Ecdysone receptor isoforms play distinct roles in larval–pupal–adult transition in Leptinotarsa decemlineata
A heterodimer of two nuclear receptors, ecdysone receptor (EcR) and ultraspiracle, mediates 20‐hydroxyecdysone (20E) signaling to modulate many aspects in insect life, such as molting and metamorphosis, reproduction, diapause and innate immunity. In the present paper, we intended to determine the is...
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description | A heterodimer of two nuclear receptors, ecdysone receptor (EcR) and ultraspiracle, mediates 20‐hydroxyecdysone (20E) signaling to modulate many aspects in insect life, such as molting and metamorphosis, reproduction, diapause and innate immunity. In the present paper, we intended to determine the isoform‐specific roles of EcR during larval–pupal–adult transition in the Colorado potato beetle. Double‐stranded RNAs (dsRNAs) were prepared using the common (dsEcR) or isoform‐specific (dsEcRA, dsEcRB1) regions of EcR as templates. Ingestion of either dsEcR or dsEcRA, rather than dsEcRB1, by the penultimate (3rd) and final (4th) instar larvae caused failure of larval–pupal and pupal–adult ecdysis. The RNA interference (RNAi) larvae remained as prepupae, or became deformed pupae and adults. Determination of messenger RNA (mRNA) levels of EcR isoforms found that LdEcRA regulates the expression of LdEcRB1. Moreover, silencing the two EcR transcripts, LdEcRA or LdEcRB1 reduced the mRNA levels of Ldspo and Ldsad, and lowered 20E titer. In contrast, the expression levels of HR3, HR4, E74 and E75 were significantly decreased in the LdEcR or LdEcRA RNAi larvae, but not in LdEcRB1 depleted specimens. Dietary supplement with 20E did not restore the expression of five 20E signaling genes (USP, HR3, HR4, E74 and E75), and only partially alleviated the pupation defects in dsEcR‐ or dsEcRA‐fed beetles. These data suggest that EcR plays isoform‐specific roles in the regulation of ecdysteroidogenesis and the transduction of 20E signal in L. decemlineata. |
doi_str_mv | 10.1111/1744-7917.12662 |
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In the present paper, we intended to determine the isoform‐specific roles of EcR during larval–pupal–adult transition in the Colorado potato beetle. Double‐stranded RNAs (dsRNAs) were prepared using the common (dsEcR) or isoform‐specific (dsEcRA, dsEcRB1) regions of EcR as templates. Ingestion of either dsEcR or dsEcRA, rather than dsEcRB1, by the penultimate (3rd) and final (4th) instar larvae caused failure of larval–pupal and pupal–adult ecdysis. The RNA interference (RNAi) larvae remained as prepupae, or became deformed pupae and adults. Determination of messenger RNA (mRNA) levels of EcR isoforms found that LdEcRA regulates the expression of LdEcRB1. Moreover, silencing the two EcR transcripts, LdEcRA or LdEcRB1 reduced the mRNA levels of Ldspo and Ldsad, and lowered 20E titer. In contrast, the expression levels of HR3, HR4, E74 and E75 were significantly decreased in the LdEcR or LdEcRA RNAi larvae, but not in LdEcRB1 depleted specimens. Dietary supplement with 20E did not restore the expression of five 20E signaling genes (USP, HR3, HR4, E74 and E75), and only partially alleviated the pupation defects in dsEcR‐ or dsEcRA‐fed beetles. These data suggest that EcR plays isoform‐specific roles in the regulation of ecdysteroidogenesis and the transduction of 20E signal in L. decemlineata.</description><identifier>ISSN: 1672-9609</identifier><identifier>EISSN: 1744-7917</identifier><identifier>DOI: 10.1111/1744-7917.12662</identifier><identifier>PMID: 30688001</identifier><language>eng</language><publisher>Australia: Wiley Subscription Services, Inc</publisher><subject>Beetles ; Diapause ; Diet ; Dietary supplements ; Ecdysone ; ecdysone receptor ; Gene expression ; Ingestion ; Innate immunity ; Insects ; Isoforms ; Larvae ; Leptinotarsa decemlineata ; Metamorphosis ; Molting ; Nuclear receptors ; Original ; Potatoes ; Prepupae ; Pupation ; Receptors ; Ribonucleic acid ; RNA ; RNA interference ; RNA-mediated interference ; Signal transduction ; Signaling</subject><ispartof>Insect science, 2020-06, Vol.27 (3), p.487-499</ispartof><rights>2019 Institute of Zoology, Chinese Academy of Sciences</rights><rights>2019 Institute of Zoology, Chinese Academy of Sciences.