Guo Pei, Lam Sik Lok
Biomol Concepts. 2016 Dec 1;7(5-6):331-340. doi: 10.1515/bmc-2016-0024.
CCTG repeat expansion in intron 1 of the cellular nucleic acid-binding protein (CNBP) gene has been identified to be the genetic cause of myotonic dystrophy type 2 (DM2). Yet the underlying reasons for the genetic instability in CCTG repeats remain elusive. In recent years, CCTG repeats have been found to form various types of unusual secondary structures including mini-dumbbell (MDB), hairpin and dumbbell, revealing that there is a high structural diversity in CCTG repeats intrinsically. Upon strand slippage, the formation of unusual structures in the nascent strand during DNA replication has been proposed to be the culprit of CCTG repeat expansions. On the one hand, the thermodynamic stability, size, and conformational dynamics of these unusual structures affect the propensity of strand slippage. On the other hand, these structural properties determine whether the unusual structure can successfully escape from DNA repair. In this short overview, we first summarize the recent advances in elucidating the solution structures of CCTG repeats. We then discuss the potential pathways by which these unusual structures bring about variable sizes of repeat expansion, high strand slippage propensity and efficient repair escape.
细胞核酸结合蛋白(CNBP)基因内含子1中的CCTG重复序列扩增已被确定为2型强直性肌营养不良(DM2)的遗传病因。然而,CCTG重复序列遗传不稳定性的根本原因仍不清楚。近年来,已发现CCTG重复序列可形成各种类型的异常二级结构,包括迷你哑铃结构(MDB)、发夹结构和哑铃结构,这表明CCTG重复序列本身具有高度的结构多样性。有人提出,在DNA复制过程中,新生链上异常结构的形成是CCTG重复序列扩增的罪魁祸首。一方面,这些异常结构的热力学稳定性、大小和构象动力学影响链滑动的倾向。另一方面,这些结构特性决定了异常结构能否成功逃避DNA修复。在本简短综述中,我们首先总结了阐明CCTG重复序列溶液结构的最新进展。然后,我们讨论了这些异常结构导致重复序列扩增大小可变、链滑动倾向高和有效逃避修复的潜在途径。