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dc.contributor.authorWang, Shoueng
dc.contributor.authorFurmanek, Tomaszeng
dc.contributor.authorKryvi, Haraldeng
dc.contributor.authorKrossøy, Christeleng
dc.contributor.authorTotland, Geir K.eng
dc.contributor.authorGrotmol, Sindreeng
dc.contributor.authorWargelius, Annaeng
dc.date.accessioned2014-03-25T09:07:54Z
dc.date.available2014-03-25T09:07:54Z
dc.date.issued2014-02-19eng
dc.identifier.issn1471-2164en_US
dc.identifier.urihttps://hdl.handle.net/1956/7889
dc.description.abstractBackground In teleosts such as Atlantic salmon (Salmo salar L.), segmentation and subsequent mineralisation of the notochord during embryonic stages are essential for normal vertebrae formation. However, the molecular mechanisms leading to segmentation and mineralisation of the notochord are poorly understood. The aim of this study was to identify genes/pathways acting in gradients over time and along the anterior-posterior axis during notochord segmentation and immediately prior to mineralisation of the vertebral bodies in Atlantic salmon. Results Notochord samples were collected from unsegmented, pre-segmented and segmented developmental stages. In each stage, the cellular core of the notochord was cut into three pieces along the longitudinal axis (anterior, mid, posterior). RNA was sequenced (22 million pair-end 100 bp/ library) and mapped to the salmon genome. 66569 transcripts were predicted and 55775 were annotated. In order to identify possible gradients leading to segmentation of the notochord, all 71 notochord-expressed hox genes were investigated, most of them displaying a typical anterior-posterior expression pattern along the notochord axis. The clustering of hox genes revealed a pattern that could be related to notochord segmentation. We further investigated how mineralisation is initiated in the notochord, and several factors related to chondrogenic lineage were identified (sox9, sox5, sox6, tgfb3, ihhb and col2a1), suggesting a cartilage-like character of the notochord. KEGG analysis of differentially expressed genes between stages revealed down-regulation of pathways associated with ECM, cell division, metabolism and development at onset of notochord segmentation. This implies that inhibitory signals produce segmentation of the notochord. One such potential inhibitory signal was identified, col11a2, which was detected in segments of non-mineralising notochord. Conclusions An incomplete salmon genome was successfully used to analyse RNA-seq data from the cellular core of the Atlantic salmon notochord. In transcriptome we found; hox gene patterns possibly linked to segmentation; down-regulation of pathways in the notochord at onset of segmentation; segmented expression of col11a2 in non-mineralised segments of the notochord; and a chondroblast-like footprint in the notochord.en_US
dc.language.isoengeng
dc.publisherBioMed Centralen_US
dc.relation.ispartof<a href="http://hdl.handle.net/1956/7888" target="blank">Notochord development in Atlantic salmon (Salmo salar L.): exploring molecular pathways and putative mechanism of segmentation</a>en_US
dc.rightsAttribution CC BYeng
dc.rights.urihttp://creativecommons.org/licenses/by/2.0eng
dc.subjectAtlantic salmoneng
dc.subjectNotochordeng
dc.subjectRNA-seqeng
dc.subjectcol11a2eng
dc.subjectHoxeng
dc.titleTranscriptome sequencing of Atlantic salmon ( Salmo salar L.) notochord prior to development of the vertebrae provides clues to regulation of positional fate, chordoblast lineage and mineralisationen_US
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2014 Wang et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.en_US
dc.source.articlenumber141
dc.identifier.doihttps://doi.org/10.1186/1471-2164-15-141
dc.identifier.cristin1165806
dc.source.journalBMC Genomics
dc.source.4015


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