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基于诱变与分子模拟结果之间的相关性,提出了一个关于(+)-反式苯并[a]芘二醇环氧化物(N2-脱氧鸟苷)主要加合物的何种构象导致G→T与G→A突变的假说。

A hypothesis for what conformation of the major adduct of (+)-anti-B[a]PDE (N2-dG) causes G-->T versus G-->A mutations based upon a correlation between mutagenesis and molecular modeling results.

作者信息

Kozack R E, Shukla R, Loechler E L

机构信息

Department of Biology, Boston University, MA 02215, USA.

出版信息

Carcinogenesis. 1999 Jan;20(1):95-102. doi: 10.1093/carcin/20.1.95.

Abstract

Molecular modeling (simulated annealing) was used to study the conformations in dsDNA of [+ta]-B[a]P-N2-dG (R.E. Kozack and E.L.Loechler, accompanying paper), which is the major benzo[a]pyrene (B[a]P) adduct. Sixteen classes of conformations were identified, and are analyzed herein vis-a-vis the two most prominent B[a]P mutations, G-->T and G-->A base substitutions. Eight conformations seem more relevant to frameshift mutagenesis, so they are excluded, leaving eight conformations as follows. Two conformations (BPmi5 and BPmi3) retain Watson-Crick G:C base pairing having the B[a]P moiety of the adduct in the minor groove. Two conformations (BPma5 and BPma3) have the Hoogsteen orientation with B[a]P in the major groove. Four conformations are base displaced and have B[a]P stacked in the helix with the dG moiety of the adduct displaced into either the major groove (Gma5 and Gma3) or the minor groove (Gmi5 and Gmi3). Three of these eight conformations (BPma5, BPma3 and Gma3) are universally high in energy. The two conformations that retain G:C base pairing potential (BPmi5 and BPmi3) are likely to be non-mutagenic. Of the three remaining conformations, Gmi5 can be relatively low in energy, but is distorted. A correlation exists between the calculated energies for the remaining two base displaced conformations and mutagenesis for [+ta]-B[a]P-N2-dG, leading to the hypothesis that Gma5 is responsible for G-->T mutations and Gmi3 is responsible for G-->A mutations. Gma5 and Gmi3 resemble each other, except that dG is in the major and minor grooves, respectively. An incipient rationale for this hypothesis is discussed: DNA polymerase might be triggered to follow a different mutagenic pathway depending upon whether a non-informational lesion has bulk protruding into the major or minor groove. A pathway for interconversion between these eight conformations is also proposed and its implications are discussed; e.g. four steps are required to interconvert between Gma5 and Gmi3.

摘要

分子建模(模拟退火)用于研究[+ta]-苯并[a]芘-N2-脱氧鸟苷(R.E.科扎克和E.L.勒克勒,随附论文)在双链DNA中的构象,该物质是主要的苯并[a]芘(B[a]P)加合物。确定了16种构象类别,并针对两种最突出的B[a]P突变,即G→T和G→A碱基替换,在此进行分析。八种构象似乎与移码诱变更相关,因此将它们排除,剩下如下八种构象。两种构象(BPmi5和BPmi3)保留了沃森-克里克G:C碱基对,加合物的B[a]P部分位于小沟中。两种构象(BPma5和BPma3)具有 hoogsteen 取向,B[a]P位于大沟中。四种构象是碱基移位的,B[a]P堆积在螺旋中,加合物的dG部分移位到要么大沟(Gma5和Gma3)要么小沟(Gmi5和Gmi3)中。这八种构象中的三种(BPma5、BPma3和Gma3)能量普遍较高。保留G:C碱基配对潜力的两种构象(BPmi5和BPmi3)可能是非诱变的。在剩下的三种构象中,Gmi5能量可能相对较低,但有畸变。剩下的两种碱基移位构象的计算能量与[+ta]-B[a]P-N2-脱氧鸟苷的诱变之间存在相关性,从而得出假设:Gma5负责G→T突变,Gmi3负责G→A突变。Gma5和Gmi3彼此相似,只是dG分别位于大沟和小沟中。讨论了这一假设的初步原理:DNA聚合酶可能会根据非信息性损伤是大量突出到大沟还是小沟中而被触发遵循不同的诱变途径。还提出了这八种构象之间相互转换的途径并讨论了其含义;例如,Gma5和Gmi3之间相互转换需要四个步骤。

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