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氟虫腈诱导的斑马鱼胚胎-幼虫的对映选择性发育毒性涉及 DNA 甲基化的改变。

Fipronil-induced enantioselective developmental toxicity to zebrafish embryo-larvae involves changes in DNA methylation.

机构信息

Beijing Advanced Innovation Center for Food Nutrition and Human Health, Key Laboratory of Microbial Technology for Industrial Pollution Control of Zhejiang Province, College of Environment, Zhejiang University of Technology, Hangzhou, Zhejiang, 310014, China.

College of Life Science, Taizhou University, Taizhou, Zhejiang, 318000, China.

出版信息

Sci Rep. 2017 May 23;7(1):2284. doi: 10.1038/s41598-017-02255-5.

Abstract

Enantioselectivity in the aquatic toxicity of chiral pesticides has been widely investigated, while the molecular mechanisms remain unclear. Thus far, few studies has focused on genomic expression related to selective toxicity in chiral pesticide, nor on epigenetic changes, such as DNA methylation. Here, we used fipronil, a broad-spectrum insecticide, as a model chemical to probe its enantioselective toxicity in embryo development. Our results showed that S-(+)-fipronil caused severer developmental toxicity in embryos. The MeDIP-Seq analysis demonstrated that S-(+)-fipronil dysregulated a higher level of genomic DNA methylation than R-(-)-fipronil. Gene Ontology analysis revealed that S-(+)-fipronil caused more differentially methylated genes that are involved in developmental processes. Compared with R-(-)-fipronil, S-(+)-fipronil significantly disrupted 7 signaling pathways (i.e., mitogen-activated protein kinases, tight junctions, focal adhesion, transforming growth factor-β, vascular smooth muscle contraction, and the hedgehog and Wnt signaling pathways) by hyper-methylation of developmentally related genes, which further induced the downregulation of those genes. Together, these data suggest that differences in DNA methylation may partly explain the enantioselectivity of fipronil to zebrafish embryos. The application of epigenetics to investigate the enantioselective toxicity mechanism of chiral chemicals would provide a further understanding of their stereoselectivity biological effects.

摘要

对映选择性在手性农药的水生毒性中已得到广泛研究,但其分子机制尚不清楚。迄今为止,很少有研究关注与手性农药选择性毒性相关的基因组表达,也很少关注 DNA 甲基化等表观遗传变化。在这里,我们使用了一种广谱杀虫剂——氟虫腈作为模型化学物质,来探究其在胚胎发育中的对映选择性毒性。结果表明,S-(+)-氟虫腈比 R-(-)-氟虫腈对胚胎的发育毒性更严重。MeDIP-Seq 分析表明,S-(+)-氟虫腈引起的基因组 DNA 甲基化失调水平高于 R-(-)-氟虫腈。GO 分析表明,S-(+)-氟虫腈引起的差异甲基化基因更多地参与了发育过程。与 R-(-)-氟虫腈相比,S-(+)-氟虫腈通过对发育相关基因的超甲基化,显著扰乱了 7 个信号通路(即丝裂原活化蛋白激酶、紧密连接、黏着斑、转化生长因子-β、血管平滑肌收缩、 hedgehog 和 Wnt 信号通路),从而进一步下调了这些基因的表达。综上所述,这些数据表明,DNA 甲基化的差异可能部分解释了氟虫腈对斑马鱼胚胎的对映选择性。将表观遗传学应用于研究手性化学品的对映选择性毒性机制,将有助于进一步了解它们的立体选择性生物效应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73a0/5442102/d440fd3bfd70/41598_2017_2255_Fig1_HTML.jpg

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