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DNA聚合酶η的生化进化:植物、人类和酵母蛋白质的特性

Biochemical evolution of DNA polymerase eta: properties of plant, human, and yeast proteins.

作者信息

Hoffman Peter D, Curtis Marc J, Iwai Shigenori, Hays John B

机构信息

Department of Environmental and Molecular Toxicology, Oregon State University, Corvallis, OR 97331-7301, USA.

出版信息

Biochemistry. 2008 Apr 22;47(16):4583-96. doi: 10.1021/bi701781p. Epub 2008 Mar 27.

Abstract

To assess how evolution might have biochemically shaped DNA polymerase eta (Poleta) in plants, we expressed in Escherichia coli proteins from Arabidopsis thaliana (At), humans (Hs), and the yeast Saccharomyces cerevisiae (Sc), purified them to near homogeneity, and compared their properties. Consistent with the multiple divergent amino acids within mostly conserved polymerase domains, the polymerases showed modest, appreciable, and marked differences, respectively, in salt and temperature optima for activity and thermostability. We compared abilities to extend synthetic primers past template cyclobutane thymine dimers (T[CPD]T) or undamaged T-T under physiological conditions (80-110 mM salt). Specific activities for "standing-start" extension of synthetic primers ending opposite the second template nucleotide 3' to T-T were roughly similar. During subsequent "running-start" insertions past T-T and the next 5' ( N + 1) nucleotide, AtPoleta and HsPoleta appeared more processive, but DNA sequence contexts strongly affected termination probabilities. Lesion-bypass studies employed four different templates containing T[CPD]Ts, and two containing pyrimidine (6-4')-pyrimidinone photoproducts ([6-4]s). AtPoleta made the three successive insertions [opposite the T[CPD]T and (N + 1) nucleotides] that define bypass nearly as well as HsPoleta and somewhat better than ScPoleta. Again, sequence context effects were profound. Interestingly, the level of insertion opposite the ( N - 1) nucleotide 3' to T[CPD]T by HsPoleta and especially AtPoleta, but not ScPoleta, was reduced (up to 4-fold) relative to the level of insertion opposite the ( N - 1) nucleotide 3' to T-T. Evolutionary conservation of efficient T[CPD]T bypass by HsPoleta and AtPoleta may reflect a high degree of exposure of human skin and plants to solar UV-B radiation. The depressed ( N - 1) insertion upstream of T[CPD]T (but not T-T) may reduce the extent of gratuitous error-prone insertion.

摘要

为了评估进化可能如何在生物化学层面塑造植物中的DNA聚合酶η(Polη),我们在大肠杆菌中表达了来自拟南芥(At)、人类(Hs)和酿酒酵母(Sc)的蛋白质,将它们纯化至近乎均一,并比较了它们的特性。与大多保守聚合酶结构域内的多个不同氨基酸一致,这些聚合酶在活性和热稳定性的盐和温度最佳条件方面分别表现出适度、明显和显著的差异。我们比较了在生理条件(80 - 110 mM盐)下将合成引物延伸越过模板环丁烷胸腺嘧啶二聚体(T[CPD]T)或未受损的T - T的能力。与T - T相对的第二个模板核苷酸3'处结束的合成引物“起始延伸”的比活性大致相似。在随后越过T - T和下一个5'(N + 1)核苷酸的“连续延伸”插入过程中,AtPolη和HsPolη似乎更具持续性,但DNA序列背景强烈影响终止概率。损伤绕过研究使用了四种不同的含有T[CPD]T的模板,以及两种含有嘧啶(6 - 4')-嘧啶酮光产物([6 - 4]s)的模板。AtPolη进行定义绕过的三个连续插入[与T[CPD]T和(N + 1)核苷酸相对]的效果几乎与HsPolη相同,并且比ScPolη略好。同样,序列背景效应很显著。有趣的是,相对于与T - T相对的3'处(N - 1)核苷酸的插入水平,HsPolη尤其是AtPolη,但不是ScPolη,在与T[CPD]T相对的3'处(N - 1)核苷酸的插入水平降低了(高达4倍)。HsPolη和AtPolη对T[CPD]T的高效绕过的进化保守性可能反映了人类皮肤和植物对太阳UV - B辐射的高度暴露。T[CPD]T(而非T - T)上游(N - 1)插入的减少可能会降低不必要的易错插入程度。

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