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丙嗪衍生物和4'-羟甲基-4,5',8-三甲基补骨脂素介导的SV 40 DNA光敏化。体外转录的抑制作用。

Photosensitization of SV 40 DNA mediated by promazine derivatives and 4'-hydroxymethyl-4,5',8-trimethylpsoralen. Inhibition of the in vitro transcription.

作者信息

Decuyper J, Piette J, Merville-Louis M P, van de Vorst A

出版信息

Biochem Pharmacol. 1987 Apr 1;36(7):1069-76. doi: 10.1016/0006-2952(87)90416-3.

Abstract

In vitro transcription by E. coli RNA polymerase was carried out on SV40 DNA photoreacted with various promazine derivatives. Inhibition of the template activity was recorded with increasing irradiation times in the presence of promazine derivatives. Promazine covalent adducts on guanine did not terminate RNA synthesis and seemed to be bypassed by the enzyme. HMT (4'-hydroxymethyl-4,5',8-trimethylpsoralen) photoreaction with DNA was carried out under two conditions: irradiation with lambda greater than 395 nm favouring monoadduction on pyrimidine residues and irradiation at 360 nm inducing a maximum of interstrand diadducts. Both adducts were able to terminate RNA synthesis on the phototreated SV40 DNA and using the O-methyl-nucleotide sequencing procedure, the termination sites were precisely mapped. Monoadducts on the coding strand and cross-links induced termination two bases away from the covalent adduct, but monoadducts on the noncoding strand did not half RNA polymerase.

摘要

用大肠杆菌RNA聚合酶对经各种丙嗪衍生物进行光反应的SV40 DNA进行体外转录。在丙嗪衍生物存在的情况下,随着照射时间的增加,记录到模板活性受到抑制。丙嗪与鸟嘌呤的共价加合物不会终止RNA合成,似乎会被该酶绕过。HMT(4'-羟甲基-4,5',8-三甲基补骨脂素)与DNA的光反应在两种条件下进行:用大于395 nm的λ光照射有利于嘧啶残基上的单加成,以及在360 nm照射诱导最大量的链间双加合物。两种加合物都能够终止经光处理的SV40 DNA上的RNA合成,并且使用O-甲基核苷酸测序程序,精确地定位了终止位点。编码链上的单加合物和交联在距离共价加合物两个碱基处诱导终止,但非编码链上的单加合物不会使RNA聚合酶失活。

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