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Evolutionary rate patterns of genes involved in the Drosophila Toll and Imd signaling pathway

BACKGROUND: To survive in a hostile environment, insects have evolved an innate immune system to defend against infection. Studies have shown that natural selection may drive the evolution of immune system-related proteins. Yet, how network architecture influences protein sequence evolution remains...

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Autores principales: Han, Ming, Qin, Sheng, Song, Xiaojun, Li, Yafang, Jin, Ping, Chen, Liming, Ma, Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3826850/
https://www.ncbi.nlm.nih.gov/pubmed/24209511
http://dx.doi.org/10.1186/1471-2148-13-245
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author Han, Ming
Qin, Sheng
Song, Xiaojun
Li, Yafang
Jin, Ping
Chen, Liming
Ma, Fei
author_facet Han, Ming
Qin, Sheng
Song, Xiaojun
Li, Yafang
Jin, Ping
Chen, Liming
Ma, Fei
author_sort Han, Ming
collection PubMed
description BACKGROUND: To survive in a hostile environment, insects have evolved an innate immune system to defend against infection. Studies have shown that natural selection may drive the evolution of immune system-related proteins. Yet, how network architecture influences protein sequence evolution remains unclear. Here, we analyzed the molecular evolutionary patterns of genes in the Toll and Imd innate immune signaling pathways across six Drosophila genomes within the context of a functional network. RESULTS: Based on published literature, we identified 50 genes that are directly involved in the Drosophila Toll and Imd signaling pathways. Of those genes, only two (Sphinx1 and Dnr1) exhibited signals of positive selection. There existed a negative correlation between the strength of purifying selection and gene position within the pathway; the downstream genes were more conserved, indicating that they were subjected to stronger evolutionary constraints. Interestingly, there was also a significantly negative correlation between the rate of protein evolution and the number of regulatory microRNAs, implying that genes regulated by more miRNAs experience stronger functional constraints and therefore evolve more slowly. CONCLUSION: Taken together, our results suggested that both network architecture and miRNA regulation affect protein sequence evolution. These findings improve our understanding of the evolutionary patterns of genes involved in Drosophila innate immune pathways.
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spelling pubmed-38268502013-11-14 Evolutionary rate patterns of genes involved in the Drosophila Toll and Imd signaling pathway Han, Ming Qin, Sheng Song, Xiaojun Li, Yafang Jin, Ping Chen, Liming Ma, Fei BMC Evol Biol Research Article BACKGROUND: To survive in a hostile environment, insects have evolved an innate immune system to defend against infection. Studies have shown that natural selection may drive the evolution of immune system-related proteins. Yet, how network architecture influences protein sequence evolution remains unclear. Here, we analyzed the molecular evolutionary patterns of genes in the Toll and Imd innate immune signaling pathways across six Drosophila genomes within the context of a functional network. RESULTS: Based on published literature, we identified 50 genes that are directly involved in the Drosophila Toll and Imd signaling pathways. Of those genes, only two (Sphinx1 and Dnr1) exhibited signals of positive selection. There existed a negative correlation between the strength of purifying selection and gene position within the pathway; the downstream genes were more conserved, indicating that they were subjected to stronger evolutionary constraints. Interestingly, there was also a significantly negative correlation between the rate of protein evolution and the number of regulatory microRNAs, implying that genes regulated by more miRNAs experience stronger functional constraints and therefore evolve more slowly. CONCLUSION: Taken together, our results suggested that both network architecture and miRNA regulation affect protein sequence evolution. These findings improve our understanding of the evolutionary patterns of genes involved in Drosophila innate immune pathways. BioMed Central 2013-11-08 /pmc/articles/PMC3826850/ /pubmed/24209511 http://dx.doi.org/10.1186/1471-2148-13-245 Text en Copyright © 2013 Han 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
Han, Ming
Qin, Sheng
Song, Xiaojun
Li, Yafang
Jin, Ping
Chen, Liming
Ma, Fei
Evolutionary rate patterns of genes involved in the Drosophila Toll and Imd signaling pathway
title Evolutionary rate patterns of genes involved in the Drosophila Toll and Imd signaling pathway
title_full Evolutionary rate patterns of genes involved in the Drosophila Toll and Imd signaling pathway
title_fullStr Evolutionary rate patterns of genes involved in the Drosophila Toll and Imd signaling pathway
title_full_unstemmed Evolutionary rate patterns of genes involved in the Drosophila Toll and Imd signaling pathway
title_short Evolutionary rate patterns of genes involved in the Drosophila Toll and Imd signaling pathway
title_sort evolutionary rate patterns of genes involved in the drosophila toll and imd signaling pathway
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3826850/
https://www.ncbi.nlm.nih.gov/pubmed/24209511
http://dx.doi.org/10.1186/1471-2148-13-245
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