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Insertion of telomere repeat sequence decreases plasmid DNA condensation by cobalt (III) hexaammine.

机译:端粒重复序列的插入减少了钴(II​​I)六胺的质粒DNA缩合。

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摘要

Telomere repeat sequence (TRS) DNA is found at the termini of most eukaryotic chromosomes. The sequences are highly repetitive and G-rich (e.g., [C(1-3)A/TG(1-3)]n for the yeast Saccharomyces cerevisiae) and are packaged into nonnucleosomal protein-DNA structures in vivo. We have used total intensity light scattering and electron microscopy to monitor the effects of yeast TRS inserts on in vitro DNA condensation by cobalt (III) hexaammine. Insertion of 72 bp of TRS into a 3.3-kb plasmid depresses condensation as seen by light scattering and results in a 22% decrease in condensate thickness as measured by electron microscopy. Analysis of toroidal condensate dimensions suggests that the growth stages of condensation are inhibited by the presence of a TRS insert. The depression in total light scattering intensity is greater when the plasmid is linearized with the TRS at an end (39-49%) than when linearized with the TRS in the interior (18-22%). Circular dichroism of a 95-bp fragment containing the TRS insert gives a spectrum that is intermediate between the A-form and B-form, and the anomalous condensation behavior of the TRS suggests a noncanonical DNA structure. We speculate that under conditions in which the plasmid DNA condenses, the telomeric insert assumes a helical geometry that is similar to the A-form and is incompatible with packing into the otherwise B-form lattice of the condensate interior.
机译:在大多数真核染色体的末端发现了端粒重复序列(TRS)DNA。该序列是高度重复的和富含G的(例如,用于酿酒酵母的[C(1-3)A / TG(1-3)] n),并在体内包装成非核小体蛋白质-DNA结构。我们已经使用总强度光散射和电子显微镜来监测酵母TRS插入物对钴(III)六胺的体外DNA缩合的影响。如通过光散射观察到的,将72bp的TRS插入3.3kb质粒中可抑制凝结,并且通过电子显微镜测得凝结物厚度降低22%。环形冷凝水尺寸的分析表明,TRS插件的存在会抑制冷凝水的生长阶段。当质粒在末端用TRS线性化时(39-49%),总光散射强度的降低要比在内部用TRS线性化时(18-22%)更大。包含TRS插入片段的95 bp片段的圆二色性给出的光谱介于A型和B型之间,TRS的异常缩合行为表明其是非规范的DNA结构。我们推测,在质粒DNA冷凝的条件下,端粒插入物呈类似于A型的螺旋几何形状,并且与包装入冷凝物内部的B型晶格不相容。

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