Biswas S B, Kornberg A
J Biol Chem. 1984 Jun 25;259(12):7990-3.
The physical basis of ATP binding and activation of DNA polymerase III holoenzyme was studied by an ultraviolet irradiation cross-linking technique. ATP and dATP were photocrosslinked to the alpha, tau, gamma, and delta subunits of holoenzyme; photocrosslinking of dATP was competitively inhibited by ATP. No photocrosslinking was observed with GTP or CTP, nor did GTP, CTP, or UTP inhibit cross-linking of ATP. ADP and adenosine 5'-O-(3-thio)-triphosphate, both potent inhibitors of ATP activation of holoenzyme, inhibited cross-linking of ATP to tau, gamma, and delta subunits, but not to the alpha subunit, suggesting that one or more of these subunits are ATP (or dATP)-binding sites. Photocrosslinking of dTTP to the ATP-activated holoenzyme was exclusively to the epsilon subunit, the dnaQ ( mutD ) gene product; dCTP and dGTP were not photocrosslinked to any subunit. Binding of dTTP was enhanced by ATP, but by no other nucleotide (or deoxynucleotide). This binding of dTTP to epsilon, a subunit likely responsible for regulation of proofreading by the holoenzyme, may function in the control of the fidelity of replication.
采用紫外线照射交联技术研究了ATP结合及DNA聚合酶III全酶激活的物理基础。ATP和dATP光交联至全酶的α、τ、γ和δ亚基;dATP的光交联被ATP竞争性抑制。未观察到GTP或CTP的光交联,GTP、CTP或UTP也不抑制ATP的交联。ADP和腺苷5'-O-(3-硫代)-三磷酸均为全酶ATP激活的强效抑制剂,它们抑制ATP与τ、γ和δ亚基的交联,但不抑制与α亚基的交联,表明这些亚基中的一个或多个是ATP(或dATP)结合位点。dTTP与ATP激活的全酶的光交联仅发生在ε亚基,即dnaQ(mutD)基因产物上;dCTP和dGTP未与任何亚基发生光交联。ATP增强了dTTP的结合,但其他核苷酸(或脱氧核苷酸)则无此作用。dTTP与ε亚基的这种结合可能在全酶校对调控中起作用,可能参与复制保真度的控制,ε亚基可能负责全酶的校对调控。