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First published online September 16, 2005
Journal of Experimental Biology 208, 3627-3636 (2005)
Published by The Company of Biologists 2005
doi: 10.1242/jeb.01820
Induction of branchial ion transporter mRNA expression during acclimation to salinity change in the euryhaline crab Chasmagnathus granulatus

1 Departamento de Biodiversidad y Biología Experimental, Facultad de
Ciencias Exactas y Naturales, Universidad de Buenos Aires, Pab. II, Ciudad
Universitaria, C1428EHA Buenos Aires, Argentina
2 CONICET (Consejo Nacional de Investigaciones Cientificas y Tecnicas),
Rivadavia 1917, C1033AAJ Buenos Aires, Argentina
3 Department of Animal Physiology, University of Osnabrueck, 49076
Osnabrueck, Germany
4 College of the Atlantic, Bar Harbor, ME 04609, USA
5 Mount Desert Island Biological Laboratory, Salsbury Cove, ME 04672,
USA
Author for correspondence (e-mail:
dtowle{at}mdibl.org)
Accepted 1 August 2005
Using quantitative real-time PCR, the expression of mRNAs encoding three
transport-related proteins and one putative housekeeping protein was analyzed
in anterior and posterior gills of the euryhaline crab Chasmagnathus
granulatus following transfer from isosmotic conditions (30
salinity) to either dilute (2
) or concentrated (45
) seawater.
Modest changes were observed in the abundance of mRNAs encoding the
housekeeping protein arginine kinase and the vacuolar-type
H+-ATPase B-subunit, both of which were highly expressed under all
conditions. By contrast, the expression of Na+/K+-ATPase
-subunit mRNA and Na+/K+/2Cl-
cotransporter mRNA was strongly responsive to external salinity. During
acclimation to dilute seawater, cotransporter mRNA increased 10-20-fold in
posterior gills within the first 24 h while
Na+/K+-ATPase
-subunit mRNA increased 35-55-fold.
During acclimation to concentrated seawater, cotransporter mRNA increased
60-fold by 96 h and Na+/K+-ATPase
-subunit
increased approximately 25-fold in posterior gills. Our results indicate a
complex pattern of transcriptional regulation dependent upon the direction of
salinity change and the developmental background of the gills.
Key words: Na+/K+-ATPase, Na+/K+/2Cl- cotransporter, V-type H+-ATPase, arginine kinase, crab, gill, gene expression, quantitative PCR
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