Reports

Population genetics of the Icelandic Nephrops norvegius stock / Stofnerfðafræði leturhumars á Íslandsmiðum

Published:

01/06/2010

Authors:

Sigurlaug Skírnisdóttir, Sigurbjörg Hauksdóttir, Kristinn Ólafsson, Christophe Pampouli, Hrafnkell Eiríksson, Steinunn Á. Magnúsdóttir, Guðmundur H. Gunnarsson, Guðmundur Ó. Hreggviðsson, Sigríður Hjörleifsdóttir

Supported by:

The Icelandic Fisheries Research Fund, the Student Innovation Fund

Contact

Sigurlaug Skírnisdóttir

Project Manager

sigurlaug.skirnisdottir@matis.is

Population genetics of the Icelandic Nephrops norvegius stock / Stofnerfðafræði leturhumars á Íslandsmiðum

As the name of the project "Stock genetics of lobster in Icelandic waters" indicates, the aim of the project was to examine the type of lobster (Nephrops norvegicus) in Icelandic waters, but stock type research is an important factor for sustainable fisheries management. The main objectives of the project were to develop new genetic boundaries to assess genetic variability within and between geographically separated hunting areas in Iceland, to define the paternity of female egg masses from separate hunting areas in order to shed light on the reproductive process of lobster breeding and to stem genetic factors. Genetic analysis involves the use of so-called genetic markers, which are based on specific DNA sequences that are somehow detectable in the genome. Genetic markers based on repeated short sequences (2-6 bases) are most commonly used, which are known to vary between individuals of the same species. These areas therefore vary in length between individuals and make them suitable options. Genetic analysis is a very powerful technology that can be used for individual analysis in a group of organisms. This method is now increasingly used for parental analysis, to assess population structure, for research traceability and to accelerate targeted breeding. Usually 5-15 different genetic markers need to be used to differentiate individuals. A large part of the development work is therefore to find the best conditions for PCR reactions, where as many genetic markers as possible can be used in one reaction (multiplex) and simultaneous runs on a sequencer. Well-made genetic analysis kits that are easy and cheap to use and provide a lot of information and good diagnostic skills are very useful for a variety of uses. They are therefore valuable products and marketers, as both genetic analysis and services based on them can be sold. The project developed eight new genetic markers for lobsters and used them to analyze samples from separate geographical fishing areas around Iceland, while Scottish lobster samples were used as a group. In addition, four previously published genetic markers were used for the analyzes. The results of analyzes with these 12 genetic markers from geographically separated regions (together with the subgroup) did not show a significant genetic difference of lobster between the regions. The results of the project have been published in articles and student projects. The student thesis is entitled "Development of microsatellite multiplex systems for Nephrops norvegicus" and is by Sóleyja Valgeirsdóttir. One article has been approved for publication in the project, which describes eight new genetic markers. The title of the article is: "Isolation and characterization of eight new microsatellite loci in the Norway lobster, Nephrops norvegicus (Linnaeus, 1758)" (approved for publication in the journal Molecular Ecology Resources, Appendix 1). Another article has been submitted for publication in the ICES Journal of Marine Science under the title "A pilot genetic study revealed the absence of spatial genetic structure of the Norway lobster (Nephrops norvegicus) at fishing grounds in Icelandic waters" but it deals with the structure of lobster in Icelandic waters where lobsters from Scotland were kept as an outing group (Appendix 2).

