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Regulation of olfactory-based sex behaviors in the silkworm by genes in the sex-determination cascade
Insect courtship and mating depend on integration of olfactory, visual, and tactile cues. Compared to other insects, Bombyx mori, the domesticated silkworm, has relatively simple sexual behaviors as it cannot fly. Here by using CRISPR/Cas9 and electrophysiological techniques we found that courtship...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7307793/ https://www.ncbi.nlm.nih.gov/pubmed/32520935 http://dx.doi.org/10.1371/journal.pgen.1008622 |
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author | Xu, Jun Liu, Wei Yang, Dehong Chen, Shuqing Chen, Kai Liu, Zulian Yang, Xu Meng, Jing Zhu, Guanheng Dong, Shuanglin Zhang, Yong Zhan, Shuai Wang, Guirong Huang, Yongping |
author_facet | Xu, Jun Liu, Wei Yang, Dehong Chen, Shuqing Chen, Kai Liu, Zulian Yang, Xu Meng, Jing Zhu, Guanheng Dong, Shuanglin Zhang, Yong Zhan, Shuai Wang, Guirong Huang, Yongping |
author_sort | Xu, Jun |
collection | PubMed |
description | Insect courtship and mating depend on integration of olfactory, visual, and tactile cues. Compared to other insects, Bombyx mori, the domesticated silkworm, has relatively simple sexual behaviors as it cannot fly. Here by using CRISPR/Cas9 and electrophysiological techniques we found that courtship and mating behaviors are regulated in male silk moths by mutating genes in the sex determination cascade belonging to two conserved pathways. Loss of Bmdsx gene expression significantly reduced the peripheral perception of the major pheromone component bombykol by reducing expression of the product of the BmOR1 gene which completely blocked courtship in adult males. Interestingly, we found that mating behavior was regulated independently by another sexual differentiation gene, Bmfru. Loss of Bmfru completely blocked mating, but males displayed normal courtship behavior. Lack of Bmfru expression significantly reduced the perception of the minor pheromone component bombykal due to the down regulation of BmOR3 expression; further, functional analysis revealed that loss of the product of BmOR3 played a key role in terminating male mating behavior. Our results suggest that Bmdsx and Bmfru are at the base of the two primary pathways that regulate olfactory-based sexual behavior. |
format | Online Article Text |
id | pubmed-7307793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-73077932020-06-25 Regulation of olfactory-based sex behaviors in the silkworm by genes in the sex-determination cascade Xu, Jun Liu, Wei Yang, Dehong Chen, Shuqing Chen, Kai Liu, Zulian Yang, Xu Meng, Jing Zhu, Guanheng Dong, Shuanglin Zhang, Yong Zhan, Shuai Wang, Guirong Huang, Yongping PLoS Genet Research Article Insect courtship and mating depend on integration of olfactory, visual, and tactile cues. Compared to other insects, Bombyx mori, the domesticated silkworm, has relatively simple sexual behaviors as it cannot fly. Here by using CRISPR/Cas9 and electrophysiological techniques we found that courtship and mating behaviors are regulated in male silk moths by mutating genes in the sex determination cascade belonging to two conserved pathways. Loss of Bmdsx gene expression significantly reduced the peripheral perception of the major pheromone component bombykol by reducing expression of the product of the BmOR1 gene which completely blocked courtship in adult males. Interestingly, we found that mating behavior was regulated independently by another sexual differentiation gene, Bmfru. Loss of Bmfru completely blocked mating, but males displayed normal courtship behavior. Lack of Bmfru expression significantly reduced the perception of the minor pheromone component bombykal due to the down regulation of BmOR3 expression; further, functional analysis revealed that loss of the product of BmOR3 played a key role in terminating male mating behavior. Our results suggest that Bmdsx and Bmfru are at the base of the two primary pathways that regulate olfactory-based sexual behavior. Public Library of Science 2020-06-10 /pmc/articles/PMC7307793/ /pubmed/32520935 http://dx.doi.org/10.1371/journal.pgen.1008622 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, Jun Liu, Wei Yang, Dehong Chen, Shuqing Chen, Kai Liu, Zulian Yang, Xu Meng, Jing Zhu, Guanheng Dong, Shuanglin Zhang, Yong Zhan, Shuai Wang, Guirong Huang, Yongping Regulation of olfactory-based sex behaviors in the silkworm by genes in the sex-determination cascade |
title | Regulation of olfactory-based sex behaviors in the silkworm by genes in the sex-determination cascade |
title_full | Regulation of olfactory-based sex behaviors in the silkworm by genes in the sex-determination cascade |
title_fullStr | Regulation of olfactory-based sex behaviors in the silkworm by genes in the sex-determination cascade |
title_full_unstemmed | Regulation of olfactory-based sex behaviors in the silkworm by genes in the sex-determination cascade |
title_short | Regulation of olfactory-based sex behaviors in the silkworm by genes in the sex-determination cascade |
title_sort | regulation of olfactory-based sex behaviors in the silkworm by genes in the sex-determination cascade |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7307793/ https://www.ncbi.nlm.nih.gov/pubmed/32520935 http://dx.doi.org/10.1371/journal.pgen.1008622 |
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