Sarraj M A, McClive P J, Szczepny A, Daggag H, Loveland K L, Sinclair A H
The ARC Centre of Excellence in Biotechnology and Development, Murdoch Children's Research Institute and the Department of Paediatrics, University of Melbourne, Royal Children's Hospital, Melbourne, Victoria, Australia.
Reproduction. 2007 Apr;133(4):753-61. doi: 10.1530/rep.1.01184.
We present a detailed study of the expression pattern of WD repeat and SOCS box-containing 2 (Wsb2) in mouse embryonic and adult gonads. Wsb2 was previously identified in a differential screen aimed at identifying the genes involved in male- and female-specific gonadal development. Wsb2 expression was analysed during mouse gonadogenesis by real-time PCR, whole-mount and section in situ hybridisation and immunofluorescence. Wsb2 mRNA expression was initially detected in gonads of both sexes from 11.5 days post coitum (dpc) until 12.0 dpc. By 12.5 dpc and thereafter, Wsb2 expression rapidly decreased in the female, while persisting in the male gonads. In foetal, newborn and juvenile testes, Wsb2 mRNA and protein were readily detected in the seminiferous cords within both Sertoli and germ cells. Wsb2 mRNA was present in spermatogonia, spermatocytes and in Sertoli cells of the adult mouse testis. The differential expression of Wsb2 in male versus female embryonic gonads suggests some male-specific role in gonad development, and its expression in the first wave of spermatogenesis indicates a role in germ cells. Real-time analysis of adult mouse testis tubules cultured in the presence of the Hedgehog signalling inhibitor, cyclopamine, showed a downregulation of Wsb2 mRNA after treatment which suggests that Wsb2 may be a target of Hedgehog signalling.
我们对含WD重复序列和SOCS盒蛋白2(Wsb2)在小鼠胚胎期和成体性腺中的表达模式进行了详细研究。Wsb2先前是在一项旨在鉴定参与雄性和雌性特异性性腺发育的基因的差异筛选中被鉴定出来的。通过实时定量PCR、全胚胎原位杂交和切片原位杂交以及免疫荧光技术,对小鼠性腺发生过程中Wsb2的表达进行了分析。Wsb2 mRNA表达最初在交配后11.5天(dpc)至12.0 dpc的两性性腺中被检测到。到12.5 dpc及之后,Wsb2在雌性性腺中的表达迅速下降,而在雄性性腺中持续存在。在胎儿、新生和幼年睾丸中,在支持细胞和生殖细胞内的生精索中很容易检测到Wsb2 mRNA和蛋白。Wsb2 mRNA存在于成年小鼠睾丸的精原细胞、精母细胞和支持细胞中。Wsb2在雄性与雌性胚胎性腺中的差异表达表明其在性腺发育中具有一些雄性特异性作用,并且其在第一波精子发生中的表达表明其在生殖细胞中发挥作用。对在存在Hedgehog信号抑制剂环杷明的情况下培养的成年小鼠睾丸小管进行实时分析,结果显示处理后Wsb2 mRNA表达下调,这表明Wsb2可能是Hedgehog信号的一个靶点。