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相邻碱基对对DNA片段中单碱基凸起和碱基对稳定性的影响。

Influence of neighboring base pairs on the stability of single base bulges and base pairs in a DNA fragment.

作者信息

Ke S H, Wartell R M

机构信息

School of Biology, Georgia Institute of Technology, Atlanta 30332, USA.

出版信息

Biochemistry. 1995 Apr 11;34(14):4593-600. doi: 10.1021/bi00014a012.

DOI:10.1021/bi00014a012
PMID:7718561
Abstract

Temperature-gradient gel electrophoresis (TGGE) was used to determine the relative thermal stabilities of 32 DNA fragments that differ by a single unpaired base (base bulge) and 17 DNAs differing by a base pair. Homologus 373 and 372 bp DNA fragments differing by a single base pair substitution or deletion were employed. Heteroduplexes containing a single base bulge were formed by melting and reannealing pairs of 372 and 373 bp DNAs. Product DNAs were separated on the basis of their thermal stability by parallel and perpendicular TGGE. The order of stability was determined for all single unpaired bases in four different nearest neighbor environments: (GXT).(AYC), (GXG).(CYC), (CXA).(TYG), and (TXT).(AYA) with X = A, T, G, or C, and Y = no base, or visa versa. DNA fragments containing a base bulge were destabilized by 2-3.6 degrees C (+/- 0.2 degrees C) with respect to homologous DNAs with complete Watson-Crick base pairing. Both the identity of the unpaired base and the sequence of the flanking base pairs influenced the degree of destabilization. The range of temperature shift correspond to estimated unfavorable free energies from 2.5 to 4.6 kcal/mol. Purine base bulges were generally not as destabilizing as pyrimidine base bulges. An unpaired base which was identical to one of its adjacent bases generally caused less destabilization than an unpaired base with an identity differing from its nearest neighbors. This implies that positional degeneracy of an unpaired base within a run of two or more identical bases is an important factor effecting stability.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

温度梯度凝胶电泳(TGGE)用于确定32个相差单个未配对碱基(碱基凸起)的DNA片段以及17个相差一个碱基对的DNA的相对热稳定性。使用了相差单个碱基对替换或缺失的同源373和372 bp DNA片段。通过将372和373 bp DNA对进行熔解和重退火形成含有单个碱基凸起的异源双链体。产物DNA通过平行和垂直TGGE根据其热稳定性进行分离。确定了在四种不同的最近邻环境中所有单个未配对碱基的稳定性顺序:(GXT).(AYC)、(GXG).(CYC)、(CXA).(TYG)和(TXT).(AYA),其中X = A、T、G或C,Y = 无碱基,反之亦然。相对于具有完全沃森-克里克碱基配对的同源DNA,含有碱基凸起的DNA片段的稳定性降低了2 - 3.6摄氏度(±0.2摄氏度)。未配对碱基的身份和侧翼碱基对的序列均影响不稳定程度。温度变化范围对应于估计的不利自由能为2.5至4.6千卡/摩尔。嘌呤碱基凸起通常不如嘧啶碱基凸起那样使稳定性降低。与其相邻碱基之一相同的未配对碱基通常比与其最近邻碱基身份不同的未配对碱基引起的稳定性降低要小。这意味着在两个或更多相同碱基的序列中未配对碱基的位置简并性是影响稳定性的一个重要因素。(摘要截短于250字)

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