Knower K C, Sim H, McClive P J, Bowles J, Koopman P, Sinclair A H, Harley V R
Human Molecular Genetics, Prince Henry's Institute of Medical Research, Clayton, Australia.
Sex Dev. 2007;1(2):114-26. doi: 10.1159/000100033.
The study of the mammalian sex-determining pathway has been hampered by the lack of cell culture systems to investigate the underlying molecular relationships between sex-determining genes. Recent approaches using high-throughput genome-wide studies have revealed a number of sexually dimorphic genes expressed in the developing mouse gonad. Here, we investigated a human testicular cell line in terms of its expression of known sex-determining genes and newly identified candidates. The human embryonal carcinoma cell line NT2/D1 was screened for the expression of 46 genes with known or potential roles in the sex-determining and differentiation pathway. Forty genes tested were expressed in NT2/D1 cells including the testis-determining genes SRY, SOX9, SF-1, DHH and FGF9. Genes not expressed included WT1, DAX1 and the ovary-specific genes FOXL2 and WNT4. Cell-specific markers demonstrate that NT2/D1 cells reflect a number of cell types in the gonad including Sertoli, Leydig and germ cells. Our results suggest that male pathways initiated by SRY, SOX9 and SF-1 remain intact in these cells. Lack of expression of ovary-specific genes is consistent with a commitment of these cells to the male lineage. Manipulation of gene expression in this cell line could be an important new in vitro tool for the discovery of new human sex-determining genes.
由于缺乏用于研究性别决定基因之间潜在分子关系的细胞培养系统,哺乳动物性别决定途径的研究受到了阻碍。最近使用高通量全基因组研究的方法揭示了许多在发育中的小鼠性腺中表达的性二态性基因。在这里,我们就已知性别决定基因和新鉴定的候选基因的表达情况对一种人类睾丸细胞系进行了研究。对人类胚胎癌细胞系NT2/D1进行了筛选,以检测46个在性别决定和分化途径中具有已知或潜在作用的基因的表达。所检测的40个基因在NT2/D1细胞中表达,包括睾丸决定基因SRY、SOX9、SF-1、DHH和FGF9。未表达的基因包括WT1、DAX1以及卵巢特异性基因FOXL2和WNT4。细胞特异性标志物表明,NT2/D1细胞反映了性腺中的多种细胞类型,包括支持细胞、间质细胞和生殖细胞。我们的结果表明,由SRY、SOX9和SF-1启动的雄性途径在这些细胞中保持完整。卵巢特异性基因的未表达与这些细胞向雄性谱系的定向分化一致。对该细胞系中基因表达的操纵可能成为发现新的人类性别决定基因的一种重要的新型体外工具。