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在塞来昔布干预下,ins-7 基因表达部分受线虫 DAF-16/IIS 信号通路调控。

ins-7 Gene expression is partially regulated by the DAF-16/IIS signaling pathway in Caenorhabditis elegans under celecoxib intervention.

机构信息

Sericulture & Agri-Food Research Institute, Guangdong Academy of Agricultural Sciences, Guangzhou, Guangdong, China.

出版信息

PLoS One. 2014 Jun 19;9(6):e100320. doi: 10.1371/journal.pone.0100320. eCollection 2014.

Abstract

DAF-16 target genes are employed as reporters of the insulin/IGF-1 like signal pathway (IIS), and this is notably true when Caenorhabditis elegans (C. elegans) is used to study the action of anti-aging compounds on IIS activity. However, some of these genes may not be specific to DAF-16, even if their expression levels are altered when DAF-16 is activated. Celecoxib was reported to extend the lifespan of C. elegans through activation of DAF-16. Our results confirmed the function of celecoxib on aging; however, we found that the expression of ins-7, a DAF-16 target gene, was abnormally regulated by celecoxib. ins-7 plays an important role in regulating aging, and its expression is suppressed in C. elegans when DAF-16 is activated. However, we found that celecoxib upregulated the expression of ins-7 in contrast to its role in DAF-16 activation. Our subsequent analysis indicated that the expression level of ins-7 in C. elegans was negatively regulated by DAF-16 activity. Additionally, its expression was also positively regulated by DAF-16-independent mechanisms, at least following external pharmacological intervention. Our study suggests that ins-7 is not a specific target gene of DAF-16, and should not be chosen as a reporter for IIS activity. This conclusion is important in the study of INSs on aging in C. elegans, especially under the circumstance of drug intervention.

摘要

DAF-16 靶基因被用作胰岛素/胰岛素样生长因子 1 样信号通路(IIS)的报告基因,当使用秀丽隐杆线虫(C. elegans)来研究抗衰老化合物对 IIS 活性的作用时,这一点尤其正确。然而,即使 DAF-16 被激活时这些基因的表达水平发生改变,其中一些基因也可能不是特异性针对 DAF-16 的。塞来昔布被报道通过激活 DAF-16 来延长 C. elegans 的寿命。我们的结果证实了塞来昔布在衰老中的作用;然而,我们发现 DAF-16 靶基因 ins-7 的表达被塞来昔布异常调控。ins-7 在调节衰老中起着重要作用,当 DAF-16 被激活时,其在 C. elegans 中的表达受到抑制。然而,我们发现塞来昔布上调了 ins-7 的表达,与 DAF-16 激活的作用相反。我们随后的分析表明,C. elegans 中 ins-7 的表达水平受 DAF-16 活性的负调控。此外,其表达还受到 DAF-16 独立机制的正调控,至少在外部药物干预后是这样。我们的研究表明,ins-7 不是 DAF-16 的特异性靶基因,不应作为 IIS 活性的报告基因。这一结论在研究 C. elegans 中 INSs 对衰老的影响,特别是在药物干预的情况下非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c956/4063773/842f30c61670/pone.0100320.g001.jpg

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