Lasko D D, Tomkinson A E, Lindahl T
Imperial Cancer Research Fund, Clare Hall Laboratories, South Mimms, Hertfordshire, United Kingdom.
J Biol Chem. 1990 Jul 25;265(21):12618-22.
Mammalian DNA ligase I is presumed to act in DNA replication. Rabbit antibodies against the homogeneous enzyme from calf thymus inhibited DNA ligase I activity and consistently recognized a single polypeptide of 125 kDa when cells from an established bovine kidney cell line (MDBK) were lysed rapidly by a variety of procedures and subjected to immunoblotting analysis. After biosynthetic labeling of MDBK cells with [35S]methionine, immunoprecipitation experiments revealed a polypeptide of 125 kDa that did not appear when purified calf thymus DNA ligase I was used in competition. A 125-kDa polypeptide was adenylated when immunoprecipitated protein from MDBK cells was incubated with [alpha-32P]ATP. Thus, the apparent molecular mass of the initial translation product is identical or nearly so to that of the purified enzyme. The half-life of the protein is 7 h as determined by pulse-chase experiments in asynchronous MDBK cells. Immunocytochemistry and indirect immunofluorescence experiments showed that DNA ligase I is localized to cell nuclei.
哺乳动物DNA连接酶I被推测在DNA复制中起作用。针对来自小牛胸腺的纯酶制备的兔抗体抑制了DNA连接酶I的活性,并且当通过多种方法快速裂解已建立的牛肾细胞系(MDBK)的细胞并进行免疫印迹分析时,始终识别出一条125 kDa的单一多肽。在用[35S]甲硫氨酸对MDBK细胞进行生物合成标记后,免疫沉淀实验揭示了一条125 kDa的多肽,当使用纯化的小牛胸腺DNA连接酶I进行竞争时该多肽未出现。当将来自MDBK细胞的免疫沉淀蛋白与[α-32P]ATP一起孵育时,一条125 kDa的多肽被腺苷酸化。因此,初始翻译产物的表观分子量与纯化酶的表观分子量相同或几乎相同。通过在异步MDBK细胞中进行脉冲追踪实验确定该蛋白质的半衰期为7小时。免疫细胞化学和间接免疫荧光实验表明DNA连接酶I定位于细胞核。