Nuclear trafficking of the POZ-ZF protein Znf131
- 作者：Nickett S. Donaldson ; Yasmin Daniel ; Kevin F. Kelly ; Monica Graham ; Juliet M. Daniel
- 关键词：Znf131 ; Transcription factor ; POZ-ZF ; Nuclear import ; NLS
- 刊名：Biochimica et Biophysica Acta (BBA)/Molecular Cell Research
- 出版年：2007
- 期刊代码：20_01674889
- 类别：bio
- 出版时间：April 2007
- 卷：1773
- 期：4
- 页码：546-555
- 文件大小：13538 K
摘要
Znf131 is a member of the BTB/POZ family of transcription factors with roles in development and carcinogenesis. Like many members of this protein family, Znf131 displays robust nuclear localization in cultured cells, but the mechanism(s) of Znf131 nuclear trafficking is unknown. Here, we report the mechanism of Znf131 nuclear localization. Visual inspection of the Znf131 amino acid sequence revealed three basic regions (BR-1, -2 and -3) with the potential to serve as nuclear localization signals (NLS). Of the three basic regions, only BR-1 functioned independently to efficiently target heterologous β-gal-GFP fusion proteins to HeLa cell nuclei. However, a Znf131 truncation mutant containing BR-2 and BR-3 efficiently targeted heterologous β-gal-GFP fusion proteins to HeLa cell nuclei. Mutational analysis of full-length GFP-tagged Znf131 revealed that loss of any one BR alone did not prevent Znf131 nuclear localization. This apparent redundancy in NLS activity was due to the fact that intact BR-1 or BR-2 alone could target full-length Znf131 to nuclei. Consequently, simultaneous mutation of BR-1 and BR-2 abolished full-length Znf131 nuclear localization. Therefore, BR-1 and BR-2 are functional NLSs for Znf131 and as such are designated NLS-1 and NLS-2. Finally, wild type Znf131, and not a Znf131 NLS-defective mutant (NLS-1m/NLS-2m) interacted preferentially with the nuclear import receptor Importin-α3 in vitro.