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DNA聚合酶:DNA复制中的Hoogsteen碱基配对?

DNA polymerases: Hoogsteen base-pairing in DNA replication?

作者信息

Wang Jimin

机构信息

Center for Structural Biology, Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06520, USA

出版信息

Nature. 2005 Sep 15;437(7057):E6-7; discussion E7. doi: 10.1038/nature04199.

Abstract

Human polymerase-iota belongs to the error-prone Y family of polymerases, which frequently incorporate incorrect nucleotides during DNA replication but can efficiently bypass DNA lesions. On the basis of X-ray diffraction data, Nair et al. propose that Hoogsteen base-pairing is adopted by DNA during its replication by this enzyme. Here I re-examine their X-ray data and find that the electron density is very weak for a Hoogsteen base pair formed between a template adenine deoxyribonucleotide in the syn conformation and a deoxythymidine 5'-triphosphate (dTTP), and that the fit is better for a normal Watson-Crick base pair. As a guanine-cytosine (G-C) base pair has no potential to form a Hoogsteen base pair at physiological pH, Hoogsteen base-pairing is unlikely to be used in replication by this polymerase.

摘要

人类聚合酶ι属于易出错的Y家族聚合酶,该家族在DNA复制过程中经常掺入错误的核苷酸,但能够有效绕过DNA损伤。基于X射线衍射数据,奈尔等人提出,该酶在DNA复制过程中采用了Hoogsteen碱基配对。在此,我重新审视了他们的X射线数据,发现处于顺式构象的模板腺嘌呤脱氧核糖核苷酸与脱氧胸苷5'-三磷酸(dTTP)之间形成的Hoogsteen碱基对的电子密度非常弱,而对于正常的沃森-克里克碱基对,拟合效果更好。由于鸟嘌呤-胞嘧啶(G-C)碱基对在生理pH值下没有形成Hoogsteen碱基对的可能性,因此这种聚合酶在复制过程中不太可能使用Hoogsteen碱基配对。

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