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Haplotypes in the promoter region of the CIDEC gene associated with growth traits in Nanyang cattle
Cell death-inducing DFFA-like effector c (CIDEC, also known as Fsp27) has emerged as an important regulator of metabolism associated with lipodystrophy, diabetes, and hepatic steatosis. It is required for unilocular lipid droplet formation and optimal energy storage. The mechanism between this gene...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4648405/ https://www.ncbi.nlm.nih.gov/pubmed/26189824 http://dx.doi.org/10.1038/srep12075 |
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author | Wang, Jing Hua, Liu-shuai Pan, Hong Zhang, Liang-zhi Li, Ming-xun Huang, Yong-zhen Li, Zhuan-jian Lan, Xian-yong Lei, Chu-zhao Li, Cong-jun Chen, Hong |
author_facet | Wang, Jing Hua, Liu-shuai Pan, Hong Zhang, Liang-zhi Li, Ming-xun Huang, Yong-zhen Li, Zhuan-jian Lan, Xian-yong Lei, Chu-zhao Li, Cong-jun Chen, Hong |
author_sort | Wang, Jing |
collection | PubMed |
description | Cell death-inducing DFFA-like effector c (CIDEC, also known as Fsp27) has emerged as an important regulator of metabolism associated with lipodystrophy, diabetes, and hepatic steatosis. It is required for unilocular lipid droplet formation and optimal energy storage. The mechanism between this gene and livestock growth traits, however, has yet to be reported. In this study, we found ten novel single nucleotide polymorphisms (SNPs) in the 5’ transcriptional region of CIDEC in Nanyang (NY) cattle, which are located in the recognition sequences (potential cis-acting elements) of 22 transcription factors, and the nine haplotypes represent nine different combinations of polymorphic potential cis-acting elements. The results indicated that individuals with the H8-H8 diplotype had heavier body weights and faster growth rates (P < 0.01) at 18th months than those with H1-H8. We evaluated the transcriptional activities of different haplotypes in vitro, the results were consistent with the association analysis. The H8 haplotype had 1.88-fold (P < 0.001) higher transcriptional activity than the H1 haplotype. We speculate that the haplotypes of the potential cis-acting elements may affect the transcriptional activity of CIDEC, thus affecting the growth traits of cattle. This information may be used in molecular marker-assisted selection of cattle breeding in the future. |
format | Online Article Text |
id | pubmed-4648405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46484052015-11-23 Haplotypes in the promoter region of the CIDEC gene associated with growth traits in Nanyang cattle Wang, Jing Hua, Liu-shuai Pan, Hong Zhang, Liang-zhi Li, Ming-xun Huang, Yong-zhen Li, Zhuan-jian Lan, Xian-yong Lei, Chu-zhao Li, Cong-jun Chen, Hong Sci Rep Article Cell death-inducing DFFA-like effector c (CIDEC, also known as Fsp27) has emerged as an important regulator of metabolism associated with lipodystrophy, diabetes, and hepatic steatosis. It is required for unilocular lipid droplet formation and optimal energy storage. The mechanism between this gene and livestock growth traits, however, has yet to be reported. In this study, we found ten novel single nucleotide polymorphisms (SNPs) in the 5’ transcriptional region of CIDEC in Nanyang (NY) cattle, which are located in the recognition sequences (potential cis-acting elements) of 22 transcription factors, and the nine haplotypes represent nine different combinations of polymorphic potential cis-acting elements. The results indicated that individuals with the H8-H8 diplotype had heavier body weights and faster growth rates (P < 0.01) at 18th months than those with H1-H8. We evaluated the transcriptional activities of different haplotypes in vitro, the results were consistent with the association analysis. The H8 haplotype had 1.88-fold (P < 0.001) higher transcriptional activity than the H1 haplotype. We speculate that the haplotypes of the potential cis-acting elements may affect the transcriptional activity of CIDEC, thus affecting the growth traits of cattle. This information may be used in molecular marker-assisted selection of cattle breeding in the future. Nature Publishing Group 2015-07-20 /pmc/articles/PMC4648405/ /pubmed/26189824 http://dx.doi.org/10.1038/srep12075 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Wang, Jing Hua, Liu-shuai Pan, Hong Zhang, Liang-zhi Li, Ming-xun Huang, Yong-zhen Li, Zhuan-jian Lan, Xian-yong Lei, Chu-zhao Li, Cong-jun Chen, Hong Haplotypes in the promoter region of the CIDEC gene associated with growth traits in Nanyang cattle |
title | Haplotypes in the promoter region of the CIDEC gene associated with growth traits in Nanyang cattle |
title_full | Haplotypes in the promoter region of the CIDEC gene associated with growth traits in Nanyang cattle |
title_fullStr | Haplotypes in the promoter region of the CIDEC gene associated with growth traits in Nanyang cattle |
title_full_unstemmed | Haplotypes in the promoter region of the CIDEC gene associated with growth traits in Nanyang cattle |
title_short | Haplotypes in the promoter region of the CIDEC gene associated with growth traits in Nanyang cattle |
title_sort | haplotypes in the promoter region of the cidec gene associated with growth traits in nanyang cattle |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4648405/ https://www.ncbi.nlm.nih.gov/pubmed/26189824 http://dx.doi.org/10.1038/srep12075 |
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