Klug A
Medical Research Council Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH, UK.
J Mol Biol. 1999 Oct 22;293(2):215-8. doi: 10.1006/jmbi.1999.3007.
Zinc fingers are small DNA-binding peptide motifs that were discovered in this laboratory. These motifs can be used as modular building blocks for the construction of larger protein domains that recognise and bind to specific DNA sequences. Phage display has been used to create a large library of different zinc fingers from which selections were made for binding to a given DNA sequence. From this database there have been elucidated elements of recognition rules that relate the amino acid sequence of a finger to its preferred DNA binding site. Control of gene expression using designed zinc finger peptides has been demonstrated by the specific inhibition of an oncogene mouse cell line and also by switching on genes in expression plasmids. These experiments demonstrate that zinc finger DNA-binding domains can be engineered de novo to recognise given DNA sequences. Five to six individual zinc fingers linked together would recognise a DNA sequence 15-18 bp in length, sufficiently long to constitute a rare address in the human genome. By adding functional groups to the engineered DNA-binding domains, e.g. silencing domains, novel transcription factors can be generated to up- or downregulate expression of a target gene. Among potential applications are the repression of oncogene expression and the disruption of the reproductive cycle of virus infection.
锌指是在本实验室发现的小型DNA结合肽基序。这些基序可作为构建更大蛋白质结构域的模块化构件,这些结构域能够识别并结合特定的DNA序列。噬菌体展示技术已被用于创建一个包含不同锌指的大型文库,并从中筛选出能够结合给定DNA序列的锌指。从这个数据库中已经阐明了识别规则的要素,这些要素将锌指的氨基酸序列与其偏好的DNA结合位点联系起来。通过对癌基因小鼠细胞系的特异性抑制以及通过开启表达质粒中的基因,已经证明了使用设计的锌指肽来控制基因表达。这些实验表明,可以从头设计锌指DNA结合结构域以识别给定的DNA序列。五到六个连接在一起的单个锌指将识别长度为15 - 18个碱基对的DNA序列,这一长度足以构成人类基因组中的一个稀有地址。通过向工程化的DNA结合结构域添加功能基团,例如沉默结构域,可以产生新的转录因子以上调或下调靶基因的表达。潜在的应用包括抑制癌基因表达以及破坏病毒感染的繁殖周期。