| First Author | Wang S | Year | 2024 |
| Journal | Adv Sci (Weinh) | Volume | 11 |
| Issue | 31 | Pages | e2403866 |
| PubMed ID | 38889293 | Mgi Jnum | J:354333 |
| Mgi Id | MGI:7731018 | Doi | 10.1002/advs.202403866 |
| Citation | Wang S, et al. (2024) CWF19L2 is Essential for Male Fertility and Spermatogenesis by Regulating Alternative Splicing. Adv Sci (Weinh) 11(31):e2403866 |
| abstractText | The progression of spermatogenesis along specific developmental trajectories depends on the coordinated regulation of pre-mRNA alternative splicing (AS) at the post-transcriptional level. However, the fundamental mechanism of AS in spermatogenesis remains to be investigated. Here, it is demonstrated that CWF19L2 plays a pivotal role in spermatogenesis and male fertility. In germline conditional Cwf19l2 knockout mice exhibiting male sterility, impaired spermatogenesis characterized by increased apoptosis and decreased differentiated spermatogonia and spermatocytes is observed. That CWF19L2 interacted with several spliceosome proteins to participate in the proper assembly and stability of the spliceosome is discovered. By integrating RNA-seq and LACE-seq data, it is further confirmed CWF19L2 directly bound and regulated the splicing of genes related to spermatogenesis (Znhit1, Btrc, and Fbxw7) and RNA splicing (Rbfox1, Celf1, and Rbm10). Additionally, CWF19L2 can indirectly amplify its effect on splicing regulation through modulating RBFOX1. Collectively, this research establishes that CWF19L2 orchestrates a splicing factor network to ensure accurate pre-mRNA splicing during the early steps of spermatogenesis. |
