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二氨基嘌呤和肌苷取代对A序列诱导的DNA弯曲的影响。3'-A序列连接处的重要性。

Effects of diaminopurine and inosine substitutions on A-tract induced DNA curvature. Importance of the 3'-A-tract junction.

作者信息

Mollegaard N E, Bailly C, Waring M J, Nielsen P E

机构信息

Center for Biomolecular Recognition, Department of Medical Biochemistry and Genetics, The Panum Institute, University of Copenhagen, Blegdamsvej 3c, 2200 Copenhagen N, Denmark.

出版信息

Nucleic Acids Res. 1997 Sep 1;25(17):3497-502. doi: 10.1093/nar/25.17.3497.

DOI:10.1093/nar/25.17.3497
PMID:9254710
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC146927/
Abstract

Gel migration and uranyl photoprobing have been used to study the effects of inosine and 2,6-diaminopurine (2,6-DAP) substitution on adenine-tract (A-tract) induced DNA curvature. Using a 10mer repeated sequence including five inosines we show by uranyl photoprobing that a narrow minor groove varying in phase with the helix repeat is not the cause of DNA curvature. Further, we have systematically studied by gel migration the effects on A-tract induced curvature of either single or full substitution with inosine and/or 2,6-DAP in a 5'-AAAAAGCCGC-3'sequence. DNA curvature is shown to increase when inosines are substituted for the guanosines in the sequence between the A-tracts. By comparing the effects of each monosubstitution it can be seen that when the G closest to the 3'-end of the A-tract is substituted the effect on DNA curvature is much stronger than when substitution is made at any other position. By contrast, curvature is abolished when 2,6-DAP residues are substituted for all adenines, and monosubstitution reveals that the effect of substituting a single adenine is strongest at the 3'-end of the A-tract. These results favor a model in which the curvature induced by an A-tract in DNA molecules is primarily located at the junction with the 3'-end of the A-tract, and this peculiar junction is created because the A-tract has a preference to form a non-B-DNA structure which builds up from the 5'-end.

摘要

凝胶迁移和铀酰光探测已被用于研究肌苷和2,6 - 二氨基嘌呤(2,6 - DAP)取代对腺嘌呤序列(A序列)诱导的DNA弯曲的影响。使用包含五个肌苷的10聚体重复序列,我们通过铀酰光探测表明,与螺旋重复相位不同的狭窄小沟不是DNA弯曲的原因。此外,我们通过凝胶迁移系统地研究了在5'-AAAAAGCCGC-3'序列中用肌苷和/或2,6 - DAP进行单取代或完全取代对A序列诱导弯曲的影响。当肌苷取代A序列之间序列中的鸟苷时,DNA弯曲度增加。通过比较每个单取代的效果可以看出,当取代靠近A序列3'-末端的G时,对DNA弯曲的影响比在任何其他位置进行取代时要强得多。相比之下,当所有腺嘌呤被2,6 - DAP残基取代时弯曲消失,单取代表明取代单个腺嘌呤的效果在A序列的3'-末端最强。这些结果支持一种模型,即DNA分子中A序列诱导的弯曲主要位于与A序列3'-末端的交界处,并且这种特殊的交界处是由于A序列倾向于形成从5'-末端开始构建的非B - DNA结构而产生的。