Cargando…

Clocks do not tick in unison: isolation of Clock and vrille shed new light on the clockwork model of the sand fly Lutzomyia longipalpis

BACKGROUND: Behavior rhythms of insect vectors directly interfere with the dynamics of pathogen transmission to humans. The sand fly Lutzomyia longipalpis is the main vector of visceral leishmaniasis in America and concentrates its activity around dusk. Despite the accumulation of behavioral data, v...

Descripción completa

Detalles Bibliográficos
Autores principales: Gesto, João Silveira Moledo, Rivas, Gustavo Bueno da Silva, Pavan, Marcio Galvão, Meireles-Filho, Antonio Carlos Alves, Amoretty, Paulo Roberto de, Souza, Nataly Araújo de, Bruno, Rafaela Vieira, Peixoto, Alexandre Afranio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4595053/
https://www.ncbi.nlm.nih.gov/pubmed/26438221
http://dx.doi.org/10.1186/s13071-015-1117-6
_version_ 1782393526135291904
author Gesto, João Silveira Moledo
Rivas, Gustavo Bueno da Silva
Pavan, Marcio Galvão
Meireles-Filho, Antonio Carlos Alves
Amoretty, Paulo Roberto de
Souza, Nataly Araújo de
Bruno, Rafaela Vieira
Peixoto, Alexandre Afranio
author_facet Gesto, João Silveira Moledo
Rivas, Gustavo Bueno da Silva
Pavan, Marcio Galvão
Meireles-Filho, Antonio Carlos Alves
Amoretty, Paulo Roberto de
Souza, Nataly Araújo de
Bruno, Rafaela Vieira
Peixoto, Alexandre Afranio
author_sort Gesto, João Silveira Moledo
collection PubMed
description BACKGROUND: Behavior rhythms of insect vectors directly interfere with the dynamics of pathogen transmission to humans. The sand fly Lutzomyia longipalpis is the main vector of visceral leishmaniasis in America and concentrates its activity around dusk. Despite the accumulation of behavioral data, very little is known about the molecular bases of the clock mechanism in this species. This study aims to characterize, within an evolutionary perspective, two important circadian clock genes, Clock and vrille. FINDINGS: We have cloned and isolated the coding sequence of L. longipalpis’ genes Clock and vrille. The former is structured in eight exons and encodes a protein of 696 amino acids, and the latter comprises three exons and translates to a protein of 469 amino acids. When compared to other insects’ orthologues, L. longipalpis CLOCK shows a high degree of conservation in the functional domains bHLH and PAS, but a much shorter glutamine-rich (poly-Q) C-terminal region. As for L. longipalpis VRILLE, a high degree of conservation was found in the bZIP domain. To support these observations and provide an elegant view of the evolution of both genes in insects, phylogenetic analyses based on maximum-likelihood and Bayesian inferences were performed, corroborating the previously known insect systematics. CONCLUSIONS: The isolation and phylogenetic analyses of Clock and vrille orthologues in L. longipalpis bring novel and important data to characterize this species’ circadian clock. Interestingly, the poly-Q shortening observed in CLOCK suggests that its transcription activity might be impaired and we speculate if this effect could be compensated by other clock factors such as CYCLE. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-015-1117-6) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4595053
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-45950532015-10-07 Clocks do not tick in unison: isolation of Clock and vrille shed new light on the clockwork model of the sand fly Lutzomyia longipalpis Gesto, João Silveira Moledo Rivas, Gustavo Bueno da Silva Pavan, Marcio Galvão Meireles-Filho, Antonio Carlos Alves Amoretty, Paulo Roberto de Souza, Nataly Araújo de Bruno, Rafaela Vieira Peixoto, Alexandre Afranio Parasit Vectors Short Report BACKGROUND: Behavior rhythms of insect vectors directly interfere with the dynamics of pathogen transmission to humans. The sand fly Lutzomyia longipalpis is the main vector of visceral leishmaniasis in America and concentrates its activity around dusk. Despite the accumulation of behavioral data, very little is known about the molecular bases of the clock mechanism in this species. This study aims to