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Cloning of urea transporters from the kidneys of two batoid elasmobranchs: evidence for a common elasmobranch urea transporter isoform
Authors:Michael G. Janech  Holly A. Gefroh  Emily E. Cwengros  James A. Sulikowski  David W. Ploth  Wayne R. Fitzgibbon
Affiliation:(1) Marine Biomedicine and Environmental Sciences Center, Medical University of South Carolina, Fort Johnson, Charleston, SC, USA;(2) Division of Nephrology, Department of Medicine, Medical University of South Carolina, 96 Jonathan Lucas St, P.O. Box 250623, Charleston, SC 29425, USA;(3) Ralph H. Johnson VAMC, Charleston, SC, USA;(4) Department of Zoology, University of New Hampshire, Durham, NH, USA;(5) Present address: Division of Nephrology, Department of Medicine, Medical University of South Carolina, 96 Jonathan Lucas St, P.O. Box 250623, Charleston, SC 29425, USA;(6) Present address: Qualyst Inc., Trinity Road, Raleigh, NC 27607, USA;(7) Present address: Division of Thoracic Oncology Research, St. Joseph’s Hospital and Medical Center, Phoenix, AZ 85013, USA;(8) Present address: Department of Biological Sciences, University of New England, Biddeford, ME 04005, USA
Abstract:One of the two phloretin-sensitive, facilitated urea transporters identified from the kidneys of the myliobatiform, euryhaline elasmobranch, Dasyatis sabina, a 379 amino acid protein ([D. sabina]strUT-2), was very similar to the 380 amino acid isoform (shUT) present in the kidney of the squaliform, dogfish shark, Squalus acanthias (a species that can be considered marginally euryhaline since it utilizes upper estuarine, as well as ocean habitats). To test the proposal that this isoform is a conserved urea transporter (UT) expressed in the kidneys of diverse elasmobranchs, UTs were cloned from the kidneys of a rajiform elasmobranch, the stenohaline skate, Leucoraja ocellata and another dasyatid stingray, the marginally euryhaline, Dasyatis say. Utilizing 5′/3′ RACE, a 2,060 nt cDNA that encoded a phloretin-sensitive, 378 amino acid skate urea transporter ([L. ocellata]skUT-2) and a 1,683 nt cDNA that encoded a stingray 379 amino acid UT ([D. say]strUT-2) were obtained. These deduced UTs have a very high sequence identity with the known elasmobranch Uts. [L. ocellata]skUT-2 was 86% identical to [D. sabina]strUT-2 and 84% identical to [S. acanthias]shUT. [D. say]strUT-2 was 97% identical to the [D. sabina]strUT-2. These findings support the hypothesis that a conserved UT isoform is present in the kidneys of marine elasmobranchs, and is an important pathway for facilitated urea transport in the kidneys of marine elasmobranchs. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. H.A. Gefroh and E.E. Cwengros contributed equally to this study.
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