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Comparative Study of Cyanobacterial and E. coli RNA Polymerases: Misincorporation, Abortive Transcription, and Dependence on Divalent Cations

机译:蓝细菌和大肠杆菌RNA聚合酶的比较研究:错误掺入,堕胎转录和对二价阳离子的依赖性

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摘要

If Mg2+ ion is replaced by Mn2+ ion, RNA polymerase tends to misincorporate noncognate nucleotide, which is thought to be one of the reasons for the toxicity of Mn2+ ion. Therefore, most cells have Mn2+ ion at low intracellular concentrations, but cyanobacteria need the ion at a millimolar concentration to maintain photosynthetic machinery. To analyse the mechanism for resistance against the abundant Mn2+ ion, we compared the properties of cyanobacterial and E. coli RNA polymerases. The cyanobacterial enzyme showed a lower level of abortive transcription and less misincorporation than the E. coli enzyme. Moreover, the cyanobacterial enzyme showed a slower rate of the whole elongation by an order of magnitude, paused more frequently, and cleaved its transcript faster in the absence of NTPs. In conclusion, cyanobacterial RNA polymerase maintains the fidelity of transcription against Mn2+ ion by deliberate incorporation of a nucleotide at the cost of the elongation rate. The cyanobacterial and the E. coli enzymes showed different sensitivities to Mg2+ ion, and the physiological role of the difference is also discussed.
机译:如果用Mn2 +离子代替Mg2 +离子,RNA聚合酶往往会掺入非同源核苷酸,这被认为是Mn2 +离子毒性的原因之一。因此,大多数细胞在较低的细胞内浓度下具有Mn2 +离子,但是蓝细菌需要以毫摩尔浓度的离子来维持光合作用机制。为了分析对丰富的Mn2 +离子的抗性机理,我们比较了蓝细菌和大肠杆菌RNA聚合酶的特性。蓝细菌酶显示出比大肠杆菌酶更低的流产转录水平和更少的错误掺入。此外,在没有NTP的情况下,蓝细菌酶的整体伸长率降低了一个数量级,暂停的频率更高,并且其转录物的切割速度更快。总之,蓝细菌RNA聚合酶通过故意掺入核苷酸来维持针对Mn2 +离子的转录保真度,但以延长速率为代价。蓝细菌和大肠杆菌酶对Mg2 +离子的敏感性不同,并且还讨论了这种差异的生理作用。

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