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单链DNA在非变性凝胶电泳中的离散迁移率。

Discrete mobility of single-stranded DNA in non-denaturing gel electrophoresis.

作者信息

Liu Q, Scaringe W A, Sommer S S

机构信息

Departments of Molecular Genetics and Molecular Diagnosis, City of Hope National Medical Center, 1500 East Duarte Road, Duarte, CA 91010-3000, USA.

出版信息

Nucleic Acids Res. 2000 Feb 15;28(4):940-3. doi: 10.1093/nar/28.4.940.

Abstract

Gel electrophoresis is the standard method to separate, identify and purify nucleic acids. SSCP detects single base changes by altered mobility of single-stranded segments electrophoresed through non-denaturing polyacrylamide gels. Herein, changes in electrophoretic mobilities due to single base substitutions were measured for single-stranded segments of lengths ranging from 333 to 547 nt. A 484 nt segment in exon H of the human factor IX gene was studied most intensively. After SSCP, mobilities were determined by scanning autoradiograms at very high resolution (1200 d.p.i.), which allowed precise measurement of mobilities. When the mobilities of 46 single base substitutions were characterized, the distribution of mutant segments relative to a wild-type control was found to be discrete, i.e. the observed mobility values occurred in distinct ranges. Discrete mobility distributions were seen at different electrophoretic temperatures, buffer concentrations, segment lengths and segment sequences. In addition: (i) single base substitutions caused discontinuous distributions between highly dispersed and sharp bands; (ii) at least one single-stranded segment produced two sharp bands of similar intensity. These observations suggest that: (i) the single base changes in DNA segments in the size range 333-547 nt result in discrete conformational changes; (ii) individual DNA molecules of the same DNA segment can occasionally adopt two or more discrete conformations.

摘要

凝胶电泳是分离、鉴定和纯化核酸的标准方法。单链构象多态性(SSCP)通过单链片段在非变性聚丙烯酰胺凝胶中电泳时迁移率的改变来检测单碱基变化。在此,对长度在333至547个核苷酸范围内的单链片段,测量了由于单碱基取代导致的电泳迁移率变化。对人凝血因子IX基因外显子H中的一个484个核苷酸的片段进行了最深入的研究。SSCP后,通过以非常高的分辨率(1200 d.p.i.)扫描放射自显影片来确定迁移率,这使得能够精确测量迁移率。当对46个单碱基取代的迁移率进行表征时,发现相对于野生型对照,突变片段的分布是离散的,即观察到的迁移率值出现在不同的范围内。在不同的电泳温度、缓冲液浓度、片段长度和片段序列下都观察到了离散的迁移率分布。此外:(i)单碱基取代导致高度分散的条带和清晰条带之间出现不连续分布;(ii)至少有一个单链片段产生了两条强度相似的清晰条带。这些观察结果表明:(i)大小在333 - 547个核苷酸范围内的DNA片段中的单碱基变化会导致离散的构象变化;(ii)同一DNA片段的单个DNA分子偶尔可以采用两种或更多种离散的构象。

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