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Identification of 20-Hydroxyecdysone Late-Response Genes in the Chitin Biosynthesis Pathway
BACKGROUND: 20-hydroxyecdysone (20E) and its receptor complex ecdysone receptor (EcR) and ultraspiracle (USP) play a crucial role in controlling development, metamorphosis, reproduction and diapause. The ligand-receptor complex 20E-EcR/USP directly activates a small set of early-response genes and a...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2987807/ https://www.ncbi.nlm.nih.gov/pubmed/21124981 http://dx.doi.org/10.1371/journal.pone.0014058 |
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author | Yao, Qiong Zhang, Daowei Tang, Bin Chen, Jie Chen, Jing Lu, Liang Zhang, Wenqing |
author_facet | Yao, Qiong Zhang, Daowei Tang, Bin Chen, Jie Chen, Jing Lu, Liang Zhang, Wenqing |
author_sort | Yao, Qiong |
collection | PubMed |
description | BACKGROUND: 20-hydroxyecdysone (20E) and its receptor complex ecdysone receptor (EcR) and ultraspiracle (USP) play a crucial role in controlling development, metamorphosis, reproduction and diapause. The ligand-receptor complex 20E-EcR/USP directly activates a small set of early-response genes and a much larger set of late-response genes. However, ecdysone-responsive genes have not been previously characterized in the context of insect chitin biosynthesis. PRINCIPAL FINDINGS: Here, we show that injection-based RNA interference (RNAi) directed towards a common region of the two isoforms of SeEcR in a lepidopteron insect Spodoptera exigua was effective, with phenotypes including a high mortality prior to pupation and developmental defects. After gene specific RNAi, chitin contents in the cuticle of an abnormal larva significantly decreased. The expression levels of five genes in the chitin biosynthesis pathway, SeTre-1, SeG6PI, SeUAP, SeCHSA and SeCHSB, were significantly reduced, while there was no difference in the expression of SeTre-2 prior to 72 hr after injection of EcR dsRNA. Meanwhile, injection of 20E in vivo induced the expression of the five genes mentioned above. Moreover, the SeTre-1, SeG6PI, SeUAP and SeCHSB genes showed late responses to the hormone and the induction of SeTre-1, SeG6PI, SeUAP and SeCHSB genes by 20E were able to be inhibited by the protein synthesis inhibitor cycloheximide in vitro indicating these genes are 20E late-response genes. CONCLUSIONS: We conclude that SeTre-1, SeG6PI, SeUAP and SeCHSB in the chitin biosynthesis pathway are 20E late-response genes and 20E and its specific receptors plays a key role in the regulation of chitin biosynthesis via inducing their expression. |
format | Text |
id | pubmed-2987807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-29878072010-12-01 Identification of 20-Hydroxyecdysone Late-Response Genes in the Chitin Biosynthesis Pathway Yao, Qiong Zhang, Daowei Tang, Bin Chen, Jie Chen, Jing Lu, Liang Zhang, Wenqing PLoS One Research Article BACKGROUND: 20-hydroxyecdysone (20E) and its receptor complex ecdysone receptor (EcR) and ultraspiracle (USP) play a crucial role in controlling development, metamorphosis, reproduction and diapause. The ligand-receptor complex 20E-EcR/USP directly activates a small set of early-response genes and a much larger set of late-response genes. However, ecdysone-responsive genes have not been previously characterized in the context of insect chitin biosynthesis. PRINCIPAL FINDINGS: Here, we show that injection-based RNA interference (RNAi) directed towards a common region of the two isoforms of SeEcR in a lepidopteron insect Spodoptera exigua was effective, with phenotypes including a high mortality prior to pupation and developmental defects. After gene specific RNAi, chitin contents in the cuticle of an abnormal larva significantly decreased. The expression levels of five genes in the chitin biosynthesis pathway, SeTre-1, SeG6PI, SeUAP, SeCHSA and SeCHSB, were significantly reduced, while there was no difference in the expression of SeTre-2 prior to 72 hr after injection of EcR dsRNA. Meanwhile, injection of 20E in vivo induced the expression of the five genes mentioned above. Moreover, the SeTre-1, SeG6PI, SeUAP and SeCHSB genes showed late responses to the hormone and the induction of SeTre-1, SeG6PI, SeUAP and SeCHSB genes by 20E were able to be inhibited by the protein synthesis inhibitor cycloheximide in vitro indicating these genes are 20E late-response genes. CONCLUSIONS: We conclude that SeTre-1, SeG6PI, SeUAP and SeCHSB in the chitin biosynthesis pathway are 20E late-response genes and 20E and its specific receptors plays a key role in the regulation of chitin biosynthesis via inducing their expression. Public Library of Science 2010-11-18 /pmc/articles/PMC2987807/ /pubmed/21124981 http://dx.doi.org/10.1371/journal.pone.0014058 Text en Yao 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Yao, Qiong Zhang, Daowei Tang, Bin Chen, Jie Chen, Jing Lu, Liang Zhang, Wenqing Identification of 20-Hydroxyecdysone Late-Response Genes in the Chitin Biosynthesis Pathway |
title | Identification of 20-Hydroxyecdysone Late-Response Genes in the Chitin Biosynthesis Pathway |
title_full | Identification of 20-Hydroxyecdysone Late-Response Genes in the Chitin Biosynthesis Pathway |
title_fullStr | Identification of 20-Hydroxyecdysone Late-Response Genes in the Chitin Biosynthesis Pathway |
title_full_unstemmed | Identification of 20-Hydroxyecdysone Late-Response Genes in the Chitin Biosynthesis Pathway |
title_short | Identification of 20-Hydroxyecdysone Late-Response Genes in the Chitin Biosynthesis Pathway |
title_sort | identification of 20-hydroxyecdysone late-response genes in the chitin biosynthesis pathway |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2987807/ https://www.ncbi.nlm.nih.gov/pubmed/21124981 http://dx.doi.org/10.1371/journal.pone.0014058 |
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