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首页> 外文期刊>Chemical research in toxicology >Epigenetic DNA Modification N-6-Methyladenine Inhibits DNA Replication by DNA Polymerase of Pseudomonas aeruginosa Phage PaP1
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Epigenetic DNA Modification N-6-Methyladenine Inhibits DNA Replication by DNA Polymerase of Pseudomonas aeruginosa Phage PaP1

机译:表观遗传DNA修饰N-6-甲基腺嘌呤抑制DNA聚合酶的DNA聚合酶PSSUDOUTONAS噬菌体PAP1

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摘要

N-6-methyladenine (6mA), a newly identified epigenetic modification, plays important roles in regulation of various biological processes. However, the effect of 6mA on DNA replication has been little addressed. In this work, we investigated how 6mA affected DNA replication by DNA polymerase of Pseudomonas aeruginosa Phage PaP1 (gp90 exo(-)). The presence of 6mA, as well as its intermediate hypoxanthine (Hyp), inhibited DNA replication by gp90 exo(-). The 6mA reduced dTTP incorporation efficiency by 10-fold and inhibited next-base extension efficiency by 100-fold. Differently, dCTP was preferentially incorporated opposite Hyp among four dNTPs. Gp90 exo(-) reduced the extension priority beyond the 6mA:T pair rather than the 6mA:C mispair and preferred to extend beyond Hyp:C rather than the Hyp:T pair. Incorporation of dTTP opposite 6mA and dCTP opposite Hyp showed fast burst phases. The burst rate and burst amplitude were both reduced for 6mA compared with unmodified A. Moreover, the total incorporation efficiency (k(poI)/K-d,K-dNTP) was decreased for dTTP incorporation opposite 6mA and dCTP incorporation opposite Hyp compared with dTTP incorporation opposite A. 6mA reduced the incorporation rate (k(poI)), and Hyp increased the dissociation constant (K-d,K-dNTP). However, 6mA or Hyp on template did not affect the binding of DNA polymerase to DNA in binary or ternary complexes. This work provides new insight into the inhibited effects of epigenetic modification of 6mA on DNA replication in PaP1.
机译:N-6-甲基腺嘌呤(6mA),新发现的表观遗传改性,在各种生物过程的调节中起重要作用。然而,6mA对DNA复制的影响几乎没有解决。在这项工作中,我们调查了Pseudomonas铜绿素PAP1(GP90 EXO()的DNA聚合酶受影响的DNA复制的DNA复制。 6mA的存在以及其中间缺氧(百下),通过GP90 EXO( - )抑制DNA复制。 6MA将DTTP掺入效率降低10倍,并抑制下一个底座延长效率100倍。不同,DCTP优先于四个DNTPS中的对面掺入。 GP90 EXO( - )将延长优先级降低超过6MA:T对而不是6mA:C错误,并且优选延伸超越:C而不是Hyp:T对。掺入DTTP相反的6MA和DCTP对面的爆发阶段。与未经修改的A相比,突发速率和突发幅度均降低6mA。此外,对于与DTTP掺入相反,DTTP结合的DTTP掺入,降低了总掺入效率(K(POI)/ Kd,K-DNTP),与DTTP掺入相反相反的A.6MA降低了掺入率(K(POI)),升高增加了解离常数(KD,K-DNTP)。然而,6mA或百下模板在二元或三元复合物中没有影响DNA聚合酶对DNA的结合。这项工作为抑制6mA对PAP1中DNA复制的表观遗传修饰抑制作用的新见解。

著录项

  • 来源
    《Chemical research in toxicology》 |2019年第5期|共10页
  • 作者单位

    Dalian Polytech Univ Sch Biol Engn Dalian 116034 Peoples R China;

    Sichuan Univ West China Sch Publ Hlth Hosp Key Lab Environm &

    Female Reprod Hlth Chengdu;

    Sichuan Univ West China Sch Publ Hlth Hosp Key Lab Environm &

    Female Reprod Hlth Chengdu;

    Sichuan Univ West China Sch Publ Hlth Hosp Key Lab Environm &

    Female Reprod Hlth Chengdu;

    Sichuan Univ West China Sch Publ Hlth Hosp Key Lab Environm &

    Female Reprod Hlth Chengdu;

    Sichuan Univ West China Sch Publ Hlth Hosp Key Lab Environm &

    Female Reprod Hlth Chengdu;

    Dalian Polytech Univ Sch Biol Engn Dalian 116034 Peoples R China;

    Guangzhou Med Univ Inst Chem Carcinogenesis Guangzhou Guangdong Peoples R China;

    Third Mil Med Univ Coll Basic Med Sci Dept Microbiol Chongqing Peoples R China;

    Dalian Polytech Univ Sch Biol Engn Dalian 116034 Peoples R China;

    Sichuan Univ West China Sch Publ Hlth Hosp Key Lab Environm &

    Female Reprod Hlth Chengdu;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 毒物学(毒理学);
  • 关键词

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