Blommers M J, Walters J A, Haasnoot C A, Aelen J M, van der Marel G A, van Boom J H, Hilbers C W
Laboratory of Biophysical Chemistry, Faculty of Science, University of Nijmegen, The Netherlands.
Biochemistry. 1989 Sep 5;28(18):7491-8. doi: 10.1021/bi00444a049.
High-resolution NMR and UV-melting experiments have been used to study the hairpin formation of partly self-complementary DNA fragments in an attempt to derive rules that describe the folding in these molecules. Earlier experiments on the hexadecanucleotide d(ATCCTA-TTTT-TAGGAT) had indicated that within the loop of four thymidines a wobble T-T pair is formed (Blommers et al., 1987). In the present paper it is shown that if the first and the last thymines of the intervening sequence are replaced by complementary bases, sometimes base pairs can be formed. Thus for the intervening sequences -CTTG- and -TTTA- with the pyrimidine in the 5'-position and the purine in the 3'-position, a base pair is formed leading to a loop consisting of two residues. For the intervening sequences -GTTC- and -ATTT- with the purine in the 5'-position and the pyrimidine in the 3'-position, this turns out not to be the case. It was found that it made no difference when the four-membered sequence was closed by a G-C base pair or an A-T base pair. Replacement of the two central thymidine residues by the more bulky adenine residues limits the hairpin to a four-membered loop scheme. Very surprisingly, it was found from 2D NOE experiments that the T-A base pair, formed in the loop consisting of the -TTTA- sequence, is a Hoogsteen pair. It is argued that the pairing of the bases in this scheme may facilitate the formation of a loop of two residues, since the distance of the C1' atoms in this base pair is 8.6 A instead of 10.4 A found in the canonical Watson-Crick base pair. Combination of the data obtained for the series of DNA fragments studied shows that the results can be explained by a simple, earlier proposed, loop folding principle which assumes that the folding of the four-membered loop is dictated by the stacking of the double-helical stem of the hairpin.
高分辨率核磁共振(NMR)和紫外熔解实验已被用于研究部分自我互补DNA片段的发夹结构形成,旨在推导描述这些分子折叠的规则。早期对十六聚体d(ATCCTA-TTTT-TAGGAT)的实验表明,在四个胸腺嘧啶组成的环内形成了一个摆动的T-T对(布洛默斯等人,1987年)。在本文中表明,如果中间序列的第一个和最后一个胸腺嘧啶被互补碱基取代,有时可以形成碱基对。因此,对于中间序列-CTTG-和-TTTA-,嘧啶在5'-位置,嘌呤在3'-位置,会形成一个碱基对,导致由两个残基组成的环。对于中间序列-GTTC-和-ATTT-,嘌呤在5'-位置,嘧啶在3'-位置,情况并非如此。结果发现,当四元序列由G-C碱基对或A-T碱基对封闭时,没有差异。用体积更大的腺嘌呤残基取代两个中心胸腺嘧啶残基将发夹限制为四元环结构。非常令人惊讶的是,从二维NOE实验中发现,在由-TTTA-序列组成的环中形成的T-A碱基对是一个Hoogsteen碱基对。有人认为,该结构中碱基的配对可能有助于形成由两个残基组成的环,因为该碱基对中C1'原子的距离为8.6 Å,而不是在经典沃森-克里克碱基对中发现的10.4 Å。对所研究的一系列DNA片段获得的数据进行综合分析表明,这些结果可以用一个简单的、先前提出的环折叠原理来解释,该原理假设四元环的折叠由发夹双螺旋茎的堆积决定。