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Parent of origin influences the cardiac expression of vascular endothelial growth factor (Vegfa)
BACKGROUND: Vascular endothelial growth factor A (VEGFA) is a major regulator of both physiological and pathological angiogenesis. Associations between polymorphisms in VEGFA and complex disease have been inconsistent. The parent from whom the allele was inherited may account for these inconsistenci...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3626619/ https://www.ncbi.nlm.nih.gov/pubmed/23560444 http://dx.doi.org/10.1186/1471-2350-14-43 |
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author | Chiu, Christine L Morgan, Chloe T Lupton, Samantha J Lind, Joanne M |
author_facet | Chiu, Christine L Morgan, Chloe T Lupton, Samantha J Lind, Joanne M |
author_sort | Chiu, Christine L |
collection | PubMed |
description | BACKGROUND: Vascular endothelial growth factor A (VEGFA) is a major regulator of both physiological and pathological angiogenesis. Associations between polymorphisms in VEGFA and complex disease have been inconsistent. The parent from whom the allele was inherited may account for these inconsistencies. This study examined the parent of origin effect on the expression of murine Vegfa. METHODS: Two homozygous, inbred mouse strains A/J (AJ) and 129x1/SvJ (129) were crossed to produce reciprocal AJ129 and 129AJ offspring, respectively. RNA was extracted from cardiac tissue of 6 week old male (n = 8) and female (n = 8) parental, and male and female F1 offspring mice (AJ129 n = 8 and 129AJ n = 8). Vegfa and Hif1a expression levels were measured by qPCR and compared between the F1 offspring from the reciprocal crosses. RESULTS: We found significant differences in the expression of Vegfa in F1 offspring (AJ129 and 129AJ mice) of the reciprocal crosses between AJ and 129 mice. Offspring of male AJ mice had significantly higher expression of Vegfa than offspring of male 129 mice (p = 0.006). This difference in expression was not the result of preferential allele expression (allelic imbalance). Expression of Hif1a, a transcriptional regulator of Vegfa expression, was also higher in F1 offspring of an AJ father (p = 0.004). CONCLUSION: Differences in Vegfa and Hif1a gene expression are likely the result of an upstream angiogenic regulator gene that is influenced by the parent of origin. These results highlight the importance of including inheritance information, such as parent of origin, when undertaking allelic association studies. |
format | Online Article Text |
id | pubmed-3626619 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36266192013-04-16 Parent of origin influences the cardiac expression of vascular endothelial growth factor (Vegfa) Chiu, Christine L Morgan, Chloe T Lupton, Samantha J Lind, Joanne M BMC Med Genet Research Article BACKGROUND: Vascular endothelial growth factor A (VEGFA) is a major regulator of both physiological and pathological angiogenesis. Associations between polymorphisms in VEGFA and complex disease have been inconsistent. The parent from whom the allele was inherited may account for these inconsistencies. This study examined the parent of origin effect on the expression of murine Vegfa. METHODS: Two homozygous, inbred mouse strains A/J (AJ) and 129x1/SvJ (129) were crossed to produce reciprocal AJ129 and 129AJ offspring, respectively. RNA was extracted from cardiac tissue of 6 week old male (n = 8) and female (n = 8) parental, and male and female F1 offspring mice (AJ129 n = 8 and 129AJ n = 8). Vegfa and Hif1a expression levels were measured by qPCR and compared between the F1 offspring from the reciprocal crosses. RESULTS: We found significant differences in the expression of Vegfa in F1 offspring (AJ129 and 129AJ mice) of the reciprocal crosses between AJ and 129 mice. Offspring of male AJ mice had significantly higher expression of Vegfa than offspring of male 129 mice (p = 0.006). This difference in expression was not the result of preferential allele expression (allelic imbalance). Expression of Hif1a, a transcriptional regulator of Vegfa expression, was also higher in F1 offspring of an AJ father (p = 0.004). CONCLUSION: Differences in Vegfa and Hif1a gene expression are likely the result of an upstream angiogenic regulator gene that is influenced by the parent of origin. These results highlight the importance of including inheritance information, such as parent of origin, when undertaking allelic association studies. BioMed Central 2013-04-05 /pmc/articles/PMC3626619/ /pubmed/23560444 http://dx.doi.org/10.1186/1471-2350-14-43 Text en Copyright © 2013 Chiu 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 Chiu, Christine L Morgan, Chloe T Lupton, Samantha J Lind, Joanne M Parent of origin influences the cardiac expression of vascular endothelial growth factor (Vegfa) |
title | Parent of origin influences the cardiac expression of vascular endothelial growth factor (Vegfa) |
title_full | Parent of origin influences the cardiac expression of vascular endothelial growth factor (Vegfa) |
title_fullStr | Parent of origin influences the cardiac expression of vascular endothelial growth factor (Vegfa) |
title_full_unstemmed | Parent of origin influences the cardiac expression of vascular endothelial growth factor (Vegfa) |
title_short | Parent of origin influences the cardiac expression of vascular endothelial growth factor (Vegfa) |
title_sort | parent of origin influences the cardiac expression of vascular endothelial growth factor (vegfa) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3626619/ https://www.ncbi.nlm.nih.gov/pubmed/23560444 http://dx.doi.org/10.1186/1471-2350-14-43 |
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