Analysis of the Gene Expression and RNAi-Mediated Knockdown of Chitin Synthase from Leaf-Cutting Ant Atta sexdens

Detalhes bibliográficos
Autor(a) principal: Moreira, Ariele C.
Data de Publicação: 2020
Outros Autores: Carneiro, Renato L., Fracola, Mariana F., Micocci, Kelli C. [UNESP], Bueno, Odair C. [UNESP], Souza, Dulce H. F.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.21577/0103-5053.20200098
http://hdl.handle.net/11449/209546
Resumo: Chitin synthase (CHS) is the enzyme specifically associated with chitin synthesis, an important component of diverse organisms including insects. Two alternative spliced transcripts of the CHS gene (AsCHS-A1 and AsCHS-A2) were identified by quantitative reverse-transcription polymerase chain reaction (RT-qPCR) during the development of the leaf-cutting ant Ana sermons. Expression profiles of AsCHS-A transcripts increased from larva to pupae and decay in workers. Phylogenetic analysis showed both transcripts are classified within class A insect CASs. AsCI IS-A1 showed the highest expression level in larvae and pupae, while AsCHS-A2 is the main CHS transcript in workers. Our results suggest that these variants should be under regulation of different promoters. AsCHS-A1 has topology expected for insect CHSs, while the predicted AsCHS-A2 topology. with a missing A domain, is similar to some fungal CHSs. CHS-B (class B) was not identified in A. sexdens transcriptome. Ribonucleic acid interference (RNAi)-mediated gene silencing in pupae revealed that low reduction in CHS transcript levels (18%) was enough to cause morphological changes in the pupa exoskeleton impairing the process of cuticle sclerotization. To our knowledge, this work was the first to use and to show the feasibility of using RNA interference techniques on leaf-cutting ants.
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spelling Analysis of the Gene Expression and RNAi-Mediated Knockdown of Chitin Synthase from Leaf-Cutting Ant Atta sexdensleaf-cutting antchitin synthase (CHS)CHS gene expressionRNAi-mediated knockdownCHS insect topologyChitin synthase (CHS) is the enzyme specifically associated with chitin synthesis, an important component of diverse organisms including insects. Two alternative spliced transcripts of the CHS gene (AsCHS-A1 and AsCHS-A2) were identified by quantitative reverse-transcription polymerase chain reaction (RT-qPCR) during the development of the leaf-cutting ant Ana sermons. Expression profiles of AsCHS-A transcripts increased from larva to pupae and decay in workers. Phylogenetic analysis showed both transcripts are classified within class A insect CASs. AsCI IS-A1 showed the highest expression level in larvae and pupae, while AsCHS-A2 is the main CHS transcript in workers. Our results suggest that these variants should be under regulation of different promoters. AsCHS-A1 has topology expected for insect CHSs, while the predicted AsCHS-A2 topology. with a missing A domain, is similar to some fungal CHSs. CHS-B (class B) was not identified in A. sexdens transcriptome. Ribonucleic acid interference (RNAi)-mediated gene silencing in pupae revealed that low reduction in CHS transcript levels (18%) was enough to cause morphological changes in the pupa exoskeleton impairing the process of cuticle sclerotization. To our knowledge, this work was the first to use and to show the feasibility of using RNA interference techniques on leaf-cutting ants.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Univ Fed Sao Carlos, Dept Quim, BR-13565905 Sao Carlos, SP, BrazilUniv Fed Sao Carlos, Dept Fis Quim & Matemat, BR-18052780 Sorocaba, SP, BrazilUniv Estadual Paulista, Ctr Estudos Insetos Sociais, BR-13506900 Rio Claro, SP, BrazilUniv Estadual Paulista, Ctr Estudos Insetos Sociais, BR-13506900 Rio Claro, SP, BrazilCNPq: 160662/2013-3FAPESP: 2014/12169-2FAPESP: 2012/25299-6FAPESP: 2017/06198-8CAPES: 001Soc Brasileira QuimicaUniversidade Federal de São Carlos (UFSCar)Universidade Estadual Paulista (Unesp)Moreira, Ariele C.Carneiro, Renato L.Fracola, Mariana F.Micocci, Kelli C. [UNESP]Bueno, Odair C. [UNESP]Souza, Dulce H. F.2021-06-25T12:21:52Z2021-06-25T12:21:52Z2020-10-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1979-1990application/pdfhttp://dx.doi.org/10.21577/0103-5053.20200098Journal Of The Brazilian Chemical Society. Sao Paulo: Soc Brasileira Quimica, v. 31, n. 10, p. 1979-1990, 2020.0103-5053http://hdl.handle.net/11449/20954610.21577/0103-5053.20200098S0103-50532020001001979WOS:000577634100003S0103-50532020001001979.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal Of The Brazilian Chemical Societyinfo:eu-repo/semantics/openAccess2024-04-11T14:57:01Zoai:repositorio.unesp.br:11449/209546Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T14:33:44.648452Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Analysis of the Gene Expression and RNAi-Mediated Knockdown of Chitin Synthase from Leaf-Cutting Ant Atta sexdens
title Analysis of the Gene Expression and RNAi-Mediated Knockdown of Chitin Synthase from Leaf-Cutting Ant Atta sexdens
spellingShingle Analysis of the Gene Expression and RNAi-Mediated Knockdown of Chitin Synthase from Leaf-Cutting Ant Atta sexdens
Moreira, Ariele C.
