A population genetic analysis of the New Zealand spotty (Notolabrus celidotus) using mitochondrial DNA and microsatellite DNA markers

Notolabrus celidotus (the New Zealand spotty) is a common rocky reef species that is endemic to New Zealand. This species is the most abundant demersal reef fish in New Zealand, and is distributed throughout the North and South Islands, and Stewart Island. Notolabrus celidotus consumes a wide variety of small invertebrates, and juveniles are reliant on coastal kelp forests as nursery habitats. Because N. celidotus is such a common species on New Zealand rocky reefs it is a good model species for population genetic studies. The primary goal of this research was to investigate new genetic markers and add new sample locations to bolster previous genetic population data from N. celidotus. The thesis research utilised DNA sequences obtained from a 454 massively parallel DNA sequencer and reports six new microsatellite loci for N. celidotus. These loci are the first microsatellite DNA markers to be developed for this species. Additional mitochondrial DNA (mtDNA) control region sequences were obtained from new samples of N. celidotus and combined with previously reported mtDNA sequences. Increasing the sample size improved the genetic coverage of N. celidotus populations around coastal New Zealand. The mtDNA sequences were analysed to examine the population connectivity and demographic history of N. celidotus. The microsatellite DNA loci reported in this study were also used to examine the levels of genetic diversity and population structure in N. celidotus. Results of the combined genetic analyses revealed extremely high levels of genetic diversity among the population sample of the mtDNA control region. Both the mitochondrial DNA and microsatellite DNA analyses showed a distinct lack of population genetic structuring, which suggests there is constant mixing of N. celidotus among sites. The results of this study have the potential to inform the expectations about the genetic structure of closely related wrasse species, such as Notolabrus fucicola, as well as other coastal species that have a similar life history, dispersal power, and New Zealand-wide distribution.

Population genetics of the school shark (Galeorhinus galeus) in New Zealand, Australian and Chilean waters

10.26686/wgtn.17005726.v1 ◽

2021 ◽

Author(s):

◽

Sebastián Ignacio Hernández Muñoz

Keyword(s):

