Cargando…
A comprehensive omics analysis and functional survey of cuticular proteins in the brown planthopper
Cuticle, mainly composed of chitin and cuticular proteins (CPs), is a multifunctional structure of arthropods. CPs usually account for >1% of the total insect proteins. Why does an insect encode so many different CP genes in the genome? In this study, we use comprehensive large-scale technologies...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960286/ https://www.ncbi.nlm.nih.gov/pubmed/29712872 http://dx.doi.org/10.1073/pnas.1716951115 |
_version_ | 1783324565073559552 |
---|---|
author | Pan, Peng-Lu Ye, Yu-Xuan Lou, Yi-Han Lu, Jia-Bao Cheng, Chen Shen, Yan Moussian, Bernard Zhang, Chuan-Xi |
author_facet | Pan, Peng-Lu Ye, Yu-Xuan Lou, Yi-Han Lu, Jia-Bao Cheng, Chen Shen, Yan Moussian, Bernard Zhang, Chuan-Xi |
author_sort | Pan, Peng-Lu |
collection | PubMed |
description | Cuticle, mainly composed of chitin and cuticular proteins (CPs), is a multifunctional structure of arthropods. CPs usually account for >1% of the total insect proteins. Why does an insect encode so many different CP genes in the genome? In this study, we use comprehensive large-scale technologies to study the full complement of CPs (i.e., the CP-ome) of the brown planthopper (BPH), Nilaparvata lugens, a major rice plant pest. Eight CP families (CPR, CPF, TWDL, CPLCP, CPG, CPAP1, CPAP3, and CPAPn) including 140 proteins in BPH, in which CPAPn is a CP family that we discovered. The CPG family that was considered to be restricted to the Lepidoptera has also been identified in BPH. As reported here, CPLCP family members are characterized by three conserved sequence motifs. In addition, we identified a testis protein family with a peritrophin A domain that we named TPAP. We authenticated the real existence of 106 proteins among the 140 CPs. RNA interference (RNAi) experiments were conducted against 135 CP genes in early- and late-instar nymphs and newly emerged female adults, demonstrating that 32 CPs were essential for BPH normal development or egg production. Combined RNAi experiments suggested redundant and complementary functions of the large number of CPs. Transcriptomic data revealed that the CP genes were expressed in a tissue-specific manner, and there were four clusters of developmental expression patterns. This study gives a comprehensive understanding of the roles of CPs in an insect cuticle. |
format | Online Article Text |
id | pubmed-5960286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-59602862018-05-21 A comprehensive omics analysis and functional survey of cuticular proteins in the brown planthopper Pan, Peng-Lu Ye, Yu-Xuan Lou, Yi-Han Lu, Jia-Bao Cheng, Chen Shen, Yan Moussian, Bernard Zhang, Chuan-Xi Proc Natl Acad Sci U S A Biological Sciences Cuticle, mainly composed of chitin and cuticular proteins (CPs), is a multifunctional structure of arthropods. CPs usually account for >1% of the total insect proteins. Why does an insect encode so many different CP genes in the genome? In this study, we use comprehensive large-scale technologies to study the full complement of CPs (i.e., the CP-ome) of the brown planthopper (BPH), Nilaparvata lugens, a major rice plant pest. Eight CP families (CPR, CPF, TWDL, CPLCP, CPG, CPAP1, CPAP3, and CPAPn) including 140 proteins in BPH, in which CPAPn is a CP family that we discovered. The CPG family that was considered to be restricted to the Lepidoptera has also been identified in BPH. As reported here, CPLCP family members are characterized by three conserved sequence motifs. In addition, we identified a testis protein family with a peritrophin A domain that we named TPAP. We authenticated the real existence of 106 proteins among the 140 CPs. RNA interference (RNAi) experiments were conducted against 135 CP genes in early- and late-instar nymphs and newly emerged female adults, demonstrating that 32 CPs were essential for BPH normal development or egg production. Combined RNAi experiments suggested redundant and complementary functions of the large number of CPs. Transcriptomic data revealed that the CP genes were expressed in a tissue-specific manner, and there were four clusters of developmental expression patterns. This study gives a comprehensive understanding of the roles of CPs in an insect cuticle. National Academy of Sciences 2018-05-15 2018-04-30 /pmc/articles/PMC5960286/ /pubmed/29712872 http://dx.doi.org/10.1073/pnas.1716951115 Text en Copyright © 2018 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Pan, Peng-Lu Ye, Yu-Xuan Lou, Yi-Han Lu, Jia-Bao Cheng, Chen Shen, Yan Moussian, Bernard Zhang, Chuan-Xi A comprehensive omics analysis and functional survey of cuticular proteins in the brown planthopper |
title | A comprehensive omics analysis and functional survey of cuticular proteins in the brown planthopper |
title_full | A comprehensive omics analysis and functional survey of cuticular proteins in the brown planthopper |
title_fullStr | A comprehensive omics analysis and functional survey of cuticular proteins in the brown planthopper |
title_full_unstemmed | A comprehensive omics analysis and functional survey of cuticular proteins in the brown planthopper |
title_short | A comprehensive omics analysis and functional survey of cuticular proteins in the brown planthopper |
title_sort | comprehensive omics analysis and functional survey of cuticular proteins in the brown planthopper |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960286/ https://www.ncbi.nlm.nih.gov/pubmed/29712872 http://dx.doi.org/10.1073/pnas.1716951115 |
work_keys_str_mv | AT panpenglu acomprehensiveomicsanalysisandfunctionalsurveyofcuticularproteinsinthebrownplanthopper AT yeyuxuan acomprehensiveomicsanalysisandfunctionalsurveyofcuticularproteinsinthebrownplanthopper AT louyihan acomprehensiveomicsanalysisandfunctionalsurveyofcuticularproteinsinthebrownplanthopper AT lujiabao acomprehensiveomicsanalysisandfunctionalsurveyofcuticularproteinsinthebrownplanthopper AT chengchen acomprehensiveomicsanalysisandfunctionalsurveyofcuticularproteinsinthebrownplanthopper AT shenyan acomprehensiveomicsanalysisandfunctionalsurveyofcuticularproteinsinthebrownplanthopper AT moussianbernard acomprehensiveomicsanalysisandfunctionalsurveyofcuticularproteinsinthebrownplanthopper AT zhangchuanxi acomprehensiveomicsanalysisandfunctionalsurveyofcuticularproteinsinthebrownplanthopper AT panpenglu comprehensiveomicsanalysisandfunctionalsurveyofcuticularproteinsinthebrownplanthopper AT yeyuxuan comprehensiveomicsanalysisandfunctionalsurveyofcuticularproteinsinthebrownplanthopper AT louyihan comprehensiveomicsanalysisandfunctionalsurveyofcuticularproteinsinthebrownplanthopper AT lujiabao comprehensiveomicsanalysisandfunctionalsurveyofcuticularproteinsinthebrownplanthopper AT chengchen comprehensiveomicsanalysisandfunctionalsurveyofcuticularproteinsinthebrownplanthopper AT shenyan comprehensiveomicsanalysisandfunctionalsurveyofcuticularproteinsinthebrownplanthopper AT moussianbernard comprehensiveomicsanalysisandfunctionalsurveyofcuticularproteinsinthebrownplanthopper AT zhangchuanxi comprehensiveomicsanalysisandfunctionalsurveyofcuticularproteinsinthebrownplanthopper |