CircKDM5B sponges miR-128 to regulate porcine blastocyst development by modulating trophectoderm barrier function

• Published in: Molecular human reproduction Vol. 29; no. 9
• Main Authors: Gao, Di, Wang, Xin, Yan, Ye-Lian, Li, Chao, Tan, Yong-Peng, Liu, Qiu-Chen, Zhang, Meng-Ya, Zhang, Jian V, Sun, Qing-Yuan, Cao, Zu-Bing, Zhang, Yun-Hai
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 30.08.2023
• Subjects: porcine; trophectoderm; embryo development; blastocyst development; circular RNAs; tight junction
• ISSN: 1460-2407; 1460-2407
• DOI: 10.1093/molehr/gaad027

Abstract Circular RNAs (circRNAs), which exert critical functions in the regulation of transcriptional and post-transcriptional gene expression, are found in mammalian cells but their functions in mammalian preimplantation embryo development remain poorly understood. Here, we showed that circKDM5B mediated miRNA-128 (miR-128) to regulate porcine early embryo development. We screened circRNAs potentially expressed in porcine embryos through an integrated analysis of sequencing data from mouse and human embryos, as well as porcine oocytes. An authentic circRNA originating from histone demethylase KDM5B (referred to as circKDM5B) was abundantly expressed in porcine embryos. Functional studies revealed that circKDM5B knockdown not only significantly reduced blastocyst formation but also decreased the number of total cells and trophectoderm (TE) cells. Moreover, the knockdown of circKDM5B resulted in the disturbance of tight junction assembly and impaired paracellular sealing within the TE epithelium. Mechanistically, miR-128 inhibitor injection could rescue the early development of circKDM5B knockdown embryos. Taken together, the findings revealed that circKDM5B functions as a miR-128 sponge, thereby facilitating early embryonic development in pigs through the modulation of gene expression linked to tight junction assembly.