Publications by authors named "Kelsie E Hunnicutt"

Hybrid incompatibilities are a critical component of species barriers and may arise due to negative interactions between divergent regulatory elements in parental species. We used a comparative approach to identify common themes in the regulatory phenotypes associated with hybrid male sterility in two divergent rodent crosses, dwarf hamsters and house mice. We investigated three potential characteristic gene expression phenotypes in hybrids including the propensity of transgressive differentially expressed genes towards over or underexpression, the influence of developmental stage on patterns of misexpression, and the role of the sex chromosomes on misexpression phenotypes.

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Hybrid incompatibilities are a critical component of species barriers and may arise due to negative interactions between divergent regulatory elements in parental species. We used a comparative approach to identify common themes in the regulatory phenotypes associated with hybrid male sterility in two divergent rodent crosses, dwarf hamsters and house mice. We investigated three potential characteristic gene expression phenotypes in hybrids including the propensity of transgressive differentially expressed genes towards over or underexpression, the influence of developmental stage on patterns of misexpression, and the role of the sex chromosomes on misexpression phenotypes.

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Sexual signals are shaped by their intended and unintended receivers as well as the signalling environment. This interplay between sexual and natural selection can lead to divergence in signals in heterogeneous environments. Yet, the extent to which gene flow is restricted when signalling phenotypes vary across environments and over what spatial scales remains an outstanding question.

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The X chromosome of therian mammals shows strong conservation among distantly related species, limiting insights into the distinct selective processes that have shaped sex chromosome evolution. We constructed a chromosome-scale de novo genome assembly for the Siberian dwarf hamster (Phodopus sungorus), a species reported to show extensive recombination suppression across an entire arm of the X chromosome. Combining a physical genome assembly based on shotgun and long-range proximity ligation sequencing with a dense genetic map, we detected widespread suppression of female recombination across ∼65% of the Phodopus X chromosome.

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Whole tissue RNASeq is the standard approach for studying gene expression divergence in evolutionary biology and provides a snapshot of the comprehensive transcriptome for a given tissue. However, whole tissues consist of diverse cell types differing in expression profiles, and the cellular composition of these tissues can evolve across species. Here, we investigate the effects of different cellular composition on whole tissue expression profiles.

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Hybrid sterility is a complex phenotype that can result from the breakdown of spermatogenesis at multiple developmental stages. Here, we disentangle two proposed hybrid male sterility mechanisms in the house mice, Mus musculus domesticus and M. m.

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Anthropogenic disturbances associated with urban ecosystems can create favorable conditions for populations of some invasive plant species. Light pollution is one of these disturbances, but how it affects the growth and establishment of invasive plant populations is unknown. Cheatgrass () is a problematic invasive species where it has displaced native grassland communities in the United States, but to our knowledge, there have been no studies of the ecological factors that affect cheatgrass presence in urban ecosystems.

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Article Synopsis
  • Mutations are essential for evolution, and understanding their frequency and distribution helps us learn about evolutionary processes over time.
  • This study estimates the mutation rate for gray mouse lemurs and finds it to be one of the highest among mammals at 1.52 mutations per site per generation, with an unexpected low number of paternal mutations.
  • The research also confirms that reported mutation rates come with uncertainty and shows consistency in mutation patterns across different primate species when comparing various analysis methods.
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  • Mouse lemurs, a diverse group of tiny primates in Madagascar, have seen a rapid increase in recognized species over the last 20 years, raising concerns about the oversplitting of this group.
  • In a study focusing on an area in northeastern Madagascar, researchers used genetic data to examine two pairs of mouse lemur lineages, discovering significant differences in their populations and genetic structures.
  • The findings support classifying one previously undescribed lineage as a separate species, while questioning the distinction of two other recognized species, indicating rapid evolution and reproductive isolation within these primates.
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  • The study focuses on the evolution of vomeronasal type-1 receptors (V1Rs), which are believed to influence species boundaries and mate choice, particularly in nocturnal mammals.
  • It explores V1R evolution in Madagascar's small-bodied nocturnal mouse and dwarf lemurs using a comparative genomic approach, doubling the genetic data for strepsirrhine primates.
  • The findings show that nocturnal lemurs have more diverse V1R repertoires compared to diurnal ones, with specific V1R subfamilies exhibiting signs of positive selection linked to their evolutionary response to different stimuli.
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  • - Madagascar's biodiversity, particularly its unique dwarf lemurs, faces severe threats from deforestation and climate change, leading to the need for genetic research due to their rarity.
  • - Researchers conducted a comparative genomic study, producing the first comprehensive genome-wide genetic diversity estimates for various dwarf lemur species, including generating a reference genome for the fat-tailed dwarf lemur (Cheirogaleus medius).
  • - The analysis revealed strong evolutionary relationships among species, identified areas of ancient genetic mixing possibly related to hibernation, and found low genetic diversity in isolated populations, emphasizing the importance of genomic studies for conservation efforts.
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Alu elements are a highly successful family of primate-specific retrotransposons that have fundamentally shaped primate evolution, including the evolution of our own species. Alus play critical roles in the formation of neurological networks and the epigenetic regulation of biochemical processes throughout the central nervous system (CNS), and thus are hypothesized to have contributed to the origin of human cognition. Despite the benefits that Alus provide, deleterious Alu activity is associated with a number of neurological and neurodegenerative disorders.

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Article Synopsis
  • Retrotransposons, particularly Alu elements, are believed to have significantly influenced primate evolution and may contribute to the development of higher cognitive functions in humans.
  • Enhanced activity of these retrotransposons can make neurons vulnerable to damaging pathways that disrupt mitochondrial function, as shown in the TOMM40 gene linked to Alzheimer's disease.
  • The Alu neurodegeneration hypothesis suggests that increased Alu content in mitochondrial genes can lead to neuronal dysfunction and is supported by extensive research on the relationship between mitochondrial health and neurodegenerative diseases.
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Phylogeographic analysis can be described as the study of the geological and climatological processes that have produced contemporary geographic distributions of populations and species. Here, we attempt to understand how the dynamic process of landscape change on Madagascar has shaped the distribution of a targeted clade of mouse lemurs (genus Microcebus) and, conversely, how phylogenetic and population genetic patterns in these small primates can reciprocally advance our understanding of Madagascar's prehuman environment. The degree to which human activity has impacted the natural plant communities of Madagascar is of critical and enduring interest.

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