Evidence map›Paper›PMID 40521666›Full record

ArticleNucleic acids research2025

Nat10 maintains the homeostasis of pluripotent and 2-cell-like states in mouse embryonic stem cells through mRNA cytidine acetylation.

Guofeng Feng, Guoxing Yin, Yusheng Liu, Chang Liu, Jie Li, Jiangtao Lu, Yongqin Yu, Ziyi Jin, Yiwei Wu, Yanbin Yue and 4 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Guofeng FengState Key Laboratory of Medicinal Chemical Biology, Nankai University, 94 Weijin Road, Tianjin 300071, China.ORCID 0009-0008-8446-8140
Guoxing YinState Key Laboratory of Medicinal Chemical Biology, Nankai University, 94 Weijin Road, Tianjin 300071, China.
Yusheng LiuCollege of Life Science, Northeast Forestry University, Harbin 150040, China.
Chang LiuState Key Laboratory of Medicinal Chemical Biology, Nankai University, 94 Weijin Road, Tianjin 300071, China.
Jie LiState Key Laboratory of Medicinal Chemical Biology, Nankai University, 94 Weijin Road, Tianjin 300071, China.
Jiangtao LuState Key Laboratory of Medicinal Chemical Biology, Nankai University, 94 Weijin Road, Tianjin 300071, China.
Yongqin YuState Key Laboratory of Medicinal Chemical Biology, Nankai University, 94 Weijin Road, Tianjin 300071, China.
Ziyi JinState Key Laboratory of Medicinal Chemical Biology, Nankai University, 94 Weijin Road, Tianjin 300071, China.
Yiwei WuState Key Laboratory of Medicinal Chemical Biology, Nankai University, 94 Weijin Road, Tianjin 300071, China.
Yanbin YueState Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.
Xiufang GaoState Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.
Jiaqiang WangCollege of Life Science, Northeast Agricultural University, Harbin 150006, China.ORCID 0000-0002-1758-3316
Falong LuState Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.ORCID 0000-0002-8321-4818
Lin LiuState Key Laboratory of Medicinal Chemical Biology, Nankai University, 94 Weijin Road, Tianjin 300071, China.ORCID 0000-0001-9881-6830

Funding

National Natural Science Foundation of China 32030033National Natural Science Foundation of China 322611605National Natural Science Foundation of China 82230052
6 · The paper itself

Abstract

Naïve mouse embryonic stem cells (mESCs) are characterized by a mixed population of cells in an interconvertible pluripotent state and a totipotent 2-cell (2C)-like state. It remains to be understood how the pluripotent state is maintained while the 2C-like state is suppressed. We show that N-acetyltransferase 10 (Nat10) maintains the pluripotent state and suppresses the 2C-like state in mESCs through mRNA modification and stabilization. Nat10 as a nucleolar protein may indirectly interact with heterochromatin through Ncl. Nat10 catalyzes the N4-acetylcytidine (ac4C) modification of mRNAs encoding the key pluripotency genes including Oct4,Esrrb and Zfp42 and enhances their mRNA stability, thus increasing their protein levels for pluripotency. Moreover, Nat10 acetylates and stabilizes heterochromatin modifiers such as Kap1 mRNA and protein to repress the 2C genes by maintaining the H3K9me3 complex. Together, these findings highlight critical roles for Nat10 in maintaining the pluripotency network and repressing the 2C-like program via mRNA ac4C modification, providing insights into the transition between pluripotent and totipotent states in mESCs.

Indexed as

CytidineMouse Embryonic Stem CellsN-Terminal Acetyltransferase EPluripotent Stem CellsRNA, MessengerAcetylationAnimalsHeterochromatinHistonesHomeostasisMiceRNA StabilityCytidineHeterochromatinHistonesN-acetylcytidineN-Terminal Acetyltransferase ERNA, Messenger

Identifiers

PMID40521666
PMCPMC12168070

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.