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EcoRII甲基化酶基因在转录水平的自身调控:5-氮杂胞苷的作用

Autogenous regulation of the EcoRII methylase gene at the transcriptional level: effect of 5-azacytidine.

作者信息

Som S, Friedman S

机构信息

Department of Pharmacology, State University of New York Health Science Center, Brooklyn 11357.

出版信息

EMBO J. 1993 Nov;12(11):4297-303. doi: 10.1002/j.1460-2075.1993.tb06114.x.

Abstract

mRNA of the EcoRII methylase (M.EcoRII), a type II modification enzyme, was induced when Escherichia coli carrying a cloned M.EcoRII gene was exposed to the bacteriocidal drug 5-azacytidine. Induction occurred only when transcription was initiated from its own promoter. When the 5' promoter sequences were deleted or replaced with the lac promoter sequences, no induction occurred. The induction was independent of the template DNA level, but the presence of an intact M.EcoRII protein was a requirement. The drug is incorporated into DNA which then inhibits M.EcoRII by binding tightly to the enzyme. A deletion within the M.EcoRII coding region caused a marked increase in the basal level of mRNA transcribed from the M.EcoRII promoter, but no induction occurred upon 5-azacytidine treatment. The level could be reduced to normal by M.EcoRII in trans. In vitro, the enzyme bound to the sequences upstream of the transcription start sites and inhibited the initiation of transcription. These experiments indicate that expression of the M.EcoRII gene was autogenously regulated at the transcriptional level. Similar regulation is also noted in another DNA (cytosine-5) methylase, M.MspI.

摘要

II型修饰酶EcoRII甲基化酶(M.EcoRII)的mRNA,在携带克隆的M.EcoRII基因的大肠杆菌暴露于杀菌药物5-氮杂胞苷时被诱导。只有当转录从其自身启动子开始时才会发生诱导。当5'启动子序列被删除或被lac启动子序列取代时,不会发生诱导。诱导与模板DNA水平无关,但完整的M.EcoRII蛋白的存在是必需的。该药物被整合到DNA中,然后通过与该酶紧密结合来抑制M.EcoRII。M.EcoRII编码区域内的一个缺失导致从M.EcoRII启动子转录的mRNA基础水平显著增加,但在5-氮杂胞苷处理后不会发生诱导。通过反式M.EcoRII可将该水平降低至正常。在体外,该酶与转录起始位点上游的序列结合并抑制转录起始。这些实验表明,M.EcoRII基因的表达在转录水平上是自身调节的。在另一种DNA(胞嘧啶-5)甲基化酶M.MspI中也观察到类似的调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffa1/413726/26e970bf3a41/emboj00083-0260-a.jpg

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