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人ZNF219蛋白DNA结合特异性的鉴定及其作为转录抑制因子的功能

Identification of the DNA binding specificity of the human ZNF219 protein and its function as a transcriptional repressor.

作者信息

Sakai Tsuyoshi, Hino Kimihiro, Wada Shinya, Maeda Hidekatsu

机构信息

Department of Bioengineering, Faculty of Engineering, Soka University, 1-236 Tangi, Hatiouji, Tokyo 192-8977, Japan.

出版信息

DNA Res. 2003 Aug 31;10(4):155-65. doi: 10.1093/dnares/10.4.155.

Abstract

The ZNF219 gene is a member of the Kruppel-like zinc finger gene family that is involved in a diverse range of biological processes. The ZNF219 gene encodes a 77-kDa nuclear protein containing nine sets of C2H2 zinc finger structures. By using a random oligonucleotide selection assay and the electromobility gel shift assay, we have revealed that the ZNF219 protein recognizes two copies of CCCCCA. The DNA binding core element is CCCCC. 3' flanking A residues enhance binding of the ZNF219 protein. Use of the various truncated ZNF219 constructs demonstrated that zinc finger 1 to 3 or zinc finger 5 and 6 domains are sufficient to allow specific DNA binding. Both domains independently recognized the same consensus sequence, CCCCCA. Proteins expressed from human cDNA clones KIAA0390 and KIAA0222, which have partial similarities to ZNF219, also showed specific binding to the same core DNA sequence. Potential ZNF219 binding sites were found in the HMGN1 promoter. To examine the function of ZNF219 in the modulation of transcription, we constructed Gal4 DNA binding domain (DBD)/ZNF219 fusion proteins and demonstrated that ZNF219 functioned as a transcriptional repressor for the HMGN1 promoter. Experiments with the truncated ZNF219 constructs suggest that the proline-rich sequence (226-272 a.a., proline content 49%) was responsible for part of the observed repression. These findings provide us with an important start point in our understanding of the functional role of ZNF219 in vivo.

摘要

ZNF219基因是Kruppel样锌指基因家族的成员,参与多种生物过程。ZNF219基因编码一种77 kDa的核蛋白,包含九组C2H2锌指结构。通过使用随机寡核苷酸筛选试验和电泳迁移率凝胶迁移试验,我们发现ZNF219蛋白识别两个CCCCCA拷贝。DNA结合核心元件是CCCCC。3'侧翼A残基增强ZNF219蛋白的结合。使用各种截短的ZNF219构建体表明,锌指1至3或锌指5和6结构域足以实现特异性DNA结合。两个结构域独立识别相同的共有序列CCCCCA。从与ZNF219有部分相似性的人类cDNA克隆KIAA0390和KIAA0222表达的蛋白质也显示出与相同核心DNA序列的特异性结合。在HMGN1启动子中发现了潜在的ZNF219结合位点。为了研究ZNF219在转录调控中的功能,我们构建了Gal4 DNA结合结构域(DBD)/ZNF219融合蛋白,并证明ZNF219作为HMGN1启动子的转录抑制因子发挥作用。用截短的ZNF219构建体进行的实验表明,富含脯氨酸的序列(226 - 272个氨基酸,脯氨酸含量49%)是观察到的部分抑制作用的原因。这些发现为我们理解ZNF219在体内的功能作用提供了一个重要的起点。

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