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Biology subjects

Mehr, S.

Publications and source records attributed to Mehr, S..

2 recordsLinked to original sources

Sex Differences in Human Music Perception are Negligible

Since Darwin1, researchers have proposed that human musicality evolved in a reproductive context in which males produce music to signal their mate quality to females. Sexually selected traits involve tradeoffs in the costs of high-quality signal production and high-fidelity signal detection2, leading to observable sexual dimorphisms across many species3,4. If musicality is a sexually selected trait in humans, males and females should then differ in their music perception ability, music production ability, or both. The evidence for this possibility is unclear, because previous reports of sex differences in human auditory perception are restricted in scope and inconsistent in direction5-15. Here, we report a test of music processing ability in 360,009 men and 194,291 women from 208 countries. In contrast to other non-musical human traits16-19, and in contrast to music-related traits in non-human animals20-23, we found no consistent advantage for either sex. The sex differences we did observe were negligible (Cohens d range: 0.009-0.111) and Bayesian analyses indicated evidence in favor of the null hypothesis of no sex difference in general musical ability (Bayes Factor = 0.6). These results suggest that it is unlikely that music evolved in the context of sexual selection.

animal behavior and cognition↗

Increased core body temperature exacerbates defective protein prenylation in mouse avatars of mevalonate kinase deficiency

Mevalonate kinase deficiency (MKD) is caused by biallelic loss-of-function mutations in MVK, leading to recurrent fevers and systemic inflammation. We describe new mouse avatars of MKD bearing p.Val377Ile (the commonest variant) or deletions in Mvk. Compound heterozygous mice recapitulated the biochemical phenotype of MKD, with build-up of unprenylated GTPases and increased plasma mevalonic acid. Mice with different deficiencies in mevalonate kinase revealed new insights into the genotype-phenotype relationship and mirrored the variability in the prenylation defect in human MKD, with p.V377I homozygous mice having a milder phenotype than compound heterozygous animals. The inflammatory response to LPS was enhanced in compound heterozygous mice in vivo and elevated serum interleukin-1{beta} was abrogated by NLRP3 inflammasome inhibition. Increased temperature dramatically but reversibly exacerbated the deficit in the mevalonate pathway and defective prenylation in vitro and in vivo, highlighting increased body temperature as a likely trigger of inflammatory flares and an additional potential target for future therapeutic approaches.

physiology↗