Cargando…

Molecular cloning, expression, and in situ hybridization analysis of MnGPx-3 and MnGPx-4 from oriental river prawn, Macrobrachium nipponense, in response to hypoxia and reoxygenation

Glutathione peroxidase (GPx) has been the focus of increased research because of its important role as an antioxidant and in reactive oxygen species (ROS) induced damage repair. Studies on GPxs have relevance with Macrobrachium nipponense because it has poor tolerance to hypoxia in Macrobrachium nip...

Descripción completa

Detalles Bibliográficos
Autores principales: Xu, Lei, Yang, Ming, Fu, Hongtuo, Sun, Shengming, Qiao, Hui, Zhang, Wenyi, Gong, Yongsheng, Jiang, Sufei, Xiong, Yiwei, Jin, Shubo, Wu, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034814/
https://www.ncbi.nlm.nih.gov/pubmed/32084182
http://dx.doi.org/10.1371/journal.pone.0229171
_version_ 1783499947421728768
author Xu, Lei
Yang, Ming
Fu, Hongtuo
Sun, Shengming
Qiao, Hui
Zhang, Wenyi
Gong, Yongsheng
Jiang, Sufei
Xiong, Yiwei
Jin, Shubo
Wu, Yan
author_facet Xu, Lei
Yang, Ming
Fu, Hongtuo
Sun, Shengming
Qiao, Hui
Zhang, Wenyi
Gong, Yongsheng
Jiang, Sufei
Xiong, Yiwei
Jin, Shubo
Wu, Yan
author_sort Xu, Lei
collection PubMed
description Glutathione peroxidase (GPx) has been the focus of increased research because of its important role as an antioxidant and in reactive oxygen species (ROS) induced damage repair. Studies on GPxs have relevance with Macrobrachium nipponense because it has poor tolerance to hypoxia in Macrobrachium nipponense. The two subunits named as MnGPx-3 and MnGPx-4 according to the glutathione peroxidase nomenclature system. Both full-length cDNAs were cloned from the hepatopancreas. In this study, we analyzed the expression of two GPxs in Macrobrachium nipponense in response to changes in environmental oxygen. Expression levels of MnGPx-3 and MnGPx-4 indicated that both have strong responses to hypoxia. In situ hybridization showed that MnGPx-3 and MnGPx-4 were located in secretory and storage cells in hepatopancreas. These results suggest that GPx gene is expressed and released by secretory cells and released response to hypoxia. In the gill tissue, however, GPxs are located in blood cells, suggesting that they perform different functions in different tissues or organs. The results of in situ hybridization were consistent with those of quantitative Real-time PCR. This study provides a basis for understanding the oxidative stress response in M. nipponense under hypoxia.
format Online
Article
Text
id pubmed-7034814
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-70348142020-02-27 Molecular cloning, expression, and in situ hybridization analysis of MnGPx-3 and MnGPx-4 from oriental river prawn, Macrobrachium nipponense, in response to hypoxia and reoxygenation Xu, Lei Yang, Ming Fu, Hongtuo Sun, Shengming Qiao, Hui Zhang, Wenyi Gong, Yongsheng Jiang, Sufei Xiong, Yiwei Jin, Shubo Wu, Yan PLoS One Research Article Glutathione peroxidase (GPx) has been the focus of increased research because of its important role as an antioxidant and in reactive oxygen species (ROS) induced damage repair. Studies on GPxs have relevance with Macrobrachium nipponense because it has poor tolerance to hypoxia in Macrobrachium nipponense. The two subunits named as MnGPx-3 and MnGPx-4 according to the glutathione peroxidase nomenclature system. Both full-length cDNAs were cloned from the hepatopancreas. In this study, we analyzed the expression of two GPxs in Macrobrachium nipponense in response to changes in environmental oxygen. Expression levels of MnGPx-3 and MnGPx-4 indicated that both have strong responses to hypoxia. In situ hybridization showed that MnGPx-3 and MnGPx-4 were located in secretory and storage cells in hepatopancreas. These results suggest that GPx gene is expressed and released by secretory cells and released response to hypoxia. In the gill tissue, however, GPxs are located in blood cells, suggesting that they perform different functions in different tissues or organs. The results of in situ hybridization were consistent with those of quantitative Real-time PCR. This study provides a basis for understanding the oxidative stress response in M. nipponense under hypoxia. Public Library of Science 2020-02-21 /pmc/articles/PMC7034814/ /pubmed/32084182 http://dx.doi.org/10.1371/journal.pone.0229171 Text en © 2020 Xu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Xu, Lei
