Characterization of critical domains within the tumor suppressor CASZ1 required for transcriptional regulation and growth suppression.

Abstract

CASZ1 is a zinc finger (ZF) transcription factor that is critical for controlling the normal differentiation of subtypes of neural and cardiac muscle cells. In neuroblastoma tumors, loss of CASZ1 is associated with poor prognosis and restoration of CASZ1 function suppresses neuroblastoma tumorigenicity. However, the key domains by which CASZ1 transcription controls developmental processes and neuroblastoma tumorigenicity have yet to be elucidated. In this study, we show that loss of any one of ZF1 to ZF4 resulted in a 58 to 79% loss in transcriptional activity, as measured by induction of tyrosine hydroxylase promoter-luciferase activity, compared to that of wild-type (WT) CASZ1b. Mutation of ZF5 or deletion of the C-terminal sequence of amino acids (aa) 728 to 1166 (a truncation of 38% of the protein) does not significantly alter transcriptional function. A series of N-terminal truncations reveals a critical transcriptional activation domain at aa 31 to 185 and a nuclear localization signal at aa 23 to 29. Soft agar colony formation assays and xenograft studies show that WT CASZ1b is more active in suppressing neuroblastoma growth than CASZ1b with a ZF4 mutation or a deletion of aa 31 to 185. This study identifies key domains needed for CASZ1b to regulate gene transcription. Furthermore, we establish a link between loss of CASZ1b transcriptional activity and attenuation of CASZ1b-mediated inhibition of neuroblastoma growth and tumorigenicity.

• Authors: Ryan A Virden, Carol J Thiele, Zhihui Liu
• Journal: Molecular and cellular biology (Mol Cell Biol) Vol. 32 Issue 8 Pg. 1518-28 (Apr 2012) ISSN: 1098-5549 [Electronic] United States
• PMID: 22331471 (Publication Type: Journal Article, Research Support, N.I.H., Intramural)

Chemical References

• CASZ1 protein, human
• DNA-Binding Proteins
• Transcription Factors

Topics

• Animals
• Cell Line, Tumor
• Cell Proliferation
• DNA-Binding Proteins (chemistry, genetics, metabolism)
• Genes, Tumor Suppressor
• Humans
• Mice
• Mice, SCID
• Mutation
• Neoplasm Transplantation
• Neuroblastoma (genetics, metabolism, pathology)
• Protein Structure, Tertiary (genetics)
• Transcription Factors (chemistry, genetics, metabolism)
• Transcription, Genetic
• Zinc Fingers