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大肠杆菌DNA聚合酶I的记忆特性。与一个模板的相互作用会影响与另一个模板的后续相互作用。

Mnemonic aspects of Escherichia coli DNA polymerase I. Interaction with one template influences the next interaction with another template.

作者信息

Papanicolaou C, Lecomte P, Ninio J

出版信息

J Mol Biol. 1986 Jun 5;189(3):435-48. doi: 10.1016/0022-2836(86)90315-3.

Abstract

When Escherichia coli DNA polymerase I (Pol I) replicates a homopolymer, the excision/polymerization (exo/pol) ratio varies with enzyme and initiator concentration. The study of this effect in the case of poly(dA).oligo(dT) replication led us to propose a mnemonic model for Pol I, in which the 3' to 5' excision activity warms up when the enzyme is actively polymerizing, and cools down when it dissociates from the template. The model predicts that the exo/pol ratio must increase with processivity length and initiator concentration and decrease with enzyme concentration. It predicts also that contact of the enzyme with one template alters its excision efficiency towards another template. The exo/pol ratio and processivities of Pol I and its Klenow fragment were studied on four templates: poly(dA).(dT)10, poly(dT).(dA)10, poly(dC).(dG)10 and poly(dI).(dC)10. We show that the Klenow fragment is usually much less processive than Pol I and when this is the case it has a much lower exo/pol ratio. At equal processivity, the exo/pol ratios are nearly equal. Furthermore, many factors that influence processivity length (e.g. manganese versus magnesium, inorganic pyrophosphate, ionic strength) influence the exo/pol ratio in the same direction. The study of deaminated poly(dC) replication, where we followed incorporation and excision of both G and A residues, allowed us to assign the origin of the dNMP variations to changes in the 3' to 5' proof-reading activity of Pol I. Similarly, the lower dNMP turnover of the Klenow fragment observed with deaminated poly(dC) was specifically assigned to a decreased 3' to 5' exonuclease activity. The exo/pol ratio generally increased with initiator and decreased with enzyme concentration, in agreement with the model, except for poly(dI).oligo(dC), where it decreased with initiator concentration. However, by terminating chain elongation with dideoxy CTP, we showed directly that, even in this system, excision is relatively inefficient at the beginning of synthesis. Interaction of Pol I with poly(dA).(dT) or with poly(dC).(dG) modifies its exo/pol characteristics in the replication of poly(dI).(dC) and poly(dA).(dT), respectively. The Klenow enzyme is not sensitive to such influences and this correlates with its reduced processivity on the influencing templates. Our results reveal the existence of differences between Pol I and its Klenow fragment that are more profound than has been thought previously.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

当大肠杆菌DNA聚合酶I(Pol I)复制同聚物时,切除/聚合(exo/pol)比率会随酶和引发剂浓度而变化。对聚(dA)·寡聚(dT)复制情况下这种效应的研究,使我们提出了一个关于Pol I的记忆模型,其中3'至5'切除活性在酶积极聚合时升温,而在其与模板解离时降温。该模型预测,exo/pol比率必定会随着持续合成能力长度和引发剂浓度的增加而升高,随着酶浓度的增加而降低。它还预测,酶与一个模板的接触会改变其对另一个模板的切除效率。在四个模板上研究了Pol I及其Klenow片段的exo/pol比率和持续合成能力:聚(dA)·(dT)10、聚(dT)·(dA)10、聚(dC)·(dG)10和聚(dI)·(dC)10。我们发现,Klenow片段的持续合成能力通常远低于Pol I,在这种情况下它的exo/pol比率也低得多。在持续合成能力相等时,exo/pol比率几乎相等。此外,许多影响持续合成能力长度的因素(如锰与镁、无机焦磷酸、离子强度)会以相同方向影响exo/pol比率。对脱氨基聚(dC)复制的研究(在此研究中我们追踪了G和A残基的掺入和切除),使我们能够将dNMP变化的根源归因于Pol I的3'至5'校对活性的变化。同样,用脱氨基聚(dC)观察到的Klenow片段较低的dNMP周转率,具体归因于3'至5'核酸外切酶活性的降低。exo/pol比率通常随引发剂增加而升高,随酶浓度降低,这与模型一致,但聚(dI)·寡聚(dC)除外,其随引发剂浓度降低。然而,通过用双脱氧CTP终止链延伸,我们直接表明,即使在这个系统中,切除在合成开始时也相对低效。Pol I与聚(dA)·(dT)或聚(dC)·(dG)的相互作用,分别改变了其在聚(dI)·(dC)和聚(dA)·(dT)复制中的exo/pol特性。Klenow酶对这种影响不敏感,这与其在影响模板上降低的持续合成能力相关。我们的结果揭示了Pol I及其Klenow片段之间存在比之前认为的更为深刻的差异。(摘要截选至400字)

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