Washington M Todd, Helquist Sandra A, Kool Eric T, Prakash Louise, Prakash Satya
Sealy Center for Molecular Science, University of Texas Medical Branch at Galveston, Galveston, Texas 77555-1061, USA.
Mol Cell Biol. 2003 Jul;23(14):5107-12. doi: 10.1128/MCB.23.14.5107-5112.2003.
Classical high-fidelity DNA polymerases discriminate between the correct and incorrect nucleotides by using geometric constraints imposed by the tight fit of the active site with the incipient base pair. Consequently, Watson-Crick (W-C) hydrogen bonding between the bases is not required for the efficiency and accuracy of DNA synthesis by these polymerases. DNA polymerase eta (Poleta) is a low-fidelity enzyme able to replicate through DNA lesions. Using difluorotoluene, a nonpolar isosteric analog of thymine unable to form W-C hydrogen bonds with adenine, we found that the efficiency and accuracy of nucleotide incorporation by Poleta are severely impaired. From these observations, we suggest that W-C hydrogen bonding is required for DNA synthesis by Poleta; in this regard, Poleta differs strikingly from classical high-fidelity DNA polymerases.
经典的高保真DNA聚合酶通过利用活性位点与起始碱基对紧密契合所施加的几何约束来区分正确和错误的核苷酸。因此,这些聚合酶进行DNA合成的效率和准确性并不需要碱基之间形成沃森-克里克(W-C)氢键。DNA聚合酶η(Polη)是一种能够绕过DNA损伤进行复制的低保真酶。我们使用二氟甲苯(一种胸腺嘧啶的非极性等排类似物,无法与腺嘌呤形成W-C氢键)发现,Polη掺入核苷酸的效率和准确性受到严重损害。基于这些观察结果,我们认为Polη进行DNA合成需要W-C氢键;在这方面,Polη与经典的高保真DNA聚合酶有显著差异。