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N6-methyladenosine methyltransferase METTL3 modulates the cell cycle of granulosa cells via CCND1 and AURKB in Haimen goats. | LitMetric

AI Article Synopsis

  • N6-methyladenosine (m6A) is important for various biological processes, but its role during oocyte maturation in domestic animals, particularly in granulosa cells, is not well understood.
  • Observations show an increase in m6A methyltransferase-like 3 (METTL3) in granulosa cells during maturation in Haimen goats, with knockdown of METTL3 causing cell cycle disruptions, increased apoptosis, and decreased hormone secretion.
  • METTL3 regulates the cell cycle by promoting Aurora kinase B (AURKB) mRNA degradation and is involved in AURKB transcription through the Cyclin D1-Retinoblastoma-E2F1 pathway, emphasizing its crucial role in granulosa cells during o

Article Abstract

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.

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Source
http://dx.doi.org/10.1096/fj.202301232RDOI Listing

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