Genetic Diversity ◽

New Zealand ◽

Dna Markers ◽

Microsatellite Dna ◽

Multiple Paternity ◽

Shark Species ◽

Microsatellite Dna Markers ◽

Minimum Number ◽

Galeorhinus Galeus ◽

Shark Fisheries

The school shark (Galeorhinus galeus) is a coastal bentho-pelagic species that is highly migratory and has a widespread distribution in temperate waters. This species matures late, has a relatively low fecundity and is slow growing, which makes it vulnerable to overfishing. They are commercially fished throughout their distribution, and some global stocks have been under pressure because of poor management. In Australia, longline and gillnet fisheries targeted pregnant females and juveniles around Victorian and Tasmanian nursery grounds, resulting in loss of historical inshore nursery habitat. School shark tagging programmes have reported migration between Australian and New Zealand stocks, but preliminary genetic studies have suggested that there are slight genetic differences between the stocks. Currently, the Australian and New Zealand school shark fisheries are assessed and managed as separate stocks. However, the question of whether this species is comprised of a single population or multiple sub-populations in the South Pacific remains unresolved. Given the commercial importance of the school shark fisheries and the concern about stock levels on the regional and trans-Tasman scales, knowledge of stock structure is essential for effective management. The aim of this thesis research was to determine the levels of genetic diversity and population structure of G. galeus in New Zealand and Australia, and compare these to a population in Chile, using mitochondrial DNA (mtDNA) sequencing and microsatellite DNA markers. The DNA sequence of an 893 base pair region of the mtDNA control region (CR) was determined using 475 school shark samples and nine microsatellite DNA loci were genotyped in 239 individuals. Analyses of the data revealed strong evidence of genetic differentiation between G. galeus populations in Australasia and Chile, suggesting restricted gene flow among populations in the western and eastern areas of the Pacific Ocean. The FST values ranged from 0.188 to 0.300 for CR mtDNA, and 0.195 to 0.247 for microsatellite DNA in G. galeus. However, there was no evidence of stock differentiation among New Zealand/Australian sample sites for either mtDNA or microsatellite DNA data. These results support the model of a single panmictic stock across the Tasman Sea. The similarity of the results obtained from the maternally inherited mtDNA and biparental inherited microsatellite loci did not support the suggestion of sex-biased dispersal of G. galeus in the New Zealand/Australia region and it was concluded that females and males had similar patterns of dispersal. Sharks can be either monogamous or polygamous, which is important when considering stock assessments and harvesting models. Multiple paternity has been reported in several shark species, however, the number of sires per litter varies considerably among species. An investigation of multiple paternity (MP) was conducted in G. galeus by assessing the levels of relatedness within progeny arrays using six polymorphic microsatellite DNA markers. Five “families” (mother and litters) were sampled from the North Island of New Zealand and a parentage analysis was conducted. The minimum number of males contributing to each progeny array was estimated by identifying the putative paternal alleles by allele counting and reconstructing multilocus genotypes method. The analysis showed the occurrence of genetic polyandry in G. galeus; two of five litters showing multiple sires involved in the progeny arrays (40%). The minimum number of sires per litter ranged from one to four. Although MP was only detected in two litters, this finding is consistent with the known reproductive characteristics of G. galeus. It can potentially store sperm for long periods of time and has a specific mating season when males and females typically mix on the edge of the continental shelf. Detecting MP within a litter has highlighted the importance of the post-copulatory selective processes in the G. galeus mating system, and this has implications for the management and conservation of genetic diversity.

Use of microsatellite DNA markers to investigate the level of genetic diversity and population genetic structure of coconut (Cocos nucifera L.)

Genome ◽

10.1139/gen-43-1-15 ◽

2000 ◽

Vol 43 (1) ◽

pp. 15-21 ◽

Cited By ~ 5

Author(s):

L. Perera ◽

J.R. Russell ◽

J. Provan ◽

W. Powell

Keyword(s):

Genetic Diversity ◽

Genetic Structure ◽

Dna Markers ◽

Microsatellite Dna ◽

Population Genetic ◽

Cocos Nucifera ◽

Characterisation of the Mitochondrial Genome and the Population Genetics of Polyprion Oxygeneios (Hapuku) from Around New Zealand

10.26686/wgtn.17011832.v1 ◽

2021 ◽

Author(s):

◽

Henry Somerset Lane

Keyword(s):

Genetic Diversity ◽

Mitochondrial Dna ◽

New Zealand ◽

Genetic Structure ◽

Mitochondrial Genome ◽

Microsatellite Dna ◽

Population Genetic ◽

The West ◽

Polyprion Oxygeneios

Polyprion oxygeneios (hapuku) is an important commercial and recreational fishery species within New Zealand. Moreover, P. oxygeneios are currently being developed as a high-value New Zealand aquaculture species. There have been no previous studies on New Zealand’s P. oxygeneios that have been able to detect genetic differences among samples, which may be of use to either broodstock or fisheries managers. An understanding of the genetic structure of commercially harvested species maximises the potential for sustainable harvesting through effective management schemes. The primary goal of this thesis was to investigate the population genetic structure of P. oxygeneios using molecular markers to analyse samples collected from sites within New Zealand’s Exclusive Economic Zone (EEZ). The DNA sequence of the whole mitochondrial genome of P. oxygeneios was determined and it showed a similar structure and gene organisation to that of other species across a wide range of taxa. A set of species-specific control region primers was developed for P. oxygeneios and Polyprion americanus, and additional primers were designed for the 16S and ND6 genes of P. oxygeneios. A ~488 bp portion of the mitochondrial DNA (mtDNA) control region sequence from 274 individuals, and genotypes from 259 individuals using nine polymorphic microsatellite loci, were used to investigate the phylogeography and population genetic structure of P. oxygeneios. The mitochondrial DNA data failed to detect any significant differentiation between sample sites. However, the microsatellite DNA analyses showed that individuals sampled from the west coast of the South Island (Hokitika) were genetically distinct from individuals sampled at all other New Zealand sites. These two groups might be representative of two discrete populations of P. oxygeneios within New Zealand’s EEZ. These results suggest that the west coast South Island P. oxygeneios fishery should continue to be managed as a separate stock, with some possible revision of the Cook Strait fishery required. Analyses of the mtDNA and microsatellite DNA data of P. oxygeneios broodstock held at NIWA’s Bream Bay Aquaculture Park showed that they were not significantly differentiated from the wild populations (excluding Hokitika). Simulations also described the appropriate sampling efforts required to capture an appropriate level of genetic diversity when either establishing a new broodstock or supplementing an existing broodstock with new individuals. Continued management of the broodstock will be required to maintain the high levels of genetic diversity that have been captured in the founding broodstock in future generations.

