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 PMID:17524391  

The transcription factor Zfp423/OAZ is required for cerebellar development and CNS midline patterning.

Li E Cheng | Jiangyang Zhang | Randall R Reed
Developmental biology | 2007

The dorsal midline structure is critical for patterning the developing central nervous system (CNS). We show here that Zfp423/OAZ, a multiple zinc-finger transcription factor involved in both OE/EBF and BMP-signaling pathways, is required for the proper formation of forebrain and hindbrain midline structures. During embryogenesis, OAZ is highly expressed at the dorsal neuroepithelium flanking the roof plate. OAZ-deficient mice are ataxic, attributed to the reduction of the cerebellar vermis and some regions of the hemispheres. Characterization of postnatal cerebellar development shows defects in Purkinje cell differentiation and granule cell proliferation. In the forebrain, dorsal telencephalic commissural neurons project axons, but these axons fail to cross the midline and midline glial cells are abnormally distributed. Moreover, there are malformations in midline structures including the septum, thalamus and hypothalamus, suggesting a pivotal role of OAZ in CNS midline patterning.

Pubmed ID: 17524391

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Associated grants

  • Agency: NIDCD NIH HHS, United States
    Id: R01 DC008295
  • Agency: NIDCD NIH HHS, United States
    Id: R01 DC008295-02
  • Agency: NIBIB NIH HHS, United States
    Id: R01EB003543

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BayGenomics (tool)

RRID:SCR_008168

THIS RESOURCE IS NO LONGER IN SERVICE, documented August 29, 2016. The BayGenomics gene-trap resource provides researchers with access to thousands of mouse embryonic stem (ES) cell lines harboring characterized insertional mutations in both known and novel genes. The major goal of BayGenomics is to identify genes relevant to cardiovascular and pulmonary disease.

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