Huang Shih-Ming, Huang Sheng-Ping, Wang Sung-Ling, Liu Pei-Yao
Department of Biochemistry and Graduate Institute of Life Sciences, National Defense Medical Center, Taipei, Taiwan 114, Republic of China.
Biochem J. 2007 Mar 1;402(2):359-66. doi: 10.1042/BJ20061295.
Zac1, a novel seven-zinc-finger transcription factor, preferentially binds GC-rich DNA elements and has intrinsic transactivation activity. To date, the NLS (nuclear localization signal) of Zac1 has not been empirically determined. We generated a series of EGFP (enhanced green fluorescence protein)-tagged deletion mutants of Zac1 and examined their subcellular localization, from which we defined two NLSs within the DNA-binding (or zinc-finger) domain. Fusion proteins consisting of the two EGFP-tagged zinc-finger clusters (zinc finger motifs 1-3 and 4-7) were located exclusively in the nucleus, demonstrating that each of the zinc-finger clusters is sufficient for nuclear localization. Physical interactions between these two zinc-finger clusters and importin alpha1 were demonstrated using an in vitro glutathione S-transferase pull-down assay. Finally, our results indicate that the association of Zac1 with importin alpha1 is also involved in regulating the transactivation activity of Zac1 on the p21WAF1/CIP1 gene and protein expression.
Zac1是一种新型的七锌指转录因子,它优先结合富含GC的DNA元件并具有内在的反式激活活性。迄今为止,Zac1的核定位信号(NLS)尚未通过实验确定。我们构建了一系列带有增强绿色荧光蛋白(EGFP)标签的Zac1缺失突变体,并检测了它们的亚细胞定位,从中我们在DNA结合(或锌指)结构域内确定了两个NLS。由两个带有EGFP标签的锌指簇(锌指基序1 - 3和4 - 7)组成的融合蛋白仅定位于细胞核,这表明每个锌指簇都足以实现核定位。使用体外谷胱甘肽S - 转移酶下拉试验证明了这两个锌指簇与输入蛋白α1之间的物理相互作用。最后,我们的结果表明,Zac1与输入蛋白α1的结合也参与调节Zac1对p21WAF1/CIP1基因的反式激活活性和蛋白质表达。