The genetic structure of population and mating behavior of exploited marine species are important criteria for effective fisheries management. The distribution of Nephrops norvegicus, Norway lobster, in Icelandic waters is limited to the warmer sea of the south coast. The distribution of the Icelandic stock can be divided into ten geographical areas but the main aim of this project was to develop microsatellite markers to use for the genetics analysis and to analyze whether the lobsters in each area are a self-contained unit stock or not. The aim was furthermore to determine the paternity of egg masses from individual females, and thus elucidate the breeding structure in Icelandic waters. The final goal was to produce a plan for the conservation and management of genetic resources in the Icelandic Norway lobster stock taking into account possible natural population diversity. Microsatellites are short sequence repeats of 2-6 bases found in all prokaryotic and eukaryotic genomes analyzed to date. Microsatellites are variable, which means the number of repeats in a specific area of the DNA variants between the different members of a species. Consequently, the alleles of the microsatellites differ by the length. The different alleles and thus the different length of the microsatellites can be caused by insertion or deletion of one or more repeats during the DNA replication. These sequences are usually under a high degree of length variability and that makes them as powerful genetic markers. Therefore, microsatellites are suitable for population genetics, for family tracing in breeding programs, genetic monitoring, and kinship studies as well as tracing of origin. Usually, 5-15 microsatellites are enough to discriminate between individuals. A microsatellite multiplex system is the use of multiple, unique primer sets in a single PCR mixture to produce amplicons of varying sizes, specific to different DNA sequences. By targeting multiple loci at once, additional information may be gained from a single reaction. It is a great advantage that microsatellite markers can be run in multiplex assay systems. Larger numbers of samples and smaller DNA quantities can then be genotyped at once, saving time and money. This also minimizes the risk of handling errors. In this study we developed eight new microsatellite markers that were used to characterize the genetic diversity of Norway lobster, in and between isolated geographical areas in Icelandic waters, and an out-group sample from Scotland. In addition, four previously published microsatellite markers were used for the analysis. The microsatellites did not detect significant genetic differentiation among the location sampled, not even among Icelandic samples and the out-group collected in Scotland. The outcomes of the project are two papers and one student report. The report is titled "Development of microsatellite multiplex systems for Nephrops norvegicus" by Sóley Valgeirsdóttir. The first paper is titled; „Isolation and characterization of eight new microsatellite loci in the Norway lobster, Nephrops norvegicus (Linnaeus, 1758)“ where the eight new loci are described (Molecular Ecology Resources; Appendix 1; accepted for publication). The second paper is titled "A pilot genetic study revealed the absence of spatial genetic structure of the Norway lobster (Nephrops norvegicus) at fishing grounds in Icelandic waters" (ICES Journal of Marine Science; Appendix 2; submitted).

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Reports

Genetics kit for char

Published:

01/02/2008

Authors:

Sigurlaug Skírnisdóttir, Alexandra M. Klonowski, Sigurbjörg Hauksdóttir, Kristinn Ólafsson, Helgi Thorarensen, Einar Svavarsson, Sigríður Hjörleifsdóttir

Supported by:

Tækniþróunarsjóður Rannsóknamiðstöð Íslands

Contact

Sigurlaug Skírnisdóttir

Project Manager

sigurlaug.skirnisdottir@matis.is

Genetics kit for char

The goal of the project was to create a powerful genetic kit for char with 15-20 genetic markers. Many genetic markers have been published for char and other salmonids, but the disadvantage is that no suitable reproduction gene set is known, which is a prerequisite for the efficient use of technology. It is important that the genetic markers show variability within the strain, are of a certain size but of different sizes, work well in a amplification reaction solution and are well readable after the sample has been run on a sequencer. The risk in the project was whether it would be possible to find a suitable genetic marker that could be combined into 2-3 reaction mixtures. 70 pairs of indicators were tested for 56 published genetic markers. The result of the project was that it was possible to combine 17 genetic markers into 3 reaction mixtures. A total of 140 fish were identified from the Hólar fish stock with these 17 genetic boundaries, but in addition, 12 wild fish were identified with them. The results showed that the genetic markers were used to differentiate between different groups of char. The processing of genetic analyzes clearly confirmed that Hólableikjan is mainly made up of two species. Some genetically modified wild charr yielded new isotopes not seen in farmed fish. Therefore, there are now genetic marketing kits that can be used in breeding work, in stock research on wild char and in traceability research. This will strengthen breeding work and is a powerful tool for research on char in the future.

The goal of the project was to develop genotyping protocols for Arctic charr containing multiplexes of 15-20 microsatellite markers. Many microsatellite markers have been published for salmonoid fishes, but no multiplexes are known which are of practical use when analyzing many samples at a time and therefore, to make the research profitable. The microsatellite markers must show variability among the fishes, they must be of certain sizes and of variable sizes, they must be amplifiable in multiplex PCR reactions and they must be easily readable from the machine. The risk of the project was to find published microsatellite markers which would fulfill these criteria and fit into 2-3 multiplex PCR reactions. Seventy primer pairs were tested for 56 published microsatellite markers. The results of the project were that 17 microsatellite markers which fit into 3 multiplex PCR reactions. A total of 140 fish from the brood stock of Arctic charr from the University at Holar was analyzed in the study as well as 12 samples from wild fish of different lakes and rivers. The results indicate that these markers can be used to analyze different stocks of Arctic charr. Furthermore, analyzes of the brood stock confirms that it mainly consists of two different stocks. New alleles were observed in the wild fish compared to the brood stock fish. A genotyping protocol to analyze Arctic charr for use in breeding industry, in wild fish research and in tractability analyzes, is now available. This will help in building up breeding programs and will be a helpful tool of the genetic research of Arctic charr.

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