Benabou Sanae, Ferreira Rubén, Aviñó Anna, González Carlos, Lyonnais Sébastien, Solà Maria, Eritja Ramon, Jaumot Joaquim, Gargallo Raimundo
Solution Equilibria and Chemometrics Group, Department of Analytical Chemistry, University of Barcelona, Diagonal 645, E-08028 Barcelona, Spain.
Biochim Biophys Acta. 2014 Jan;1840(1):41-52. doi: 10.1016/j.bbagen.2013.08.028. Epub 2013 Sep 6.
Cytosine- and guanine-rich regions of DNA are capable of forming complex structures named i-motifs and G-quadruplexes, respectively. In the present study the solution equilibria at nearly physiological conditions of a 34-base long cytosine-rich sequence and its complementary guanine-rich strand corresponding to the first intron of the n-myc gene were studied. Both sequences, not yet studied, contain a 12-base tract capable of forming stable hairpins inside the i-motif and G-quadruplex structures, respectively.
Spectroscopic, mass spectrometry and separation techniques, as well as multivariate data analysis methods, were used to unravel the species and conformations present.
The cytosine-rich sequence forms two i-motifs that differ in the protonation of bases located in the loops. A stable Watson-Crick hairpin is formed by the bases in the first loop, stabilizing the i-motif structure. The guanine-rich sequence adopts a parallel G-quadruplex structure that is stable throughout the pH range 3-7, despite the protonation of cytosine and adenine bases at lower pH values. The presence of G-quadruplex aggregates was confirmed using separation techniques. When mixed, G-quadruplex and i-motif coexist with the Watson-Crick duplex across a pH range from approximately 3.0 to 6.5.
Two cytosine- and guanine-rich sequences in n-myc gene may form stable i-motif and G-quadruplex structures even in the presence of long loops. pH modulates the equilibria involving the intramolecular structures and the intermolecular Watson-Crick duplex.
Watson-Crick hairpins located in the intramolecular G-quadruplexes and i-motifs in the promoter regions of oncogenes could play a role in stabilizing these structures.
DNA中富含胞嘧啶和鸟嘌呤的区域能够分别形成名为i-基序和G-四链体的复杂结构。在本研究中,对一段34个碱基长的富含胞嘧啶序列及其对应于n-myc基因第一个内含子的富含鸟嘌呤互补链在接近生理条件下的溶液平衡进行了研究。这两个尚未被研究的序列分别包含一个12个碱基的片段,该片段能够在i-基序和G-四链体结构内部形成稳定的发夹结构。
使用光谱学、质谱和分离技术以及多变量数据分析方法来解析存在的物种和构象。
富含胞嘧啶的序列形成了两个i-基序,它们在环中碱基的质子化情况上有所不同。第一个环中的碱基形成了一个稳定的沃森-克里克发夹结构,稳定了i-基序结构。富含鸟嘌呤的序列采用了一种平行G-四链体结构,尽管在较低pH值下胞嘧啶和腺嘌呤碱基会发生质子化,但该结构在pH值3 - 7的整个范围内都是稳定的。使用分离技术证实了G-四链体聚集体的存在。当混合时,G-四链体和i-基序在大约3.0至6.5的pH范围内与沃森-克里克双链体共存。
n-myc基因中的两个富含胞嘧啶和鸟嘌呤的序列即使在存在长环的情况下也可能形成稳定的i-基序和G-四链体结构。pH调节涉及分子内结构和分子间沃森-克里克双链体的平衡。
位于癌基因启动子区域的分子内G-四链体和i-基序中的沃森-克里克发夹结构可能在稳定这些结构中发挥作用。