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Two new splice variants in porcine PPARGC1A
BACKGROUND: Peroxisome proliferator-activated receptor γ coactivator 1α (PPARGC1A) is a coactivator with a vital and central role in fat and energy metabolism. It is considered to be a candidate gene for meat quality in pigs and is involved in the development of obesity and diabetes in humans. How i...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2631024/ https://www.ncbi.nlm.nih.gov/pubmed/19114011 http://dx.doi.org/10.1186/1756-0500-1-138 |
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author | Erkens, Tim Bilek, Karel Van Zeveren, Alex Peelman, Luc J |
author_facet | Erkens, Tim Bilek, Karel Van Zeveren, Alex Peelman, Luc J |
author_sort | Erkens, Tim |
collection | PubMed |
description | BACKGROUND: Peroxisome proliferator-activated receptor γ coactivator 1α (PPARGC1A) is a coactivator with a vital and central role in fat and energy metabolism. It is considered to be a candidate gene for meat quality in pigs and is involved in the development of obesity and diabetes in humans. How its many functions are regulated, is however still largely unclear. Therefore a transcription profile of PPARGC1A in 32 tissues and 4 embryonic developmental stages in the pig was constructed by screening its cDNA for possible splice variants with exon-spanning primers. FINDINGS: This led to the discovery of 2 new splice variants in the pig, which were subsequently also detected in human tissues. In these variants, exon 8 was either completely or partly (the last 66 bp were conserved) spliced out, potentially coding for a much shorter protein of respectively 337 and 359 amino acids (aa), of which the first 291 aa would be the same compared to the complete protein (796 aa). CONCLUSION: Considering the functional domains of the PPARGC1A protein, it is very likely these splice variants considerably affect the function of the protein and alternative splicing could be one of the mechanisms by which the diverse functions of PPARGC1A are regulated. |
format | Text |
id | pubmed-2631024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26310242009-01-27 Two new splice variants in porcine PPARGC1A Erkens, Tim Bilek, Karel Van Zeveren, Alex Peelman, Luc J BMC Res Notes Short Report BACKGROUND: Peroxisome proliferator-activated receptor γ coactivator 1α (PPARGC1A) is a coactivator with a vital and central role in fat and energy metabolism. It is considered to be a candidate gene for meat quality in pigs and is involved in the development of obesity and diabetes in humans. How its many functions are regulated, is however still largely unclear. Therefore a transcription profile of PPARGC1A in 32 tissues and 4 embryonic developmental stages in the pig was constructed by screening its cDNA for possible splice variants with exon-spanning primers. FINDINGS: This led to the discovery of 2 new splice variants in the pig, which were subsequently also detected in human tissues. In these variants, exon 8 was either completely or partly (the last 66 bp were conserved) spliced out, potentially coding for a much shorter protein of respectively 337 and 359 amino acids (aa), of which the first 291 aa would be the same compared to the complete protein (796 aa). CONCLUSION: Considering the functional domains of the PPARGC1A protein, it is very likely these splice variants considerably affect the function of the protein and alternative splicing could be one of the mechanisms by which the diverse functions of PPARGC1A are regulated. BioMed Central 2008-12-29 /pmc/articles/PMC2631024/ /pubmed/19114011 http://dx.doi.org/10.1186/1756-0500-1-138 Text en Copyright © 2008 Erkens 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 | Short Report Erkens, Tim Bilek, Karel Van Zeveren, Alex Peelman, Luc J Two new splice variants in porcine PPARGC1A |
title | Two new splice variants in porcine PPARGC1A |
title_full | Two new splice variants in porcine PPARGC1A |
title_fullStr | Two new splice variants in porcine PPARGC1A |
title_full_unstemmed | Two new splice variants in porcine PPARGC1A |
title_short | Two new splice variants in porcine PPARGC1A |
title_sort | two new splice variants in porcine ppargc1a |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2631024/ https://www.ncbi.nlm.nih.gov/pubmed/19114011 http://dx.doi.org/10.1186/1756-0500-1-138 |
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