scholarly journals Wnt Inhibitory Factor 1 Binds to and Inhibits the Activity of Sonic Hedgehog

Cells ◽  
2021 ◽  
Vol 10 (12) ◽  
pp. 3496
Author(s):  
Krisztina Kerekes ◽  
Mária Trexler ◽  
László Bányai ◽  
László Patthy

The hedgehog (Hh) and Wnt pathways, crucial for the embryonic development and stem cell proliferation of Metazoa, have long been known to have similarities that argue for their common evolutionary origin. A surprising additional similarity of the two pathways came with the discovery that WIF1 proteins are involved in the regulation of both the Wnt and Hh pathways. Originally, WIF1 (Wnt Inhibitory Factor 1) was identified as a Wnt antagonist of vertebrates, but subsequent studies have shown that in Drosophila, the WIF1 ortholog serves primarily to control the distribution of Hh. In the present, work we have characterized the interaction of the human WIF1 protein with human sonic hedgehog (Shh) using Surface Plasmon Resonance spectroscopy and reporter assays monitoring the signaling activity of human Shh. Our studies have shown that human WIF1 protein binds human Shh with high affinity and inhibits its signaling activity efficiently. Our observation that the human WIF1 protein is a potent antagonist of human Shh suggests that the known tumor suppressor activity of WIF1 may not be ascribed only to its role as a Wnt inhibitor.

2018 ◽  
Vol 14 (9) ◽  
pp. 381 ◽  
Author(s):  
Jianliang Zhang ◽  
Yong Zhou ◽  
Zhaohua Li ◽  
Yinlu Ding ◽  
Peng Zhang ◽  
...  

2006 ◽  
Vol 54 (1) ◽  
pp. S104.6-S105
Author(s):  
E. G. Thung ◽  
J. Chou ◽  
L. You ◽  
Z. Xu ◽  
D. M. Jablons

Oncogene ◽  
2005 ◽  
Vol 24 (53) ◽  
pp. 7946-7952 ◽  
Author(s):  
Hiroaki Taniguchi ◽  
Hiroyuki Yamamoto ◽  
Tamaki Hirata ◽  
Nobuki Miyamoto ◽  
Mariko Oki ◽  
...  

2009 ◽  
Vol 69 (22) ◽  
pp. 8603-8610 ◽  
Author(s):  
K. Kawakami ◽  
H. Hirata ◽  
S. Yamamura ◽  
N. Kikuno ◽  
S. Saini ◽  
...  

Endocrinology ◽  
2012 ◽  
Vol 153 (12) ◽  
pp. 6091-6103 ◽  
Author(s):  
Kimberly P. Keil ◽  
Vatsal Mehta ◽  
Amanda M. Branam ◽  
Lisa L. Abler ◽  
Rita A. Buresh-Stiemke ◽  
...  

Abstract Fetal prostate development from urogenital sinus (UGS) epithelium requires androgen receptor (AR) activation in UGS mesenchyme (UGM). Despite growing awareness of sexually dimorphic gene expression in the UGS, we are still limited in our knowledge of androgen-responsive genes in UGM that initiate prostate ductal development. We found that WNT inhibitory factor 1 (Wif1) mRNA is more abundant in male vs. female mouse UGM in which its expression temporally and spatially overlaps androgen-responsive steroid 5α-reductase 2 (Srd5a2). Wif1 mRNA is also present in prostatic buds during their elongation and branching morphogenesis. Androgens are necessary and sufficient for Wif1 expression in mouse UGS explant mesenchyme, and testicular androgens remain necessary for normal Wif1 expression in adult mouse prostate stroma. WIF1 contributes functionally to prostatic bud formation. In the presence of androgens, exogenous WIF1 protein increases prostatic bud number and UGS basal epithelial cell proliferation without noticeably altering the pattern of WNT/β-catenin-responsive Axin2 or lymphoid enhancer binding factor 1 (Lef1) mRNA. Wif1 mutant male UGSs exhibit increased (Sfrp)2 and (Sfrp)3 expression and form the same number of prostatic buds as the wild-type control males. Collectively our results reveal Wif1 as one of the few known androgen-responsive genes in the fetal mouse UGM and support the hypothesis that androgen-dependent Wif1 expression is linked to the mechanism of androgen-induced prostatic bud formation.


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