</rights><rights>2019. 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In the present paper, we intended to determine the isoform‐specific roles of EcR during larval–pupal–adult transition in the Colorado potato beetle. Double‐stranded RNAs (dsRNAs) were prepared using the common (dsEcR) or isoform‐specific (dsEcRA, dsEcRB1) regions of EcR as templates. Ingestion of either dsEcR or dsEcRA, rather than dsEcRB1, by the penultimate (3rd) and final (4th) instar larvae caused failure of larval–pupal and pupal–adult ecdysis. The RNA interference (RNAi) larvae remained as prepupae, or became deformed pupae and adults. Determination of messenger RNA (mRNA) levels of EcR isoforms found that LdEcRA regulates the expression of LdEcRB1. Moreover, silencing the two EcR transcripts, LdEcRA or LdEcRB1 reduced the mRNA levels of Ldspo and Ldsad, and lowered 20E titer. In contrast, the expression levels of HR3, HR4, E74 and E75 were significantly decreased in the LdEcR or LdEcRA RNAi larvae, but not in LdEcRB1 depleted specimens. Dietary supplement with 20E did not restore the expression of five 20E signaling genes (USP, HR3, HR4, E74 and E75), and only partially alleviated the pupation defects in dsEcR‐ or dsEcRA‐fed beetles. These data suggest that EcR plays isoform‐specific roles in the regulation of ecdysteroidogenesis and the transduction of 20E signal in L. decemlineata.</description><subject>Beetles</subject><subject>Diapause</subject><subject>Diet</subject><subject>Dietary supplements</subject><subject>Ecdysone</subject><subject>ecdysone receptor</subject><subject>Gene expression</subject><subject>Ingestion</subject><subject>Innate immunity</subject><subject>Insects</subject><subject>Isoforms</subject><subject>Larvae</subject><subject>Leptinotarsa decemlineata</subject><subject>Metamorphosis</subject><subject>Molting</subject><subject>Nuclear receptors</subject><subject>Original</subject><subject>Potatoes</subject><subject>Prepupae</subject><subject>Pupation</subject><subject>Receptors</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA interference</subject><subject>RNA-mediated interference</subject><subject>Signal transduction</subject><subject>Signaling</subject><issn>1672-9609</issn><issn>1744-7917</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><recordid>eNqFkU9vFCEYh4nR2Lp69mZIvHjZln87DBcT01RtstGDeiYs86I0DIzA1OzN7-A39JPIdOtGvcgFAg9Pfm9-CD2l5Iy2dU6lEGupqDyjrOvYPXR6vLnfzp1ka9URdYIelXJNCFdMsYfohJOu7wmhp2i6tMO-pAg4g4Wppox9SS7lseApmD0efKk-2opzClCwjziYfGPCz-8_pnm63c0wh4prNrH46lNcoG1z-ZiqycXgoanH4COYah6jB86EAk_u9hX69Pry48Xb9fb9m6uLV9u1FUtqBzsgVjjGe-ekIz0TwDduIAZ62tIzPlhlZCd2hktmd5b3BKy0bMMGtjGWr9DLg3eadyMMFmILGPSU_WjyXifj9d8v0X_Rn9ONlkxKIlgTvLgT5PR1hlL16IuFEEyENBfNqFRC8K5XDX3-D3qd5hzbeJpxJbiSS-AVOj9QNqdSMrhjGEr00qZeutNLd_q2zfbj2Z8zHPnf9TVgcwC--QD7__n01bsPB_EvqTCvMw</recordid><startdate>202006</startdate><enddate>202006</enddate><creator>Xu, Qing‐Yu</creator><creator>Deng, Pan</creator><creator>Zhang, Qiong</creator><creator>Li, Ang</creator><creator>Fu, Kai‐Yun</creator><creator>Guo, Wen‐Chao</creator><creator>Li, Guo‐Qing</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-7449-8433</orcidid></search><sort><creationdate>202006</creationdate><title>Ecdysone receptor isoforms play distinct roles in larval–pupal–adult transition in Leptinotarsa decemlineata</title><author>Xu, Qing‐Yu ; Deng, Pan ; Zhang, Qiong ; Li, Ang ; Fu, Kai‐Yun ; Guo, Wen‐Chao ; Li, Guo‐Qing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4672-febe0c4f238ff7f0824e35fd0ae8106823dc9a764ba372cbc380ec7c252d25ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Beetles</topic><topic>Diapause</topic><topic>Diet</topic><topic>Dietary supplements</topic><topic>Ecdysone</topic><topic>ecdysone