Exploring the distribution of genetic variants:neutral, ancestral and derived variants in natural populations of warfarin resistant Norway rats

dc.contributor.advisorKohn, Michael Hen_US
dc.creatorBiswas, Sreyasien_US
dc.date.accessioned2019-05-17T16:22:15Zen_US
dc.date.available2019-05-17T16:22:15Zen_US
dc.date.created2018-08en_US
dc.date.issued2018-08-30en_US
dc.date.submittedAugust 2018en_US
dc.date.updated2019-05-17T16:22:16Zen_US
dc.description.abstractNatural selection acts on variation that occurs by spontaneous mutation, and the fate of mutations depends on their selective value and drift. Moreover, mutations are distributed within and amongst populations due to demographic events, and often reflect historical biogeography and migration. The evolution of traits by natural selection in local populations depends on the rate of mutational input and draws upon standing variation. Quantifying the relative importance of both is of interest especially in complex traits encoded by interacting genes where major adaptive mutations may require allelic reconfiguration at interacting loci. Here I address the role of complex demographics and standing variations in assembly of a polygenic adaptive trait – warfarin resistance in natural populations of Norway rat (Rattus norvegicus). Warfarin is used both as a rodenticide and a prescribed blood thinning medicine in humans. It works by inhibiting the vitamin K cycle, specifically blocking Vkorc1 (vitamin K epoxide reductase complex subunit 1). Warfarin resistance mainly encoded by Y139C mutation in the Vkorc1 evolved quickly in wild Norway rats. In humans, warfarin has a narrow therapeutic window and depends upon variation in at least 2 additional genes suggesting a complex genetic architecture. In this dissertation, I show that association study and population genetics of any variant in the study area would need to consider the population structure at local and regional scales. A major contribution of this dissertation is a fully sequenced, mapped and annotated genome sequence of out-group species, the roof-rat (Rattus rattus) which enables the polarization of variants in the Norway rat as either ancestral or derived. This work also showed that the causative variation in Vkorc1 is a new mutation and such instances of new mutations are rare in the genome of Norway rats. Interestingly, I found that the majority of other genes participating in Vitamin K cycle carry common standing variants whose local occurrences may have been affected by demographics more strongly than by selection. Selection on interacting putative candidate genes underlying warfarin resistance in rats may have favored a main de novo mutation in Vkorc1, and previously rare standing derived variants in interacting genes.en_US
dc.format.mimetypeapplication/pdfen_US
dc.identifier.citationBiswas, Sreyasi. "Exploring the distribution of genetic variants:neutral, ancestral and derived variants in natural populations of warfarin resistant Norway rats." (2018) Diss., Rice University. <a href="https://hdl.handle.net/1911/105864">https://hdl.handle.net/1911/105864</a>.en_US
dc.identifier.urihttps://hdl.handle.net/1911/105864en_US
dc.language.isoengen_US
dc.rightsCopyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder.en_US
dc.subjectpolygenic adaptive traiten_US
dc.subjectstanding variantsen_US
dc.subjectvitamin K cycleen_US
dc.subjectNorway raten_US
dc.titleExploring the distribution of genetic variants:neutral, ancestral and derived variants in natural populations of warfarin resistant Norway ratsen_US
dc.typeThesisen_US
dc.type.dcmiDataseten_US
dc.type.materialTexten_US
thesis.degree.departmentEcology and Evolutionary Biologyen_US
thesis.degree.disciplineNatural Sciencesen_US
thesis.degree.grantorRice Universityen_US
thesis.degree.levelDoctoralen_US
thesis.degree.nameDoctor of Philosophyen_US
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