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史无前例的C-选择性跨链交叉连接通过在位氧化原改性寡氧核酸
Marieke Op de Beeck1, Annemieke Madder
1Laboratory for Organic and Biomimetic Chemistry, University of Ghent, Krijgslaan 281 S4, B-9000 Ghent, Belgium.
Journal of the American Chemical Society
|December 18, 2010
概括
研究人员开发了一种新的方法,使用改性寡核酸制造特定的DNA交叉链接. 这一突破为研究DNA修复机制和改进癌症治疗提供了必要的稳定DNA复合体.
科学领域:
- 化学生物学 化学生物学
- 分子生物学分子生物学
- 药用化学 医学化学
背景情况:
- 跨链交叉链在癌症治疗中至关重要,因为它阻断了DNA转录.
- 抗癌药物的耐药性源于交叉链修复酶,其机制尚不清楚.
- 研究DNA修复酶受到缺乏稳定,明确的交叉链接DNA复合体的阻碍.
研究的目的:
- 开发一种新的策略,用于创建稳定,特定的交叉链接的DNA复合体.
- 促进对DNA交叉链路修复机制的研究.
主要方法:
- 在尿素的2'-位置通过胺或尿素连接器将 furan 部分纳入寡度氧核酸 (ODN) 中.
- 使用N-bromosuccinimide选择性氧化法兰部分以诱导跨链交叉链接.
- 由此产生的交叉连接的双层住宅的隔离和特征.
主要成果:
- 成功合成了能够形成跨链跨链的原修饰ODN.
- 证明了前所未有的选择性,用于与修改后的残留物相反的cytidine进行交叉链接.
- 获得了一个特定的交叉连接的双层住宅,具有良好的收益率和明确的结构特征.
结论:
- 开发的基于的交叉链接策略产生了稳定和特定的交叉链接DNA复合体.
- 这种方法克服了以前在获得适合用于研究DNA修复酶的基质方面的局限性.
- 这些发现为深入研究DNA修复途径和开发更有效的癌症疗法铺平了道路.
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Nucleotide Excision Repair
Overview
Nucleotide Excision Repair
DNA Distortion and Damage
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
Long-patch Base Excision Repair
Since the discovery of the two BER pathways, there has been a debate about how a cell chooses one pathway over the other and the factors determining this selection. Numerous in vitro experiments have pointed out multiple determinants for the sub-pathway selection. These are:
Homologous Recombination
The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
Spontaneous and Induced Mutations
Spontaneous mutations arise infrequently during DNA replication due to errors in the process. A key factor behind these errors is tautomeric shifts in nitrogenous bases, where bases transition from keto to enol forms or amino to imino forms. This shift can alter base-pairing rules, leading to mutations. Additionally, reactive oxygen species (ROS) arising from aerobic metabolism can damage DNA, resulting in depurination (loss of a purine base) or depyrimidination (loss of a pyrimidine base).
Base Excision Repair
One of the common DNA damages is the chemical alteration of single bases by alkylation, oxidation, or deamination. The altered bases cause mispairing and strand breakage during replication. This type of damage causes minimal change to the DNA double helix structure and can be repaired by the base excision repair (BER) pathways. BER corrects damaged DNA sequences by removing the damaged base and restoring the original base sequence using the complementary strand as a template.
The first step of...
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