Cargando…

The mitogen-activated protein kinome from Anopheles gambiae: identification, phylogeny and functional characterization of the ERK, JNK and p38 MAP kinases

BACKGROUND: Anopheles gambiae is the primary mosquito vector of human malaria parasites in sub-Saharan Africa. To date, three innate immune signaling pathways, including the nuclear factor (NF)-kappaB-dependent Toll and immune deficient (IMD) pathways and the Janus kinase/signal transducers and acti...

Descripción completa

Detalles Bibliográficos
Autores principales: Horton, Ashley A, Wang, Bo, Camp, Lauren, Price, Mark S, Arshi, Arora, Nagy, Mate, Nadler, Steven A, Faeder, James R, Luckhart, Shirley
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3233564/
https://www.ncbi.nlm.nih.gov/pubmed/22111877
http://dx.doi.org/10.1186/1471-2164-12-574
_version_ 1782218432958169088
author Horton, Ashley A
Wang, Bo
Camp, Lauren
Price, Mark S
Arshi, Arora
Nagy, Mate
Nadler, Steven A
Faeder, James R
Luckhart, Shirley
author_facet Horton, Ashley A
Wang, Bo
Camp, Lauren
Price, Mark S
Arshi, Arora
Nagy, Mate
Nadler, Steven A
Faeder, James R
Luckhart, Shirley
author_sort Horton, Ashley A
collection PubMed
description BACKGROUND: Anopheles gambiae is the primary mosquito vector of human malaria parasites in sub-Saharan Africa. To date, three innate immune signaling pathways, including the nuclear factor (NF)-kappaB-dependent Toll and immune deficient (IMD) pathways and the Janus kinase/signal transducers and activators of transcription (Jak-STAT) pathway, have been extensively characterized in An. gambiae. However, in addition to NF-kappaB-dependent signaling, three mitogen-activated protein kinase (MAPK) pathways regulated by JNK, ERK and p38 MAPK are critical mediators of innate immunity in other invertebrates and in mammals. Our understanding of the roles of the MAPK signaling cascades in anopheline innate immunity is limited, so identification of the encoded complement of these proteins, their upstream activators, and phosphorylation profiles in response to relevant immune signals was warranted. RESULTS: In this study, we present the orthologs and phylogeny of 17 An. gambiae MAPKs, two of which were previously unknown and two others that were incompletely annotated. We also provide detailed temporal activation profiles for ERK, JNK, and p38 MAPK in An. gambiae cells in vitro to immune signals that are relevant to malaria parasite infection (human insulin, human transforming growth factor-beta1, hydrogen peroxide) and to bacterial lipopolysaccharide. These activation profiles and possible upstream regulatory pathways are interpreted in light of known MAPK signaling cascades. CONCLUSIONS: The establishment of a MAPK "road map" based on the most advanced mosquito genome annotation can accelerate our understanding of host-pathogen interactions and broader physiology of An. gambiae and other mosquito species. Further, future efforts to develop predictive models of anopheline cell signaling responses, based on iterative construction and refinement of data-based and literature-based knowledge of the MAP kinase cascades and other networked pathways will facilitate identification of the "master signaling regulators" in biomedically important mosquito species.
format Online
Article
Text
id pubmed-3233564
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-32335642011-12-08 The mitogen-activated protein kinome from Anopheles gambiae: identification, phylogeny and functional characterization of the ERK, JNK and p38 MAP kinases Horton, Ashley A Wang, Bo Camp, Lauren Price, Mark S Arshi, Arora Nagy, Mate Nadler, Steven A Faeder, James R Luckhart, Shirley BMC Genomics Research Article BACKGROUND: Anopheles gambiae is the primary mosquito vector of human malaria parasites in sub-Saharan Africa. To date, three innate immune signaling pathways, including the nuclear factor (NF)-kappaB-dependent Toll and immune deficient (IMD) pathways and the Janus kinase/signal transducers and activators of transcription (Jak-STAT) pathway, have been extensively characterized in An. gambiae. However, in addition to NF-kappaB-dependent signaling, three mitogen-activated protein kinase (MAPK) pathways regulated by JNK, ERK and p38 MAPK are critical mediators of innate immunity in other invertebrates and in mammals. Our understanding of the roles of the MAPK signaling cascades in anopheline innate immunity is limited, so identification of the encoded complement of these proteins, their upstream activators, and phosphorylation profiles in response to relevant immune signals was warranted. RESULTS: In this study, we present the orthologs and phylogeny of 17 An. gambiae MAPKs, two of which were previously unknown and two others that were incompletely annotated. We also provide detailed temporal activation profiles for ERK, JNK, and p38 MAPK in An. gambiae cells in vitro to immune signals that are relevant to malaria parasite infection (human insulin, human transforming growth factor-beta1, hydrogen