首页> 美国卫生研究院文献>Biophysical Journal >Nature of the Complementary Strands Synthesized in Vitro upon the Single-Stranded Circular DNA of Bacteriophage øX174 after Ultraviolet Irradiation
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Nature of the Complementary Strands Synthesized in Vitro upon the Single-Stranded Circular DNA of Bacteriophage øX174 after Ultraviolet Irradiation

机译:噬菌体øX174的单链环状DNA在紫外线照射后体外合成的互补链的性质

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摘要

This paper describes experiments intended to decide whether UV lesions in DNA act as absolute blocks to chain elongation by the Escherichia coli DNA polymerase or only slow down the polymerization process. Ultraviolet (UV)-irradiated, single-stranded (SS) circular DNA of bacteriophage øX174 was used as template for the polymerase in a reaction mixture in vitro, under conditions allowing synthesis of not more than one complementary strand per template molecule. The mean length of the newly synthesized complementary strands (as determined by velocity sedimentation in alkaline CsCl gradients), as well as the over-all template activity (as measured by deoxyadenosine monophosphate [dAMP] incorporation) was found to decrease with the number of biologically lethal hits sustained by the irradiated templates. With the increase of time or temperature of reaction, the net synthesis of complementary strands increased (as a consequence of increased initiation), but their mean length remained constant. The mean length of synthesized strands was greater than would be expected if all biologically lethal hits were to block the polymerization process. The lethal hits which serve as blocking lesions are inferred to be pyrimidine dimers because it is possible to obtain synthesis of full-length complementary strands if, when heat-denatured, UV-irradiated, double-stranded replicative form (RF II) DNA of bacteriophage øX174 is used as a template, it is pretreated with yeast photoreactivating enzyme (YPRE) in presence of visible light.
机译:本文描述了旨在确定DNA中的UV损伤是否充当大肠杆菌DNA聚合酶链延长的绝对嵌段或仅减慢聚合过程的实验。噬菌体øX174的紫外线(UV)辐照,单链(SS)环状DNA用作体外反应混合物中聚合酶的模板,条件是每个模板分子最多可合成一条互补链。发现新合成的互补链的平均长度(由碱性CsCl梯度中的速度沉淀确定)以及总体模板活性​​(由脱氧腺苷单磷酸[dAMP]掺入测量)随着生物学数量的增加而减少辐照模板承受致命的命中。随着反应时间或温度的增加,互补链的净合成增加(由于引发增加),但它们的平均长度保持恒定。如果所有具有生物学致命性的命中点都将阻止聚合过程,则合成链的平均长度将大于预期长度。可以推断,作为阻断性病变的致死命中是嘧啶二聚体,因为如果热变性,紫外线照射,噬菌体的双链复制形式(RF II)DNA能够获得全长互补链的合成øX174作为模板,在可见光下用酵母光活化酶(YPRE)进行了预处理。

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