Suppr超能文献

核激素受体调控秀丽隐杆线虫对外源应激的适应性和特化转录反应。

Adaptive and specialised transcriptional responses to xenobiotic stress in Caenorhabditis elegans are regulated by nuclear hormone receptors.

机构信息

School of Biology, University of Leeds, Leeds, United Kingdom.

出版信息

PLoS One. 2013 Jul 26;8(7):e69956. doi: 10.1371/journal.pone.0069956. Print 2013.

Abstract

Characterisation of the pathways by which xenobiotics are metabolised and excreted in both target and non-target organisms is crucial for the rational design of effective and specific novel bioactive molecules. Consequently, we have investigated the induced responses of the model nematode Caenorhabditis elegans to a variety of xenobiotics which represent a range of putative modes of action. The majority of genes that were specifically induced in preliminary microarray analyses encoded enzymes from Phase I and II metabolism, including cytochrome P450s, short chain dehydrogenases, UDP-glucuronosyl transferases and glutathione transferases. Changes in gene expression were confirmed by quantitative PCR and GFP induction in reporter strains driven by promoters for transcription of twelve induced enzymes was investigated. The particular complement of metabolic genes induced was found to be highly contingent on the xenobiotic applied. The known regulators of responses to applied chemicals ahr-1, hif-1, mdt-15 and nhr-8 were not required for any of these inducible responses and skn-1 regulated GFP expression from only two of the promoters. Reporter strains were used in conjunction with systematic RNAi screens to identify transcription factors which drive expression of these genes under xenobiotic exposure. These transcription factors appeared to regulate specific xenobiotic responses and have no reported phenotypes under standard conditions. Focussing on nhr-176 we demonstrate the role of this transcription factor in mediating the resistance to thiabendazole.

摘要

阐明外源化学物在目标生物和非目标生物中的代谢和排泄途径对于合理设计有效和特异的新型生物活性分子至关重要。因此,我们研究了模式线虫秀丽隐杆线虫对多种外源化学物的诱导反应,这些化学物代表了一系列可能的作用模式。初步微阵列分析中特异性诱导的大多数基因编码来自 I 相和 II 相代谢的酶,包括细胞色素 P450s、短链脱氢酶、UDP-葡糖醛酸基转移酶和谷胱甘肽转移酶。通过定量 PCR 证实了基因表达的变化,并研究了由 12 种诱导酶转录启动子驱动的报告菌株中 GFP 的诱导。发现诱导的代谢基因的特定补体高度依赖于所应用的外源化学物。已知的化学物质应答调节剂 ahr-1、hif-1、mdt-15 和 nhr-8 对于这些可诱导应答中的任何一种都不是必需的,而 skn-1 仅调控两个启动子中的 GFP 表达。报告菌株与系统 RNAi 筛选相结合,用于鉴定在暴露于外源化学物下驱动这些基因表达的转录因子。这些转录因子似乎调节特定的外源化学物反应,并且在标准条件下没有报道的表型。我们专注于 nhr-176,证明了该转录因子在介导噻菌灵抗性中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f52/3724934/dde20a90715d/pone.0069956.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验