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pUC质粒的高拷贝数源于RNA II中一个可被Rom/Rop抑制的点突变。

High copy number of the pUC plasmid results from a Rom/Rop-suppressible point mutation in RNA II.

作者信息

Lin-Chao S, Chen W T, Wong T T

机构信息

Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan, Republic of China.

出版信息

Mol Microbiol. 1992 Nov;6(22):3385-93. doi: 10.1111/j.1365-2958.1992.tb02206.x.

Abstract

The plasmids pUC18 and pUC19 are pBR322 derivatives that replicate at a copy number several fold higher than the parent during growth of Escherichia coli at 37 degrees C. We show here that the high copy number of pUC plasmids results from a single point mutation in the replication primer, RNA II, and that the phenotypic effects of this mutation can be suppressed by the Rom (RNA one modulator)/Rop protein or by lowering the growth temperature to 30 degrees C. The mutation's effects are enhanced by cell growth at 42 degrees C, at which copy number is further increased. During normal cell growth, the pUC mutation does not affect the length or function of RNA I, the antisense repressor of plasmid DNA replication, but may, as computer analysis suggests, alter the secondary structure of pUC RNA II. We suggest that the pUC mutation impedes interactions between the repressor and the primer by producing a temperature-dependent alteration of the RNA II conformation. The Rom/Rop protein may either promote normal folding of the mutated RNA II or, alternatively, may enable the interaction of sub-optimally folded RNA II with the repressor.

摘要

质粒pUC18和pUC19是pBR322的衍生物,在37℃培养大肠杆菌时,它们的复制拷贝数比亲本高出数倍。我们在此表明,pUC质粒的高拷贝数源于复制引物RNA II中的一个单点突变,并且该突变的表型效应可被Rom(RNA一调节剂)/Rop蛋白抑制,或者通过将生长温度降至30℃来抑制。在42℃下细胞生长会增强该突变的效应,此时拷贝数会进一步增加。在正常细胞生长过程中,pUC突变不会影响RNA I(质粒DNA复制的反义阻遏物)的长度或功能,但如计算机分析所示,可能会改变pUC RNA II的二级结构。我们认为,pUC突变通过产生RNA II构象的温度依赖性改变来阻碍阻遏物与引物之间的相互作用。Rom/Rop蛋白可能会促进突变的RNA II正常折叠,或者使折叠欠佳的RNA II与阻遏物相互作用。

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