Washington M Todd, Wolfle William T, Spratt Thomas E, Prakash Louise, Prakash Satya
Sealy Center for Molecular Science, University of Texas Medical Branch, 6.104 Blocker Medical Research Building, 11th and Mechanic Streets, Galveston, TX 77555-1061, USA.
Proc Natl Acad Sci U S A. 2003 Apr 29;100(9):5113-8. doi: 10.1073/pnas.0837578100. Epub 2003 Apr 11.
DNA polymerase eta (Pol eta) functions in the proficient bypass of a variety of DNA lesions. Relative to the replicative polymerases, Pol eta has a greater tolerance for distorted DNA geometries and possesses a low fidelity. X-ray crystal structures and studies with nucleotide analogs have implicated interactions with the DNA minor groove as being crucial for the high fidelity of replicative DNA polymerases. To determine whether Pol eta also makes such functionally important contacts with the DNA minor groove, here we examine the effects on Pol eta-catalyzed nucleotide incorporation when 3-deazaguanine, a base analog that lacks the ability to form minor-groove hydrogen bonds with the protein, is substituted for guanine at various positions in the DNA. From these studies, we conclude that Pol eta makes only a single functional contact with the DNA minor groove at the position of the incoming nucleotide; in this regard, Pol eta differs from high-fidelity DNA polymerases that are unable to replicate through DNA lesions. These results help explain the proficient ability of Pol eta for bypassing distorting DNA lesions.
DNA聚合酶η(Pol η)在多种DNA损伤的高效绕过中发挥作用。相对于复制性聚合酶,Pol η对扭曲的DNA几何结构具有更高的耐受性,且保真度较低。X射线晶体结构以及对核苷酸类似物的研究表明,与DNA小沟的相互作用对于复制性DNA聚合酶的高保真度至关重要。为了确定Pol η是否也与DNA小沟形成这种功能上重要的接触,我们在此研究了当3-脱氮鸟嘌呤(一种缺乏与蛋白质形成小沟氢键能力的碱基类似物)在DNA的不同位置取代鸟嘌呤时,对Pol η催化的核苷酸掺入的影响。从这些研究中,我们得出结论,Pol η仅在进入核苷酸的位置与DNA小沟进行单一功能接触;在这方面,Pol η不同于无法通过DNA损伤进行复制的高保真DNA聚合酶。这些结果有助于解释Pol η绕过扭曲DNA损伤的高效能力。