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Biology subjects

Wearing, O.

Publications and source records attributed to Wearing, O..

2 recordsLinked to original sources

Genetic variation in haemoglobin regulates breathing in high-altitude deer mice

Physiological systems often have emergent properties but the effects of genetic variation on physiology are often unknown, which presents a major challenge to understanding the mechanisms of phenotypic evolution. We investigated the in vivo effects on respiratory physiology of genetic variants in haemoglobin (Hb) that contribute to hypoxia adaptation in high-altitude deer mice (Peromyscus maniculatus). We created F2 inter-population hybrids of highland and lowland deer mice to test the phenotypic effects of - and {beta}-globin variants on a mixed genetic background. High-altitude genotypes were associated with breathing phenotypes that enhance O2 uptake in hypoxia, including a deeper more effective breathing pattern and an augmented hypoxic ventilatory response. These effects could not be explained by erythrocyte Hb-O2 affinity or globin gene expression in the brainstem. Therefore, adaptive variation in haemoglobin can have unexpected effects on physiology that are distinct from the canonical function of this protein in circulatory O2 transport.

evolutionary biology↗

Grb10a knockdown in Danio rerio during early life alters growth and cardiometabolic function associated with a remodelled transcriptome

Embryonic growth trajectory is a risk factor for chronic metabolic and cardiovascular disorder. Grb10 is a negative regulator of the main pathways driving embryonic growth. This study investigates the long-term cardiometabolic consequences and transcriptomic profiles of transient disruption of grb10a expression in Danio rerio. Knockdown was associated with increased embryonic growth (+7%) and metabolic rate (+25%), and decreased heart rate (- 50%) in early life. Juvenile growth and respiratory rate were also elevated (+30% and 7-fold increase respectively). The transcriptome was permanently remodelled by this transient disruption, with dysregulation of multiple growth, cardiac, and metabolic pathways. Phenotypic alteration persisted into adulthood, resulting in a leaner body with elevated skeletal and cardiac muscle content and aerobic scope (43%). This study not only confirms for the first time that transient disruption of a single gene can result in permanent transcriptomic remodelling but correlates this remodelling with persistent alterations to the adult cardiometabolic phenotype.

developmental biology↗