2. Academic Validation
  3. SPT6 regulates H3K14Ac deposition in mouse embryonic stem cells

SPT6 regulates H3K14Ac deposition in mouse embryonic stem cells

  • Cell Rep. 2025 Jun 24;44(6):115757. doi: 10.1016/j.celrep.2025.115757.
Daixuan Zhang 1,  Li Dong 1,  Ying Cai 1,  Peng Zhao 1,  Qingqing Cai 1,  Jian Zhang 1,  Yajun Hu 1,  Mandi Mu 1,  Siyi Cheng 1,  Jin Wang 1,  Min Zeng 1,  Chenxi He 1,  Lei Zhang 1,  Hui Yang 2,  Fei Xavier Chen 1,  Li Tan 3,  Feizhen Wu 4,  Yujiang Geno Shi 1,  Wenqi Xu 5,  Hongjie Shen 6
Affiliations

Affiliations

  • 1 Longevity and Aging Institute, The Shanghai Key Laboratory of Medical Epigenetics, Institutes of Biomedical Sciences, Department of Pancreatic Surgery, Zhongshan Hospital, Fudan University, Shanghai 200030, China.
  • 2 Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai 200040, China.
  • 3 Longevity and Aging Institute, The Shanghai Key Laboratory of Medical Epigenetics, Institutes of Biomedical Sciences, Department of Pancreatic Surgery, Zhongshan Hospital, Fudan University, Shanghai 200030, China; Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Fudan University, Shanghai 201300, China.
  • 4 Laboratory of Epi-Informatics, Intelligent Medicine Institute, Fudan University, Shanghai 200030, China.
  • 5 Longevity and Aging Institute, The Shanghai Key Laboratory of Medical Epigenetics, Institutes of Biomedical Sciences, Department of Pancreatic Surgery, Zhongshan Hospital, Fudan University, Shanghai 200030, China. Electronic address: wenqixu@fudan.edu.cn.
  • 6 Longevity and Aging Institute, The Shanghai Key Laboratory of Medical Epigenetics, Institutes of Biomedical Sciences, Department of Pancreatic Surgery, Zhongshan Hospital, Fudan University, Shanghai 200030, China. Electronic address: hongjieshen@fudan.edu.cn.
PMID: 40450685 DOI: 10.1016/j.celrep.2025.115757
Abstract

SPT6 (suppressor of Ty 6) is a conserved histone chaperone that plays critical roles in RNA Pol II progression and nucleosome reassembly. However, the functions of SPT6 in chromatin regulation remain incompletely understood. Here, we show that SPT6 localizes to histone H3 lysine 14 acetylation (H3K14Ac)-enriched regions in mouse embryonic stem cells (mESCs). Loss of SPT6 leads to reduced H3K14Ac levels and diminished transcription. Mechanistically, we show that SPT6 enhances the chromatin binding of the acetyltransferases KAT7 and KAT6A/KAT6B, which are responsible for H3K14Ac deposition, but SPT6-facilitated H3K14Ac can also occur in a KAT7/6A/6B independent manner. Our findings highlight a vital role for SPT6 in preserving the H3K14Ac landscape in mESCs, providing new insights into the crosstalk between transcription machinery and H3K14Ac regulation in mammals.

Keywords

CP: Stem cell research; H3K14Ac; SPT6; epigenetics; histone modification; transcription.

Figures
Products