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Gene expression profiling in the developing secondary palate in the absence of Tbx1 function
BACKGROUND: Microdeletion of chromosome 22q11 is associated with significant developmental anomalies, including disruption of the cardiac outflow tract, thymic/parathyroid aplasia and cleft palate. Amongst the genes within this region, TBX1 is a major candidate for many of these developmental defect...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987606/ https://www.ncbi.nlm.nih.gov/pubmed/29866044 http://dx.doi.org/10.1186/s12864-018-4782-y |
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author | Zoupa, Maria Xavier, Guilherme Machado Bryan, Stephanie Theologidis, Ioannis Arno, Matthew Cobourne, Martyn T. |
author_facet | Zoupa, Maria Xavier, Guilherme Machado Bryan, Stephanie Theologidis, Ioannis Arno, Matthew Cobourne, Martyn T. |
author_sort | Zoupa, Maria |
collection | PubMed |
description | BACKGROUND: Microdeletion of chromosome 22q11 is associated with significant developmental anomalies, including disruption of the cardiac outflow tract, thymic/parathyroid aplasia and cleft palate. Amongst the genes within this region, TBX1 is a major candidate for many of these developmental defects. Targeted deletion of Tbx1 in the mouse has provided significant insight into the function of this transcription factor during early development of the cardiac and pharyngeal systems. However, less is known about its role during palatogenesis. To assess the influence of Tbx1 function on gene expression profile within the developing palate we performed a microarray screen using total RNA isolated from the secondary palate of E13.5 mouse embryos wild type, heterozygous and mutant for Tbx1. RESULTS: Expression-level filtering and statistical analysis revealed a total of 577 genes differentially expressed across genotypes. Data were clustered into 3 groups based on comparison between genotypes. Group A was composed of differentially expressed genes in mutant compared to wild type (n = 89); Group B included differentially expressed genes in heterozygous compared to wild type (n = 400) and Group C included differentially expressed genes in mutant compared to heterozygous (n = 88). High-throughput quantitative real-time PCR (RT-PCR) confirmed a total of 27 genes significantly changed between wild type and mutant; and 27 genes between heterozygote and mutant. Amongst these, the majority were present in both groups A and C (26 genes). Associations existed with hypertrophic cardiomyopathy, cardiac muscle contraction, dilated cardiomyopathy, focal adhesion, tight junction and calcium signalling pathways. No significant differences in gene expression were found between wild type and heterozygous palatal shelves. CONCLUSIONS: Significant differences in gene expression profile within the secondary palate of wild type and mutant embryos is consistent with a primary role for Tbx1 during palatogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-4782-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5987606 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59876062018-06-20 Gene expression profiling in the developing secondary palate in the absence of Tbx1 function Zoupa, Maria Xavier, Guilherme Machado Bryan, Stephanie Theologidis, Ioannis Arno, Matthew Cobourne, Martyn T. BMC Genomics Research Article BACKGROUND: Microdeletion of chromosome 22q11 is associated with significant developmental anomalies, including disruption of the cardiac outflow tract, thymic/parathyroid aplasia and cleft palate. Amongst the genes within this region, TBX1 is a major candidate for many of these developmental defects. Targeted deletion of Tbx1 in the mouse has provided significant insight into the function of this transcription factor during early development of the cardiac and pharyngeal systems. However, less is known about its role during palatogenesis. To assess the influence of Tbx1 function on gene expression profile within the developing palate we performed a microarray screen using total RNA isolated from the secondary palate of E13.5 mouse embryos wild type, heterozygous and mutant for Tbx1. RESULTS: Expression-level filtering and statistical analysis revealed a total of 577 genes differentially expressed across genotypes. Data were clustered into 3 groups based on comparison between genotypes. Group A was composed of differentially expressed genes in mutant compared to wild type (n = 89); Group B included differentially expressed genes in heterozygous compared to wild type (n = 400) and Group C included differentially expressed genes in mutant compared to heterozygous (n = 88). High-throughput quantitative real-time PCR (RT-PCR) confirmed a total of 27 genes significantly changed between wild type and mutant; and 27 genes between heterozygote and mutant. Amongst these, the majority were present in both groups A and C (26 genes). Associations existed with hypertrophic cardiomyopathy, cardiac muscle contraction, dilated cardiomyopathy, focal adhesion, tight junction and calcium signalling pathways. No significant differences in gene expression were found between wild type and heterozygous palatal shelves. CONCLUSIONS: Significant differences in gene expression profile within the secondary palate of wild type and mutant embryos is consistent with a primary role for Tbx1 during palatogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-4782-y) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-04 /pmc/articles/PMC5987606/ /pubmed/29866044 http://dx.doi.org/10.1186/s12864-018-4782-y Text en © The Author(s). 2018 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 Article Zoupa, Maria Xavier, Guilherme Machado Bryan, Stephanie Theologidis, Ioannis Arno, Matthew Cobourne, Martyn T. Gene expression profiling in the developing secondary palate in the absence of Tbx1 function |
title | Gene expression profiling in the developing secondary palate in the absence of Tbx1 function |
title_full | Gene expression profiling in the developing secondary palate in the absence of Tbx1 function |
title_fullStr | Gene expression profiling in the developing secondary palate in the absence of Tbx1 function |
title_full_unstemmed | Gene expression profiling in the developing secondary palate in the absence of Tbx1 function |
title_short | Gene expression profiling in the developing secondary palate in the absence of Tbx1 function |
title_sort | gene expression profiling in the developing secondary palate in the absence of tbx1 function |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987606/ https://www.ncbi.nlm.nih.gov/pubmed/29866044 http://dx.doi.org/10.1186/s12864-018-4782-y |
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