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抗生素抗性质粒R100 - 1的转移基因traY和traM的转录是相关联的。

Transcription of the transfer genes traY and traM of the antibiotic resistance plasmid R100-1 is linked.

作者信息

Stockwell D, Lelianova V, Thompson T, Dempsey W B

机构信息

Veterans Affairs Medical Center and University of Texas Southwestern Medical Center, Dallas, Texas, 75216, USA.

出版信息

Plasmid. 2000 Jan;43(1):35-48. doi: 10.1006/plas.1999.1435.

Abstract

Three separate traY deletion mutants of R100-1 were prepared by allele replacement. These mutants retained the ability to transfer at a level 100 times greater than R100 and 1/50 that of the parental R100-1. The mutants were complemented to normal R100-1 transfer levels by pDSP06, a multicopy traY clone. Comparison of transcripts initiated at the traY promoter, P(Y), by primer extension experiments showed that there was no detectable P(Y) activity in R100 and that the level of P(Y) activity in the traY deletion mutants was lower than that in R100-1. Similar measurements performed on RNA from a set of previously described traM deletion mutants showed that those traM deletion mutants that produced more traM and finM (M) transcripts than the parental R100-1 also produced more traY transcripts than R100-1 and that those traM mutants that produced fewer M transcripts than R100-1 also produced fewer traY transcripts than R100-1. We conclude that in R100, TraY regulates P(Y) activity and that transcripts originating in traM affect P(Y) activity.

摘要

通过等位基因替换构建了R100-1的三个独立的traY缺失突变体。这些突变体保持了转移能力,其转移水平比R100高100倍,是亲本R100-1的1/50。通过多拷贝traY克隆pDSP06,这些突变体的转移水平恢复到正常R100-1的水平。通过引物延伸实验比较在traY启动子P(Y)起始的转录本,结果显示在R100中未检测到P(Y)活性,并且traY缺失突变体中的P(Y)活性水平低于R100-1。对一组先前描述的traM缺失突变体的RNA进行的类似测量表明,那些产生比亲本R100-1更多traM和finM (M)转录本的traM缺失突变体也比R100-1产生更多的traY转录本,而那些产生比R100-1更少M转录本的traM突变体也比R100-1产生更少的traY转录本。我们得出结论,在R100中,TraY调节P(Y)活性,并且源自traM的转录本影响P(Y)活性。

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