Yang, Ming
Fu, Hongtuo
Sun, Shengming
Qiao, Hui
Zhang, Wenyi
Gong, Yongsheng
Jiang, Sufei
Xiong, Yiwei
Jin, Shubo
Wu, Yan
Molecular cloning, expression, and in situ hybridization analysis of MnGPx-3 and MnGPx-4 from oriental river prawn, Macrobrachium nipponense, in response to hypoxia and reoxygenation
title Molecular cloning, expression, and in situ hybridization analysis of MnGPx-3 and MnGPx-4 from oriental river prawn, Macrobrachium nipponense, in response to hypoxia and reoxygenation
title_full Molecular cloning, expression, and in situ hybridization analysis of MnGPx-3 and MnGPx-4 from oriental river prawn, Macrobrachium nipponense, in response to hypoxia and reoxygenation
title_fullStr Molecular cloning, expression, and in situ hybridization analysis of MnGPx-3 and MnGPx-4 from oriental river prawn, Macrobrachium nipponense, in response to hypoxia and reoxygenation
title_full_unstemmed Molecular cloning, expression, and in situ hybridization analysis of MnGPx-3 and MnGPx-4 from oriental river prawn, Macrobrachium nipponense, in response to hypoxia and reoxygenation
title_short Molecular cloning, expression, and in situ hybridization analysis of MnGPx-3 and MnGPx-4 from oriental river prawn, Macrobrachium nipponense, in response to hypoxia and reoxygenation
title_sort molecular cloning, expression, and in situ hybridization analysis of mngpx-3 and mngpx-4 from oriental river prawn, macrobrachium nipponense, in response to hypoxia and reoxygenation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034814/
https://www.ncbi.nlm.nih.gov/pubmed/32084182
http://dx.doi.org/10.1371/journal.pone.0229171
work_keys_str_mv AT xulei molecularcloningexpressionandinsituhybridizationanalysisofmngpx3andmngpx4fromorientalriverprawnmacrobrachiumnipponenseinresponsetohypoxiaandreoxygenation
AT yangming molecularcloningexpressionandinsituhybridizationanalysisofmngpx3andmngpx4fromorientalriverprawnmacrobrachiumnipponenseinresponsetohypoxiaandreoxygenation
AT fuhongtuo molecularcloningexpressionandinsituhybridizationanalysisofmngpx3andmngpx4fromorientalriverprawnmacrobrachiumnipponenseinresponsetohypoxiaandreoxygenation
AT sunshengming molecularcloningexpressionandinsituhybridizationanalysisofmngpx3andmngpx4fromorientalriverprawnmacrobrachiumnipponenseinresponsetohypoxiaandreoxygenation
AT qiaohui molecularcloningexpressionandinsituhybridizationanalysisofmngpx3andmngpx4fromorientalriverprawnmacrobrachiumnipponenseinresponsetohypoxiaandreoxygenation
AT zhangwenyi molecularcloningexpressionandinsituhybridizationanalysisofmngpx3andmngpx4fromorientalriverprawnmacrobrachiumnipponenseinresponsetohypoxiaandreoxygenation
AT gongyongsheng molecularcloningexpressionandinsituhybridizationanalysisofmngpx3andmngpx4fromorientalriverprawnmacrobrachiumnipponenseinresponsetohypoxiaandreoxygenation
AT jiangsufei molecularcloningexpressionandinsituhybridizationanalysisofmngpx3andmngpx4fromorientalriverprawnmacrobrachiumnipponenseinresponsetohypoxiaandreoxygenation
AT xiongyiwei molecularcloningexpressionandinsituhybridizationanalysisofmngpx3andmngpx4fromorientalriverprawnmacrobrachiumnipponenseinresponsetohypoxiaandreoxygenation
AT jinshubo molecularcloningexpressionandinsituhybridizationanalysisofmngpx3andmngpx4fromorientalriverprawnmacrobrachiumnipponenseinresponsetohypoxiaandreoxygenation
AT wuyan molecularcloningexpressionandinsituhybridizationanalysisofmngpx3andmngpx4fromorientalriverprawnmacrobrachiumnipponenseinresponsetohypoxiaandreoxygenation