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人端粒DNA分子间和分子内G-四链体形成的序列特异性

Sequence specificity of inter- and intramolecular G-quadruplex formation by human telomeric DNA.

作者信息

Pedroso Ilene M, Duarte Luis F, Yanez Giscard, Burkewitz Kris, Fletcher Terace M

机构信息

Department of Biochemistry and Molecular Biology, University of Miami School of Medicine, Miami, FL 33101-6129, USA.

出版信息

Biopolymers. 2007 Sep;87(1):74-84. doi: 10.1002/bip.20790.

Abstract

Human telomeric DNA consists of tandem repeats of the sequence 5'-d(TTAGGG)-3'. Guanine-rich DNA, such as that seen at telomeres, forms G-quadruplex secondary structures. Alternative forms of G-quadruplex structures can have differential effects on activities involved in telomere maintenance. With this in mind, we analyzed the effect of sequence and length of human telomeric DNA on G-quadruplex structures by native polyacrylamide gel electrophoresis and circular dichroism. Telomeric oligonucleotides shorter than four, 5'-d(TTAGGG)-3' repeats formed intermolecular G-quadruplexes. However, longer telomeric repeats formed intramolecular structures. Altering the 5'-d(TTAGGG)-3' to 5'-d(TTAGAG)-3' in any one of the repeats of 5'-d(TTAGGG)(4)-3' converted an intramolecular structure to intermolecular G-quadruplexes with varying degrees of parallel or anti-parallel-stranded character, depending on the length of incubation time and DNA sequence. These structures were most abundant in K(+)-containing buffers. Higher-order structures that exhibited ladders on polyacrylamide gels were observed only for oligonucleotides with the first telomeric repeat altered. Altering the sequence of 5'-d(TTAGGG)(8)-3' did not result in the substantial formation of intermolecular structures even when the oligonucleotide lacked four consecutive telomeric repeats. However, many of these intramolecular structures shared common features with intermolecular structures formed by the shorter oligonucleotides. The wide variability in structure formed by human telomeric sequence suggests that telomeric DNA structure can be easily modulated by proteins, oxidative damage, or point mutations resulting in conversion from one form of G-quadruplex to another.

摘要

人类端粒DNA由5'-d(TTAGGG)-3'序列的串联重复组成。富含鸟嘌呤的DNA,如在端粒处所见,形成G-四链体二级结构。G-四链体结构的不同形式对端粒维持所涉及的活性可能有不同影响。考虑到这一点,我们通过非变性聚丙烯酰胺凝胶电泳和圆二色性分析了人类端粒DNA的序列和长度对G-四链体结构的影响。短于四个5'-d(TTAGGG)-3'重复序列的端粒寡核苷酸形成分子间G-四链体。然而,较长的端粒重复序列形成分子内结构。在5'-d(TTAGGG)(4)-3'的任何一个重复序列中将5'-d(TTAGGG)-3'改变为5'-d(TTAGAG)-3',会将分子内结构转变为具有不同程度平行或反平行链特征的分子间G-四链体,这取决于孵育时间和DNA序列的长度。这些结构在含K(+)的缓冲液中最为丰富。仅在第一个端粒重复序列改变的寡核苷酸中观察到在聚丙烯酰胺凝胶上呈现梯状的高阶结构。改变5'-d(TTAGGG)(8)-3'的序列即使在寡核苷酸缺少四个连续端粒重复序列时也不会导致分子间结构的大量形成。然而,许多这些分子内结构与较短寡核苷酸形成的分子间结构具有共同特征。人类端粒序列形成的结构的广泛变异性表明,端粒DNA结构可以很容易地被蛋白质、氧化损伤或点突变调节,从而导致从一种G-四链体形式转变为另一种形式。

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