receptor</topic><topic>Gene expression</topic><topic>Ingestion</topic><topic>Innate immunity</topic><topic>Insects</topic><topic>Isoforms</topic><topic>Larvae</topic><topic>Leptinotarsa decemlineata</topic><topic>Metamorphosis</topic><topic>Molting</topic><topic>Nuclear receptors</topic><topic>Original</topic><topic>Potatoes</topic><topic>Prepupae</topic><topic>Pupation</topic><topic>Receptors</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>RNA interference</topic><topic>RNA-mediated interference</topic><topic>Signal transduction</topic><topic>Signaling</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Qing‐Yu</creatorcontrib><creatorcontrib>Deng, Pan</creatorcontrib><creatorcontrib>Zhang, Qiong</creatorcontrib><creatorcontrib>Li, Ang</creatorcontrib><creatorcontrib>Fu, Kai‐Yun</creatorcontrib><creatorcontrib>Guo, Wen‐Chao</creatorcontrib><creatorcontrib>Li, Guo‐Qing</creatorcontrib><collection>Wiley Online Library (Open Access Collection)</collection><collection>Wiley Online Library (Open Access Collection)</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Insect science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Qing‐Yu</au><au>Deng, Pan</au><au>Zhang, Qiong</au><au>Li, Ang</au><au>Fu, Kai‐Yun</au><au>Guo, Wen‐Chao</au><au>Li, Guo‐Qing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ecdysone receptor isoforms play distinct roles in larval–pupal–adult transition in Leptinotarsa decemlineata</atitle><jtitle>Insect science</jtitle><addtitle>Insect Sci</addtitle><date>2020-06</date><risdate>2020</risdate><volume>27</volume><issue>3</issue><spage>487</spage><epage>499</epage><pages>487-499</pages><issn>1672-9609</issn><eissn>1744-7917</eissn><abstract>A heterodimer of two nuclear receptors, ecdysone receptor (EcR) and ultraspiracle, mediates 20‐hydroxyecdysone (20E) signaling to modulate many aspects in insect life, such as molting and metamorphosis, reproduction, diapause and innate immunity. In the present paper, we intended to determine the isoform‐specific roles of EcR during larval–pupal–adult transition in the Colorado potato beetle. Double‐stranded RNAs (dsRNAs) were prepared using the common (dsEcR) or isoform‐specific (dsEcRA, dsEcRB1) regions of EcR as templates. Ingestion of either dsEcR or dsEcRA, rather than dsEcRB1, by the penultimate (3rd) and final (4th) instar larvae caused failure of larval–pupal and pupal–adult ecdysis. The RNA interference (RNAi) larvae remained as prepupae, or became deformed pupae and adults. Determination of messenger RNA (mRNA) levels of EcR isoforms found that LdEcRA regulates the expression of LdEcRB1. Moreover, silencing the two EcR transcripts, LdEcRA or LdEcRB1 reduced the mRNA levels of Ldspo and Ldsad, and lowered 20E titer. In contrast, the expression levels of HR3, HR4, E74 and E75 were significantly decreased in the LdEcR or LdEcRA RNAi larvae, but not in LdEcRB1 depleted specimens. Dietary supplement with 20E did not restore the expression of five 20E signaling genes (USP, HR3, HR4, E74 and E75), and only partially alleviated the pupation defects in dsEcR‐ or dsEcRA‐fed beetles. These data suggest that EcR plays isoform‐specific roles in the regulation of ecdysteroidogenesis and the transduction of 20E signal in L. decemlineata.</abstract><cop>Australia</cop><pub>Wiley Subscription Services, Inc</pub><pmid>30688001</pmid><doi>10.1111/1744-7917.12662</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-7449-8433</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Beetles Diapause Diet Dietary supplements Ecdysone ecdysone receptor Gene expression Ingestion Innate immunity Insects Isoforms Larvae Leptinotarsa decemlineata Metamorphosis Molting Nuclear receptors Original Potatoes Prepupae Pupation Receptors Ribonucleic acid RNA RNA interference RNA-mediated interference Signal transduction Signaling |
title | Ecdysone receptor isoforms play distinct roles in larval–pupal–adult transition in Leptinotarsa decemlineata |
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