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Madagascar's biodiversity is notoriously threatened by deforestation and climate change. Many of these organisms are rare, cryptic, and severely threatened, making population-level sampling unrealistic. Such is the case with Madagascar's dwarf lemurs (genus Cheirogaleus), the only obligate hibernating primate. We here apply comparative genomic approaches to generate the first genome-wide estimates of genetic diversity within dwarf lemurs. We generate a reference genome for the fat-tailed dwarf lemur, Cheirogaleus medius, and use this resource to facilitate analyses of high-coverage (~30×) genome sequences for wild-caught individuals representing species: C. sp. cf. medius, C. major, C. crossleyi, and C. sibreei. This study represents the largest contribution to date of novel genomic resources for Madagascar's lemurs. We find concordant phylogenetic relationships among the four lineages of Cheirogaleus across most of the genome, and yet detect a number of discordant genomic regions consistent with ancient admixture. We hypothesized that these regions could have resulted from adaptive introgression related to hibernation, indeed finding that genes associated with hibernation are present, though most significantly, that gene ontology categories relating to transcription are over-represented. We estimate levels of heterozygosity and find particularly low levels in an individual sampled from an isolated population of C. medius that we refer to as C. sp. cf. medius. Results are consistent with a recent decline in effective population size, which is evident across species. Our study highlights the power of comparative genomic analysis for identifying species and populations of conservation concern, as well as for illuminating possible mechanisms of adaptive phenotypic evolution.
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http://dx.doi.org/10.1038/s41437-019-0260-9 | DOI Listing |
Evolution
September 2025
Center for the Evolutionary Origins of Human Behavior, Kyoto University, 41-2, Kanrin, Inuyama, Aichi, Japan.
Malagasy lemurs are diverse primates that underwent adaptive radiation. While this radiation promotes modifications in cranium for niche partitioning, evolutionary constraints impose common craniofacial patterns among smaller lemurs: they are predicted to be constrained to have a shorter upper jaw and laterally-facing orbits to compensate for small masticatory muscles and accommodate relatively large orbits, regardless of niche. This study aims to elucidate how these evolutionary constraints operate during the adaptive radiation of lemurs.
View Article and Find Full Text PDFCurr Cardiol Rep
August 2025
Department of Biochemistry, Stanford University School of Medicine, Beckman Center B400, 279 Campus Drive, Stanford, CA, USA.
Purpose Of Review: Due to differences in cardiac structure and function, it has become increasingly clear that many aspects of cardiovascular anatomy, physiology, biochemistry, and disease are not well modeled in mice. This has spurred a search for new model organisms with the practical advantages of mice but that more closely mimic human biology and disease.
Recent Findings: Until recently, little was known of lemur cardiovascular physiology, cell types, or pathology.
Nature
August 2025
Department of Biochemistry, Stanford University School of Medicine, Stanford, CA, USA.
Mouse lemurs are the smallest and fastest reproducing primates, as well as one of the most abundant, and they are emerging as a model organism for primate biology, behaviour, health and conservation. Although much has been learnt about their ecology and phylogeny in Madagascar and their physiology, little is known about their cellular and molecular biology. Here we used droplet-based and plate-based single-cell RNA sequencing to create Tabula Microcebus, a transcriptomic atlas of 226,000 cells from 27 mouse lemur organs opportunistically obtained from four donors clinically and histologically characterized.
View Article and Find Full Text PDFNature
August 2025
Department of Biochemistry, Stanford University School of Medicine, Stanford, CA, USA.
Mouse lemurs (Microcebus spp.) are an emerging primate model organism, but their genetics, cellular and molecular biology remain largely unexplored. In an accompanying paper, we performed large-scale single-cell RNA sequencing of 27 organs from mouse lemurs.
View Article and Find Full Text PDFBrain Struct Funct
July 2025
Neuromorphology Laboratory, Pavlov Institute of Physiology Russian Academy of Sciences, Saint-Petersburg, 199034, Russia.
Acomys cahirinus is an increasingly utilized model in various biological disciplines, particularly for studying the regeneration and developmental plasticity of the central nervous system due to its remarkable ability for neural tissue repair and early neurodevelopmental milestones. Despite its growing prominence in neuroscience, the lack of comprehensive neuroanatomical data hinders precise experimental design, especially in injury and regeneration studies. To address this gap, we present a neuroanatomical and neurochemical atlas of the Acomys cahirinus spinal cord, integrating anatomical, cytoarchitectonic, neurochemical, and morphometric data.
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