https://ogma.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 Dynamic Hedgehog signalling pathway activity in germline stem cells https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:20442 Sat 24 Mar 2018 08:06:54 AEDT ]]> The chemokine CXCL12 and its receptor CXCR4 are implicated in human seminoma metastasis https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:20270 Sat 24 Mar 2018 07:59:54 AEDT ]]> Differential expression profiles of conserved Snail transcription factors in the mouse testis https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:42608 Snai2‐deficient mice provided evidence of deficient spermatogenesis. To address the hypothesis that Snail proteins are important for male fertility, this study provides the first comprehensive cellular expression profiles of all three mammalian Snail genes in the post‐natal mouse testis. To evaluate Snail transcript expression profiles, droplet digital (dd) PCR and in situ hybridization were employed. Snai1, 2 and 3 transcripts are readily detected at 7, 14, 28 days post‐partum (dpp) and 7 weeks (adult). Unique cellular expression was demonstrated for each by in situ hybridization and immunohistochemistry using Western blot‐validated antibodies. SNAI1 and SNAI2 are in the nucleus of the most mature germ cell types at post‐natal ages 10, 15 and 26. SNAI3 is only detected from 15 dpp onwards and is localized in the Sertoli cell cytoplasm. In the adult testis, Snai1 and Snai2 transcripts are detected in spermatogonia and spermatocytes, while Snai3 is in both germ and Sertoli cells. SNAI1 protein is evident in nuclei of spermatogonia, spermatocytes, round spermatids and elongated spermatids (Stages IX–XII). SNAI2 is present in the nuclei of spermatogonia and spermatocytes, with a faint signal detected in round spermatids. SNAI3 was detected only in Sertoli cell cytoplasm, as in juvenile testes. Additionally, colocalization of SNAI1 and SNAI2 with previously identified key binding partners, LSD1 and PRC2 complex components, provides strong evidence that these important functional interactions are conserved during spermatogenesis to control gene activity. These distinct expression profiles suggest that each Snail family member has unique functions during spermatogenesis.]]> Fri 26 Aug 2022 14:44:17 AEST ]]>