Wei K, Huber B E
Department of Cell Biology, Wellcome Research Laboratories, Research Triangle Park, North Carolina 27709, USA.
J Biol Chem. 1996 Feb 16;271(7):3812-6.
Cytosine deaminase (EC 3.5.4.1), a non-mammalian enzyme, catalyzes the deamination of cytosine and 5-fluorocytosine to form uracil and 5-fluorouracil, respectively. Eukaryotic cells have been genetically modified with a bacterial cytosine deaminase gene to express a functional enzyme. When the genetically modified cells are combined with 5-fluorocytosine, it creates a potent negative selection system, which may have important applications in cancer gene therapy. In this paper, we introduce a novel positive selection method based upon the expression of the cytosine deaminase gene. This method utilizes inhibitors in the pyrimidine de novo synthesis pathway to create a condition in which cells are dependent on the conversion of pyrimidine supplements to uracil by cytosine deaminase. Thus, only cells expressing the cytosine deaminase gene can be rescued in a positive selection medium.
胞嘧啶脱氨酶(EC 3.5.4.1)是一种非哺乳动物酶,可催化胞嘧啶和5-氟胞嘧啶脱氨,分别形成尿嘧啶和5-氟尿嘧啶。真核细胞已通过细菌胞嘧啶脱氨酶基因进行基因改造,以表达功能性酶。当基因改造后的细胞与5-氟胞嘧啶结合时,会创建一个强大的阴性选择系统,这在癌症基因治疗中可能具有重要应用。在本文中,我们介绍了一种基于胞嘧啶脱氨酶基因表达的新型阳性选择方法。该方法利用嘧啶从头合成途径中的抑制剂来创造一种条件,使细胞依赖于胞嘧啶脱氨酶将嘧啶补充物转化为尿嘧啶。因此,只有表达胞嘧啶脱氨酶基因的细胞才能在阳性选择培养基中获救。