Population genetic structure of New Zealand blue cod (Parapercis colias) based on mitochondrial and microsatellite DNA markers

10.26686/wgtn.17009387 ◽

2021 ◽

Author(s):

◽

Clare Louise Gebbie

Keyword(s):

New Zealand ◽

Genetic Structure ◽

Dna Markers ◽

Microsatellite Dna ◽

Population Genetic ◽

Current Knowledge ◽

Isolation By Distance ◽

Genetic Connectivity ◽

Parapercis colias (blue cod) is an endemic temperate reef fish that supports an important commercial and recreational fishery in New Zealand. However, concerns have been raised about localized stock depletion, and multiple lines of evidence have suggested P. colias may form several biologically distinct populations within the New Zealand Exclusive Economic Zone. Mark and recapture studies along with otolith and stable isotope studies have indicated that individuals are sedentary with very limited movement beyond the scale of 10-20km. The primary goal of this research was to advance the current knowledge of P. colias population genetic structure. This information can be incorporated into stock assessment models with the aim of improving the management of the P. colias fishery. This study made use of 454 pyrosequencing technology to isolate and develop the first set of microsatellite DNA markers for P. colias. These seven microsatellite loci, along with mitochondrial control region sequences, were used to determine the levels of genetic variation and differentiation between sites around the New Zealand coastline, including the Chatham Islands. Significant differentiation was observed between the Chatham Islands and mainland New Zealand sample sites, indicating that these two regions form distinct populations. Interpretation of the results for the mainland sites was more complex. Mitochondrial sequence data detected no significant pairwise differentiation between mainland sites, although a pattern of isolation-by-distance was observed. However, evidence for genetic differentiation among mainland sites was weak based on the microsatellite DNA analysis. Although pairwise Gѕт levels were significant in some sites, this was not reflected in principal component analysis or Bayesian structure analysis. It is likely that through long range dispersal, migration is at or above the threshold for genetic connectivity, but below a level necessary for demographic connectivity. This is indicated by both the genetic structure reported here, along with previous studies showing limited dispersal of P. colias.

Characterisation of the Mitochondrial Genome and the Population Genetics of Polyprion Oxygeneios (Hapuku) from Around New Zealand

10.26686/wgtn.17011832 ◽

2021 ◽

Author(s):

◽

Henry Somerset Lane

Keyword(s):

