Srivastava V K, Tilley R D, Hart R W, Busbee D L
Department of Anatomy, College of Veterinary Medicine, Texas A & M University, College Station 77843.
Exp Gerontol. 1991;26(5):453-66. doi: 10.1016/0531-5565(91)90034-j.
DNA polymerases purified from hepatic tissues of C57BL/6 mice showed an age-related decrease in both specific activity and fidelity of the various enzyme forms. Polymerases from dietary restricted mice exhibited less of a decline in specific activity and copied synthetic DNA templates with relatively higher fidelity than did enzymes from animals fed ad libitum. Polymerases treated with inositol-1,4-bisphosphate [I(1,4)P2] showed varying levels of increased activity, with fidelity increases up to 3-fold. These data indicate that aging is associated with decreases in both specific activity and fidelity of DNA polymerases isolated from a nondividing tissue, and that dietary restriction impedes the age-related decline in both specific activity and fidelity of these polymerases. The data further indicate that DNA polymerases may interact with phosphoinositide hydrolysis products resulting in increased specific activity and fidelity of the enzymes. Phosphoinositide interactions with polymerases could constitute an important mechanism moderating the age-related decrease in function and accuracy of DNA polymerases.
从C57BL/6小鼠肝脏组织中纯化的DNA聚合酶,其各种酶形式的比活性和保真度均呈现与年龄相关的下降。来自饮食限制小鼠的聚合酶比活性下降较少,并且与自由进食动物的酶相比,在复制合成DNA模板时具有相对更高的保真度。用肌醇-1,4-二磷酸[I(1,4)P2]处理的聚合酶显示出不同程度的活性增加,保真度提高了3倍。这些数据表明,衰老与从非分裂组织中分离的DNA聚合酶的比活性和保真度下降有关,饮食限制可阻碍这些聚合酶比活性和保真度与年龄相关的下降。数据还进一步表明,DNA聚合酶可能与磷酸肌醇水解产物相互作用,从而导致酶的比活性和保真度增加。磷酸肌醇与聚合酶的相互作用可能构成一种重要机制,调节DNA聚合酶与年龄相关的功能和准确性下降。