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Woolfolk, M. L.

Publications and source records attributed to Woolfolk, M. L..

2 recordsLinked to original sources

The Genetic Architecture of Neonatal Deer Mouse Cries Implicates the Cerebellum in the Temporal Control of an Infant Social Behavior

Vocal communication is a conserved vertebrate social behavior that begins at birth with the cries of infants. These neonatal vocal signals vary across contexts to elicit parental care that matches infant needs, and across species to match species-specific ecologies and social systems. This natural variation presents an opportunity to identify proximate mechanisms supporting flexible neonatal vocal behaviors and their evolution. To this end, we recently described neonatal vocalizations in North American deer mice, a model system for behavioral evolution, and identified heritable interspecific differences in features of these vocalizations. Here, we examine one of these features, temporal structure, which in humans and rodents contains information about infant distress. We find that temporal features of neonatal deer mouse cries have diverged more across deer mouse species than spectral features, and that in a playback assay cry duration affects the ability of pup vocalizations to elicit parental approach. To test proximate mechanisms underlying natural variation in cry duration, we first focus on the cerebellar system, a conserved hindbrain region that contributes to the temporal structure of motor rhythms. We identify interspecies variation in the gross anatomy of the neonatal cerebellum and inferior olive and show that pharmacological perturbation of olivocerebellar function alters the temporal structure of neonatal cries in deer mice. Next, we use an interspecies cross to map the genetic architecture underlying neonatal cry duration in deer mice. We identify a single quantitative trait locus significantly associated with cry duration, as well as candidate genes in this locus that could plausibly underlie species differences in the temporal structure of infant crying. Among these candidates are genes that are differentially expressed between species, function in the developing cerebellum, and have been linked to the duration of neonatal vocal signals in house mice. Taken as a whole, this work identifies contributions of the cerebellar system to neonatal social behaviors and suggests testable neural and genetic hypotheses about the evolution of infant crying.

evolutionary biology↗

Two pup vocalization types are genetically and functionally separable in deer mice

Vocalization is a widespread vertebrate social behavior that is essential for fitness in the wild. While many vocal behaviors are highly conserved, heritable features of specific vocalization types can vary both within and between species, raising the questions of why and how some vocal behaviors evolve. Here, using new computational tools to automatically detect and cluster vocalizations into distinct acoustic categories, we compare pup isolation calls across neonatal development in eight taxa of deer mice (genus Peromyscus) and compare them to laboratory mice (C57Bl6/j strain) and free-living, wild house mice (Mus musculus musculus). Whereas both Peromyscus and Mus pups produce ultrasonic vocalizations (USVs), Peromyscus pups also produce a second call type with acoustic features, temporal rhythms, and developmental trajectories that are distinct from those of USVs. In deer mice, these tonal and low frequency "cries" are predominantly emitted in postnatal days one through nine, while USVs are primarily made after day nine. Using playback assays, we show that cries result in a more rapid approach by Peromyscus mothers than USVs, suggesting a role for cries in eliciting parental care early in neonatal development. Using genetic crosses between two sister species of deer mice exhibiting large, innate differences in the acoustic structure of cries and USVs, we find that variation in vocalization rate, duration, and pitch display different degrees of genetic dominance and that cry and USV features can be uncoupled in second-generation hybrids. Taken together, this work shows that vocal behavior can evolve quickly between closely related rodent species in which vocalization types, likely serving distinct functions in communication, are controlled by distinct genetic loci.

evolutionary biology↗