Genetic Diversity ◽

Mitochondrial Dna ◽

New Zealand ◽

Genetic Structure ◽

Mitochondrial Genome ◽

Microsatellite Dna ◽

Population Genetic ◽

The West ◽

Polyprion Oxygeneios

Polyprion oxygeneios (hapuku) is an important commercial and recreational fishery species within New Zealand. Moreover, P. oxygeneios are currently being developed as a high-value New Zealand aquaculture species. There have been no previous studies on New Zealand’s P. oxygeneios that have been able to detect genetic differences among samples, which may be of use to either broodstock or fisheries managers. An understanding of the genetic structure of commercially harvested species maximises the potential for sustainable harvesting through effective management schemes. The primary goal of this thesis was to investigate the population genetic structure of P. oxygeneios using molecular markers to analyse samples collected from sites within New Zealand’s Exclusive Economic Zone (EEZ). The DNA sequence of the whole mitochondrial genome of P. oxygeneios was determined and it showed a similar structure and gene organisation to that of other species across a wide range of taxa. A set of species-specific control region primers was developed for P. oxygeneios and Polyprion americanus, and additional primers were designed for the 16S and ND6 genes of P. oxygeneios. A ~488 bp portion of the mitochondrial DNA (mtDNA) control region sequence from 274 individuals, and genotypes from 259 individuals using nine polymorphic microsatellite loci, were used to investigate the phylogeography and population genetic structure of P. oxygeneios. The mitochondrial DNA data failed to detect any significant differentiation between sample sites. However, the microsatellite DNA analyses showed that individuals sampled from the west coast of the South Island (Hokitika) were genetically distinct from individuals sampled at all other New Zealand sites. These two groups might be representative of two discrete populations of P. oxygeneios within New Zealand’s EEZ. These results suggest that the west coast South Island P. oxygeneios fishery should continue to be managed as a separate stock, with some possible revision of the Cook Strait fishery required. Analyses of the mtDNA and microsatellite DNA data of P. oxygeneios broodstock held at NIWA’s Bream Bay Aquaculture Park showed that they were not significantly differentiated from the wild populations (excluding Hokitika). Simulations also described the appropriate sampling efforts required to capture an appropriate level of genetic diversity when either establishing a new broodstock or supplementing an existing broodstock with new individuals. Continued management of the broodstock will be required to maintain the high levels of genetic diversity that have been captured in the founding broodstock in future generations.

Population genetics of the school shark (Galeorhinus galeus) in New Zealand, Australian and Chilean waters

10.26686/wgtn.17005726 ◽

2021 ◽

Author(s):

◽

Sebastián Ignacio Hernández Muñoz

Keyword(s):

Genetic Diversity ◽

New Zealand ◽

Dna Markers ◽

Microsatellite Dna ◽

Multiple Paternity ◽

Shark Species ◽

Microsatellite Dna Markers ◽

Minimum Number ◽

Galeorhinus Galeus ◽

Shark Fisheries

The school shark (Galeorhinus galeus) is a coastal bentho-pelagic species that is highly migratory and has a widespread distribution in temperate waters. This species matures late, has a relatively low fecundity and is slow growing, which makes it vulnerable to overfishing. They are commercially fished throughout their distribution, and some global stocks have been under pressure because of poor management. In Australia, longline and gillnet fisheries targeted pregnant females and juveniles around Victorian and Tasmanian nursery grounds, resulting in loss of historical inshore nursery habitat. School shark tagging programmes have reported migration between Australian and New Zealand stocks, but preliminary genetic studies have suggested that there are slight genetic differences between the stocks. Currently, the Australian and New Zealand school shark fisheries are assessed and managed as separate stocks. However, the question of whether this species is comprised of a single population or multiple sub-populations in the South Pacific remains unresolved. Given the commercial importance of the school shark fisheries and the concern about stock levels on the regional and trans-Tasman scales, knowledge of stock structure is essential for effective management. The aim of this thesis research was to determine the levels of genetic diversity and population structure of G. galeus in New Zealand and Australia, and compare these to a population in Chile, using mitochondrial DNA (mtDNA) sequencing and microsatellite DNA markers. The DNA sequence of an 893 base pair region of the mtDNA control region (CR) was determined using 475 school shark samples and nine microsatellite DNA loci were genotyped in 239 individuals. Analyses of the data revealed strong evidence of genetic differentiation between G. galeus populations in Australasia and Chile, suggesting restricted gene flow among populations in the western and eastern areas of the Pacific Ocean. The FST values ranged from 0.188 to 0.300 for CR mtDNA, and 0.195 to 0.247 for microsatellite DNA in G. galeus. However, there was no evidence of stock differentiation among New Zealand/Australian sample sites for either mtDNA or microsatellite DNA data. These results support the model of a single panmictic stock across the Tasman Sea. The similarity of the results obtained from the maternally inherited mtDNA and biparental inherited microsatellite loci did not support the suggestion of sex-biased dispersal of G. galeus in the New Zealand/Australia region and it was concluded that females and males had similar patterns of dispersal. Sharks can be either monogamous or polygamous, which is important when considering stock assessments and harvesting models. Multiple paternity has been reported in several shark species, however, the number of sires per litter varies considerably among species. An investigation of multiple paternity (MP) was conducted in G. galeus by assessing the levels of relatedness within progeny arrays using six polymorphic microsatellite DNA markers. Five “families” (mother and litters) were sampled from the North Island of New Zealand and a parentage analysis was conducted. The minimum number of males contributing to each progeny array was estimated by identifying the putative paternal alleles by allele counting and reconstructing multilocus genotypes method. The analysis showed the occurrence of genetic polyandry in G. galeus; two of five litters showing multiple sires involved in the progeny arrays (40%). The minimum number of sires per litter ranged from one to four. Although MP was only detected in two litters, this finding is consistent with the known reproductive characteristics of G. galeus. It can potentially store sperm for long periods of time and has a specific mating season when males and females typically mix on the edge of the continental shelf. Detecting MP within a litter has highlighted the importance of the post-copulatory selective processes in the G. galeus mating system, and this has implications for the management and conservation of genetic diversity.

