Physiol. Genomics AJP: Endocrinology and Metabolism
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Physiol. Genomics 31: 385-401, 2007. First published July 31, 2007; doi:10.1152/physiolgenomics.00059.2007
1094-8341/07 $8.00
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Received 9 March 2007; accepted in final form 27 July 2007.
Physiological Genomics 31:385-401 (2007)
1094-8341/06 $8.00 © 2007 American Physiological Society

Transcriptomic approach to the study of osmoregulation in the European eel Anguilla anguilla

Svetlana Kalujnaia 1, Iain S. McWilliam 1, Vitalii A. Zaguinaiko 2, Anja L. Feilen 1, John Nicholson 1, Neil Hazon 1, Christopher P. Cutler 3 and Gordon Cramb 1

1 School of Biology, University of St. Andrews, Fife, United Kingdom
2 Moscow State University of Instrument Engineering and Computer Science, Moscow, Russia
3 Department of Biology, University of Southern Georgia, Statesboro, Georgia

In euryhaline teleosts, osmoregulation is a fundamental and dynamic process that is essential for the maintenance of ion and water balance, especially when fish migrate between fresh water (FW) and sea water (SW) environments. The European eel has proved to be an excellent model species to study the molecular and physiological adaptations associated with this osmoregulatory plasticity. The life cycle of the European eel includes two migratory periods, the second being the migration of FW eels back to the Sargasso Sea for reproduction. Various anatomical and physiological changes allow the successful transition to SW. The aim of this study was to use a microarray approach to screen the osmoregulatory tissues of the eel for changes in gene expression following acclimation to SW. Tissues were sampled from fish at selected intervals over a 5-mo period following FW/SW transfer, and RNA was isolated. Suppressive subtractive hybridization was used for enrichment of differentially expressed genes. Microarrays comprising 6,144 cDNAs from brain, gill, intestine, and kidney libraries were hybridized with appropriate targets and analyzed; 229 differentially expressed clones with unique sequences were identified. These clones represented the sequences for 95 known genes, with the remaining sequences (59%) being unknown. The results of the microarray analysis were validated by quantification of 28 differentially expressed genes by Northern blotting. A number of the differentially expressed genes were already known to be involved in osmoregulation, but the functional roles of many others, not normally associated with ion or water transport, remain to be characterized.

microarray; genes; differential expression




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