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Structure and functional impact of seed region variant in MIR-499 gene family in bronchial asthma

BACKGROUND: Small non-coding RNAs (microRNAs) have been evolved to master numerous cellular processes. Genetic variants within microRNA seed region might influence microRNA biogenesis and function. The study aimed at determining the role of microRNA-499 (MIR-499) gene family polymorphism as a marker...

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Autores principales: Toraih, Eman A., Hussein, Mohammad H., Al Ageeli, Essam, Riad, Eman, AbdAllah, Nouran B., Helal, Ghada M., Fawzy, Manal S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5591547/
https://www.ncbi.nlm.nih.gov/pubmed/28886711
http://dx.doi.org/10.1186/s12931-017-0648-0
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author Toraih, Eman A.
Hussein, Mohammad H.
Al Ageeli, Essam
Riad, Eman
AbdAllah, Nouran B.
Helal, Ghada M.
Fawzy, Manal S.
author_facet Toraih, Eman A.
Hussein, Mohammad H.
Al Ageeli, Essam
Riad, Eman
AbdAllah, Nouran B.
Helal, Ghada M.
Fawzy, Manal S.
author_sort Toraih, Eman A.
collection PubMed
description BACKGROUND: Small non-coding RNAs (microRNAs) have been evolved to master numerous cellular processes. Genetic variants within microRNA seed region might influence microRNA biogenesis and function. The study aimed at determining the role of microRNA-499 (MIR-499) gene family polymorphism as a marker for susceptibility and progression of bronchial asthma and to analyze the structural and functional impact of rs3746444 within the seed region. METHODS: Genotyping for 192 participants (96 patients and 96 controls) in the discovery phase and 319 subjects (115 patients and 204 controls) in the replication phase was performed via Real Time-Polymerase Chain Reaction technology. Patients underwent the methacholine challenge test and biochemical analysis. Gene structural and functional analysis, target prediction, annotation clustering, and pathway enrichment analysis were executed. Predicted functional effect of rs37464443 SNP was analyzed. RESULTS: miR-499 gene family is highly implicated in inflammation-related signaling pathways. Rs374644 (A > G) in MIR499A and MIR499B within the seed region could disrupt target genes and create new genes. The G variant was associated with high risk of developing asthma under all genetic association models (G versus A: OR = 3.27, 95% CI = 2.53–4.22; GG versus AA: OR = 9.52, 95% CI = 5.61–16.5; AG versus AA: OR = 2.13, 95% CI = 1.24–3.46; GG + AG versus AA: OR = 4.43, 95% CI = 2.88–6.82). GG genotype was associated with poor pre-bronchodilator FEV(1) (p = 0.047) and the worst bronchodilator response after Salbutamol inhalation, represented in low peaked expiratory flow rate (p = 0.035). CONCLUSIONS: miR-499 rs3746444 (A > G) polymorphism was associated with asthma susceptibility and bronchodilator response in Egyptian children and adolescents. Further functional analysis is warranted to develop more specific theranostic agents for selecting targeted therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12931-017-0648-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-55915472017-09-13 Structure and functional impact of seed region variant in MIR-499 gene family in bronchial asthma Toraih, Eman A. Hussein, Mohammad H. Al Ageeli, Essam Riad, Eman AbdAllah, Nouran B. Helal, Ghada M. Fawzy, Manal S. Respir Res Research BACKGROUND: Small non-coding RNAs (microRNAs) have been evolved to master numerous cellular processes. Genetic variants within microRNA seed region might influence microRNA biogenesis and function. The study aimed at determining the role of microRNA-499 (MIR-499) gene family polymorphism as a marker for susceptibility and progression of bronchial asthma and to analyze the structural and functional impact of rs3746444 within the seed region. METHODS: Genotyping for 192 participants (96 patients and 96 controls) in the discovery phase and 319 subjects (115 patients and 204 controls) in the replication phase was performed via Real Time-Polymerase Chain Reaction technology. Patients underwent the methacholine challenge test and biochemical analysis. Gene structural and functional analysis, target prediction, annotation clustering, and pathway enrichment analysis were executed. Predicted functional effect of rs37464443 SNP was analyzed. RESULTS: miR-499 gene family is highly implicated in inflammation-related signaling pathways. Rs374644 (A > G) in MIR499A and MIR499B within the seed region could disrupt target genes and create new genes. The G variant was associated with high risk of developing asthma under all genetic association models (G versus A: OR = 3.27, 95% CI = 2.53–4.22; GG versus AA: OR = 9.52, 95% CI = 5.61–16.5; AG versus AA: OR = 2.13, 95% CI = 1.24–3.46; GG + AG versus AA: OR = 4.43, 95% CI = 2.88–6.82). GG genotype was associated with poor pre-bronchodilator FEV(1) (p = 0.047) and the worst bronchodilator response after Salbutamol inhalation, represented in low peaked expiratory flow rate (p = 0.035). CONCLUSIONS: miR-499 rs3746444 (A > G) polymorphism was associated with asthma susceptibility and bronchodilator response in Egyptian children and adolescents. Further functional analysis is warranted to develop more specific theranostic agents for selecting targeted therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12931-017-0648-0) contains supplementary material, which is available to authorized users. BioMed Central 2017-09-08 2017 /pmc/articles/PMC5591547/ /pubmed/28886711 http://dx.doi.org/10.1186/s12931-017-0648-0 Text en © The Author(s). 2017 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 Research
Toraih, Eman A.
Hussein, Mohammad H.
Al Ageeli, Essam
Riad, Eman
AbdAllah, Nouran B.
Helal, Ghada M.
Fawzy, Manal S.
Structure and functional impact of seed region variant in MIR-499 gene family in bronchial asthma
title Structure and functional impact of seed region variant in MIR-499 gene family in bronchial asthma
title_full Structure and functional impact of seed region variant in MIR-499 gene family in bronchial asthma
title_fullStr Structure and functional impact of seed region variant in MIR-499 gene family in bronchial asthma
title_full_unstemmed Structure and functional impact of seed region variant in MIR-499 gene family in bronchial asthma
title_short Structure and functional impact of seed region variant in MIR-499 gene family in bronchial asthma
title_sort structure and functional impact of seed region variant in mir-499 gene family in bronchial asthma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5591547/
https://www.ncbi.nlm.nih.gov/pubmed/28886711
http://dx.doi.org/10.1186/s12931-017-0648-0
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