EXAMINING HIBERNATION IN THE BIG BROWN BAT THROUGH DNA METHYLATION

dc.contributor.advisorWilkinson, Gerald Sen_US
dc.contributor.authorSullivan, Isabelen_US
dc.contributor.departmentMarine-Estuarine-Environmental Sciencesen_US
dc.contributor.publisherDigital Repository at the University of Marylanden_US
dc.contributor.publisherUniversity of Maryland (College Park, Md.)en_US
dc.date.accessioned2021-09-16T05:39:19Z
dc.date.available2021-09-16T05:39:19Z
dc.date.issued2021en_US
dc.description.abstractHibernation allows individuals to conserve energy during seasonal low temperatures. As the physiological regulation of hibernation is inadequately understood, I examine hibernation using DNA methylation (DNAm). DNAm is the addition of a methyl group to cytosine at cytosine guanine dinucleotide (CpG) sites in the genome. DNAm in promoters can repress gene expression and be influenced by histone modifications. Using the big brown bat, Eptesicus fuscus, I examined how hibernation influences DNAm, independent of age, through comparing DNAm from bats that differed in hibernation history and comparing DNAm from the same individual between hibernating and active seasons. Both comparisons found evidence of differential enrichment of genes near significant CpG sites resulting from hibernation. The latter analysis found evidence consistent with a histone mark, associated with active transcription, is likely enriched in hibernating bats. These results suggest that DNAm and histone modifications associated with transcription factor binding regulate gene expression during hibernation.en_US
dc.identifierhttps://doi.org/10.13016/n7sa-jfmd
dc.identifier.urihttp://hdl.handle.net/1903/27762
dc.language.isoenen_US
dc.subject.pqcontrolledBiologyen_US
dc.subject.pqcontrolledBioinformaticsen_US
dc.subject.pqcontrolledGeneticsen_US
dc.subject.pquncontrolledCumulative hibernationen_US
dc.subject.pquncontrolledDNA methylationen_US
dc.subject.pquncontrolledHibernationen_US
dc.subject.pquncontrolledThe big brown baten_US
dc.titleEXAMINING HIBERNATION IN THE BIG BROWN BAT THROUGH DNA METHYLATIONen_US
dc.typeThesisen_US

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