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Ccdc3: A New P63 Target Involved in Regulation Of Liver Lipid Metabolism

TAp63, a member of the p53 family, has been shown to regulate energy metabolism. Here, we report coiled coil domain-containing 3 (CCDC3) as a new TAp63 target. TAp63, but not ΔNp63, p53 or p73, upregulates CCDC3 expression by directly binding to its enhancer region. The CCDC3 expression is markedly...

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Autores principales: Liao, Wenjuan, Liu, Hongbing, Zhang, Yiwei, Jung, Ji Hoon, Chen, Jiaxiang, Su, Xiaohua, Kim, Yeong C., Flores, Elsa R, Wang, San Ming, Czarny-Ratajczak, Malwina, Li, Wen, Zeng, Shelya X., Lu, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566403/
https://www.ncbi.nlm.nih.gov/pubmed/28827783
http://dx.doi.org/10.1038/s41598-017-09228-8
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author Liao, Wenjuan
Liu, Hongbing
Zhang, Yiwei
Jung, Ji Hoon
Chen, Jiaxiang
Su, Xiaohua
Kim, Yeong C.
Flores, Elsa R
Wang, San Ming
Czarny-Ratajczak, Malwina
Li, Wen
Zeng, Shelya X.
Lu, Hua
author_facet Liao, Wenjuan
Liu, Hongbing
Zhang, Yiwei
Jung, Ji Hoon
Chen, Jiaxiang
Su, Xiaohua
Kim, Yeong C.
Flores, Elsa R
Wang, San Ming
Czarny-Ratajczak, Malwina
Li, Wen
Zeng, Shelya X.
Lu, Hua
author_sort Liao, Wenjuan
collection PubMed
description TAp63, a member of the p53 family, has been shown to regulate energy metabolism. Here, we report coiled coil domain-containing 3 (CCDC3) as a new TAp63 target. TAp63, but not ΔNp63, p53 or p73, upregulates CCDC3 expression by directly binding to its enhancer region. The CCDC3 expression is markedly reduced in TAp63-null mouse embryonic fibroblasts and brown adipose tissues and by tumor necrosis factor alpha that reduces p63 transcriptional activity, but induced by metformin, an anti-diabetic drug that activates p63. Also, the expression of CCDC3 is positively correlated with TAp63 levels, but conversely with ΔNp63 levels, during adipocyte differentiation. Interestingly, CCDC3, as a secreted protein, targets liver cancer cells and increases long chain polyunsaturated fatty acids, but decreases ceramide in the cells. CCDC3 alleviates glucose intolerance, insulin resistance and steatosis formation in transgenic CCDC3 mice on high-fat diet (HFD) by reducing the expression of hepatic PPARγ and its target gene CIDEA as well as other genes involved in de novo lipogenesis. Similar results are reproduced by hepatic expression of ectopic CCDC3 in mice on HFD. Altogether, these results demonstrate that CCDC3 modulates liver lipid metabolism by inhibiting liver de novo lipogenesis as a downstream player of the p63 network.
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spelling pubmed-55664032017-08-23 Ccdc3: A New P63 Target Involved in Regulation Of Liver Lipid Metabolism Liao, Wenjuan Liu, Hongbing Zhang, Yiwei Jung, Ji Hoon Chen, Jiaxiang Su, Xiaohua Kim, Yeong C. Flores, Elsa R Wang, San Ming Czarny-Ratajczak, Malwina Li, Wen Zeng, Shelya X. Lu, Hua Sci Rep Article TAp63, a member of the p53 family, has been shown to regulate energy metabolism. Here, we report coiled coil domain-containing 3 (CCDC3) as a new TAp63 target. TAp63, but not ΔNp63, p53 or p73, upregulates CCDC3 expression by directly binding to its enhancer region. The CCDC3 expression is markedly reduced in TAp63-null mouse embryonic fibroblasts and brown adipose tissues and by tumor necrosis factor alpha that reduces p63 transcriptional activity, but induced by metformin, an anti-diabetic drug that activates p63. Also, the expression of CCDC3 is positively correlated with TAp63 levels, but conversely with ΔNp63 levels, during adipocyte differentiation. Interestingly, CCDC3, as a secreted protein, targets liver cancer cells and increases long chain polyunsaturated fatty acids, but decreases ceramide in the cells. CCDC3 alleviates glucose intolerance, insulin resistance and steatosis formation in transgenic CCDC3 mice on high-fat diet (HFD) by reducing the expression of hepatic PPARγ and its target gene CIDEA as well as other genes involved in de novo lipogenesis. Similar results are reproduced by hepatic expression of ectopic CCDC3 in mice on HFD. Altogether, these results demonstrate that CCDC3 modulates liver lipid metabolism by inhibiting liver de novo lipogenesis as a downstream player of the p63 network. Nature Publishing Group UK 2017-08-21 /pmc/articles/PMC5566403/ /pubmed/28827783 http://dx.doi.org/10.1038/s41598-017-09228-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Liao, Wenjuan
Liu, Hongbing
Zhang, Yiwei
Jung, Ji Hoon
Chen, Jiaxiang
Su, Xiaohua
Kim, Yeong C.
Flores, Elsa R
Wang, San Ming
Czarny-Ratajczak, Malwina
Li, Wen
Zeng, Shelya X.
Lu, Hua
Ccdc3: A New P63 Target Involved in Regulation Of Liver Lipid Metabolism
title Ccdc3: A New P63 Target Involved in Regulation Of Liver Lipid Metabolism
title_full Ccdc3: A New P63 Target Involved in Regulation Of Liver Lipid Metabolism
title_fullStr Ccdc3: A New P63 Target Involved in Regulation Of Liver Lipid Metabolism
title_full_unstemmed Ccdc3: A New P63 Target Involved in Regulation Of Liver Lipid Metabolism
title_short Ccdc3: A New P63 Target Involved in Regulation Of Liver Lipid Metabolism
title_sort ccdc3: a new p63 target involved in regulation of liver lipid metabolism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566403/
https://www.ncbi.nlm.nih.gov/pubmed/28827783
http://dx.doi.org/10.1038/s41598-017-09228-8
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