The application of new technologies in conservation genetics
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Authors
Labuschagne, Christiaan De Jager
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University of the Free State
Abstract
Showing abstract in English
English: Over the past decade, the development of high-throughput DNA techniques has expanded the
scope of conservation genetics and molecular markers have become indispensable tools for the
management of wildlife species and populations. There are several molecular markers available for
biodiversity analysis, but their selection depends on the objective of the study, the molecular
information sought (and reliability thereof) and the facilities and/or resources available. In order to
develop and apply new genetic techniques I have decided on using one bird and one mammal
species of interest in South Africa. The bird species chosen is the African Penguin (Spheniscus
demersus) which has suffered serious population declines and is listed in the IUCN Red Data Book
as an endangered species. Due to world-wide attention to rhinoceros conservation and population
decline, the white rhinoceros (Ceratotherium simum) was selected as mammal species. Three
different markers and their utility in aid of South African wildlife biodiversity conservation were
investigated in these diverse species. The complete mitochondrial genome of the African Penguin
was sequenced. The Spheniscus demersus mtDNA genome is very similar, both in composition
and length, to both the Eudyptes chrysocome and E. minor genomes. This is the first report of the
complete nucleotide sequence for the mitochondrial genome of the African Penguin. These results
can be subsequently used to provide information for penguin phylogenetic studies and insights into
the evolution of genomes. Furthermore, the study reported eight species specific microsatellite
markers as well as 31 SNP markers as new molecular tools for the investigation, management and
reintroduction of African penguin. Utilising these new tools, the study generated molecular genetic
information to verify/complement studbook-based pedigree data from ex-situ populations of African
Penguin. In addition, we compared the relative and combined utility of MS and SNP markers for
parentage assignment. We found that a combined subset of these two types of markers attained a
> 99% correct cumulative parentage assignment probability. This study further reported on 34
novel SNP markers for the white rhinoceros, identified through sequencing of CATS loci as well as
SNP enriched libraries. The utility of 33 Single Nucleotide Polymorphisms and 10 microsatellites in
isolation and in combination for assigning parentage in captive white rhinoceros were compared. It
was found that a combined dataset of SNPs and microsatellites was most informative and showed
the highest confidence level. This study thus provides a useful set of SNP and MS markers for
parentage and relatedness testing in white rhinoceros. Furthermore, assessment of the utility of
SNP and MS markers over multiple (> three) generations and the incorporation of a larger variety
of relationships among individuals (e.g. half-siblings or cousins) is strongly recommended.
Developed SNP markers could be used to define the genetic mating system of this species, for
forensic applications and to determine population structure and variability when other markers
prove problematic.