Target intelligence / Profile preview

Ovo-like zinc finger transcription factor 2 (OVOL2)

Target
OVOL2
Molecular classification
Transcription factor, Zinc finger protein, DNA-binding protein
01

Overview

Ovo-like zinc finger transcription factor 2 (OVOL2) is a DNA-binding transcription factor belonging to the evolutionarily conserved ovo-like protein family, characterized by a conserved set of C2H2-type zinc finger domains[1][2][4]. It is essential in maintaining epithelial cell lineage identity, mainly by suppressing epithelial-to-mesenchymal transition (EMT)[1][3][4]. OVOL2 also regulates neuronal differentiation, adipogenesis, and the development of primordial germ cells[1][3][4]. As a transcriptional repressor, it inhibits the expression of key EMT inducers (such as ZEB1) and other factors promoting cell proliferation and differentiation[1][3]. Loss of OVOL2 function in mice is embryonic lethal and causes defects in neuroectoderm, vascular, and cardiac development[1]. In humans, loss-of-function mutations in OVOL2 are associated with posterior polymorphous corneal dystrophy, and emerging data suggest tumor suppressor roles via regulation of EMT and cell cycle-related genes[1][3][5]. OVOL2 does not currently have known approved or clinical-stage drugs targeting it directly, but it is considered a therapeutic target, especially in oncology and regenerative medicine applications where modulation of EMT and epithelial lineage specification are of interest[3].

Other names
Ovo like zinc finger 2OVOL2Zinc finger protein 339CHED1ZNF339
02

Biological functions

Epithelial development and differentiationSuppression of epithelial-to-mesenchymal transition (EMT)Regulation of neuronal differentiationSuppression of cell cycling and terminal differentiation of keratinocytesRegulation of germ cell developmentRegulation of thermogenesis and adipogenesis
03

Disease associations

Cancer (tumor suppressor function)Corneal dystrophy (posterior polymorphous corneal dystrophy)Developmental disorders
04

Biomarkers

Mutations in OVOL2 can serve as biomarkers for posterior polymorphous corneal dystrophy

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