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10.1073/pnas.90.7.2749

http://scihub22266oqcxt.onion/10.1073/pnas.90.7.2749
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suck abstract from ncbi


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pmid8464884      Proc+Natl+Acad+Sci+U+S+A 1993 ; 90 (7): 2749-53
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  • Primary structure and functional expression of a cDNA encoding the thiazide-sensitive, electroneutral sodium-chloride cotransporter #MMPMID8464884
  • Gamba G; Saltzberg SN; Lombardi M; Miyanoshita A; Lytton J; Hediger MA; Brenner BM; Hebert SC
  • Proc Natl Acad Sci U S A 1993[Apr]; 90 (7): 2749-53 PMID8464884show ga
  • Electroneutral Na+:Cl- cotransport systems are involved in a number of important physiological processes including salt absorption and secretion by epithelia and cell volume regulation. One group of Na+:Cl- cotransporters is specifically inhibited by the benzothiadiazine (thiazide) class of diuretic agents and can be distinguished from Na+:K+:2Cl- cotransporters based on a lack of K+ requirement and insensitivity to sulfamoylbenzoic acid diruetics like bumetanide. We report here the isolation of a cDNA encoding a thiazide-sensitive, electroneutral sodium-chloride cotransporter from the winter flounder urinary bladder using an expression cloning strategy. The pharmacological and kinetic characteristics of the cloned cotransporter are consistent with the properties of native thiazide-sensitive sodium-chloride cotransporters in teleost urinary bladder and mammalian renal distal tubule epithelia. The nucleotide sequence predicts a protein of 1023 amino acids (112 kDa) with 12 putative membrane-spanning regions, which is not related to other previously cloned sodium or chloride transporters. Northern hybridization shows two different gene products: a 3.7-kb mRNA localized only to the urinary bladder and a 3.0-kb mRNA present in several non-bladder/kidney tissues.
  • |*Symporters[MESH]
  • |Amino Acid Sequence[MESH]
  • |Animals[MESH]
  • |Base Sequence[MESH]
  • |Benzothiadiazines/*pharmacology[MESH]
  • |Carrier Proteins/drug effects/*genetics/*physiology[MESH]
  • |DNA/*genetics/isolation & purification[MESH]
  • |Flounder[MESH]
  • |Intestines/physiology[MESH]
  • |Kinetics[MESH]
  • |Models, Structural[MESH]
  • |Molecular Sequence Data[MESH]
  • |Oocytes/drug effects/*physiology[MESH]
  • |Open Reading Frames[MESH]
  • |Organ Specificity[MESH]
  • |Protein Structure, Secondary[MESH]
  • |Recombinant Proteins/drug effects/metabolism[MESH]
  • |Sodium Chloride Symporters[MESH]
  • |Sodium/*metabolism[MESH]
  • |Urinary Bladder/*physiology[MESH]


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