| First Author | Cooke PS | Year | 2021 |
| Journal | Cell Rep | Volume | 36 |
| Issue | 7 | Pages | 109557 |
| PubMed ID | 34407397 | Mgi Jnum | J:310653 |
| Mgi Id | MGI:6764038 | Doi | 10.1016/j.celrep.2021.109557 |
| Citation | Cooke PS, et al. (2021) Male fertility in mice requires classical and nonclassical androgen signaling. Cell Rep 36(7):109557 |
| abstractText | Molecular mechanisms by which androgens signal through the androgen receptor (AR) to maintain male fertility are poorly understood. Transgenic mice were produced expressing mutant ARs that can only (1) alter gene transcription through the classical response pathway (AR-C) or (2) activate kinase signaling cascades via the nonclassical pathway (AR-NC). AR-C is sufficient to produce sperm and fertility. Haploid germ cell production, the blood-testis barrier, and spermatid migration are supported by AR-NC. Gene expression essential for chromosome synapsis during meiosis requires AR-C. We identify targets of androgen signaling required for male fertility and provide a mechanistic explanation for meiotic germ cell arrest in the absence of androgen signaling. Prostate differentiation occurs with AR-C alone, but full development requires synergistic nonclassical signaling. Both AR signaling pathways are necessary for normal male reproductive tract development and function, validating our mouse models for studies of AR functions in other target tissues. |
