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Author

Julie Colleter

Bio: Julie Colleter is an academic researcher. The author has contributed to research in topics: Sea bass. The author has an hindex of 1, co-authored 1 publications receiving 6 citations.
Topics: Sea bass

Papers
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Dissertation
13 Feb 2015
TL;DR: Gynogenesis was reported successful to produce clonal founders in the sea bass, but high numbers of meiotic individuals contaminating fully homozygous progenies highlighted the need for efficient DNA markers to distinguish mitotic gynogenetic individuals.
Abstract: Clonal lines are a powerful scientific tool for improved genetic characterization of organisms used in research. Inbred fish lines can be produced in only two generations using uniparental reproduction techniques. Androgenesis, achieved with variable success in several freshwater species, has been attempted in the European sea bass (Dicentrarchus labrax L), a marine fish of commercial and scientific interest. The low yields of progenies inheriting only the paternal genome after UV-irradiation of eggs led to considerations on the occurrence of UV screening compounds in pelagic eggs. Mycosporine-like amino acids and gadusol were found in many marine and freshwater organisms, but their occurrence in fish eggs was not clearly related to a behavioral pattern and while gadusol appeared in higher proportions in pelagic marine eggs compared to benthic species, this statement did not apply in freshwater, and moreover the kind of compounds was related to phylogeny. Further studies on DNA photorepair could enlighten hypotheses to understand the mechanisms underlying the disparate results obtained in inducing androgenesis in different fish species. Gynogenesis was reported successful to produce clonal founders in the sea bass, but high numbers of meiotic individuals contaminating fully homozygous progenies highlighted the need for efficient DNA markers to distinguish mitotic gynogenetic individuals. Furthermore, gonad development was highly delayed in gynogenetic progenies enhancing the difficulties to produce clonal lines. A high variability between individuals in the success of uniparental reproduction brought out gamete characterization and quality as a prerequisite.

6 citations


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Journal Article
TL;DR: In this article, the authors report experiments to assess the competitive and reproductive abilities of fifth-generation farmed salmon and their potential impacts upon wild salmon and conclude that farmed females had less than one-third of the reproductive success of wild females.
Abstract: 1. Escape of cultured organisms into natural ecosystems may threaten wild populations both ecologically and genetically. In the aquaculture industry, farmed Atlantic salmon (Salmo salar L.) often escape and enter the spawning grounds of wild salmon. We report experiments to assess the competitive and reproductive abilities of fifth-generation farmed salmon and their potential impacts upon wild salmon. 2. The farmed and wild females had similar levels of competitive behaviour; however, they differed in reproductive behaviour and success. Farmed females displayed less breeding behaviour, constructed fewer nests, retained a greater weight of eggs unspawned, were less efficient at nest covering, incurred more nest destruction, and suffered greater egg mortality than wild females. As a result, farmed females had less than one-third of the reproductive success of wild females. 3. The farmed males were even less successful than the farmed females in competition with the wild fish. They were less aggressive, courted less, partook in fewer spawnings, and achieved only an estimated one to three percentage of the reproductive success of the wild males. 4. The farmed males exhibited inappropriate mating behaviour, that led to poor fertilization success, even in the absence of competition with wild males. 5. Adult farmed fish are thus likely to be relatively unsuccessful in natural environments due to a competitive and reproductive inferiority apparently resulting from domestication.

301 citations

Journal ArticleDOI
TL;DR: Genome-wide screening enabled substantive verification of the production of the gynogenetic family used in this study, and the large number of telomeric and subtelomeric markers with high heterozygosity values in the meiotic gynagenetic family indicate that such markers could be used to clearly distinguish between meiotic and mitotic gwnogenetics.
Abstract: Fully isogenic lines in fish can be developed using “mitotic” gynogenesis (suppression of first zygotic mitosis following inactivation of the sperm genome). However, genome-wide verification of the steps in this process has seldom been applied. We used ddRADseq to generate SNP markers in a meiotic gynogenetic family of European seabass (Dicentrarchus labrax): (i) to verify the lack of paternal contribution in a meiotic gynogenetic family; (ii) to generate a gene-centromere map from this family; (iii) to identify telomeric markers that could distinguish mitotic gynogenetics from meiotic gynogenetics, which sometimes arise spontaneously in mitotic gynogenetic families. From a single meiotic gynogenetic family consisting of 79 progeny, 42 million sequencing reads (Illumina, trimmed to 148 bases) resolved 6866 unique RAD-tags. The 340 male-informative SNP markers that were identified confirmed the lack of paternal contribution. A gene-centromere map was constructed based on 804 female-informative SNPs in 24 linkage groups (2n = 48) with a total length of 1251.02 cM (initial LG assignment was based on the seabass genome assembly, dicLab v1). Chromosome arm structure could be clearly discerned from the pattern of heterozygosity in each linkage group in 18 out of 24 LGs: the other six showed anomalies that appeared to be related to issues in the genome assembly. Genome-wide screening enabled substantive verification of the production of the gynogenetic family used in this study. The large number of telomeric and subtelomeric markers with high heterozygosity values in the meiotic gynogenetic family indicate that such markers could be used to clearly distinguish between meiotic and mitotic gynogenetics.

10 citations

13 Jul 2016
TL;DR: The nuclear DNA content in 10 species of chondrostean fishes was measured by flow cytometry and the sterlet Acipenser ruthenus blood cells were used as an internal standard.
Abstract: DNA Content in Eurasian Sturgeon Species Determined by flow cytomery , DNA Content in Eurasian Sturgeon Species Determined by flow cytomery , مرکز فناوری اطلاعات و اطلاع رسانی کشاورزی

2 citations