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首页> 外文期刊>Nucleosides, Nucleotides and Nucleic Acids >Simple and Rapid Enzymatic Method for the Synthesis of Single-Strand Oligonucleotides Containing Trifluorothymidine
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Simple and Rapid Enzymatic Method for the Synthesis of Single-Strand Oligonucleotides Containing Trifluorothymidine

机译:简单快速的酶法合成含三氟胸苷的单链寡核苷酸

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摘要

To investigate the mechanism of trifluorothymidine (TFT)-induced DNA damage, we developed an enzymatic method for the synthesis of single-strand oligonucleotides containing TFT-monophosphate residues. Sixteen-mer oligonucleotides and 14-mer 5′-phosphorylated oligonucleotides were annealed to the template of 25-mer, so as to empty one nucleotide site. TFT-triphosphate was incorporated into the site by DNA polymerase and then ligated to 5′-phosphorylated oligonucleotides by DNA ligase. The synthesized 31-mer oligonucleotides containing TFT residues were isolated from the 25-mer complementary template by denaturing polyacrylamide electrophoresis. Using these single-strand oligonucleotides containing TFT residues, the cleavage of TFT residues from DNA, using mismatch uracil-DNA glycosylase (MUG) of E.coli origin, was compared with that of 5-fluorouracil (5FU) and 5-bromodeoxyuridine (BrdU). The TFT/A pair was not cleaved by MUG, while the other pairs, namely, 5FU/A, 5FU/G, BrdU/A, BrdU/G, and TFT/G, were easily cleaved from each synthesized DNA. Thus, this method is useful for obtaining some site-specifically modified oligonucleotides.
机译:为了研究三氟胸苷(TFT)诱导的DNA损伤的机制,我们开发了一种酶法来合成含有TFT-单磷酸酯残基的单链寡核苷酸。将16-mer寡核苷酸和14-mer 5'-磷酸化的寡核苷酸退火到25-mer模板上,以清空一个核苷酸位点。 TFT三磷酸通过DNA聚合酶并入该位点,然后通过DNA连接酶与5'-磷酸化的寡核苷酸连接。通过变性聚丙烯酰胺电泳从25-mer互补模板中分离出含有TFT残基的31-mer合成寡核苷酸。使用这些含有TFT残基的单链寡核苷酸,使用大肠杆菌来源的错配尿嘧啶-DNA糖基化酶(MUG)从DNA切割TFT残基与5-氟尿嘧啶(5FU)和5-溴脱氧尿苷(BrdU)进行了比较。 )。 TFT / A对未被MUG切割,而其他对,即5FU / A,5FU / G,BrdU / A,BrdU / G和TFT / G则易于从每个合成的DNA切割。因此,该方法可用于获得某些位点特异性修饰的寡核苷酸。

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