The Wnt/JNK signaling target gene alcam is required for embryonic kidney development

Author:

Cizelsky Wiebke12,Tata Aleksandra123,Kühl Michael1,Kühl Susanne J.1

Affiliation:

1. Institute for Biochemistry and Molecular Biology, Ulm University, Albert-Einstein-Allee 11, Ulm 89081, Germany

2. International Graduate School in Molecular Medicine Ulm, Ulm 89081, Germany

3. Department of Neurobiology, Harvard Medical School, 220 Longwood Ave, Boston, MA 02115, USA

Abstract

Proper development of nephrons is essential for kidney function. β-Catenin-independent Wnt signaling through Fzd8, Inversin, Daam1, RhoA and Myosin is required for nephric tubule morphogenesis. Here, we provide a novel mechanism through which non-canonical Wnt signaling contributes to tubular development. Using Xenopus laevis as a model system, we found that the cell-adhesion molecule Alcam is required for proper nephrogenesis and functions downstream of Fzd3 during embryonic kidney development. We found alcam expression to be independent of Fzd8 or Inversin, but to be transcriptionally regulated by the β-Catenin-independent Wnt/JNK pathway involving ATF2 and Pax2 in a direct manner. These novel findings indicate that several branches of Wnt signaling are independently required for proximal tubule development. Moreover, our data indicate that regulation of morphogenesis by non-canonical Wnt ligands also involves direct transcriptional responses in addition to the effects on a post-translational level.

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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