Non-catalytic mechanisms of KMT5C regulating hepatic gluconeogenesis

Lysine methyltransferase KMT5C catalyzes deposition of trimethylation on histone H4 lysine 20 (H4K20me3), an epigenetic marker usually associated with gene repression and maintenance of heterochromatin. KMT5C is widely expressed in a variety of tissues, however, its functional role in liver has not been explored. Here, we show Kmt5c is a fasting- and glucagon-induced gene in liver which regulates hepatic gluconeogenesis. Loss of KMT5C in hepatocytes results in downregulated gluconeogenic gene expression and compromised glucose output during fasting. KMT5C fosters gluconeogenesis through decreasing ubiquitination-mediated PGC-1α degradation, which is unexpectedly independent of its methyltransferase activity. In fact, KMT5C impedes the E3 ligase RNF34 binding to the C-terminal of PGC-1α and subsequent ubiquitination-associated degradation. The diabetic mice models and patients show elevated KMT5C levels in the livers, and KMT5C knockdown beneficially reduces gluconeogenesis and fasting blood glucose levels. In conclusion, the present study identifies KMT5C as a hepatic gluconeogenesis regulator by affecting PGC-1α stability.

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Journal
Nature Communications
Published
2025-02-10
DOI
https://doi.org/10.1038/s41467-025-56696-y
Citations
5
Primary Topic
Metabolism, Diabetes, and Cancer
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article
Field-Weighted Citation Impact
4.03

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article

Non-catalytic mechanisms of KMT5C regulating hepatic gluconeogenesis

Xuan Cui, Qingwen Zhao, Qi‐Qun Tang, Haojie Liu et al.
5 citations
Nature Communications
Metabolism, Diabetes, and Cancer
4.03
article

Non-catalytic mechanisms of KMT5C regulating hepatic gluconeogenesis

Xuan Cui, Qingwen Zhao, Qi‐Qun Tang, Haojie Liu, Feiyan Li, Dongning Pan, Wenjing Lv, Min Zhang, Qi Zhu, Yingjiang Xu, Ting Shi, Yue Gao, Ran Bao
article en
5 citations

Abstract

Lysine methyltransferase KMT5C catalyzes deposition of trimethylation on histone H4 lysine 20 (H4K20me3), an epigenetic marker usually associated with gene repression and maintenance of heterochromatin. KMT5C is widely expressed in a variety of tissues, however, its functional role in liver has not been explored. Here, we show Kmt5c is a fasting- and glucagon-induced gene in liver which regulates hepatic gluconeogenesis. Loss of KMT5C in hepatocytes results in downregulated gluconeogenic gene expression and compromised glucose output during fasting. KMT5C fosters gluconeogenesis through decreasing ubiquitination-mediated PGC-1α degradation, which is unexpectedly independent of its methyltransferase activity. In fact, KMT5C impedes the E3 ligase RNF34 binding to the C-terminal of PGC-1α and subsequent ubiquitination-associated degradation. The diabetic mice models and patients show elevated KMT5C levels in the livers, and KMT5C knockdown beneficially reduces gluconeogenesis and fasting blood glucose levels. In conclusion, the present study identifies KMT5C as a hepatic gluconeogenesis regulator by affecting PGC-1α stability.

Nature CommunicationsVol. 16(1)
Shanghai Medical College of Fudan University (CN), Binzhou Medical University (CN), Shandong University of Aeronautics (CN), Fudan University (CN), Westlake University (CN), Wuhan Wudong Hospital (CN), Zhongshan Hospital (CN), Affiliated Hangzhou First People's Hospital, Westlake University, School of Medicine (CN)
National Natural Science Foundation of China, Ministry of Education of the People's Republic of China, Program of Shanghai Academic Research Leader, Natural Science Foundation of Zhejiang Province
Zero hunger
Openalex Percentile: Top 7%
Metabolism, Diabetes, and Cancer
4.03
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