TY - JOUR
T1 - PTBP1 mediates Sertoli cell actin cytoskeleton organization by regulating alternative splicing of actin regulators
AU - Wang, Yuexi
AU - Chembazhi, Ullas Valiya
AU - Yee, Danielle
AU - Chen, Sijie
AU - Ji, Jie
AU - Wang, Yujie
AU - Nguyen, Ka Lam
AU - Lin, PoChing
AU - Ratti, Antonia
AU - Hess, Rex A
AU - Qiao, Huanyu
AU - Ko, CheMyong
AU - Yang, Jing
AU - Kalsotra, Auinash
AU - Mei, Wenyan
PY - 2024/11/11
Y1 - 2024/11/11
N2 - Spermatogenesis is a biological process within the testis that produces haploid spermatozoa for the continuity of species. Sertoli cells are somatic cells in the seminiferous epithelium that orchestrate spermatogenesis. Cyclic reorganization of the Sertoli cell actin cytoskeleton is vital for spermatogenesis, but the underlying mechanism remains largely unclear. Here, we report that the RNA-binding protein PTBP1 controls Sertoli cell actin cytoskeleton reorganization by programming alternative splicing of actin cytoskeleton regulators. This splicing control enables ectoplasmic specializations, the actin-based adhesion junctions, to maintain the blood-testis barrier and support spermatid transport and transformation. Particularly, we show that PTBP1 promotes actin bundle formation by repressing the inclusion of exon 14 of Tnik, a kinase present at the ectoplasmic specialization. Our results thus reveal a novel mechanism wherein Sertoli cell actin cytoskeleton dynamics are controlled post-transcriptionally by utilizing functionally distinct isoforms of actin regulatory proteins, and PTBP1 is a critical regulatory factor in generating such isoforms.
AB - Spermatogenesis is a biological process within the testis that produces haploid spermatozoa for the continuity of species. Sertoli cells are somatic cells in the seminiferous epithelium that orchestrate spermatogenesis. Cyclic reorganization of the Sertoli cell actin cytoskeleton is vital for spermatogenesis, but the underlying mechanism remains largely unclear. Here, we report that the RNA-binding protein PTBP1 controls Sertoli cell actin cytoskeleton reorganization by programming alternative splicing of actin cytoskeleton regulators. This splicing control enables ectoplasmic specializations, the actin-based adhesion junctions, to maintain the blood-testis barrier and support spermatid transport and transformation. Particularly, we show that PTBP1 promotes actin bundle formation by repressing the inclusion of exon 14 of Tnik, a kinase present at the ectoplasmic specialization. Our results thus reveal a novel mechanism wherein Sertoli cell actin cytoskeleton dynamics are controlled post-transcriptionally by utilizing functionally distinct isoforms of actin regulatory proteins, and PTBP1 is a critical regulatory factor in generating such isoforms.
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U2 - 10.1093/nar/gkae862
DO - 10.1093/nar/gkae862
M3 - Article
C2 - 39373517
SN - 0305-1048
VL - 52
SP - 12244
EP - 12261
JO - Nucleic acids research
JF - Nucleic acids research
IS - 20
M1 - gkae862
ER -