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RNA测序分析表明解毒途径与绵羊对霉菌毒素的抗性有关。

RNA-Seq analysis implicates detoxification pathways in ovine mycotoxin resistance.

作者信息

Zhang Jinbi, Pan Zengxiang, Moloney Stephanie, Sheppard Allan

机构信息

Liggins Institute, University of Auckland, Auckland, New Zealand.

出版信息

PLoS One. 2014 Jun 17;9(6):e99975. doi: 10.1371/journal.pone.0099975. eCollection 2014.

DOI:10.1371/journal.pone.0099975
PMID:24936865
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4061066/
Abstract

Mycotoxin induced hepatoxocity has been linked to oxidative stress, resulting from either an increase in levels of reactive oxygen species (ROS) above normal levels and/or the suppression of antioxidant protective pathways. However, few detailed molecular studies of mycotoxicoses in animals have been carried out. This study use current RNA-seq based approaches to investigate the effects of mycotoxin exposure in a ruminant model. Having first assembled a de novo reference transcriptome, we use RNA-Seq technology to define in vivo hepatic gene expression changes resulting from mycotoxin exposure in relationship to pathological effect. As expected, characteristic oxidative stress related gene expression is markedly different in animals exhibiting poorer outcomes. However, expression of multiple genes critical for detoxification, particularly members of the cytochrome P450 gene family, was significantly higher in animals exhibiting mycotoxin tolerance ('resistance'). Further, we present novel evidence for the amplification of Wnt signalling pathway activity in 'resistant' animals, resulting from the marked suppression of multiple key Wnt inhibitor genes. Notably, 'resistance' may be determined primarily by the ability of an individual to detoxify secondary metabolites generated by the metabolism of mycotoxins and the potentiation of Wnt signalling may be pivotal to achieving a favourable outcome upon challenge.

摘要

霉菌毒素诱导的肝毒性与氧化应激有关,这是由于活性氧(ROS)水平高于正常水平和/或抗氧化保护途径受到抑制所致。然而,针对动物霉菌毒素中毒的详细分子研究却很少。本研究采用基于RNA测序的方法来研究霉菌毒素暴露对反刍动物模型的影响。在首次组装了一个从头参考转录组后,我们使用RNA测序技术来确定霉菌毒素暴露导致的体内肝脏基因表达变化及其与病理效应的关系。正如预期的那样,在表现出较差结果的动物中,与氧化应激相关的特征性基因表达明显不同。然而,在表现出霉菌毒素耐受性(“抗性”)的动物中,多个对解毒至关重要的基因,特别是细胞色素P450基因家族成员的表达显著更高。此外,我们提供了新的证据表明,由于多个关键Wnt抑制剂基因受到显著抑制,“抗性”动物中Wnt信号通路活性增强。值得注意的是,“抗性”可能主要取决于个体对霉菌毒素代谢产生的次生代谢产物进行解毒的能力,而Wnt信号的增强可能是在受到挑战时取得良好结果的关键。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6990/4061066/00eebaf2aaee/pone.0099975.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6990/4061066/554a70954f29/pone.0099975.g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6990/4061066/a41c4e675451/pone.0099975.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6990/4061066/4b212dec9d42/pone.0099975.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6990/4061066/dbf46defca9b/pone.0099975.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6990/4061066/00eebaf2aaee/pone.0099975.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6990/4061066/554a70954f29/pone.0099975.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6990/4061066/0d625679335d/pone.0099975.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6990/4061066/a41c4e675451/pone.0099975.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6990/4061066/4b212dec9d42/pone.0099975.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6990/4061066/dbf46defca9b/pone.0099975.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6990/4061066/00eebaf2aaee/pone.0099975.g006.jpg

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