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首页> 外文期刊>The Journal of Biochemistry >A Palindromic Repeat Sequence Adopts a Stable Fold Back Structure under Supercoiling.
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A Palindromic Repeat Sequence Adopts a Stable Fold Back Structure under Supercoiling.

机译:回文重复序列在超螺旋下采用稳定的折返结构。

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摘要

A synthetic deoxyoligonucleotide containing five palindromic repeats of GGATCC self assembles to form a parallel four-stranded structure held together by G-tetrads that shows slower mobility than duplex DNA. This structure is hypersensitive to S1 nuclease and resistant to DMS modification. The same oligonucleotide when cloned in a plasmid forms a different structure under supercoiling that persists stably even in the cleaved out insert. On polyacrylamide gel electrophoresis, the cleaved out insert moves to a position midway between the duplex and parallel four-stranded forms of the oligonucleotide. Upon S1 nuclease treatment, the cleaved out insert shows a discreet band of 18 base pairs, suggesting an unfolded region in the middle. All the guanines in the cleaved out insert are sensitive to DMS modification and produce a positive peak at 285 nM in the circular dichroism spectrum, a signature of fold back tetraplex structures. We propose a fold back quadruplex structure for the insert under supercoilingwith only A.T.A.T and G.C.G.C tetrads. This is the first suggestive evidence of a general tetraplex motif without G quartets as that proposed for generalized recombination.
机译:包含GGATCC的五个回文重复序列的合成脱氧寡核苷酸可自行组装,形成由G-tetrads保持在一起的平行四链结构,其移动性比双链DNA慢。该结构对S1核酸酶高度敏感,并且对DMS修饰具有抗性。当克隆到质粒中时,相同的寡核苷酸会在超螺旋下形成不同的结构,即使在切出的插入片段中也能稳定存在。在聚丙烯酰胺凝胶电泳中,切出的插入片段移动到寡核苷酸的双链和平行四链形式之间的中间位置。在S1核酸酶处理后,裂解的插入片段显示18条碱基对的离散带,表明中间存在未折叠区域。裂解的插入片段中的所有鸟嘌呤均对DMS修饰敏感,并在圆二色性光谱中于285 nM处产生正峰,这是折返四链体结构的特征。我们为仅在A.T.A.T和G.C.G.C四分之一的超螺旋下的刀片提出了一种折返四边形结构。这是不具有G四重奏的通用四重基序的第一个暗示性证据,如针对广义重组所提出的。

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