Bae Kwang-Hee, Kwon Young Do, Shin Hyun-Chul, Hwang Moon-Sun, Ryu Eun-Hyun, Park Kyung-Soon, Yang Hyo-Young, Lee Dong-Ki, Lee Yangsoon, Park Jinwoo, Kwon Heung Sun, Kim Hyun-Won, Yeh Byung-Il, Lee Hyean-Woo, Sohn Soon Hyung, Yoon Joonho, Seol Wongi, Kim Jin-Soo
ToolGen Inc., 461-6 Jeonmin-Dong, Yusung-Gu, Daejeon, 305-390, South Korea.
Nat Biotechnol. 2003 Mar;21(3):275-80. doi: 10.1038/nbt796. Epub 2003 Feb 18.
We describe methods for generating artificial transcription factors capable of up- or downregulating the expression of genes whose promoter regions contain the target DNA sequences. To accomplish this, we screened zinc fingers derived from sequences in the human genome and isolated 56 zinc fingers with diverse DNA-binding specificities. We used these zinc fingers as modular building blocks in the construction of novel, sequence-specific DNA-binding proteins. Fusion of these zinc-finger proteins with either a transcriptional activation or repression domain yielded potent transcriptional activators or repressors, respectively. These results show that the human genome encodes zinc fingers with diverse DNA-binding specificities and that these domains can be used to design sequence-specific DNA-binding proteins and artificial transcription factors.
我们描述了生成能够上调或下调其启动子区域包含靶DNA序列的基因表达的人工转录因子的方法。为实现这一点,我们筛选了源自人类基因组序列的锌指,并分离出56个具有不同DNA结合特异性的锌指。我们将这些锌指用作构建新型序列特异性DNA结合蛋白的模块化构件。将这些锌指蛋白与转录激活或抑制结构域融合,分别产生了有效的转录激活剂或抑制剂。这些结果表明,人类基因组编码具有不同DNA结合特异性的锌指,并且这些结构域可用于设计序列特异性DNA结合蛋白和人工转录因子。