Gaynutdinov Timur I, Brown Patrick, Neumann Ronald D, Panyutin Igor G
Department of Radiology and Imaging Sciences, Clinical Center, National Institutes of Health, Bethesda, Maryland 20892-1180, USA.
Biochemistry. 2009 Dec 1;48(47):11169-77. doi: 10.1021/bi901063g.
Human telomeres contain numerous copies of the (TTAGGG)(n).(AATCCC)(n) repeated sequence with multiple TTAGGG repeats in 3' single-stranded overhangs. Single-stranded oligonucleotides consisting of four TTAGGG repeats can fold into various intramolecular quadruplex structures stabilized by quartets of guanines. The quadruplex structures are believed to play a role in telomere functions and considered as targets for anticancer drug design. In an effort to create a more realistic model of telomeric DNA, we designed oligonucleotides containing a duplex region at the 5' end and four telomeric repeats in the 3' overhang. We applied CD spectroscopy and (125)I radioprobing to determine the conformation of the quadruplexes formed in the 3' overhangs. We found that in the presence of NaCl the conformation of the quadruplex changes with formation of the 5' duplex and depends on the position of the interface between the duplex and the 3' telomeric sequence. When the duplex region extended to the first T of the first TTAGGG repeat, both CD and radioprobing data are consistent with the parallel propeller conformation of the overhang. In the presence of KCl, formation of the duplex at the 5' end of DNA molecules did not change the fold of the quadruplex in the overhang which was interpreted as a mixture of two isomers of 3+1 conformation regardless of the duplex-overhang interface position. Our results demonstrate that the interface between the duplex and single-stranded overhang can affect the conformation of the telomeric quadruplex.
人类端粒包含大量(TTAGGG)(n).(AATCCC)(n)重复序列的拷贝,其3'单链突出端含有多个TTAGGG重复序列。由四个TTAGGG重复序列组成的单链寡核苷酸可折叠成多种分子内四重结构,这些结构由鸟嘌呤四联体稳定。人们认为四重结构在端粒功能中发挥作用,并被视为抗癌药物设计的靶点。为了构建更逼真的端粒DNA模型,我们设计了在5'端含有双链区域且在3'突出端含有四个端粒重复序列的寡核苷酸。我们应用圆二色光谱法(CD光谱法)和¹²⁵I放射性探测来确定在3'突出端形成的四重结构的构象。我们发现,在氯化钠存在的情况下,四重结构的构象会随着5'双链的形成而改变,并且取决于双链与3'端粒序列之间界面的位置。当双链区域延伸至第一个TTAGGG重复序列的第一个T时,CD光谱数据和放射性探测数据均与突出端的平行螺旋桨构象一致。在氯化钾存在的情况下,DNA分子5'端双链的形成并未改变突出端四重结构的折叠方式,无论双链 - 突出端界面位置如何,该折叠方式均被解释为3 + 1构象的两种异构体的混合物。我们的结果表明,双链与单链突出端之间的界面可影响端粒四重结构的构象。