THE MITOCHONDRIAL GENOME OF THE BLUE CRAB (CALLINECTES SAPIDUS), AN INFORMATIVE GENETIC MARKER FOR THE EVOLUTIONARY BIOLOGY AND POPULATION GENETICS OF THE SPECIES

dc.contributor.advisorPlace, Allen Ren_US
dc.contributor.authorFeng, Xiaojunen_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.accessioned2009-10-06T06:08:56Z
dc.date.available2009-10-06T06:08:56Z
dc.date.issued2009en_US
dc.description.abstractThe blue crab (Callinectes sapidus) is a widely distributed decapod which ranges from Nova Scotia to the northern Argentina coasts. It is one of the most abundant estuarine invertebrates, supporting both commercial and recreational fisheries along the Atlantic and Gulf coasts. This thesis presents data clearly establishing the unprecedented hyper-variability in the mitochondrial genome of C. sapidus. This variation extended to multiple regions, including the cox1, nad2, and nad4 protein coding loci as well as ribosomal 12s RNA molecule. The haplotype diversity of the nad2 gene approached 1, with a nucleotide diversity approaching 1%. This hyper-variability in the mtDNA allows using a single mtDNA gene (nad2) to distinguish hatchery-produced crabs from wild crabs after release to the wild. I found no dominant mtDNA haplotypes in wild populations but instead a distribution of a few low-frequency recurrent haplotypes with a large number of singletons. Because of this high diversity and extensive population mixing, the geographic structure in wild populations exhibits panmixia from the Atlantic to Gulf of Mexico. Some of the high genetic diversity found seems to stem from the heteroplasmic nature of the blue crab mtDNA. By cloning high fidelity PCR products, I confirmed single individual crab and megalopa harbored dozens of copies of mitochondrial haplotypes. A copy number analysis indicates discovery of unique haplotypes was probably not saturated with the possibility of inadequate sampling. The heteroplasmy in the blue crab appears to be under maternal inheritance without paternal contribution. While minor haplotypes are represented in wild populations, other minor haplotypes contained stop codons and/or non-synonymous substitutions which may influence the viability of the mitochondria. Given the blue crab inhabits a broad variety of environments and that the mtDNA genome appears to be under selective pressure, the potential for mtDNA functional correlates with this genetic diversity maybe at the basis for the robust physiological capability of the species.en_US
dc.format.extent33197118 bytes
dc.format.mimetypeapplication/pdf
dc.identifier.urihttp://hdl.handle.net/1903/9559
dc.language.isoen_US
dc.subject.pqcontrolledBiology, Geneticsen_US
dc.subject.pquncontrolledblue craben_US
dc.subject.pquncontrolledgenetic diversityen_US
dc.subject.pquncontrolledheteroplasmyen_US
dc.subject.pquncontrolledmitochondrial DNAen_US
dc.subject.pquncontrollednad2en_US
dc.titleTHE MITOCHONDRIAL GENOME OF THE BLUE CRAB (CALLINECTES SAPIDUS), AN INFORMATIVE GENETIC MARKER FOR THE EVOLUTIONARY BIOLOGY AND POPULATION GENETICS OF THE SPECIESen_US
dc.typeDissertationen_US

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