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Role of juvenile hormone receptor Methoprene-tolerant 1 in silkworm larval brain development and domestication
The insect brain is the central part of the neurosecretory system, which controls morphology, physiology, and behavior during the insect’s lifecycle. Lepidoptera are holometabolous insects, and their brains develop during the larval period and metamorphosis into the adult form. As the only fully dom...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Science Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455460/ https://www.ncbi.nlm.nih.gov/pubmed/34472225 http://dx.doi.org/10.24272/j.issn.2095-8137.2021.126 |
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author | Cui, Yong Liu, Zu-Lian Li, Cen-Cen Wei, Xiang-Min Lin, Yong-Jian You, Lang Zhu, Zi-Dan Deng, Hui-Min Feng, Qi-Li Huang, Yong-Ping Xiang, Hui |
author_facet | Cui, Yong Liu, Zu-Lian Li, Cen-Cen Wei, Xiang-Min Lin, Yong-Jian You, Lang Zhu, Zi-Dan Deng, Hui-Min Feng, Qi-Li Huang, Yong-Ping Xiang, Hui |
author_sort | Cui, Yong |
collection | PubMed |
description | The insect brain is the central part of the neurosecretory system, which controls morphology, physiology, and behavior during the insect’s lifecycle. Lepidoptera are holometabolous insects, and their brains develop during the larval period and metamorphosis into the adult form. As the only fully domesticated insect, the Lepidoptera silkworm Bombyx mori experienced changes in larval brain morphology and certain behaviors during the domestication process. Hormonal regulation in insects is a key factor in multiple processes. However, how juvenile hormone (JH) signals regulate brain development in Lepidoptera species, especially in the larval stage, remains elusive. We recently identified the JH receptor Methoprene tolerant 1 (Met1) as a putative domestication gene. How artificial selection on Met1 impacts brain and behavioral domestication is another important issue addressing Darwin’s theory on domestication. Here, CRISPR/Cas9-mediated knockout of Bombyx Met1 caused developmental retardation in the brain, unlike precocious pupation of the cuticle. At the whole transcriptome level, the ecdysteroid (20-hydroxyecdysone, 20E) signaling and downstream pathways were overactivated in the mutant cuticle but not in the brain. Pathways related to cell proliferation and specialization processes, such as extracellular matrix (ECM)-receptor interaction and tyrosine metabolism pathways, were suppressed in the brain. Molecular evolutionary analysis and in vitro assay identified an amino acid replacement located in a novel motif under positive selection in B. mori, which decreased transcriptional binding activity. The B. mori MET1 protein showed a changed structure and dynamic features, as well as a weakened co-expression gene network, compared with B. mandarina. Based on comparative transcriptomic analyses, we proposed a pathway downstream of JH signaling (i.e., tyrosine metabolism pathway) that likely contributed to silkworm larval brain development and domestication and highlighted the importance of the biogenic amine system in larval evolution during silkworm domestication. |
format | Online Article Text |
id | pubmed-8455460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Science Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-84554602021-09-22 Role of juvenile hormone receptor Methoprene-tolerant 1 in silkworm larval brain development and domestication Cui, Yong Liu, Zu-Lian Li, Cen-Cen Wei, Xiang-Min Lin, Yong-Jian You, Lang Zhu, Zi-Dan Deng, Hui-Min Feng, Qi-Li Huang, Yong-Ping Xiang, Hui Zool Res Article The insect brain is the central part of the neurosecretory system, which controls morphology, physiology, and behavior during the insect’s lifecycle. Lepidoptera are holometabolous insects, and their brains develop during the larval period and metamorphosis into the adult form. As the only fully domesticated insect, the Lepidoptera silkworm Bombyx mori experienced changes in larval brain morphology and certain behaviors during the domestication process. Hormonal regulation in insects is a key factor in multiple processes. However, how juvenile hormone (JH) signals regulate brain development in Lepidoptera species, especially in the larval stage, remains elusive. We recently identified the JH receptor Methoprene tolerant 1 (Met1) as a putative domestication gene. How artificial selection on Met1 impacts brain and behavioral domestication is another important issue addressing Darwin’s theory on domestication. Here, CRISPR/Cas9-mediated knockout of Bombyx Met1 caused developmental retardation in the brain, unlike precocious pupation of the cuticle. At the whole transcriptome level, the ecdysteroid (20-hydroxyecdysone, 20E) signaling and downstream pathways were overactivated in the mutant cuticle but not in the brain. Pathways related to cell proliferation and specialization processes, such as extracellular matrix (ECM)-receptor interaction and tyrosine metabolism pathways, were suppressed in the brain. Molecular evolutionary analysis and in vitro assay identified an amino acid replacement located in a novel motif under positive selection in B. mori, which decreased transcriptional binding activity. The B. mori MET1 protein showed a changed structure and dynamic features, as well as a weakened co-expression gene network, compared with B. mandarina. Based on comparative transcriptomic analyses, we proposed a pathway downstream of JH signaling (i.e., tyrosine metabolism pathway) that likely contributed to silkworm larval brain development and domestication and highlighted the importance of the biogenic amine system in larval evolution during silkworm domestication. Science Press 2021-09-18 /pmc/articles/PMC8455460/ /pubmed/34472225 http://dx.doi.org/10.24272/j.issn.2095-8137.2021.126 Text en Editorial Office of Zoological Research, Kunming Institute of Zoology, Chinese Academy of Sciences https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Cui, Yong Liu, Zu-Lian Li, Cen-Cen Wei, Xiang-Min Lin, Yong-Jian You, Lang Zhu, Zi-Dan Deng, Hui-Min Feng, Qi-Li Huang, Yong-Ping Xiang, Hui Role of juvenile hormone receptor Methoprene-tolerant 1 in silkworm larval brain development and domestication |
title | Role of juvenile hormone receptor Methoprene-tolerant 1 in silkworm larval brain development and domestication
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title_full | Role of juvenile hormone receptor Methoprene-tolerant 1 in silkworm larval brain development and domestication
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title_fullStr | Role of juvenile hormone receptor Methoprene-tolerant 1 in silkworm larval brain development and domestication
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title_full_unstemmed | Role of juvenile hormone receptor Methoprene-tolerant 1 in silkworm larval brain development and domestication
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title_short | Role of juvenile hormone receptor Methoprene-tolerant 1 in silkworm larval brain development and domestication
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title_sort | role of juvenile hormone receptor methoprene-tolerant 1 in silkworm larval brain development and domestication |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455460/ https://www.ncbi.nlm.nih.gov/pubmed/34472225 http://dx.doi.org/10.24272/j.issn.2095-8137.2021.126 |
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