François J C, Saison-Behmoaras T, Thuong N T, Hélène C
Laboratoire de Biophysique, INSERM U.201, CNRS UA.481, Muséum National d'Histoire Naturelle, Paris, France.
Biochemistry. 1989 Dec 12;28(25):9617-9. doi: 10.1021/bi00451a011.
A 17-mer homopyrimidine oligonucleotide was designed to bind to the major groove of SV40 DNA at a 17 base pair homopurine-homopyrimidine sequence via Hoogsteen base pairing. This sequence contains the recognition site for the class II-S restriction enzyme Ksp 632-I. The oligonucleotide was shown to inhibit enzymatic cleavage under conditions that allow for triple helix formation. Inhibition is sequence-specific and occurs in the micromolar concentration range. Triple helix formation by oligonucleotides opens new possibilities for sequence-specific regulation of gene expression.
设计了一种17聚体同嘧啶寡核苷酸,通过Hoogsteen碱基配对,在一个17碱基对的同嘌呤-同嘧啶序列处与SV40 DNA的大沟结合。该序列包含II-S类限制性内切酶Ksp 632-I的识别位点。在允许形成三链螺旋的条件下,该寡核苷酸可抑制酶切作用。抑制作用具有序列特异性,且发生在微摩尔浓度范围内。寡核苷酸形成三链螺旋为基因表达的序列特异性调控开辟了新的可能性。