Sam68 promotes hepatic gluconeogenesis via CRTC2

Hepatic gluconeogenesis is important for glucose homeostasis and a therapeutic target for type 2 diabetes. Here, the authors show that the RNA-binding adaptor protein Sam68 promotes the expression level of gluconeogenic genes and increases blood glucose levels by stabilizing the transcriptional coac...

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Autores principales: Aijun Qiao, Junlan Zhou, Shiyue Xu, Wenxia Ma, Chan Boriboun, Teayoun Kim, Baolong Yan, Jianxin Deng, Liu Yang, Eric Zhang, Yuhua Song, Yongchao C. Ma, Stephane Richard, Chunxiang Zhang, Hongyu Qiu, Kirk M. Habegger, Jianyi Zhang, Gangjian Qin
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Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/06ee0683d6c7406d8c7218d61e9eae37
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spelling oai:doaj.org-article:06ee0683d6c7406d8c7218d61e9eae372021-12-02T17:38:25ZSam68 promotes hepatic gluconeogenesis via CRTC210.1038/s41467-021-23624-92041-1723https://doaj.org/article/06ee0683d6c7406d8c7218d61e9eae372021-06-01T00:00:00Zhttps://doi.org/10.1038/s41467-021-23624-9https://doaj.org/toc/2041-1723Hepatic gluconeogenesis is important for glucose homeostasis and a therapeutic target for type 2 diabetes. Here, the authors show that the RNA-binding adaptor protein Sam68 promotes the expression level of gluconeogenic genes and increases blood glucose levels by stabilizing the transcriptional coactivator CRTC2, while hepatic Sam68 deletion alleviates hyperglycemia in mice.Aijun QiaoJunlan ZhouShiyue XuWenxia MaChan BoribounTeayoun KimBaolong YanJianxin DengLiu YangEric ZhangYuhua SongYongchao C. MaStephane RichardChunxiang ZhangHongyu QiuKirk M. HabeggerJianyi ZhangGangjian QinNature PortfolioarticleScienceQENNature Communications, Vol 12, Iss 1, Pp 1-14 (2021)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Aijun Qiao
Junlan Zhou
Shiyue Xu
Wenxia Ma
Chan Boriboun
Teayoun Kim
Baolong Yan
Jianxin Deng
Liu Yang
Eric Zhang
Yuhua Song
Yongchao C. Ma
Stephane Richard
Chunxiang Zhang
Hongyu Qiu
Kirk M. Habegger
Jianyi Zhang
Gangjian Qin
Sam68 promotes hepatic gluconeogenesis via CRTC2
description Hepatic gluconeogenesis is important for glucose homeostasis and a therapeutic target for type 2 diabetes. Here, the authors show that the RNA-binding adaptor protein Sam68 promotes the expression level of gluconeogenic genes and increases blood glucose levels by stabilizing the transcriptional coactivator CRTC2, while hepatic Sam68 deletion alleviates hyperglycemia in mice.
format article
author Aijun Qiao
Junlan Zhou
Shiyue Xu
Wenxia Ma
Chan Boriboun
Teayoun Kim
Baolong Yan
Jianxin Deng
Liu Yang
Eric Zhang
Yuhua Song
Yongchao C. Ma
Stephane Richard
Chunxiang Zhang
Hongyu Qiu
Kirk M. Habegger
Jianyi Zhang
Gangjian Qin
author_facet Aijun Qiao
Junlan Zhou
Shiyue Xu
Wenxia Ma
Chan Boriboun
Teayoun Kim
Baolong Yan
Jianxin Deng
Liu Yang
Eric Zhang
Yuhua Song
Yongchao C. Ma
Stephane Richard
Chunxiang Zhang
Hongyu Qiu
Kirk M. Habegger
Jianyi Zhang
Gangjian Qin
author_sort Aijun Qiao
title Sam68 promotes hepatic gluconeogenesis via CRTC2
title_short Sam68 promotes hepatic gluconeogenesis via CRTC2
title_full Sam68 promotes hepatic gluconeogenesis via CRTC2
title_fullStr Sam68 promotes hepatic gluconeogenesis via CRTC2
title_full_unstemmed Sam68 promotes hepatic gluconeogenesis via CRTC2
title_sort sam68 promotes hepatic gluconeogenesis via crtc2
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/06ee0683d6c7406d8c7218d61e9eae37
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