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Originally published In Press as doi:10.1074/jbc.M803025200 on July 1, 2008
J. Biol. Chem., Vol. 283, Issue 35, 23677-23684, August 29, 2008
Both WFIKKN1 and WFIKKN2 Have High Affinity for Growth and Differentiation Factors 8 and 11*
Katalin Kondás,
György Szláma,
Mária Trexler, and
László Patthy1
From the
Institute of Enzymology, Biological Research Center, Hungarian Academy of Sciences, H-1113 Budapest, Hungary
WFIKKN1 and WFIKKN2 are large extracellular multidomain proteins consisting of a WAP, a follistatin, an immunoglobulin, two Kunitz-type protease inhibitor domains, and an NTR domain. Recent experiments have shown that WFIKKN2 protein binds mature GDF8/myostatin and myostatin propeptide and inhibits the biological activity of myostatin (Hill, J. J., Qiu, Y., Hewick, R. M., and Wolfman, N. M. (2003) Mol. Endocrinol. 17, 1144–1154). Here we show that the paralogue of this protein, WFIKKN1, also binds to both myostatin and myostatin propeptide and that both WFIKKN1 and WFIKKN2 bind GDF11, the growth and differentiation factor most closely related to myostatin, with high affinity. Structure-function studies on WFIKKN1 have revealed that the follistatin domain is primarily responsible for the binding of mature growth factor, whereas the NTR domain contributes most significantly to the interaction with myostatin propeptide. Analysis of the evolutionary histories of WFIKKN1/WFIKKN2 and GDF8/GDF11 proteins indicates that the functional association of an ancestral WFIKKN protein with an ancestor of GDF8/11 may date back to cephalochordates/urochordates. Although duplication of the corresponding genes gave rise to WFIKKN1/WFIKKN2 and GDF8/GDF11 in early vertebrates, the data presented here suggest that there is significant functional overlap of the paralogous proteins.
Received for publication, April 21, 2008
, and in revised form, June 25, 2008.
* This work was supported by Grants 49890 and 72125 from the National Scientific Research Fund of Hungary and by Grant RET14/2005 from the National Office for Research and Technology of Hungary. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement"in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
The on-line version of this article (available at http://www.jbc.org) contains l a supplemental data file, Tables S1 and S2, and supplemental Fig. 1.
1 To whom correspondence should be addressed. Tel.: 361-209-3537; Fax: 361-466-5465; E-mail: patthy{at}enzim.hu.

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Copyright © 2008 by the American Society for Biochemistry and Molecular Biology.
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