首页> 外文期刊>Nucleic acids research >The high stability of the triple helices formed between short purine oligonucleotides and SIV/HIV-2 vpx genes is determined by the targeted DNA structure
【24h】

The high stability of the triple helices formed between short purine oligonucleotides and SIV/HIV-2 vpx genes is determined by the targeted DNA structure

机译:短嘌呤寡核苷酸和SIV / HIV-2 vpx基因之间形成的三重螺旋的高稳定性取决于目标DNA结构

获取原文
           

摘要

In our previous works we have shown that the oligonucleotides 5′-GGGGAGGGGGAGG-3′ and 5′-GGAGGGGGAGGGG-3′ give very stable and specific triplexes with their target double stranded DNAs [Svinarchuk, F., Bertrand, J.-R. and Malvy, C. (1994) Nucleic Acids Res., 22, 3742-3747; Svinarchuk, F., Paoletti, J. and Malvy, C. (1995) J. Biol Chem., 270, 14 068-14 071]. The target for the invariable part of these oligonucleotldes, 5′-GGAGGGGGAGG-3′, is found in a highly conserved 20 bp long purine/pyrimidine tract of the vpx gene of the SIV and HIV-2 viruses and could be a target for oligonucleotide directed antivirus therapy. Here we report on the ability of four purine oligonucieotides with different lengths (11-, 14-, 17- and 20-mer) to form triplexes with the purine/pyrimidine stretch of the vpx gene. Triplex formation was tested by Joint dimethyl sulfate (DMS) footprint, gel-retardation assay, circular dichrolsm (CD) and UV-melting studies. Dimethyl sulfate footprint studies revealed the antiparallel orientation of the third strand to the purine strand of the Watson-Crick duplex. However, the protection of the guanines at the ends of the target sequence decreased as the length of the third strand oligonucleotide increased. Melting temperature studies provided profiles with only one transition for all of the tripiexes. The melting tenpe t werei as for the targeted duplex in the case of the 11- and 14-mer third strands while for the 17- and 20-mer third strands the melting temperature of the triplexes were correspondingly 4 and 8°C higher than for the duplex. Heating and cooling melting curves were reversible for all of the tested triplexes except one with the 20-mer third strand oligonucleo tide. Circular dichroism spectra showed the ability of the target DNA to adopt an A-like DNA conformation.Upon triplex formation the A-DNA form becomes even more pronounced. This effect depends on the length of the thlrd strand oligonucleotide: the CD spectrum shows a ‘classical' A-DNA shape wtth the 20-mer. This is not observed wtth the purin/pyrimidine stretch of the HN-1 DNA which keeps an-like spectrum even after triplex formation. We suggest, that an A-like duplex DNA is required for the formation of a stable DNA purlne(purine-pyrimidine) triplex.
机译:在我们以前的工作中,我们已经表明寡核苷酸5′-GGGGAGGGGGAGG-3′和5′-GGAGGGGGAGGGG-3′与它们的靶标双链DNA给出了非常稳定和特异的三链体[Svinarchuk,F.,Bertrand,J.-R.Acad.Sci.USA,88,3593]。和Malvy,C.(1994)Nucleic Acids Res。,22,3742-3747; Svinarchuk,F.,Paoletti,J。和Malvy,C。(1995)J.Biol Chem。,270,14068-14071]。这些寡核苷酸的恒定部分5'-GGAGGGGGAGG-3'的靶标存在于SIV和HIV-2病毒vpx基因的高度保守的20 bp长的嘌呤/嘧啶区中,可能是寡核苷酸的靶标定向抗病毒治疗。在这里,我们报告了四种不同长度(11-,14-,17-和20-mer)的嘌呤寡核苷酸形成与vpx基因的嘌呤/嘧啶伸展序列形成三链体的能力。通过联合硫酸二甲酯(DMS)足迹,凝胶延迟测定,圆二色酚(CD)和UV熔融研究测试了三链体的形成。硫酸二甲酯的足迹研究表明,Watson-Crick双链体的第三条链与嘌呤链呈反平行取向。然而,随着第三链寡核苷酸的长度增加,靶序列末端的鸟嘌呤的保护作用降低。熔融温度研究为所有三联体提供了仅具有一个过渡的曲线。对于11聚体和14聚体的第三链,目标双链体的熔解温度为30℃,而对于17聚体和20聚体的第三链,三链体的熔解温度分别比4链和8℃高。双工。对于所有测试的三链体,加热和冷却熔解曲线是可逆的,除了具有20-mer第三链寡核苷酸核苷酸的三链体。圆二色性光谱显示了目标DNA能够采用A样DNA构象的能力。在三链体形成后,A-DNA形式变得更加明显。这种效应取决于第三链寡核苷酸的长度:CD光谱显示20聚体具有“经典” A-DNA形状。没有观察到HN-1 DNA的嘌呤/嘧啶片段,即使在三链体形成后仍保持类似的光谱。我们建议,A样双链体DNA是形成稳定的DNA l(嘌呤-嘧啶)三链体所必需的。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号