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Importin α1 is involved in the nuclear localization of Zac1 and the induction of p21WAF1/CIP1 by Zac1

机译:Importinα1参与Zac1的核定位和Zac1对p21WAF1 / CIP1的诱导。

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摘要

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 α1 were demonstrated using an in vitro glutathione S-transferase pull-down assay. Finally, our results indicate that the association of Zac1 with importin α1 is also involved in regulating the transactivation activity of Zac1 on the p21WAF1/CIP1 gene and protein expression.
机译:Zac1,一种新型的七锌指转录因子,优先结合富含GC的DNA元件,并具有固有的反式激活活性。迄今为止,尚未凭经验确定Zac1的NLS(核定位信号)。我们生成了Zac1的一系列EGFP(增强型绿色荧光蛋白)标签的缺失突变体,并检查了其亚细胞定位,从中我们在DNA结合(或锌指)域内定义了两个NLS。由两个带有EGFP标签的锌指簇(锌指基序1-3和4-7)组成的融合蛋白仅位于细胞核中,表明每个锌指簇都足以进行核定位。使用体外谷胱甘肽S-转移酶下拉测定法证明了这两个锌指簇和importinα1之间的物理相互作用。最后,我们的结果表明Zac1与importinα1的关联还参与调节Zac1对p21WAF1 / CIP1基因和蛋白质表达的反式激活活性。

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