FUS driven circCNOT6L biogenesis in mouse and human spermatozoa supports zygote development

• Published in: Cellular and molecular life sciences : CMLS 2022-01, Vol.79 (1), p.50-50, Article 50
• Main Authors: Chioccarelli, Teresa, Falco, Geppino, Cappetta, Donato, De Angelis, Antonella, Roberto, Luca, Addeo, Martina, Ragusa, Marco, Barbagallo, Davide, Berrino, Liberato, Purrello, Michele, Ambrosino, Concetta, Cobellis, Gilda, Pierantoni, Riccardo, Chianese, Rosanna, Manfrevola, Francesco
• Format: Article
• Language: English
• Subjects: Animal models; Animals; Biochemistry; Biomedical and Life Sciences; Biomedicine; Biosynthesis; Cannabinoid CB1 receptors; Cell Biology; Circular RNA; DNA-directed RNA polymerase; Epididymis; Female; Fertilization; Gametocytes; Gene expression; Gene sequencing; Humans; Life Sciences; Male; Mice; Mice, Knockout; Oocytes; Original; Original Article; Ribonucleases - genetics; RNA polymerase; RNA polymerase II; RNA, Circular - metabolism; RNA-binding protein; RNA-Binding Protein FUS - metabolism; RNA-mediated interference; Sperm; Spermatogenesis; Spermatozoa; Spermatozoa - cytology; Spermatozoa - metabolism; Stem cells; Zygote - metabolism; Zygotes
• ISSN: 1420-682X; 1420-9071
• DOI: 10.1007/s00018-021-04054-8

Circular RNA (circRNA) biogenesis requires a backsplicing reaction, promoted by inverted repeats in cis -flanking sequences and trans factors, such as RNA-binding proteins (RBPs). Among these, FUS plays a key role. During spermatogenesis and sperm maturation along the epididymis such a molecular mechanism has been poorly explored. With this in mind, we chose circCNOT6L as a study case and wild-type (WT) as well as cannabinoid receptor type-1 knock-out ( Cb1 −/− ) male mice as animal models to analyze backsplicing mechanisms. Our results suggest that spermatozoa (SPZ) have an endogenous skill to circularize mRNAs, choosing FUS as modulator of backsplicing and under CB1 stimulation. A physical interaction between FUS and CNOT6L as well as a cooperation among FUS, RNA Polymerase II (RNApol2) and Quaking (QKI) take place in SPZ. Finally, to gain insight into FUS involvement in circCNOT6L biogenesis, FUS expression was reduced through RNA interference approach. Paternal transmission of FUS and CNOT6L to oocytes during fertilization was then assessed by using murine unfertilized oocytes (NF), one-cell zygotes (F) and murine oocytes undergoing parthenogenetic activation (PA) to exclude a maternal contribution. The role of circCNOT6L as an active regulator of zygote transition toward the 2-cell-like state was suggested using the Embryonic Stem Cell (ESC) system. Intriguingly, human SPZ exactly mirror murine SPZ.