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首页> 外文期刊>BMC Genomics >Identification of Sertoli cell-specific transcripts in the mouse testis and the role of FSH and androgen in the control of Sertoli cell activity
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Identification of Sertoli cell-specific transcripts in the mouse testis and the role of FSH and androgen in the control of Sertoli cell activity

机译:小鼠睾丸中支持细胞特异性转录物的鉴定以及FSH和雄激素在控制支持细胞活性中的作用

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The Sertoli cells act to induce testis differentiation and subsequent development in fetal and post-natal life which makes them key to an understanding of testis biology. As a major step towards characterisation of factors involved in Sertoli cell function we have identified Sertoli cell-specific transcripts in the mouse testis and have used the data to identify Sertoli cell-specific transcripts altered in mice lacking follicle-stimulating hormone receptors (FSHRKO) and/or androgen receptors (AR) in the Sertoli cells (SCARKO). Adult iDTR mice were injected with busulfan to ablate the germ cells and 50?days later they were treated with diphtheria toxin (DTX) to ablate the Sertoli cells. RNAseq carried out on testes from control, busulfan-treated and busulfan + DTX-treated mice identified 701 Sertoli-specific transcripts and 4302 germ cell-specific transcripts. This data was mapped against results from microarrays using testicular mRNA from 20?day-old FSHRKO, SCARKO and FSHRKO.SCARKO mice. Results show that of the 534 Sertoli cell-specific transcripts present on the gene chips, 85% were altered in the FSHRKO mice and 94% in the SCARKO mice (mostly reduced in both cases). In the FSHRKO.SCARKO mice additive or synergistic effects were seen for most transcripts. Age-dependent studies on a selected number of Sertoli cell-specific transcripts, showed that the marked effects in the FSHRKO at 20?days had largely disappeared by adulthood although synergistic effects of FSHR and AR knockout were seen. These studies have identified the Sertoli cell-specific transcriptome in the mouse testis and have shown that most genes in the transcriptome are FSH- and androgen-dependent at puberty although the importance of FSH diminishes towards adulthood.
机译:睾丸支持细胞的作用是诱导睾丸的分化以及胎儿和产后生活的发育,这使其成为了解睾丸生物学的关键。作为表征Sertoli细胞功能相关因子的重要步骤,我们在小鼠睾丸中鉴定了Sertoli细胞特异性转录本,并使用该数据鉴定了在缺乏促卵泡激素受体(FSHRKO)和或支持细胞中的雄激素受体(AR)。给成年iDTR小鼠注射白消安以消融生殖细胞,然后在50天后用白喉毒素(DTX)处理以消灭Sertoli细胞。在对照,白消安处理和白消安+ DTX处理的​​小鼠的睾丸上进行的RNAseq鉴定出701个Sertoli特异性转录本和4302个生殖细胞特异性转录本。使用20天大的FSHRKO,SCARKO和FSHRKO.SCARKO小鼠的睾丸mRNA,将这些数据与微阵列的结果作图。结果显示,在基因芯片上存在的534个Sertoli细胞特异转录本中,FSHRKO小鼠的85%发生了改变,而SCARKO小鼠的94%发生了改变(两种情况下大多数都减少了)。在FSHRKO.SCARKO小鼠中,大多数转录本都具有累加或协同作用。对特定数量的支持细胞特异转录物的年龄依赖性研究表明,成年后20天FSHRKO的显着作用已基本消失,尽管已观察到FSHR和AR基因敲除的协同作用。这些研究已经在小鼠睾丸中鉴定了Sertoli细胞特异的转录组,并显示了该转录组中的大多数基因在青春期都依赖FSH和雄激素,尽管FSH对成年的重要性降低了。

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