Population genetic structure of New Zealand blue cod (Parapercis colias) based on mitochondrial and microsatellite DNA markers

10.26686/wgtn.17009387.v1 ◽

2021 ◽

Author(s):

◽

Clare Louise Gebbie

Keyword(s):

New Zealand ◽

Genetic Structure ◽

Dna Markers ◽

Microsatellite Dna ◽

Population Genetic ◽

Current Knowledge ◽

Isolation By Distance ◽

Genetic Connectivity ◽

Parapercis colias (blue cod) is an endemic temperate reef fish that supports an important commercial and recreational fishery in New Zealand. However, concerns have been raised about localized stock depletion, and multiple lines of evidence have suggested P. colias may form several biologically distinct populations within the New Zealand Exclusive Economic Zone. Mark and recapture studies along with otolith and stable isotope studies have indicated that individuals are sedentary with very limited movement beyond the scale of 10-20km. The primary goal of this research was to advance the current knowledge of P. colias population genetic structure. This information can be incorporated into stock assessment models with the aim of improving the management of the P. colias fishery. This study made use of 454 pyrosequencing technology to isolate and develop the first set of microsatellite DNA markers for P. colias. These seven microsatellite loci, along with mitochondrial control region sequences, were used to determine the levels of genetic variation and differentiation between sites around the New Zealand coastline, including the Chatham Islands. Significant differentiation was observed between the Chatham Islands and mainland New Zealand sample sites, indicating that these two regions form distinct populations. Interpretation of the results for the mainland sites was more complex. Mitochondrial sequence data detected no significant pairwise differentiation between mainland sites, although a pattern of isolation-by-distance was observed. However, evidence for genetic differentiation among mainland sites was weak based on the microsatellite DNA analysis. Although pairwise Gѕт levels were significant in some sites, this was not reflected in principal component analysis or Bayesian structure analysis. It is likely that through long range dispersal, migration is at or above the threshold for genetic connectivity, but below a level necessary for demographic connectivity. This is indicated by both the genetic structure reported here, along with previous studies showing limited dispersal of P. colias.

