Center for Reproductive Biology, School of Biological Sciences, Washington State University, Pullman, Washington, United States of America.
PLoS One. 2012;7(9):e43380. doi: 10.1371/journal.pone.0043380. Epub 2012 Sep 12.
A major event in mammalian male sex determination is the induction of the testis determining factor Sry and its downstream gene Sox9. The current study provides one of the first genome wide analyses of the downstream gene binding targets for SRY and SOX9 to help elucidate the molecular control of Sertoli cell differentiation and testis development. A modified ChIP-Chip analysis using a comparative hybridization was used to identify 71 direct downstream binding targets for SRY and 109 binding targets for SOX9. Interestingly, only 5 gene targets overlapped between SRY and SOX9. In addition to the direct response element binding gene targets, a large number of atypical binding gene targets were identified for both SRY and SOX9. Bioinformatic analysis of the downstream binding targets identified gene networks and cellular pathways potentially involved in the induction of Sertoli cell differentiation and testis development. The specific DNA sequence binding site motifs for both SRY and SOX9 were identified. Observations provide insights into the molecular control of male gonadal sex determination.
哺乳动物雄性性别决定的一个主要事件是睾丸决定因子 Sry 的诱导及其下游基因 Sox9。本研究提供了对 SRY 和 Sox9 的下游基因结合靶标的全基因组分析之一,以帮助阐明支持细胞分化和睾丸发育的分子控制。使用比较杂交的改良 ChIP-Chip 分析用于鉴定 71 个直接下游的 SRY 结合靶标和 109 个 Sox9 的结合靶标。有趣的是,仅在 SRY 和 Sox9 之间有 5 个基因靶标重叠。除了直接反应元件结合基因靶标外,还鉴定了大量针对 SRY 和 Sox9 的非典型结合基因靶标。对下游结合靶标的生物信息学分析确定了可能参与诱导支持细胞分化和睾丸发育的基因网络和细胞途径。确定了 SRY 和 Sox9 的特定 DNA 序列结合位点基序。这些观察结果为男性性腺性别决定的分子控制提供了深入了解。