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Vol. 19, Issue 11, 4660-4674, November 2008

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A Novel Functional Screen in Human Cells Identifies MOCA as a Negative Regulator of Wnt Signaling

Department of Anatomy and Anthropology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv 69978, Israel

Submitted October 17, 2007; Revised July 30, 2008; Accepted August 7, 2008
Monitoring Editor: Benjamin Margolis

Aberrant Wnt signal transduction is involved in many human diseases such as cancer and neurodegenerative disorders. The key effector protein of the canonical Wnt pathway is β-catenin, which functions with T-cell factor/lymphoid enhancer factor (TCF/LEF) to activate gene transcription that leads to expression of Wnt target genes. In this study we provide results obtained from a novel functional screen of a human brain cDNA library used to identify 63 genes that are putative negative Wnt regulators. These genes were divided into eight functional groups that include known canonical and noncanonical Wnt pathway components and genes that had not yet been assigned to the Wnt pathway. One of the groups, the presenilin-binding proteins, contains the modifier of cell adhesion (MOCA) gene. We show that MOCA is a novel inhibitor of Wnt/β-catenin signaling. MOCA forms a complex with β-catenin and inhibits transcription of known Wnt target genes. Epistasis experiments indicate that MOCA acts to reduce the levels of nuclear β-catenin, increase the levels of membrane-bound β-catenin, and enhances cell–cell adhesion. Therefore, our data indicate that MOCA is a novel Wnt negative regulator and demonstrate that this screening approach can be a rapid means for isolation of new Wnt regulators.

Address correspondence to: Rina Rosin-Arbesfeld (arina{at}tau.ac.il)

Abbreviations used: AD, Alzheimer's disease; MOCA, modifier of cell adhesion; PS, presenilin; TCF/LEF, T-cell factor/lymphoid enhancer factor.