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近紫外光照射的大肠杆菌中转运RNA的代谢。转运RNA修复假说。

Metabolism of tRNA in near-ultraviolet-illuminated Escherichia coli. The tRNA repair hypothesis.

作者信息

Blanchetot A, Hajnsdorf E, Favre A

出版信息

Eur J Biochem. 1984 Mar 15;139(3):547-52. doi: 10.1111/j.1432-1033.1984.tb08040.x.

Abstract

The relA+-dependent stringent response is an important component of the mechanism of the near-ultraviolet-induced growth delay. However, the behaviour of the intracellular level of ppGpp is unexpected [Thomas et al. (1981) Eur. J. Biochem. 118, 381-387] and this led us to examine the metabolism of tRNAs during the illumination period and the growth lag that follows. Analysis of the gel electrophoresis migration profiles of tRNA molecules, synthesized prior to the illumination period, provides no evidence for tRNA degradation. Rather, it is suggestive of the rearrangement of some cross-linked tRNA species during the growth lag. By the same technique the neosynthesis of one or several tRNA species escaping the stringent response could be ruled out at the beginning of the growth lag. The behaviour of the cross-linked tRNAs was followed by a chromatographic procedure allowing the quantitative evaluation of the 8-13 link present in vivo. Upon illumination of growing cells, one observes an initial linear increase of the 8-13 link content. Unexpectedly this is followed during the illumination period by an abrupt decrease. The 8-13 link content then remains stable. The data above suggest that part of the 8-13 link (25-40%) is eliminated from tRNA without degradation of the molecules involved. A tRNA repair hypothesis is proposed: elimination of the 8-13 link would occur by scission of the N1-C1' glycosidic bonds at positions 8 and 13 of tRNA. It would be followed by reinsertion of uracil and cytosine in their respective positions.

摘要

RelA⁺依赖性严谨反应是近紫外线诱导生长延迟机制的重要组成部分。然而,ppGpp细胞内水平的行为出乎意料[托马斯等人(1981年),《欧洲生物化学杂志》118卷,381 - 387页],这促使我们研究光照期间及随后生长滞后期间tRNA的代谢情况。对光照期之前合成的tRNA分子进行凝胶电泳迁移图谱分析,没有发现tRNA降解的证据。相反,这表明在生长滞后期间一些交联的tRNA种类发生了重排。通过同样的技术,可以排除在生长滞后开始时一种或几种逃避严谨反应的tRNA种类的重新合成。通过一种色谱程序跟踪交联tRNA的行为,该程序可以对体内存在的8 - 13连接进行定量评估。当对生长中的细胞进行光照时,可以观察到8 - 13连接含量最初呈线性增加。出乎意料的是,在光照期间随后会突然下降。然后8 - 13连接含量保持稳定。上述数据表明,部分8 - 13连接(25% - 40%)从tRNA中被消除,而不涉及相关分子的降解。提出了一种tRNA修复假说:8 - 13连接的消除将通过tRNA第8位和第13位的N1 - C1'糖苷键断裂而发生。随后尿嘧啶和胞嘧啶将重新插入各自的位置。

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