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体内d(CGG).d(CCG)重复序列中两种优选发夹折叠模式的证据。

Evidence for two preferred hairpin folding patterns in d(CGG).d(CCG) repeat tracts in vivo.

作者信息

Darlow J M, Leach D R

机构信息

Institute of Cell and Molecular Biology, University of Edinburgh, UK.

出版信息

J Mol Biol. 1998 Jan 9;275(1):17-23. doi: 10.1006/jmbi.1997.1452.

DOI:10.1006/jmbi.1997.1452
PMID:9451435
Abstract

Unusual DNA secondary structures have been implicated in the expansion of trinucleotide repeat tracts that has been found to be responsible for a growing number of human inherited disorders and folate-sensitive fragile chromosome sites. By inserting trinucleotide repeat sequences into a palindromic clamp in lambda phage we are able to investigate their tendencies to form hairpins in vivo in any particular alignment and with odd or even numbers of repeat units in the hairpin. We previously showed that with d(CAG).d(CTG) repeat tracts there was a markedly greater tendency to form hairpins with even numbers of repeat units than with odd numbers, whereas d(GAC).d(GTC) repeats showed no such alternation despite having the same base composition. We expected that d(CGG).d(CCG) repeats, might show the same pattern as d(CAG).(CTG) repeats since they are also involved in trinucleotide repeat expansion disorders. The pattern was not so clear and we wondered whether this might be because d(CGG).d(CCG) repeats have more than one possible alignment in which they could self-anneal. We now present results for all three alignments, which suggest that while even-membered hairpins are preferred in the frame d(CGG).d(CCG), hairpins with odd numbers of trinucleotides are more stable in the frame d(GGC).d(GCC). In both cases the base-pair predicted to close the terminal loop of unpaired bases is 5'C.3'G which has previously been found to be a favoured loop-closing pair.

摘要

异常的DNA二级结构与三核苷酸重复序列的扩增有关,现已发现三核苷酸重复序列的扩增是导致越来越多人类遗传性疾病和叶酸敏感型脆性染色体位点的原因。通过将三核苷酸重复序列插入λ噬菌体的回文夹中,我们能够研究它们在体内以任何特定排列方式形成发夹的倾向,以及发夹中重复单元的奇数或偶数情况。我们之前表明,对于d(CAG).d(CTG)重复序列,偶数个重复单元形成发夹的倾向明显大于奇数个重复单元,而d(GAC).d(GTC)重复序列尽管碱基组成相同,但并未表现出这种交替现象。我们预计d(CGG).d(CCG)重复序列可能会表现出与d(CAG).d(CTG)重复序列相同的模式,因为它们也与三核苷酸重复扩增疾病有关。但这种模式并不那么清晰,我们想知道这是否可能是因为d(CGG).d(CCG)重复序列有不止一种可能的自我退火排列方式。我们现在展示了所有三种排列方式的结果,结果表明,虽然在d(CGG).d(CCG)框架中偶数成员的发夹更受青睐,但在d(GGC).d(GCC)框架中奇数个三核苷酸的发夹更稳定。在这两种情况下,预计会封闭未配对碱基末端环的碱基对都是5'C.3'G,此前已发现这是一种常见的环封闭碱基对。

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