N6‐methyladenosine methyltransferase METTL3 modulates the cell cycle of granulosa cells via CCND1 and AURKB in Haimen goats

N6‐methyladenosine (m6A) plays a crucial role in many bioprocesses across species, but its function in granulosa cells during oocyte maturation is not well understood in animals, especially domestic animals. We observed an increase in m6A methyltransferase‐like 3 (METTL3) in granulosa cells during o...

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Veröffentlicht in:The FASEB journal 2023-11, Vol.37 (11), p.e23273-n/a
Hauptverfasser: Liu, Zifei, Zhou, Lei, Li, Dongxu, Lu, Honghui, Liu, Liang, Mao, Weijia, Yu, Xiaoqing, Fan, Yixuan, Huang, Qunhao, Wang, Feng, Wan, Yongjie
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Sprache:eng
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Zusammenfassung:N6‐methyladenosine (m6A) plays a crucial role in many bioprocesses across species, but its function in granulosa cells during oocyte maturation is not well understood in animals, especially domestic animals. We observed an increase in m6A methyltransferase‐like 3 (METTL3) in granulosa cells during oocyte maturation in Haimen goats. Our results showed that knockdown of METTL3 disrupted the cell cycle in goat granulosa cells, leading to aggravated cell apoptosis and inhibition of cell proliferation and hormone secretion. Mechanistically, METTL3 may regulate the cell cycle in goat granulosa cells by mediating Aurora kinase B (AURKB) mRNA degradation in an m6A‐YTH N6‐methyladenosine RNA binding protein 2 (YTHDF2) manner and participating in AURKB transcription via the Cyclin D1 (CCND1)‐Retinoblastoma protein (RB)‐E2F transcription factor 1 (E2F1) pathway. Overall, our study highlights the essential role of METTL3 in granulosa cells during oocyte maturation in Haimen goats. These findings provide a theoretical basis and technical means for understanding how RNA methylation participates in oocyte maturation through granulosa cells. METTL3 knockdown led to a decrease in the m6A level and suppressed the expression of CCND1 and AURKB, thereby disturbing the cell cycle, resulting the inhibition of cell survival in Haimen goat granulosa cells.
ISSN:0892-6638
1530-6860
DOI:10.1096/fj.202301232R