FTO Controls Endometrial Receptivity and Embryo Implantation through Regulating m6A and H3K27me3

A on SUZ12 mRNA, lowering its stability, weakening PRC2 function and de-repressing WNT5B. Functionally, FTO depletion impaired spheroid adhesion and Wnt signaling, reversible by SUZ12 restoration or WNT5B inhibition. Thus, FTO preserves epithelial integrity and endometrial receptivity by stabilizing SUZ12 mRNA and maintaining H3K27me3 mediated repression of WNT5B, implicating the FTO/SUZ12/WNT5B axis in implantation failure.

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Publication Details

Journal
Communications Biology
Published
2026-05-11
DOI
https://doi.org/10.1038/s42003-026-10247-3
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
0.00

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article

FTO Controls Endometrial Receptivity and Embryo Implantation through Regulating m6A and H3K27me3

Boxian Huang, Qingxia Meng, Fengjia Guo, Linlin Tan et al.
Communications Biology
RNA modifications and cancer
article

FTO Controls Endometrial Receptivity and Embryo Implantation through Regulating m6A and H3K27me3

Boxian Huang, Qingxia Meng, Fengjia Guo, Linlin Tan, Hong Li, Wenjuan Xia, Xiujuan Hu, Jincheng Li, Ming Zhang, Jiafeng Lu
article en

Abstract

A on SUZ12 mRNA, lowering its stability, weakening PRC2 function and de-repressing WNT5B. Functionally, FTO depletion impaired spheroid adhesion and Wnt signaling, reversible by SUZ12 restoration or WNT5B inhibition. Thus, FTO preserves epithelial integrity and endometrial receptivity by stabilizing SUZ12 mRNA and maintaining H3K27me3 mediated repression of WNT5B, implicating the FTO/SUZ12/WNT5B axis in implantation failure.

Communications Biology
Suzhou Municipal Hospital (CN)
National Natural Science Foundation of China
Zero hunger
Openalex Percentile: Top 9%
RNA modifications and cancer
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