SPT6 regulates H3K14Ac deposition in mouse embryonic stem cells

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.

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Publication Details

Journal
Cell Reports
Published
2025-05-30
DOI
https://doi.org/10.1016/j.celrep.2025.115757
Primary Topic
Genomics and Chromatin Dynamics
Type
article
Field-Weighted Citation Impact
0.00

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article

SPT6 regulates H3K14Ac deposition in mouse embryonic stem cells

Li Tan, Qingqing Cai, Chenxi He, Hongjie Shen et al.
Cell Reports
Genomics and Chromatin Dynamics
article

SPT6 regulates H3K14Ac deposition in mouse embryonic stem cells

Li Tan, Qingqing Cai, Chenxi He, Hongjie Shen, Min Zeng, Feizhen Wu, Yujiang Geno Shi, Daixuan Zhang, Fei Chen, Hui Yang, Jun Hu, Mandi Mu, Jin Wang, Peng Zhao, Dong Li, Lei Zhang, Yan Cai, Siyi Cheng, Wenqi Xu, Jian Zhang
article en

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.

Cell ReportsVol. 44(6)
Shanghai Medical College of Fudan University (CN), Fudan University (CN), Pudong Medical Center (CN), Huashan Hospital (CN)
National Natural Science Foundation of China, China Postdoctoral Science Foundation, Fudan University, Science and Technology Commission of Shanghai Municipality, National Key Research and Development Program of China
Zero hunger
Openalex Percentile: Top 89%
Genomics and Chromatin Dynamics
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