.

Publications and source records attributed to McConnell, E..

5 recordsLinked to original sources

bioRxiv2026

Forging an evolutionary individual from separate replicators

Major evolutionary transitions occur when independently replicating particles unite into a higher-level individual. How selection comes to work on particle collectives and generates reliable heredity is unresolved. By packaging red and green plasmids in yeast cells we made plasmid communities units of selection: cell boundaries supplied discreteness, segregation generated variation, and cell division reproduced communities. Communities colouring cells yellow were preferentially propagated. Initially, yellow parents rarely produced yellow offspring, but continued selection aligned replicative fates of the two plasmids favouring recombinants that fused with the endogenous 2-micron element. Chimera stability was secured by mutations in FLP1, which encodes a recombinase that otherwise resolves fused replicons. Reliable collective heredity, here, a derived product of higher-level selection, marked completion of an evolutionary transition in individuality.

evolutionary biology↗

bioRxiv2025

From rest to focus: Pharmacological modulation of the relationship between resting state dynamics and task-based brain activation

Dynamic resting-state brain activity provides insight into intrinsic neural function and holds promise for predicting individual responses to cognitive demands and pharmacological interventions. This research could ultimately guide medication selection, yet links between network dynamics and medication effects on cognitive function require further validation. Here, we examined whether dynamic activity of an attentional network at rest relates to task-evoked brain activation on the Multi Source Interference Task (MSIT) following administration of methylphenidate (20mg) and haloperidol (2mg), which have opposing effects on attention and catecholaminergic function. Fifty-nine healthy adults completed resting-state and task-based fMRI on three separate days on which they received methylphenidate, haloperidol, or placebo in a double-blind placebo-controlled design. Coactivation pattern analysis determined time spent in the dorsal attention network (DAN) under placebo at rest. Linear mixed-effects modelling assessing the relationship between MSIT task activation under drug and time spent in DAN at rest under placebo and MSIT task activation under drug identified a significant interaction in the dorsolateral prefrontal cortex (dlPFC; p<0.001). Post-hoc analyses indicated that more time in the DAN at rest under placebo was associated with decreased MSIT dlPFC activation under methylphenidate and increased dlPFC activation under haloperidol. Findings demonstrate that resting dynamics of an attentional network are linked to task-related brain responses under different drug conditions within a region implicated in attentional control and sensitive to catecholaminergic variance. Resting-state dynamics may predict pharmacological modulation of goal-directed cognition, highlighting the potential clinical utility of resting-state dynamics in predicting medication response and supporting individualized treatment.

neuroscience↗

bioRxiv2023

Rapid dissemination of host-metabolism-manipulating transposon-like entities via integrative and conjugative elements

Integrative and conjugative elements (ICEs) are self-transmissible mobile elements that transfer functional genetic units across broad phylogenetic distances. Accessory genes shuttled by ICEs can make significant contributions to bacterial fitness, yet ICEs that carry accessory genes encoding functions other than antimicrobial resistance remain poorly characterized. Recent observation of the rapid acquisition of ICEs in a pandemic lineage of Pseudomonas syringae pv. actinidae led to investigation of the structural and functional diversity of these elements among a diverse array of P. syringae. Fifty-three unique ICE types were identified across multiple phylogroups. These ICEs display distinct evolutionary histories compared to their bacterial hosts, are highly recombinogenic, exhibit a conserved structure and are punctuated by hotspots of accessory gene integration. Many carry a 16 kb transposon-like entity (Tn6212) that shows little polymorphism indicating recent dissemination. Deletion of Tn6212 did not alter pathogen growth in planta, but mutants displayed significant fitness defects when grown on TCA cycle intermediates. These were largely attributable to a single LysR regulator. RNA-seq analysis of a set of nested Tn6212 deletions confirmed a central role of LysR in enhanced expression of more than 300 genes and down-regulation of genes controlling expression of energetically demanding loci. Together the transcriptional data indicate a major role for Tn6212 in manipulation of bacterial metabolism with primary effects on RNA degradation, protein synthesis and potential diversion of ATP to growth.

microbiology↗

bioRxiv2022

Fruitful female fecundity after feeding Gryllodes sigillatus royal jelly

Dietary honey bee royal jelly increases insect growth rates and adult body size. Royal jelly could enhance mass insect production as a dietary supplement, but it is costly to produce. The mechanisms underlying the effects of royal jelly on growth remain unclear, and so it is valuable to understand the effects of royal jelly on a mass reared model species to try and augment body size in a more cost-effective manner. To determine the effect of royal jelly on a cricket species (Gryllodes sigillatus) farmed on mass for human consumption, we ran two experiments. In one experiment we tested the dose-dependent response of Gryllodes sigillatus to royal jelly using a range of diets across 0-30% w/w royal jelly. In another experiment we measured the individual-level life history responses of Gryllodes sigillatus to royal jelly over time by individually rearing freshly-hatched Gryllodes sigillatus on two separate diets: half were fed a commercially available cricket diet, while the other half were fed the same diet mixed with 15% w/w fresh royal jelly. Body size and mass measurements were recorded weekly for five weeks. We found the effects of royal jelly to be sex-dependent within crickets: females fed the royal jelly diet grew to be 30% heavier, and this effect was driven by significantly longer abdomens containing 67% more eggs compared to those fed the basal diet. There was a higher probability of crickets reaching adulthood after 35 days when fed royal jelly, and female mass was optimised at approximately 17% w/w royal jelly. Our results reveal that while a royal jelly dietary supplement can increase the yield of mass-reared insects, the life-history responses are species- and sex-specific.

ecology↗

bioRxiv2019

Independent evolution towards large body size in the distinctive Faroe Island mice

Most traits in nature involve the collective action of many genes. Traits that evolve repeatedly are particularly revealing about how selection may act on traits. In mice, large body size has evolved repeatedly on islands and under artificial selection in the laboratory. Identifying the loci and genes involved in this process may shed light on the evolution of complex, polygenic traits. Here, we have mapped the genetic basis of body size variation by making a genetic cross between mice from the Faroe Islands, which are among the largest and most distinctive populations of mice in the world, and a laboratory mouse strain selected for small body size, SM/J. Using this F2 intercross of 841 animals, we have identified 102 loci controlling various aspects of body size, weight and growth hormone levels. By comparing against other studies, including the use of a joint meta-analysis, we found that the loci involved in the evolution of large size in the Faroese mice were largely independent from those of a different island population or other laboratory strains. We conclude that colonization bottleneck, historical hybridization, or the redundancy between multiple loci have resulted in the Faroese mice achieving an outwardly similar phenotype through a distinct evolutionary path.

evolutionary biology↗