5'CAG and 5'CTG Repeats Create Differential Impediment to the Progression of a Minimal Reconstituted T4 Replisome Depending on the Concentration of dNTPs.

Molecular biology international Pub Date : 2011-01-01 Epub Date: 2011-08-10 DOI:10.4061/2011/213824
Emmanuelle Delagoutte, Giuseppe Baldacci
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Abstract

Instability of repetitive sequences originates from strand misalignment during repair or replicative DNA synthesis. To investigate the activity of reconstituted T4 replisomes across trinucleotide repeats (TNRs) during leading strand DNA synthesis, we developed a method to build replication miniforks containing a TNR unit of defined sequence and length. Each minifork consists of three strands, primer, leading strand template, and lagging strand template with a 5' single-stranded (ss) tail. Each strand is prepared independently, and the minifork is assembled by hybridization of the three strands. Using these miniforks and a minimal reconstituted T4 replisome, we show that during leading strand DNA synthesis, the dNTP concentration dictates which strand of the structure-forming 5'CAG/5'CTG repeat creates the strongest impediment to the minimal replication complex. We discuss this result in the light of the known fluctuation of dNTP concentration during the cell cycle and cell growth and the known concentration balance among individual dNTPs.

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5'CAG和5'CTG重复对最小重构T4复制体的进展产生差异障碍,这取决于dNTPs的浓度。
重复序列的不稳定性源于修复或复制DNA合成过程中的链错位。为了研究重组的T4复制体在前导链DNA合成过程中跨三核苷酸重复序列(TNR)的活性,我们开发了一种方法来构建包含定义序列和长度的TNR单元的复制迷你叉。每个迷你叉由三股组成,引物,前导链模板,后导链模板与一个5'单链(ss)尾巴。每条链都是独立制备的,迷你叉是由三条链杂交而成的。通过使用这些迷你叉和最小重构的T4复制体,我们发现在前导链DNA合成过程中,dNTP浓度决定了形成结构的5'CAG/5'CTG重复序列的哪条链对最小复制复合体产生最大的障碍。我们根据已知的dNTP浓度在细胞周期和细胞生长过程中的波动以及已知的单个dNTP之间的浓度平衡来讨论这一结果。
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