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Guest, D.

Publications and source records attributed to Guest, D..

2 recordsLinked to original sources

Profile analysis in listeners with sensorineural hearing loss: behavioral data and computational models

Many sounds contain spectral modulations at multiple scales, but much is still unknown about how such spectral features are represented in the auditory system. One behavioral task that provides insight into this question is profile analysis. In a typical profile-analysis task, listeners are asked to discriminate between a complex tone with equal-amplitude components and a complex tone with a single incremented component. Because listeners can perform profile analysis even when the overall sound level of the stimuli is randomized from interval to interval, this task is thought to be a useful index of relative processing of spectral shape, rather than just sensitivity to absolute level changes. Here, we measured profile analysis across the frequency range in a group of listeners that varied widely in their hearing status. We then modeled the resulting behavioral data by decoding responses to the stimuli from computational models of the auditory nerve and inferior colliculus. We found that both hearing loss at the target frequency and increases in the target frequency were associated with poorer profile-analysis thresholds, and that these results could both be explained as the result of corresponding changes in sensitivity of temporal modulation-sensitive cells at the level of the inferior colliculus. These results suggest that key features of profile-analysis may reflect the limits of central neural tuning to temporal modulations.

neuroscience↗

A functional single nucleotide polymorphism upstream of the collagen type III gene may contribute to catastrophic fracture risk in Thoroughbred horses.

Fractures caused by bone overloading are a leading cause of euthanasia in Thoroughbred racehorses. The risk of fatal fracture has been shown to be influenced by both environmental and genetic factors but, to date, no specific genetic mechanisms underpinning fracture have been identified. The aim of this study was to utilise a genome-wide polygenic risk score to establish an in vitro cell system to study bone gene regulation in horses at high and low genetic risk of fracture. Candidate gene expression analysis revealed differential expression of COL3A1 and STAT1 genes in osteoblasts derived from high and low risk horses. Whole genome sequencing of fracture case and control horses revealed a single nucleotide polymorphism (SNP) upstream of COL3A1 that was confirmed in a larger cohort to be significantly associated with fracture. Bioinformatics tools predicted that this SNP may impact the binding of the transcription factor SOX11. Gene modulation demonstrated SOX11 is upstream of COL3A1 and the region binds to nuclear proteins. Furthermore, luciferase assays demonstrated that the region containing the SNP has promoter activity. However, the specific effect of the SNP depends on the broader genetic background of the cells and suggest other factors may also be involved in regulating COL3A1 expression. In conclusion, this approach provides a powerful means to identify novel DNA variants and understand their mechanism of action to enable the development of new ways to identify and treat horses at high risk of a catastrophic fracture.

genetics↗