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Sharp, S. J.

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

2 recordsLinked to original sources

Daily rewiring of a neural circuit generates a predictive model of environmental light

Ongoing sensations are compared to internal, experience-based, reference models; mismatch between reality and expectation can signal opportunity or danger, and can shape behavior. The nature of internal reference models is largely unknown. We describe a model that enables moment-to-moment luminance evaluation in flies. Abrupt shifts to lighting conditions inconsistent with the subjective time-of-day trigger locomotion, whereas shifts to appropriate conditions induce quiescence. The time-of-day prediction is generated by a slowly shifting activity balance between opposing neuronal populations, LNvs and DN1as. The two populations undergo structural changes in axon length that accord with, and are required for, conveying time-of-day information. Each day, in each population, the circadian clock directs cellular remodeling such that the maximum axonal length in one population coincides with the minimum in the other; preventing remodeling prevents transitioning between opposing internal states. We propose that a dynamic predictive model resides in the shifting connectivities of the LNv- DN1a circuit.

neuroscience↗

Genome-wide scan and fine-mapping of rare nonsynonymous associations implicates intracellular lipolysis genes in fat distribution and cardio-metabolic risk

Difficulties in identifying causal variants and genes underlying genetic associations have limited the translational potential of genetic studies of body fat distribution, an important, partly-heritable risk factor for cardio-metabolic disease. Rare variant associations facilitate fine-mapping of causal alleles, but their contribution to fat distribution is understudied. We performed a genome-wide scan of rare nonsynonymous variants for body mass index-adjusted waist-to-hip-ratio (BMI-adjusted WHR; a widely-used measure of fat distribution) in 450,562 European ancestry individuals, followed by systematic Bayesian fine-mapping at six genome-wide (p<5x10-08; main-analysis) and two subthreshold signals (significant at a Bonferroni-corrected p<1.3x10-06). We found strong statistical evidence of causal association for nonsynonymous alleles in CALCRL (p.L87P, pconditional=5.9x10-12; posterior-probability of association [PPA]=52%), PLIN1 (p.L90P, pconditional=5.5x10-13; PPA>99%), PDE3B (p.R783X, pconditional=6.2x10-15; PPA>99%), ACVR1C (p.I195T; pconditional=5.4x10-12; PPA>99%), and FGF1 (p.G21E, pconditional=1.6x10-07; PPA=98%). Alleles at the four likely-causal main-analysis genes affected fat distribution primarily via larger hip-rather than smaller waist-circumference and six of nine conditionally-independent WHR-lowering index-variants were associated with protection from cardiovascular or metabolic disease. All four genes are expressed in adipose tissue and have been linked with the regulation of intracellular lipolysis, which controls fat retention in mature cells. Targeted follow-up analyses of key intracellular-lipolysis genes revealed associations for a variant in the initiator of intracellular lipolysis PNPLA2 (p.N252K) with higher BMI-adjusted-WHR and higher cardio-metabolic risk. This study provides human genetic evidence of a link between intracellular lipolysis, fat-distribution and its cardio-metabolic complications in the general population.

genetics↗