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RecA介导的由2-氨基腺嘌呤和2-硫代胸腺嘧啶取代的寡核苷酸对DNA的链入侵。

RecA-mediated strand invasion of DNA by oligonucleotides substituted with 2-aminoadenine and 2-thiothymine.

作者信息

Lahoud Georges, Arar Khalil, Hou Ya-Ming, Gamper Howard

机构信息

Department of Biochemistry and Molecular Biology, Thomas Jefferson University, Philadelphia, PA 19107, USA.

出版信息

Nucleic Acids Res. 2008 Dec;36(21):6806-15. doi: 10.1093/nar/gkn755. Epub 2008 Oct 25.

Abstract

Sequence-specific recognition of DNA is a critical step in gene targeting. Here we describe unique oligonucleotide (ON) hybrids that can stably pair to both strands of a linear DNA target in a RecA-dependent reaction with ATP or ATPgammaS. One strand of the hybrids is a 30-mer DNA ON that contains a 15-nt-long A/T-rich central core. The core sequence, which is substituted with 2-aminoadenine and 2-thiothymine, is weakly hybridized to complementary locked nucleic acid or 2'-OMe RNA ONs that are also substituted with the same base analogs. Robust targeting reactions took place in the presence of ATPgammaS and generated metastable double D-loop joints. Since the hybrids had pseudocomplementary character, the component ONs hybridized less strongly to each other than to complementary target DNA sequences composed of regular bases. This difference in pairing strength promoted the formation of joints capable of accommodating a single mismatch. If similar joints can form in vivo, virtually any A/T-rich site in genomic DNA could be selectively targeted. By designing the constructs so that the DNA ON is mismatched to its complementary sequence in DNA, joint formation might allow the ON to function as a template for targeted point mutation and gene correction.

摘要

DNA的序列特异性识别是基因靶向中的关键步骤。在此,我们描述了独特的寡核苷酸(ON)杂交体,其在与ATP或ATPγS的RecA依赖性反应中能够与线性DNA靶标的两条链稳定配对。杂交体的一条链是30聚体DNA寡核苷酸,其包含15个核苷酸长的富含A/T的中央核心。该核心序列被2-氨基腺嘌呤和2-硫代胸腺嘧啶取代,与同样被相同碱基类似物取代的互补锁核酸或2'-O-甲基RNA寡核苷酸弱杂交。在ATPγS存在下发生了稳健的靶向反应,并产生了亚稳双D环接头。由于杂交体具有假互补特性,与由常规碱基组成的互补靶DNA序列相比,组成杂交体的寡核苷酸彼此之间的杂交强度较弱。这种配对强度的差异促进了能够容纳单个错配的接头的形成。如果类似的接头能够在体内形成,基因组DNA中几乎任何富含A/T的位点都可以被选择性靶向。通过设计构建体,使DNA寡核苷酸与其在DNA中的互补序列错配,接头形成可能允许寡核苷酸作为靶向点突变和基因校正的模板发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7f5/2588519/417b33311cd8/gkn755f1.jpg

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