AJP - Regu Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Regul Integr Comp Physiol 293: R1400-R1409, 2007. First published June 13, 2007; doi:10.1152/ajpregu.00781.2006
0363-6119/07 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
293/3/R1400    most recent
00781.2006v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (4)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Cai, S.-Y.
Right arrow Articles by Boyer, J. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cai, S.-Y.
Right arrow Articles by Boyer, J. L.

COMPARATIVE AND EVOLUTIONARY PHYSIOLOGY

The farnesoid X receptor FXR{alpha}/NR1H4 acquired ligand specificity for bile salts late in vertebrate evolution

Shi-Ying Cai,1,3 Liangshi Xiong,1 Charles G. Wray,3 Nazzareno Ballatori,2,3 and James L. Boyer1,3

1Liver 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{alpha} (NR1H4) plays a pivotal role in maintaining bile salt and lipid homeostasis by functioning as a bile salt sensor in mammals. In contrast, FXRbeta (NR1H5) from mouse is activated by lanosterol and does not share common ligands with FXR{alpha}. 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 FXRbeta. There is an extra sequence in the middle of the sFxr ligand binding domain (LBD) compared with the LBD of FXR{alpha}. Luciferase reporter assays demonstrated that sFxr responds weakly to scymnol sulfate, bile salts, and synthetic FXR{alpha} ligands, in striking difference from human FXR{alpha} (hFXR{alpha}). Interestingly, all-trans retinoic acid was capable of transactivating both hFXR{alpha} and sFxr. When the extra amino acids in the sFxr LBD were deleted and replaced with the corresponding sequence from hFXR{alpha}, 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{alpha} 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



Address for reprint requests and other correspondence: S.-Y. Cai, Liver Center, Yale Univ. School of Medicine, 333 Cedar St., 1080LMP, New Haven, CT 06520 (e-mail: shi-ying.cai{at}yale.edu)




This article has been cited by other articles:


Home page
Mol Biol EvolHome page
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]


Home page
J. Lipid Res.Home page
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
Copyright © 2007 by the American Physiological Society.