characterize, within an evolutionary perspective, two important circadian clock genes, Clock and vrille. FINDINGS: We have cloned and isolated the coding sequence of L. longipalpis’ genes Clock and vrille. The former is structured in eight exons and encodes a protein of 696 amino acids, and the latter comprises three exons and translates to a protein of 469 amino acids. When compared to other insects’ orthologues, L. longipalpis CLOCK shows a high degree of conservation in the functional domains bHLH and PAS, but a much shorter glutamine-rich (poly-Q) C-terminal region. As for L. longipalpis VRILLE, a high degree of conservation was found in the bZIP domain. To support these observations and provide an elegant view of the evolution of both genes in insects, phylogenetic analyses based on maximum-likelihood and Bayesian inferences were performed, corroborating the previously known insect systematics. CONCLUSIONS: The isolation and phylogenetic analyses of Clock and vrille orthologues in L. longipalpis bring novel and important data to characterize this species’ circadian clock. Interestingly, the poly-Q shortening observed in CLOCK suggests that its transcription activity might be impaired and we speculate if this effect could be compensated by other clock factors such as CYCLE. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-015-1117-6) contains supplementary material, which is available to authorized users. BioMed Central 2015-10-06 /pmc/articles/PMC4595053/ /pubmed/26438221 http://dx.doi.org/10.1186/s13071-015-1117-6 Text en © Gesto et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Gesto, João Silveira Moledo
Rivas, Gustavo Bueno da Silva
Pavan, Marcio Galvão
Meireles-Filho, Antonio Carlos Alves
Amoretty, Paulo Roberto de
Souza, Nataly Araújo de
Bruno, Rafaela Vieira
Peixoto, Alexandre Afranio
Clocks do not tick in unison: isolation of Clock and vrille shed new light on the clockwork model of the sand fly Lutzomyia longipalpis
title Clocks do not tick in unison: isolation of Clock and vrille shed new light on the clockwork model of the sand fly Lutzomyia longipalpis
title_full Clocks do not tick in unison: isolation of Clock and vrille shed new light on the clockwork model of the sand fly Lutzomyia longipalpis
title_fullStr Clocks do not tick in unison: isolation of Clock and vrille shed new light on the clockwork model of the sand fly Lutzomyia longipalpis
title_full_unstemmed Clocks do not tick in unison: isolation of Clock and vrille shed new light on the clockwork model of the sand fly Lutzomyia longipalpis
title_short Clocks do not tick in unison: isolation of Clock and vrille shed new light on the clockwork model of the sand fly Lutzomyia longipalpis
title_sort clocks do not tick in unison: isolation of clock and vrille shed new light on the clockwork model of the sand fly lutzomyia longipalpis
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4595053/
https://www.ncbi.nlm.nih.gov/pubmed/26438221
http://dx.doi.org/10.1186/s13071-015-1117-6
work_keys_str_mv AT gestojoaosilveiramoledo clocksdonottickinunisonisolationofclockandvrilleshednewlightontheclockworkmodelofthesandflylutzomyialongipalpis
AT rivasgustavobuenodasilva clocksdonottickinunisonisolationofclockandvrilleshednewlightontheclockworkmodelofthesandflylutzomyialongipalpis
AT pavanmarciogalvao clocksdonottickinunisonisolationofclockandvrilleshednewlightontheclockworkmodelofthesandflylutzomyialongipalpis
AT meirelesfilhoantoniocarlosalves clocksdonottickinunisonisolationofclockandvrilleshednewlightontheclockworkmodelofthesandflylutzomyialongipalpis
AT amorettypaulorobertode clocksdonottickinunisonisolationofclockandvrilleshednewlightontheclockworkmodelofthesandflylutzomyialongipalpis
AT souzanatalyaraujode clocksdonottickinunisonisolationofclockandvrilleshednewlightontheclockworkmodelofthesandflylutzomyialongipalpis
AT brunorafaelavieira clocksdonottickinunisonisolationofclockandvrilleshednewlightontheclockworkmodelofthesandflylutzomyialongipalpis
AT peixotoalexandreafranio clocksdonottickinunisonisolationofclockandvrilleshednewlightontheclockworkmodelofthesandflylutzomyialongipalpis