Multi-walled carbon nanotubes-induced alterations in microRNA let-7 and its targets activate a protection mechanism by conferring a developmental timing control

Abstract Background Multi-walled carbon nanotubes (MWCNTs) have been produced and applied for diverse purposes. MWCNTs can potentially cause the adverse effects on organisms. MicroRNA let-7 and its targets of HBL-1 and LIN-41 play a central role in regulating developmental timing by acting as a deve...

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Main Authors: Li Zhao, Hanxiao Wan, Qizhan Liu, Dayong Wang
Format: Article
Language:English
Published: BMC 2017-07-01
Series:Particle and Fibre Toxicology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12989-017-0208-2
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spelling doaj-53d6e3e00a4040d4b52b77aa22d03f8e2020-11-25T00:45:33ZengBMCParticle and Fibre Toxicology1743-89772017-07-0114111110.1186/s12989-017-0208-2Multi-walled carbon nanotubes-induced alterations in microRNA let-7 and its targets activate a protection mechanism by conferring a developmental timing controlLi Zhao0Hanxiao Wan1Qizhan Liu2Dayong Wang3Key Laboratory of Environmental Medicine Engineering in Ministry of Education, Medical School, Southeast UniversityKey Laboratory of Environmental Medicine Engineering in Ministry of Education, Medical School, Southeast UniversitySchool of Public Health, Nanjing Medical UniversityKey Laboratory of Environmental Medicine Engineering in Ministry of Education, Medical School, Southeast UniversityAbstract Background Multi-walled carbon nanotubes (MWCNTs) have been produced and applied for diverse purposes. MWCNTs can potentially cause the adverse effects on organisms. MicroRNA let-7 and its targets of HBL-1 and LIN-41 play a central role in regulating developmental timing by acting as a developmental switch. The sequence of let-7 and the underlying mechanisms for let-7 in the control of developmental timing are conserved among different species. In this study, we investigated the potential effect of MWCNTs exposure on the molecular basis for developmental timing mediated by let-7 and its targets of HBL-1 and LIN-41. Results MWCNTs exposure decreased let-7 expression, and increased expressions of hbl-1 and lin-41. let-7 mutant was resistant to MWCNTs toxicity, whereas hbl-1 or lin-41 mutant was susceptible to MWCNTs toxicity. hbl-1 or lin-41 mutant suppressed the resistance of let-7 mutant to MWCNTs toxicity. HBL-1 acted upstream of TIR-1, an adaptor protein, and SYM-1, a protein containing leucine-rich repeats, and ALG-1 and ALG-2, two RDE-1 proteins related to RNA interference (RNAi) pathway, acted upstream of LIN-41 to regulate MWCNTs toxicity. Moreover, we identified a feedback loop between let-7 and its targets of HBL-1 and LIN-41 in the regulation of MWCNTs toxicity. The observed increase in let-7::GFP expression in MWCNTs exposed nematodes with mutation of hbl-1 or lin-41 implied that a feedback mechanism may exist to strengthen the function of let-7 suppression in protecting the animals from MWCNTs toxicity. Conclusions Our results demonstrate the protection function of let-7 suppression for animals from MWCNTs toxicity by conferring a robust developmental timing control. Our results highlight the importance of molecular basis for developmental timing in influencing MWCNTs toxicity.http://link.springer.com/article/10.1186/s12989-017-0208-2let-7Multi-walled carbon nanotubesDevelopmental timingNanotoxicityCaenorhabditis elegans
collection DOAJ
language English
format Article
sources DOAJ
author Li Zhao
Hanxiao Wan
Qizhan Liu
Dayong Wang
spellingShingle Li Zhao
Hanxiao Wan
Qizhan Liu
Dayong Wang
Multi-walled carbon nanotubes-induced alterations in microRNA let-7 and its targets activate a protection mechanism by conferring a developmental timing control
Particle and Fibre Toxicology
let-7
Multi-walled carbon nanotubes
Developmental timing
Nanotoxicity
Caenorhabditis elegans
author_facet Li Zhao
Hanxiao Wan
Qizhan Liu
Dayong Wang
author_sort Li Zhao
title Multi-walled carbon nanotubes-induced alterations in microRNA let-7 and its targets activate a protection mechanism by conferring a developmental timing control
title_short Multi-walled carbon nanotubes-induced alterations in microRNA let-7 and its targets activate a protection mechanism by conferring a developmental timing control
title_full Multi-walled carbon nanotubes-induced alterations in microRNA let-7 and its targets activate a protection mechanism by conferring a developmental timing control
title_fullStr Multi-walled carbon nanotubes-induced alterations in microRNA let-7 and its targets activate a protection mechanism by conferring a developmental timing control
title_full_unstemmed Multi-walled carbon nanotubes-induced alterations in microRNA let-7 and its targets activate a protection mechanism by conferring a developmental timing control
title_sort multi-walled carbon nanotubes-induced alterations in microrna let-7 and its targets activate a protection mechanism by conferring a developmental timing control
publisher BMC
series Particle and Fibre Toxicology
issn 1743-8977
publishDate 2017-07-01
description Abstract Background Multi-walled carbon nanotubes (MWCNTs) have been produced and applied for diverse purposes. MWCNTs can potentially cause the adverse effects on organisms. MicroRNA let-7 and its targets of HBL-1 and LIN-41 play a central role in regulating developmental timing by acting as a developmental switch. The sequence of let-7 and the underlying mechanisms for let-7 in the control of developmental timing are conserved among different species. In this study, we investigated the potential effect of MWCNTs exposure on the molecular basis for developmental timing mediated by let-7 and its targets of HBL-1 and LIN-41. Results MWCNTs exposure decreased let-7 expression, and increased expressions of hbl-1 and lin-41. let-7 mutant was resistant to MWCNTs toxicity, whereas hbl-1 or lin-41 mutant was susceptible to MWCNTs toxicity. hbl-1 or lin-41 mutant suppressed the resistance of let-7 mutant to MWCNTs toxicity. HBL-1 acted upstream of TIR-1, an adaptor protein, and SYM-1, a protein containing leucine-rich repeats, and ALG-1 and ALG-2, two RDE-1 proteins related to RNA interference (RNAi) pathway, acted upstream of LIN-41 to regulate MWCNTs toxicity. Moreover, we identified a feedback loop between let-7 and its targets of HBL-1 and LIN-41 in the regulation of MWCNTs toxicity. The observed increase in let-7::GFP expression in MWCNTs exposed nematodes with mutation of hbl-1 or lin-41 implied that a feedback mechanism may exist to strengthen the function of let-7 suppression in protecting the animals from MWCNTs toxicity. Conclusions Our results demonstrate the protection function of let-7 suppression for animals from MWCNTs toxicity by conferring a robust developmental timing control. Our results highlight the importance of molecular basis for developmental timing in influencing MWCNTs toxicity.
topic let-7
Multi-walled carbon nanotubes
Developmental timing
Nanotoxicity
Caenorhabditis elegans
url http://link.springer.com/article/10.1186/s12989-017-0208-2
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