INSERM, U676, Hôpital Robert-Debré, 75935 Paris Cedex 19, France; Paris Diderot University, 75018 Paris, France.
Mol Cell Endocrinol. 2012 Apr 4;351(2):239-48. doi: 10.1016/j.mce.2011.12.014. Epub 2011 Dec 30.
KISS1R and its ligand, the kisspeptins, are key hypothalamic factors that regulate GnRH hypothalamic secretion and therefore the pubertal timing. During studies analysing KiSS1 as a candidate gene in pubertal onset disorders, two SNP and one nucleotide insertion were observed in a 23 nucleotides G-rich sequence located 65 nucleotides downstream of the stop codon. The polymorphisms formed four haplotypes. Biophysical experiments revealed the ability of this G-rich sequence to fold into G-quadruplex structures and demonstrated that the three DNA polymorphisms did not perturb the folding into G-quadruplex but affected G-quadruplex conformation. A functional luciferase reporter-based assay revealed functional differences between 3'UTR haplotypes. These data show that polymorphisms in a G-rich sequence of the 3'UTR of KISS1, able to fold into G-quadruplex structures, can modulate gene expression. They highlight the potential role of this G-quadruplex in the regulation of KISS1 expression and in the timing of pubertal onset.
KISS1R 及其配体 kisspeptins 是调节 GnRH 下丘脑分泌的关键下丘脑因子,因此也是青春期开始的关键因素。在研究分析 KiSS1 作为青春期启动障碍候选基因时,在位于终止密码子下游 65 个核苷酸的 23 个核苷酸富含 G 序列中观察到两个 SNP 和一个核苷酸插入。这些多态性形成了四个单倍型。生物物理实验揭示了这个富含 G 的序列能够折叠成 G-四链体结构,并证明这三个 DNA 多态性并没有扰乱 G-四链体的折叠,但影响了 G-四链体的构象。基于荧光素酶报告基因的功能检测显示 3'UTR 单倍型之间存在功能差异。这些数据表明,KISS1 3'UTR 中富含 G 的序列中的多态性能够折叠成 G-四链体结构,能够调节基因表达。它们突出了这种 G-四链体在调节 KISS1 表达和青春期启动时间中的潜在作用。