Studwell-Vaughan P S, O'Donnell M
Microbiology Department, Hearst Research Foundation, Cornell University Medical College, New York, New York 10021.
J Biol Chem. 1993 Jun 5;268(16):11785-91.
The polIII core subassembly of DNA polymerase III holoenzyme is composed of the alpha (DNA polymerase), epsilon (editing exonuclease), and theta subunits. We have identified holE encoding theta (8.6 kDa) at 40.4 min, expressed and purified 300 mg of theta, and have studied its function by constituting the polIII core from pure alpha, epsilon, and theta subunits. The theta subunit binds the epsilon proofreader tightly, but it does not form a detectable complex with alpha. The epsilon subunit also binds to alpha (Maki, H., and Kornberg, A. (1987) Proc. Natl. Acad. Sci. U. S. A. 84, 4389-4392). Hence, the subunit arrangement of the polIII core is linear, alpha epsilon theta. Interaction of theta with epsilon slightly stimulated epsilon in excision of a 3' terminal mismatched nucleotide, suggesting a possible role for theta in fidelity.
DNA聚合酶III全酶的polIII核心亚组件由α(DNA聚合酶)、ε(校正外切核酸酶)和θ亚基组成。我们在40.4分钟处鉴定出编码θ(8.6 kDa)的holE,表达并纯化了300 mg的θ,并通过由纯α、ε和θ亚基构成polIII核心来研究其功能。θ亚基与ε校对酶紧密结合,但它与α不形成可检测到的复合物。ε亚基也与α结合(牧木,H.,和科恩伯格,A.(1987年)美国国家科学院院刊84,4389 - 4392)。因此,polIII核心的亚基排列是线性的,即αεθ。θ与ε的相互作用在切除3'末端错配核苷酸时略微刺激了ε,这表明θ在保真度方面可能发挥作用。