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首页> 外文期刊>DNA and Cell Biology >Detection of circular telomeric DNA without 2D gel electrophoresis.
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Detection of circular telomeric DNA without 2D gel electrophoresis.

机译:无需2D凝胶电泳即可检测圆形端粒DNA。

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摘要

The end of linear chromosomes forms a lasso-like structure called the t-loop. Such t-loops resemble a DNA recombination intermediate, where the single-stranded 3' overhang is arrested in a stretch of duplex DNA. Presumably, such a t-loop can also be deleted via a recombination process. This would result in the occurrence of circular extrachromosomal telomeric DNA (t-circles), which are known to be abundantly present in immortal cells engaging the recombination-based alternative lengthening of telomeres pathway (ALT pathway). Little is known about the basic mechanism of telomeric recombination in these cells and what ultimately causes the generation of such t-circles. Current standard procedures for detecting these molecules involve 2D gel electrophoresis or electron microscopy. However, both methods are labor intense and sophisticated to perform. Here, we present a simpler, faster, and equally sensitive method for detecting t-circles. Our approach is a telomere restriction fragment assay that involves the enzymatic preservation of circular DNA with Klenow enzyme followed by Bal31 degradation of the remaining linear DNA molecules. We show that with this approach t-circles can be detected in ALT cell lines, whereas no t-circles are present in telomerase-positive cell lines. We consider our approach a valid method in which t-circle generation is the experimental readout.
机译:线性染色体的末端形成称为t环的套索状结构。此类t环类似于DNA重组中间体,其中单链3'突出端被阻滞在一段双链DNA中。据推测,这种t环也可以通过重组过程删除。这将导致环状染色体外端粒DNA(t环)的发生,已知该环状端粒DNA大量存在于参与基于重组的端粒途径(ALT途径)的延长的永生细胞中。对于这些细胞中端粒重组的基本机制以及最终导致这种t环生成的原因,人们所知甚少。用于检测这些分子的当前标准程序包括2D凝胶电泳或电子显微镜。但是,这两种方法都很费力并且执行起来很复杂。在这里,我们提出了一种检测t圆的更简单,更快,同样敏感的方法。我们的方法是端粒限制性片段测定,其中涉及用Klenow酶将环状DNA酶法保存,然后将剩余的线性DNA分子Bal31降解。我们显示,通过这种方法,可以在ALT细胞系中检测到t环,而在端粒酶阳性细胞系中则没有t环。我们认为我们的方法是一种有效的方法,其中t圆生成是实验读数。

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