Abstract

The coordinated interplay between extrinsic activating and repressing cell signaling molecules is pivotal for embryonic development and subsequent tissue homeostasis. This is well exemplified by studies on the evolutionarily conserved Wnt signaling pathways. Tight temporal and spatial regulation of Wnt signaling activity is required throughout lifetime, from maternal stages before gastrulation until and throughout adulthood. Outside cells, the action of numerous Wnt ligands is counteracted and fine-tuned by only a handful of well characterized secreted inhibitors, such as for instance Dickkopf, secreted Frizzled Related Proteins and Cerberus. Here, we give an overview of our current understanding of another secreted Wnt signaling antagonist, the Wnt inhibitory factor Wif1. Wif1 can directly interact with various Wnt ligands and inhibits their binding to membrane bound receptors. Epigenetic promoter methylation of Wif1, leading to silencing of its transcription and concomitant up-regulation of Wnt signaling, is a common feature during cancer progression. Furthermore, an increasing number of reports describe Wif1 involvement in regulating processes during embryonic development, which so far has not received as much attention. We will summarize our knowledge on Wif1 function and its mode of action with a particular focus on the zebrafish (Danio rerio). In addition, we highlight the potential of Wif1 research to understand and possibly influence mechanisms underlying eye diseases and regeneration.

Highlights

  • Gene regulatory mechanisms facilitate the fundamental necessity that not all cells express and activate all genes and signaling pathways at the same time

  • Wnt inhibitory factor 1 (Wif1) was identified as an expressed sequence tag in the human retina and was functionally described as a negative regulator of canonical or Wnt/beta-catenin signaling in 1999 (Hsieh et al, 1999)

  • The antagonistic interaction between Wif1 and Olfactomedin 1 in the extracellular space may fine tune retinal ganglion cell axon growth through modulation of Wnt signaling (Nakaya et al, 2008)

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Summary

Introduction

Gene regulatory mechanisms facilitate the fundamental necessity that not all cells express and activate all genes and signaling pathways at the same time. Wif1 was identified as an expressed sequence tag in the human retina and was functionally described as a negative regulator of canonical or Wnt/beta-catenin signaling in 1999 (Hsieh et al, 1999). In addition to Wnt ligand binding, Wif1 might well influence the generation of morphogen gradients and/or protect cells within such gradients from signal cascade activation.

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