leaf-cutting ant
chitin synthase (CHS)
CHS gene expression
RNAi-mediated knockdown
CHS insect topology
title_short Analysis of the Gene Expression and RNAi-Mediated Knockdown of Chitin Synthase from Leaf-Cutting Ant Atta sexdens
title_full Analysis of the Gene Expression and RNAi-Mediated Knockdown of Chitin Synthase from Leaf-Cutting Ant Atta sexdens
title_fullStr Analysis of the Gene Expression and RNAi-Mediated Knockdown of Chitin Synthase from Leaf-Cutting Ant Atta sexdens
title_full_unstemmed Analysis of the Gene Expression and RNAi-Mediated Knockdown of Chitin Synthase from Leaf-Cutting Ant Atta sexdens
title_sort Analysis of the Gene Expression and RNAi-Mediated Knockdown of Chitin Synthase from Leaf-Cutting Ant Atta sexdens
author Moreira, Ariele C.
author_facet Moreira, Ariele C.
Carneiro, Renato L.
Fracola, Mariana F.
Micocci, Kelli C. [UNESP]
Bueno, Odair C. [UNESP]
Souza, Dulce H. F.
author_role author
author2 Carneiro, Renato L.
Fracola, Mariana F.
Micocci, Kelli C. [UNESP]
Bueno, Odair C. [UNESP]
Souza, Dulce H. F.
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Carlos (UFSCar)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Moreira, Ariele C.
Carneiro, Renato L.
Fracola, Mariana F.
Micocci, Kelli C. [UNESP]
Bueno, Odair C. [UNESP]
Souza, Dulce H. F.
dc.subject.por.fl_str_mv leaf-cutting ant
chitin synthase (CHS)
CHS gene expression
RNAi-mediated knockdown
CHS insect topology
topic leaf-cutting ant
chitin synthase (CHS)
CHS gene expression
RNAi-mediated knockdown
CHS insect topology
description Chitin synthase (CHS) is the enzyme specifically associated with chitin synthesis, an important component of diverse organisms including insects. Two alternative spliced transcripts of the CHS gene (AsCHS-A1 and AsCHS-A2) were identified by quantitative reverse-transcription polymerase chain reaction (RT-qPCR) during the development of the leaf-cutting ant Ana sermons. Expression profiles of AsCHS-A transcripts increased from larva to pupae and decay in workers. Phylogenetic analysis showed both transcripts are classified within class A insect CASs. AsCI IS-A1 showed the highest expression level in larvae and pupae, while AsCHS-A2 is the main CHS transcript in workers. Our results suggest that these variants should be under regulation of different promoters. AsCHS-A1 has topology expected for insect CHSs, while the predicted AsCHS-A2 topology. with a missing A domain, is similar to some fungal CHSs. CHS-B (class B) was not identified in A. sexdens transcriptome. Ribonucleic acid interference (RNAi)-mediated gene silencing in pupae revealed that low reduction in CHS transcript levels (18%) was enough to cause morphological changes in the pupa exoskeleton impairing the process of cuticle sclerotization. To our knowledge, this work was the first to use and to show the feasibility of using RNA interference techniques on leaf-cutting ants.
publishDate 2020
dc.date.none.fl_str_mv 2020-10-01
2021-06-25T12:21:52Z
2021-06-25T12:21:52Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.21577/0103-5053.20200098
Journal Of The Brazilian Chemical Society. Sao Paulo: Soc Brasileira Quimica, v. 31, n. 10, p. 1979-1990, 2020.
0103-5053
http://hdl.handle.net/11449/209546
10.21577/0103-5053.20200098
S0103-50532020001001979
WOS:000577634100003
S0103-50532020001001979.pdf
url http://dx.doi.org/10.21577/0103-5053.20200098
http://hdl.handle.net/11449/209546
identifier_str_mv Journal Of The Brazilian Chemical Society. Sao Paulo: Soc Brasileira Quimica, v. 31, n. 10, p. 1979-1990, 2020.
0103-5053
10.21577/0103-5053.20200098
S0103-50532020001001979
WOS:000577634100003
S0103-50532020001001979.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal Of The Brazilian Chemical Society
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1979-1990
application/pdf
dc.publisher.none.fl_str_mv Soc Brasileira Quimica
publisher.none.fl_str_mv Soc Brasileira Quimica
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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