Paritala Hanumantharao, Firestine Steven M
Department of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, MI 48201, USA.
Nucleosides Nucleotides Nucleic Acids. 2010 Feb;29(2):81-90. doi: 10.1080/15257771003597691.
A major genetic factor linked to the progression of type 1 diabetes occurs in the insulin-linked polymorphic repeat region (ILPR) located 363 bp upstream of the human insulin gene. Genetic studies have shown that individuals with class I repeats (30-60) are predisposed to the development of type 1 diabetes while individuals with longer repeats are protected. Previous research has suggested that some sequences found within the ILPR can adopt a G-quadruplex structure, and this finding has lead to speculation that G-quadruplexes may control insulin expression in certain circumstances. Unfortunately, relatively little study has been done on whether sequences found in the ILPR can adopt a quadruplex fold. In this study, we have utilized circular dichroism, thermal difference spectroscopy and ultraviolet (UV) melting studies to examine the first seven common repeat sequences (A-G) found in the ILPR. We find that sequences A-E adopt a quadruplex fold while sequences F and G likely do not. Examination of sequence B and a single nucleotide variant, B2, revealed that both folded into a G-quadruplex. This result casts doubt on previous studies suggesting that the formation of a quadruplex was related to the ability of ILPR sequences to regulate transcription.
与1型糖尿病进展相关的一个主要遗传因素出现在人类胰岛素基因上游363 bp处的胰岛素连锁多态性重复区域(ILPR)。遗传学研究表明,具有I类重复序列(30 - 60)的个体易患1型糖尿病,而具有较长重复序列的个体则受到保护。先前的研究表明,在ILPR内发现的一些序列可以形成G - 四链体结构,这一发现引发了推测,即G - 四链体可能在某些情况下控制胰岛素的表达。不幸的是,关于ILPR中发现的序列是否能形成四链体折叠的研究相对较少。在本研究中,我们利用圆二色性、热差光谱和紫外(UV)熔解研究来检测在ILPR中发现的前七个常见重复序列(A - G)。我们发现序列A - E形成了四链体折叠,而序列F和G可能没有。对序列B和一个单核苷酸变体B2的检测表明,两者都折叠成了G - 四链体。这一结果对先前认为四链体的形成与ILPR序列调节转录能力有关的研究提出了质疑。