Publications
NIBIOs employees contribute to several hundred scientific articles and research reports every year. You can browse or search in our collection which contains references and links to these publications as well as other research and dissemination activities. The collection is continously updated with new and historical material.
2010
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Emmanuel Lapied Claire Coutris Elara Moudilou Jean-Marie Exbrayat Deborah H. Oughton Erik JonerAbstract
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Authors
Hans Geir Eiken Rune Andreassen Alexander Kopatz I WartiainenAbstract
The use of non-invasive sampling of hairs and scats in wildlife genetics opens the possibility for sampling and analyzing living populations of brown bears (Ursus arctos). The aims of this study have been to develop a quality assured approach for genetic assignment of individual identity of brown bears and to generate a population database that can be used for research, conservation management and forensics. Non-invasive genetic sampling was performed by collection of scats and hairs in the field during the time period from 2004 to 2008. Hair traps were applied to collect hairs from bears in selected geographical areas in 2007 and 2008. Genotypes from 13 STR loci were determined for 232 Norwegian bears. Initial analysis of the entire sample indicated a high level of substructure, and the sample was divided in four geographically different populations consisting of 206 individuals for further validation of the markers. Ten STRs (G1D, G10L, Mu05, Mu09, Mu10, Mu15, Mu23, Mu50, Mu51 and Mu59) conformed to Hardy-Weinberg equilibrium expectations with only minor deviations, while the remaining three STR loci (G1A, Mu26 and G10B) were subjected to further molecular analysis. The average estimate of population substructure for Norwegian bears using 10 STRs (FST) was determined to be 0.1, while the estimate for inbreeding (FIS) was -0.02. Accounting for the FST-value, the average probability of identity (PIave) was 5.67 x 10-10 and the average probability of sibling identity (PIsib) was 1.68 x 10-4. Accreditation in accordance with the international standard ISO17025 was achieved for the described laboratory approach in 2009. We suggest that this approach and STR markers should also be considered to be used for other populations of brown bears in Northern Europe in order to ensure a common quality of the data as well as to facilitate exchange of information in conservation genetics.
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Authors
Jens Rohloff Per Winge Jahn Davik May Bente Brurberg Keithanne Mockaitis Vladimir Shulaev Stephen K, Randall Atle M. Bones Muath AlsheikhAbstract
In order to support functional genomics research in octoploid (Fragaria x ananassa Duch.) and diploid (F. vesca) strawberry, a customized Fragaria microarray chip was developed as a joint collaboration between Graminor Breeding Ltd. and NTNU. F. vesca cDNA sequences were provided by The Center for Genomics and Bioinformatics, Indiana University (an assembly of >3 million reads from GS-FLX Titanium - Roche/454 Life Sciences sequencing), and about 59,000 publicly available Fragaria EST sequences were uploaded from NCBI. In addition, ~190 Mb of preliminary draft genome sequences from F. vesca were provided by the Strawberry Genome Sequencing Consortium (courtesy to V. Shulaev). cDNAs used as templates for probe design were validated by BlastN against the F. vesca draft genome excluding cDNAs of microbial origin. Genes not represented in the cDNA collection were identified by screening F. vesca draft genome against protein sequences from Arabidopsis thaliana, Vitis vinifera, Ricinus communis and Populus trichocarpa. Exon sequences from genes not found in the cDNAs were included. In total, 43723 unique 60-mer probes were designed and the Agilent eARRAY tool was used to produce a 4x44k format microarray chip. Fragaria chip applicability and feasibility for transcriptional profiling was investigated using either abiotic (low temperature) or biotic (pathogenic fungi) stress treatment. Microarray data will be subsequently integrated with other omics data to address gene-regulatory networks and biological functions. Cold acclimation experiments were focused on short- and long-term effects in meristematic tissue, and revealed the up-regulation of ~100 cold-responsive genes (transcription factors, dehydrins, enzymes), and transcripts involved in starch breakdown and raffinose biosynthesis. Beside central metabolism, secondary metabolism was also strongly modulated as seen by changes in the expression of flavonoid biosynthesis-related genes. Time-course studies of transcriptional responses in F. vesca accessions showing contrasting resistance toward the pathogen Phytophthora cactorum are in progress, and will be presented in-depth.
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Authors
Ingunn ØvsthusAbstract
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