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Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on January 13, 2005; DOI: 10.1124/jpet.104.079533


0022-3565/05/3132-668-676$20.00
JPET 313:668-676, 2005
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INFLAMMATION AND IMMUNOPHARMACOLOGY

Cloning and Characterization of Cyclooxygenase-1b (Putative Cyclooxygenase-3) in Rat

James A. Snipes1, Bela Kis1, Gregory S. Shelness, James A. Hewett, and David W. Busija

Departments of Physiology and Pharmacology (J.A.S., B.K., D.W.B.) and Pathology (G.S.S.), Wake Forest University Health Sciences, Winston-Salem, North Carolina; and Department of Neuroscience (J.A.H.), University of Connecticut Health Center, Farmington, Connecticut

A splice variant of cyclooxygenase-1 (COX-1), COX-1b (previously termed as COX-3), has been identified in canine tissues as an acetaminophen-sensitive isoform, but the sequence of COX-1b mRNA and the encoded protein are not known in rats. We cloned and sequenced rat COX-1b mRNA from cerebral endothelial cells. Sequence analysis indicated that the 98-base pair intron-1 of COX-1 gene remains unprocessed in the COX-1b mRNA, causing a frameshift mutation and a 127-amino acid open reading frame with no sequence similarity with known cyclooxygenases. Transient and permanent transfection of COS-7 cells with a vector containing the rat COX-1b cDNA resulted in synthesis of a protein of the expected size. We generated an affinity-purified polyclonal antibody against the rat COX-1b protein. Western blot analysis of rat tissues using this antibody demonstrated the likely existence of rat COX-1b protein in vivo with the highest expression in heart, kidney, and neuronal tissues. Our results on both stable and on transiently transfected COS-7 cells suggest that rat COX-1b does not have cyclooxygenase activity and does not have any effect on the inhibition of prostaglandin production by acetaminophen. Because this protein has a completely different amino acid sequence than COX-1 and COX-2 and it does not have cyclooxygenase activity, we suggest a name cyclooxygenase variant protein to distinguish it from the known prostaglandin-synthesizing cyclooxygenase isoforms.


Received October 19, 2004; accepted January 12, 2005.

Address correspondence to: Dr. Bela Kis, Department of Physiology and Pharmacology, Wake Forest University Health Sciences, Medical Center Blvd., Winston-Salem, NC 27157. E-mail: bkis{at}wfubmc.edu




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