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Analysis of Schistosoma mansoni genes shared with Deuterostomia and with possible roles in host interactions

BACKGROUND: Schistosoma mansoni is a blood helminth parasite that causes schistosomiasis, a disease that affects 200 million people in the world. Many orthologs of known mammalian genes have been discovered in this parasite and evidence is accumulating that some of these genes encode proteins linked...

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Autores principales: Venancio, Thiago M, DeMarco, Ricardo, Almeida, Giulliana T, Oliveira, Katia C, Setubal, João C, Verjovski-Almeida, Sergio
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2194728/
https://www.ncbi.nlm.nih.gov/pubmed/17996068
http://dx.doi.org/10.1186/1471-2164-8-407
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author Venancio, Thiago M
DeMarco, Ricardo
Almeida, Giulliana T
Oliveira, Katia C
Setubal, João C
Verjovski-Almeida, Sergio
author_facet Venancio, Thiago M
DeMarco, Ricardo
Almeida, Giulliana T
Oliveira, Katia C
Setubal, João C
Verjovski-Almeida, Sergio
author_sort Venancio, Thiago M
collection PubMed
description BACKGROUND: Schistosoma mansoni is a blood helminth parasite that causes schistosomiasis, a disease that affects 200 million people in the world. Many orthologs of known mammalian genes have been discovered in this parasite and evidence is accumulating that some of these genes encode proteins linked to signaling pathways in the parasite that appear to be involved with growth or development, suggesting a complex co-evolutionary process. RESULTS: In this work we found 427 genes conserved in the Deuterostomia group that have orthologs in S. mansoni and no members in any nematodes and insects so far sequenced. Among these genes we have identified Insulin Induced Gene (INSIG), Interferon Regulatory Factor (IRF) and vasohibin orthologs, known to be involved in mammals in mevalonate metabolism, immune response and angiogenesis control, respectively. We have chosen these three genes for a more detailed characterization, which included extension of their cloned messages to obtain full-length sequences. Interestingly, SmINSIG showed a 10-fold higher expression in adult females as opposed to males, in accordance with its possible role in regulating egg production. SmIRF has a DNA binding domain, a tryptophan-rich N-terminal region and several predicted phosphorylation sites, usually important for IRF activity. Fourteen different alternatively spliced forms of the S. mansoni vasohibin (SmVASL) gene were detected that encode seven different protein isoforms including one with a complete C-terminal end, and other isoforms with shorter C-terminal portions. Using S. mansoni homologs, we have employed a parsimonious rationale to compute the total gene losses/gains in nematodes, arthropods and deuterostomes under either the Coelomata or the Ecdysozoa evolutionary hypotheses; our results show a lower losses/gains number under the latter hypothesis. CONCLUSION: The genes discussed which are conserved between S. mansoni and deuterostomes, probably have an ancient origin and were lost in Ecdysozoa, being still present in Lophotrochozoa. Given their known functions in Deuterostomia, it is possible that some of them have been co-opted to perform functions related (directly or indirectly) to host adaptation or interaction with host signaling processes.
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spelling pubmed-21947282008-01-12 Analysis of Schistosoma mansoni genes shared with Deuterostomia and with possible roles in host interactions Venancio, Thiago M DeMarco, Ricardo Almeida, Giulliana T Oliveira, Katia C Setubal, João C Verjovski-Almeida, Sergio BMC Genomics Research Article BACKGROUND: Schistosoma mansoni is a blood helminth parasite that causes schistosomiasis, a disease that affects 200 million people in the world. Many orthologs of known mammalian genes have been discovered in this parasite and evidence is accumulating that some of these genes encode proteins linked to signaling pathways in the parasite that appear to be involved with growth or development, suggesting a complex co-evolutionary process. RESULTS: In this work we found 427 genes conserved in the Deuterostomia group that have orthologs in S. mansoni and no members in any nematodes and insects so far sequenced. Among these genes we have identified Insulin Induced Gene (INSIG), Interferon Regulatory Factor (IRF) and vasohibin orthologs, known to be involved in mammals in mevalonate metabolism, immune response and angiogenesis control, respectively. We have chosen these three genes for a more detailed characterization, which included extension of their cloned messages to obtain full-length sequences. Interestingly, SmINSIG showed a 10-fold higher expression in adult females as opposed to males, in accordance with its possible role in regulating egg production. SmIRF has a DNA binding domain, a tryptophan-rich N-terminal region and several predicted phosphorylation sites, usually important for IRF activity. Fourteen different alternatively spliced forms of the S. mansoni vasohibin (SmVASL) gene were detected that encode seven different protein isoforms including one with a complete C-terminal end, and other isoforms with shorter C-terminal portions. Using S. mansoni homologs, we have employed a parsimonious rationale to compute the total gene losses/gains in nematodes, arthropods and deuterostomes under either the Coelomata or the Ecdysozoa evolutionary hypotheses; our results show a lower losses/gains number under the latter hypothesis. CONCLUSION: The genes discussed which are conserved between S. mansoni and deuterostomes, probably have an ancient origin and were lost in Ecdysozoa, being still present in Lophotrochozoa. Given their known functions in Deuterostomia, it is possible that some of them have been co-opted to perform functions related (directly or indirectly) to host adaptation or interaction with host signaling processes. BioMed Central 2007-11-08 /pmc/articles/PMC2194728/ /pubmed/17996068 http://dx.doi.org/10.1186/1471-2164-8-407 Text en Copyright © 2007 Venancio 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
Venancio, Thiago M
DeMarco, Ricardo
Almeida, Giulliana T
Oliveira, Katia C
Setubal, João C
Verjovski-Almeida, Sergio
Analysis of Schistosoma mansoni genes shared with Deuterostomia and with possible roles in host interactions
title Analysis of Schistosoma mansoni genes shared with Deuterostomia and with possible roles in host interactions
title_full Analysis of Schistosoma mansoni genes shared with Deuterostomia and with possible roles in host interactions
title_fullStr Analysis of Schistosoma mansoni genes shared with Deuterostomia and with possible roles in host interactions
title_full_unstemmed Analysis of Schistosoma mansoni genes shared with Deuterostomia and with possible roles in host interactions
title_short Analysis of Schistosoma mansoni genes shared with Deuterostomia and with possible roles in host interactions
title_sort analysis of schistosoma mansoni genes shared with deuterostomia and with possible roles in host interactions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2194728/
https://www.ncbi.nlm.nih.gov/pubmed/17996068
http://dx.doi.org/10.1186/1471-2164-8-407
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