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对经MNNG处理的大肠杆菌进行的基因芯片研究揭示了广泛的转录反应。

Tiling array study of MNNG treated Escherichia coli reveals a widespread transcriptional response.

作者信息

Booth James A, Thomassen Gard O S, Rowe Alexander D, Weel-Sneve Ragnhild, Lagesen Karin, Kristiansen Knut I, Bjørås Magnar, Rognes Torbjørn, Lindvall Jessica M

机构信息

1] Centre for Molecular Biology and Neuroscience (CMBN) and Department of Microbiology, Oslo University Hospital, Rikshospitalet, PO Box 4950 Nydalen, NO-0424 Oslo, Norway [2] Department of Microbiology, University of Oslo, PO Box 4950 Nydalen, NO-0424 Oslo, Norway [3].

出版信息

Sci Rep. 2013 Oct 25;3:3053. doi: 10.1038/srep03053.

Abstract

The alkylating agent N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) is known to trigger the adaptive response by inducing the ada-regulon - consisting of three DNA repair enzymes Ada, AlkB, AlkA and the enigmatic AidB. We have applied custom designed tiling arrays to study transcriptional changes in Escherichia coli following a MNNG challenge. Along with the expected upregulation of the adaptive response genes (ada, alkA and alkB), we identified a number of differentially expressed transcripts, both novel and annotated. This indicates a wider regulatory response than previously documented. There were 250 differentially-expressed and 2275 similarly-expressed unannotated transcripts. We found novel upregulation of several stress-induced transcripts, including the SOS inducible genes recN and tisAB, indicating a novel role for these genes in alkylation repair. Furthermore, the ada-regulon A and B boxes were found to be insufficient to explain the regulation of the adaptive response genes after MNNG exposure, suggesting that additional regulatory elements must be involved.

摘要

已知烷基化剂N-甲基-N'-硝基-N-亚硝基胍(MNNG)通过诱导ada调控子(由三种DNA修复酶Ada、AlkB、AlkA和神秘的AidB组成)来触发适应性反应。我们应用定制设计的平铺阵列来研究MNNG攻击后大肠杆菌中的转录变化。除了适应性反应基因(ada、alkA和alkB)预期的上调外,我们还鉴定了许多差异表达的转录本,既有新的也有已注释的。这表明调控反应比以前记录的更广泛。有250个差异表达和2275个相似表达的未注释转录本。我们发现几种应激诱导转录本有新的上调,包括SOS诱导基因recN和tisAB,表明这些基因在烷基化修复中具有新作用。此外,发现ada调控子的A盒和B盒不足以解释MNNG暴露后适应性反应基因的调控,这表明必须涉及其他调控元件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a919/6505713/99def209db29/srep03053-f1.jpg

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