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Glycine cleavage system determines the fate of pluripotent stem cells via the regulation of senescence and epigenetic modifications

Metabolic remodelling has emerged as critical for stem cell pluripotency; however, the underlying mechanisms have yet to be fully elucidated. Here, we found that the glycine cleavage system (GCS) is highly activated to promote stem cell pluripotency and during somatic cell reprogramming. Mechanistic...

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Detalles Bibliográficos
Autores principales: Tian, Shengya, Feng, Junru, Cao, Yang, Shen, Shengqi, Cai, Yongping, Yang, Dongdong, Yan, Ronghui, Wang, Lihua, Zhang, Huafeng, Zhong, Xiuying, Gao, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Life Science Alliance LLC 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6765226/
https://www.ncbi.nlm.nih.gov/pubmed/31562192
http://dx.doi.org/10.26508/lsa.201900413
Descripción
Sumario:Metabolic remodelling has emerged as critical for stem cell pluripotency; however, the underlying mechanisms have yet to be fully elucidated. Here, we found that the glycine cleavage system (GCS) is highly activated to promote stem cell pluripotency and during somatic cell reprogramming. Mechanistically, we revealed that the expression of Gldc, a rate-limiting GCS enzyme regulated by Sox2 and Lin28A, facilitates this activation. We further found that the activated GCS catabolizes glycine to fuel H3K4me3 modification, thus promoting the expression of pluripotency genes. Moreover, the activated GCS helps to cleave excess glycine and prevents methylglyoxal accumulation, which stimulates senescence in stem cells and during reprogramming. Collectively, our results demonstrate a novel mechanism whereby GCS activation controls stem cell pluripotency by promoting H3K4me3 modification and preventing cellular senescence.