|
|
||||||||
COMPARATIVE AND EVOLUTIONARY PHYSIOLOGY
/NR1H4 acquired ligand specificity for bile salts late in vertebrate evolution1Liver Center, Yale University School of Medicine, New Haven, Connecticut; 2Department of Environmental Medicine, University of Rochester School of Medicine, Rochester, New York; and 3Mount Desert Island Biological Laboratory, Salisbury Cove, Maine
Submitted 9 November 2006 ; accepted in final form 11 June 2007
The nuclear receptor FXR
(NR1H4) plays a pivotal role in maintaining bile salt and lipid homeostasis by functioning as a bile salt sensor in mammals. In contrast, FXR
(NR1H5) from mouse is activated by lanosterol and does not share common ligands with FXR
. To further elucidate FXR ligand/receptor and structure/function relationships, we characterized a FXR gene from the marine skate, Leucoraja erinacea, representing a vertebrate lineage that diverged over 400 million years ago. Phylogenetic analysis of sequence data indicated that skate Fxr (sFxr) is a FXR
. There is an extra sequence in the middle of the sFxr ligand binding domain (LBD) compared with the LBD of FXR
. Luciferase reporter assays demonstrated that sFxr responds weakly to scymnol sulfate, bile salts, and synthetic FXR
ligands, in striking difference from human FXR
(hFXR
). Interestingly, all-trans retinoic acid was capable of transactivating both hFXR
and sFxr. When the extra amino acids in the sFxr LBD were deleted and replaced with the corresponding sequence from hFXR
, the mutant sFxr gained responsiveness to ursodeoxycholic acid, GW4064, and fexaramine. Surprisingly, chenodeoxycholic acid antagonized this activation. Together, these results indicate that FXR is an ancient nuclear receptor and suggest that FXR
may have acquired ligand specificity for bile acids later in evolution by deletion of a sequence from its LBD. Acquisition of this property may be an example of molecular exploitation, where an older molecule is recruited for a new functional role.
nuclear receptor; structure/function relationship
This article has been cited by other articles:
![]() |
K. B. Harikumar, A. B. Kunnumakkara, K. S. Ahn, P. Anand, S. Krishnan, S. Guha, and B. B. Aggarwal Modification of the cysteine residues in I{kappa}B{alpha} kinase and NF-{kappa}B (p65) by xanthohumol leads to suppression of NF-{kappa}B-regulated gene products and potentiation of apoptosis in leukemia cells Blood, February 26, 2009; 113(9): 2003 - 2013. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. M. Carroll, J. T. Bridgham, and J. W. Thornton Evolution of Hormone Signaling in Elasmobranchs by Exploitation of Promiscuous Receptors Mol. Biol. Evol., December 1, 2008; 25(12): 2643 - 2652. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. J. Reschly, N. Ai, S. Ekins, W. J. Welsh, L. R. Hagey, A. F. Hofmann, and M. D. Krasowski Evolution of the bile salt nuclear receptor FXR in vertebrates J. Lipid Res., July 1, 2008; 49(7): 1577 - 1587. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |