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Identification of cis-regulatory sequences reveals potential participation of lola and Deaf1 transcription factors in Anopheles gambiae innate immune response

The innate immune response of Anopheles gambiae involves the transcriptional upregulation of effector genes. Therefore, the cis-regulatory sequences and their cognate binding factors play essential roles in the mosquito’s immune response. However, the genetic control of the mosquito’s innate immune...

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Autores principales: Pérez-Zamorano, Bernardo, Rosas-Madrigal, Sandra, Lozano, Oscar Arturo Migueles, Castillo Méndez, Manuel, Valverde-Garduño, Verónica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640250/
https://www.ncbi.nlm.nih.gov/pubmed/29028826
http://dx.doi.org/10.1371/journal.pone.0186435
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author Pérez-Zamorano, Bernardo
Rosas-Madrigal, Sandra
Lozano, Oscar Arturo Migueles
Castillo Méndez, Manuel
Valverde-Garduño, Verónica
author_facet Pérez-Zamorano, Bernardo
Rosas-Madrigal, Sandra
Lozano, Oscar Arturo Migueles
Castillo Méndez, Manuel
Valverde-Garduño, Verónica
author_sort Pérez-Zamorano, Bernardo
collection PubMed
description The innate immune response of Anopheles gambiae involves the transcriptional upregulation of effector genes. Therefore, the cis-regulatory sequences and their cognate binding factors play essential roles in the mosquito’s immune response. However, the genetic control of the mosquito’s innate immune response is not yet fully understood. To gain further insight on the elements, the factors and the potential mechanisms involved, an open chromatin profiling was carried out on A. gambiae-derived immune-responsive cells. Here, we report the identification of cis-regulatory sites, immunity-related transcription factor binding sites, and cis-regulatory modules. A de novo motif discovery carried out on this set of cis-regulatory sequences identified immunity-related motifs and cis-regulatory modules. These modules contain motifs that are similar to binding sites for REL-, STAT-, lola- and Deaf1-type transcription factors. Sequence motifs similar to the binding sites for GAGA were found within a cis-regulatory module, together with immunity-related transcription factor binding sites. The presence of Deaf1- and lola-type binding sites, along with REL- and STAT-type binding sites, suggests that the immunity function of these two factors could have been conserved both in Drosophila and Anopheles gambiae.
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spelling pubmed-56402502017-10-30 Identification of cis-regulatory sequences reveals potential participation of lola and Deaf1 transcription factors in Anopheles gambiae innate immune response Pérez-Zamorano, Bernardo Rosas-Madrigal, Sandra Lozano, Oscar Arturo Migueles Castillo Méndez, Manuel Valverde-Garduño, Verónica PLoS One Research Article The innate immune response of Anopheles gambiae involves the transcriptional upregulation of effector genes. Therefore, the cis-regulatory sequences and their cognate binding factors play essential roles in the mosquito’s immune response. However, the genetic control of the mosquito’s innate immune response is not yet fully understood. To gain further insight on the elements, the factors and the potential mechanisms involved, an open chromatin profiling was carried out on A. gambiae-derived immune-responsive cells. Here, we report the identification of cis-regulatory sites, immunity-related transcription factor binding sites, and cis-regulatory modules. A de novo motif discovery carried out on this set of cis-regulatory sequences identified immunity-related motifs and cis-regulatory modules. These modules contain motifs that are similar to binding sites for REL-, STAT-, lola- and Deaf1-type transcription factors. Sequence motifs similar to the binding sites for GAGA were found within a cis-regulatory module, together with immunity-related transcription factor binding sites. The presence of Deaf1- and lola-type binding sites, along with REL- and STAT-type binding sites, suggests that the immunity function of these two factors could have been conserved both in Drosophila and Anopheles gambiae. Public Library of Science 2017-10-13 /pmc/articles/PMC5640250/ /pubmed/29028826 http://dx.doi.org/10.1371/journal.pone.0186435 Text en © 2017 Pérez-Zamorano 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
Pérez-Zamorano, Bernardo
Rosas-Madrigal, Sandra
Lozano, Oscar Arturo Migueles
Castillo Méndez, Manuel
Valverde-Garduño, Verónica
Identification of cis-regulatory sequences reveals potential participation of lola and Deaf1 transcription factors in Anopheles gambiae innate immune response
title Identification of cis-regulatory sequences reveals potential participation of lola and Deaf1 transcription factors in Anopheles gambiae innate immune response
title_full Identification of cis-regulatory sequences reveals potential participation of lola and Deaf1 transcription factors in Anopheles gambiae innate immune response
title_fullStr Identification of cis-regulatory sequences reveals potential participation of lola and Deaf1 transcription factors in Anopheles gambiae innate immune response
title_full_unstemmed Identification of cis-regulatory sequences reveals potential participation of lola and Deaf1 transcription factors in Anopheles gambiae innate immune response
title_short Identification of cis-regulatory sequences reveals potential participation of lola and Deaf1 transcription factors in Anopheles gambiae innate immune response
title_sort identification of cis-regulatory sequences reveals potential participation of lola and deaf1 transcription factors in anopheles gambiae innate immune response
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640250/
https://www.ncbi.nlm.nih.gov/pubmed/29028826
http://dx.doi.org/10.1371/journal.pone.0186435
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