ANALYSIS OF GENETIC STRUCTURE OF DOGS OF FRENCH BULLDOG BREED USING MICROSATELLITE DNA MARKERS

Animal Breeding and Genetics ◽

10.31073/abg.51.25 ◽

2018 ◽

Vol 51 ◽

pp. 185-192

Author(s):

S. Kruhlyk ◽

V. Dzitsiuk ◽

V. Spyrydonov

Keyword(s):

Genetic Diversity ◽

Genetic Variability ◽

Dna Markers ◽

Microsatellite Dna ◽

High Variability ◽

Molecular Diagnostic ◽

Allelic Variants ◽

Microsatellite Dna Markers ◽

Gene Complexes ◽

French Bulldog

Genetic variability of domestic dogs is a source for effective process of breed formation and creating unique gene complexes. In the world, for preservation of genetic resources of dogs, there are dog training associations which have great confidence: American Club Dog Breeders (AKC), the British Kennel Club (KC) and the Federation Cynologique Internationale (FCI), aimed at protecting breeding dogs, standards creation, registration of a breed, and issuance of accurate pedigrees. Evaluation of the genetic diversity of dog breeds is able to significantly complement and improve their breeding programs. Since breeds of dog differ in morphological and economic characteristics, the problem of finding of the breed features in the genome of animals is becoming more topical. From this point of view, French Bulldog is an interesting breed of dog (FRANC.BULLDOGGE, FCI standard number 101) which belongs by the classification of breeds, adopted in FCI, to the group IX – a dog-companion for health and fun, but to a subgroup of fighting dogs of a small format. French Bulldog breed has been researched slightly not only in Ukraine and also abroad, as the main work of all dog association is focused on solving theoretical and practical issues of breeding, keeping, feeding, veterinary protection and others. The study was conducted at Research Department of Molecular Diagnostic Tests of Ukrainian Laboratory of Quality and Safety of Agricultural Products. 33 animals of French Bulldog breed, admitted to use in dog breeding of Ukrainian Kennel Union (UKU), were involved for the genetic analysis using DNA markers. The materials of the research were buccal epithelial cells, selected before the morning feeding of animals by scraping mucous membrane of oral cavity with disposable, dry, sterile cotton swab. Genomic DNA was extracted using KIT-set of reagents for DNA isolation according to the manufacturer's instructions. PEZ1, PEZ3, PEZ6, PEZ8, FHC 2010, FHC 2054 markers, recommended by International Society for Animal Genetics (ISAG), ACN, КC and FCI, were used for research. As a result of research 25 alleles for all the loci were detected in the experimental sample of dogs. The average number of alleles at the locus Na, obtained by direct counting, was 4.16. The most polymorphic loci for this breed were PEZ6 and PEZ3 with 8 and 6 allelic variants. Monomorphic loci were PEZ8 and FHC 2054 which had 4 and 3 alleles and the lowest level of polymorphism was observed for PEZ 1 and FHC 2010 loci in which only 2 alleles were identified. On analyzing the molecular genetic characteristics of dogs of French Bulldog breed, we found a high variability of genotype on rare alleles, which included alleles: M, C, D, E, J, K, L, O, N and representing 60% of the total number of the identified alleles. C, D, E alleles for PEZ3 locus and O allele at PEZ6 locus are unique to the sampling of dogs because they are not repeated in other loci. Typical alleles: N, F, R, I, P, K, M are 40% of the total. But F, R alleles for PEZ3 locus and P allele for locus PEZ6 are not repeated either in standard allelic variants or in rare one, indicating a high information content of these alleles and loci to be used for further monitoring of allele pool, genetic certification and identification of dogs. Microsatellite DNA loci were analyzed as a result of investigations of French Bulldogs and the most informative: PEZ3, PEZ6 and PEZ8 were found, which have high efficiency in individual and breed certification of dogs due to high variability. These data allow further monitoring of the state of genetic diversity of the breed and the development of measures for improvement of breeding to preserve the structure of breeding material. The study of individual and population genetic variability is advisable to continue for breeding of French Bulldogs "in purity" and preserving valuable gene complexes. The results are the basis for further monitoring of the proposed informative panels of microsatellite DNA markers for genotyping dog of French Bulldog breed and their complex evaluation.