Song, Y.; Zhang, N.; Zhang, Y.; Wang, J.; Lv, Q.; Zhang, J. Single-Cell Transcriptome Analysis Reveals Development-Specific Networks at Distinct Antral Follicle Stages in Sheep Oocytes. Preprints2023, 2023110180. https://doi.org/10.20944/preprints202311.0180.v1
APA Style
Song, Y., Zhang, N., Zhang, Y., Wang, J., Lv, Q., & Zhang, J. (2023). Single-Cell Transcriptome Analysis Reveals Development-Specific Networks at Distinct Antral Follicle Stages in Sheep Oocytes. Preprints. https://doi.org/10.20944/preprints202311.0180.v1
Chicago/Turabian Style
Song, Y., Qi Lv and Jiaxin Zhang. 2023 "Single-Cell Transcriptome Analysis Reveals Development-Specific Networks at Distinct Antral Follicle Stages in Sheep Oocytes" Preprints. https://doi.org/10.20944/preprints202311.0180.v1
Abstract
The development of the ovarian antral follicle is a complex, highly regulated process. Oocytes orchestrate and coordinate the development of mammalian ovarian follicles, and the rate of follicular development is governed by a developmental program intrinsic to the oocyte. Characterizing oocyte signatures during this dynamic process is critical for understanding oocyte maturation and follicular development. Although the transcriptional signature of sheep oocytes matured in vitro and preovulatory oocytes have been previously described, the transcriptional changes of oocytes in antral follicles have not. Here, we used single-cell transcriptomics (SmartSeq2) to characterize sheep oocytes from small, medium, and large antral follicles. We characterized the transcriptomic landscape of sheep oocytes during antral follicle development, identifying unique features in the transcriptional atlas, stage-specific molecular signatures, oocyte-secreted factors, and transcription factor networks. Notably, we identified specific gene and signaling pathways in each antral follicle stage that may reflect oocyte quality and in vitro maturation competency. Additionally, we discovered key biological processes that drive the transition from small to large antral follicles, revealing hub genes involved in follicle recruitment and selection. Thus, our work provides a comprehensive characterization of the single-oocyte transcriptome, filling a gap in the mapping of the molecular landscape of sheep oogenesis. We also provide key insights into the transcriptional regulation of the critical stages of antral follicular development, which is essential for understanding how the oocyte orchestrates follicular development.
Biology and Life Sciences, Animal Science, Veterinary Science and Zoology
Copyright:
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
