Analysis of microRNA expression in embryonic developmental toxicity induced by MC-RR.

As cynobacterial blooms frequently occur in fresh waters throughout the world, microcystins (MCs) have caused serious damage to both wildlife and human health. MCs are known to have developmental toxicity, however, the possible molecular mechanism is largely unknown. This is the first toxicological...

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Autores principales: Yanyan Zhao, Qian Xiong, Ping Xie
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Publicado: Public Library of Science (PLoS) 2011
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Acceso en línea:https://doaj.org/article/647876c5ed9b46f69f9c78c0273e8354
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spelling oai:doaj.org-article:647876c5ed9b46f69f9c78c0273e83542021-11-18T06:49:03ZAnalysis of microRNA expression in embryonic developmental toxicity induced by MC-RR.1932-620310.1371/journal.pone.0022676https://doaj.org/article/647876c5ed9b46f69f9c78c0273e83542011-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21829477/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203As cynobacterial blooms frequently occur in fresh waters throughout the world, microcystins (MCs) have caused serious damage to both wildlife and human health. MCs are known to have developmental toxicity, however, the possible molecular mechanism is largely unknown. This is the first toxicological study to integrate post-transcriptomic, proteomic and bioinformatics analysis to explore molecular mechanisms for developmental toxicity of MCs in zebrafish. After being microinjected directly into embryos, MC-RR dose-dependently decreased survival rates and increased malformation rates of embryos, causing various embryo abnormalities including loss of vascular integrity and hemorrhage. Expressions of 31 microRNAs (miRNAs) and 78 proteins were significantly affected at 72 hours post-fertilisation (hpf). Expressions of miR-430 and miR-125 families were also significantly changed. The altered expressions of miR-31 and miR-126 were likely responsible for the loss of vascular integrity. MC-RR significantly reduced the expressions of a number of proteins involved in energy metabolism, cell division, protein synthesis, cytoskeleton maintenance, response to stress and DNA replication. Bioinformatics analysis shows that several aberrantly expressed miRNAs and proteins (involved in various molecular pathways) were predicted to be potential MC-responsive miRNA-target pairs, and that their aberrant expressions should be the possible molecular mechanisms for the various developmental defects caused by MC-RR.Yanyan ZhaoQian XiongPing XiePublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 6, Iss 7, p e22676 (2011)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Yanyan Zhao
Qian Xiong
Ping Xie
Analysis of microRNA expression in embryonic developmental toxicity induced by MC-RR.
description As cynobacterial blooms frequently occur in fresh waters throughout the world, microcystins (MCs) have caused serious damage to both wildlife and human health. MCs are known to have developmental toxicity, however, the possible molecular mechanism is largely unknown. This is the first toxicological study to integrate post-transcriptomic, proteomic and bioinformatics analysis to explore molecular mechanisms for developmental toxicity of MCs in zebrafish. After being microinjected directly into embryos, MC-RR dose-dependently decreased survival rates and increased malformation rates of embryos, causing various embryo abnormalities including loss of vascular integrity and hemorrhage. Expressions of 31 microRNAs (miRNAs) and 78 proteins were significantly affected at 72 hours post-fertilisation (hpf). Expressions of miR-430 and miR-125 families were also significantly changed. The altered expressions of miR-31 and miR-126 were likely responsible for the loss of vascular integrity. MC-RR significantly reduced the expressions of a number of proteins involved in energy metabolism, cell division, protein synthesis, cytoskeleton maintenance, response to stress and DNA replication. Bioinformatics analysis shows that several aberrantly expressed miRNAs and proteins (involved in various molecular pathways) were predicted to be potential MC-responsive miRNA-target pairs, and that their aberrant expressions should be the possible molecular mechanisms for the various developmental defects caused by MC-RR.
format article
author Yanyan Zhao
Qian Xiong
Ping Xie
author_facet Yanyan Zhao
Qian Xiong
Ping Xie
author_sort Yanyan Zhao
title Analysis of microRNA expression in embryonic developmental toxicity induced by MC-RR.
title_short Analysis of microRNA expression in embryonic developmental toxicity induced by MC-RR.
title_full Analysis of microRNA expression in embryonic developmental toxicity induced by MC-RR.
title_fullStr Analysis of microRNA expression in embryonic developmental toxicity induced by MC-RR.
title_full_unstemmed Analysis of microRNA expression in embryonic developmental toxicity induced by MC-RR.
title_sort analysis of microrna expression in embryonic developmental toxicity induced by mc-rr.
publisher Public Library of Science (PLoS)
publishDate 2011
url https://doaj.org/article/647876c5ed9b46f69f9c78c0273e8354
work_keys_str_mv AT yanyanzhao analysisofmicrornaexpressioninembryonicdevelopmentaltoxicityinducedbymcrr
AT qianxiong analysisofmicrornaexpressioninembryonicdevelopmentaltoxicityinducedbymcrr
AT pingxie analysisofmicrornaexpressioninembryonicdevelopmentaltoxicityinducedbymcrr
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