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The histone deacetylase NlHDAC1 regulates both female and male fertility in the brown planthopper, Nilaparvata lugens

Histone acetylation is a specific type of chromatin modification that serves as a key regulatory mechanism for many cellular processes in mammals. However, little is known about its biological function in invertebrates. Here, we identified 12 members of histone deacetylases (NlHDACs) in the brown pl...

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Autores principales: Zhang, Jin-Li, Yuan, Xiao-Bo, Chen, Sun-Jie, Chen, Hao-Hao, Xu, Nan, Xue, Wen-Hua, Fu, Sheng-Jie, Zhang, Chuan-Xi, Xu, Hai-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303786/
https://www.ncbi.nlm.nih.gov/pubmed/30977704
http://dx.doi.org/10.1098/rsob.180158
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author Zhang, Jin-Li
Yuan, Xiao-Bo
Chen, Sun-Jie
Chen, Hao-Hao
Xu, Nan
Xue, Wen-Hua
Fu, Sheng-Jie
Zhang, Chuan-Xi
Xu, Hai-Jun
author_facet Zhang, Jin-Li
Yuan, Xiao-Bo
Chen, Sun-Jie
Chen, Hao-Hao
Xu, Nan
Xue, Wen-Hua
Fu, Sheng-Jie
Zhang, Chuan-Xi
Xu, Hai-Jun
author_sort Zhang, Jin-Li
collection PubMed
description Histone acetylation is a specific type of chromatin modification that serves as a key regulatory mechanism for many cellular processes in mammals. However, little is known about its biological function in invertebrates. Here, we identified 12 members of histone deacetylases (NlHDACs) in the brown planthopper (BPH), Nilaparvata lugens. RNAi-mediated silencing assay showed that NlHdac1, NlHdac3 and NlHdac4 played critical roles in female fertility via regulating ovary maturation or ovipositor development. Silencing of NlHdac1 substantially increased acetylation level of histones H3 and H4 in ovaries, indicating NlHDAC1 is the main histone deacetylase in ovaries of BPH. RNA sequencing (RNA-seq) analysis showed that knockdown of NlHdac1 impaired ovary development via multiple signalling pathways including the TOR pathway. Acoustic recording showed that males with NlHdac1 knockdown failed to make courtship songs, and thus were unacceptable to wild-type females, resulting in unfertilized eggs. Competition mating assay showed that wild-type females overwhelmingly preferred to mate with control males over NlHdac1-knockdown males. These findings improve our understanding of reproductive strategies controlled by HDACs in insects and provide a potential target for pest control.
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spelling pubmed-63037862019-01-18 The histone deacetylase NlHDAC1 regulates both female and male fertility in the brown planthopper, Nilaparvata lugens Zhang, Jin-Li Yuan, Xiao-Bo Chen, Sun-Jie Chen, Hao-Hao Xu, Nan Xue, Wen-Hua Fu, Sheng-Jie Zhang, Chuan-Xi Xu, Hai-Jun Open Biol Research Histone acetylation is a specific type of chromatin modification that serves as a key regulatory mechanism for many cellular processes in mammals. However, little is known about its biological function in invertebrates. Here, we identified 12 members of histone deacetylases (NlHDACs) in the brown planthopper (BPH), Nilaparvata lugens. RNAi-mediated silencing assay showed that NlHdac1, NlHdac3 and NlHdac4 played critical roles in female fertility via regulating ovary maturation or ovipositor development. Silencing of NlHdac1 substantially increased acetylation level of histones H3 and H4 in ovaries, indicating NlHDAC1 is the main histone deacetylase in ovaries of BPH. RNA sequencing (RNA-seq) analysis showed that knockdown of NlHdac1 impaired ovary development via multiple signalling pathways including the TOR pathway. Acoustic recording showed that males with NlHdac1 knockdown failed to make courtship songs, and thus were unacceptable to wild-type females, resulting in unfertilized eggs. Competition mating assay showed that wild-type females overwhelmingly preferred to mate with control males over NlHdac1-knockdown males. These findings improve our understanding of reproductive strategies controlled by HDACs in insects and provide a potential target for pest control. The Royal Society 2018-12-12 /pmc/articles/PMC6303786/ /pubmed/30977704 http://dx.doi.org/10.1098/rsob.180158 Text en © 2018 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Research
Zhang, Jin-Li
Yuan, Xiao-Bo
Chen, Sun-Jie
Chen, Hao-Hao
Xu, Nan
Xue, Wen-Hua
Fu, Sheng-Jie
Zhang, Chuan-Xi
Xu, Hai-Jun
The histone deacetylase NlHDAC1 regulates both female and male fertility in the brown planthopper, Nilaparvata lugens
title The histone deacetylase NlHDAC1 regulates both female and male fertility in the brown planthopper, Nilaparvata lugens
title_full The histone deacetylase NlHDAC1 regulates both female and male fertility in the brown planthopper, Nilaparvata lugens
title_fullStr The histone deacetylase NlHDAC1 regulates both female and male fertility in the brown planthopper, Nilaparvata lugens
title_full_unstemmed The histone deacetylase NlHDAC1 regulates both female and male fertility in the brown planthopper, Nilaparvata lugens
title_short The histone deacetylase NlHDAC1 regulates both female and male fertility in the brown planthopper, Nilaparvata lugens
title_sort histone deacetylase nlhdac1 regulates both female and male fertility in the brown planthopper, nilaparvata lugens
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303786/
https://www.ncbi.nlm.nih.gov/pubmed/30977704
http://dx.doi.org/10.1098/rsob.180158
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