peroxide) and to bacterial lipopolysaccharide. These activation profiles and possible upstream regulatory pathways are interpreted in light of known MAPK signaling cascades. CONCLUSIONS: The establishment of a MAPK "road map" based on the most advanced mosquito genome annotation can accelerate our understanding of host-pathogen interactions and broader physiology of An. gambiae and other mosquito species. Further, future efforts to develop predictive models of anopheline cell signaling responses, based on iterative construction and refinement of data-based and literature-based knowledge of the MAP kinase cascades and other networked pathways will facilitate identification of the "master signaling regulators" in biomedically important mosquito species. BioMed Central 2011-11-23 /pmc/articles/PMC3233564/ /pubmed/22111877 http://dx.doi.org/10.1186/1471-2164-12-574 Text en Copyright ©2011 Horton et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Horton, Ashley A
Wang, Bo
Camp, Lauren
Price, Mark S
Arshi, Arora
Nagy, Mate
Nadler, Steven A
Faeder, James R
Luckhart, Shirley
The mitogen-activated protein kinome from Anopheles gambiae: identification, phylogeny and functional characterization of the ERK, JNK and p38 MAP kinases
title The mitogen-activated protein kinome from Anopheles gambiae: identification, phylogeny and functional characterization of the ERK, JNK and p38 MAP kinases
title_full The mitogen-activated protein kinome from Anopheles gambiae: identification, phylogeny and functional characterization of the ERK, JNK and p38 MAP kinases
title_fullStr The mitogen-activated protein kinome from Anopheles gambiae: identification, phylogeny and functional characterization of the ERK, JNK and p38 MAP kinases
title_full_unstemmed The mitogen-activated protein kinome from Anopheles gambiae: identification, phylogeny and functional characterization of the ERK, JNK and p38 MAP kinases
title_short The mitogen-activated protein kinome from Anopheles gambiae: identification, phylogeny and functional characterization of the ERK, JNK and p38 MAP kinases
title_sort mitogen-activated protein kinome from anopheles gambiae: identification, phylogeny and functional characterization of the erk, jnk and p38 map kinases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3233564/
https://www.ncbi.nlm.nih.gov/pubmed/22111877
http://dx.doi.org/10.1186/1471-2164-12-574
work_keys_str_mv AT hortonashleya themitogenactivatedproteinkinomefromanophelesgambiaeidentificationphylogenyandfunctionalcharacterizationoftheerkjnkandp38mapkinases
AT wangbo themitogenactivatedproteinkinomefromanophelesgambiaeidentificationphylogenyandfunctionalcharacterizationoftheerkjnkandp38mapkinases
AT camplauren themitogenactivatedproteinkinomefromanophelesgambiaeidentificationphylogenyandfunctionalcharacterizationoftheerkjnkandp38mapkinases
AT pricemarks themitogenactivatedproteinkinomefromanophelesgambiaeidentificationphylogenyandfunctionalcharacterizationoftheerkjnkandp38mapkinases
AT arshiarora themitogenactivatedproteinkinomefromanophelesgambiaeidentificationphylogenyandfunctionalcharacterizationoftheerkjnkandp38mapkinases
AT nagymate themitogenactivatedproteinkinomefromanophelesgambiaeidentificationphylogenyandfunctionalcharacterizationoftheerkjnkandp38mapkinases
AT nadlerstevena themitogenactivatedproteinkinomefromanophelesgambiaeidentificationphylogenyandfunctionalcharacterizationoftheerkjnkandp38mapkinases
AT faederjamesr themitogenactivatedproteinkinomefromanophelesgambiaeidentificationphylogenyandfunctionalcharacterizationoftheerkjnkandp38mapkinases
AT luckhartshirley themitogenactivatedproteinkinomefromanophelesgambiaeidentificationphylogenyandfunctionalcharacterizationoftheerkjnkandp38mapkinases
AT hortonashleya mitogenactivatedproteinkinomefromanophelesgambiaeidentificationphylogenyandfunctionalcharacterizationoftheerkjnkandp38mapkinases
AT wangbo mitogenactivatedproteinkinomefromanophelesgambiaeidentificationphylogenyandfunctionalcharacterizationoftheerkjnkandp38mapkinases
AT camplauren mitogenactivatedproteinkinomefromanophelesgambiaeidentificationphylogenyandfunctionalcharacterizationoftheerkjnkandp38mapkinases
AT pricemarks mitogenactivatedproteinkinomefromanophelesgambiaeidentificationphylogenyandfunctionalcharacterizationoftheerkjnkandp38mapkinases
AT arshiarora mitogenactivatedproteinkinomefromanophelesgambiaeidentificationphylogenyandfunctionalcharacterizationoftheerkjnkandp38mapkinases
AT nagymate mitogenactivatedproteinkinomefromanophelesgambiaeidentificationphylogenyandfunctionalcharacterizationoftheerkjnkandp38mapkinases
AT nadlerstevena mitogenactivatedproteinkinomefromanophelesgambiaeidentificationphylogenyandfunctionalcharacterizationoftheerkjnkandp38mapkinases
AT faederjamesr mitogenactivatedproteinkinomefromanophelesgambiaeidentificationphylogenyandfunctionalcharacterizationoftheerkjnkandp38mapkinases
AT luckhartshirley mitogenactivatedproteinkinomefromanophelesgambiaeidentificationphylogenyandfunctionalcharacterizationoftheerkjnkandp38mapkinases