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B6.Y(TIR) 性腺中 SRY 对 SOX9 的上调效率低下且延迟,从而允许卵巢发生分化。

SRY upregulation of SOX9 is inefficient and delayed, allowing ovarian differentiation, in the B6.Y(TIR) gonad.

机构信息

Department of Biology, McGill University, Royal Victoria Hospital, 687 Pine Avenue West, Montreal, Quebec, Canada H3A 1A1.

出版信息

Differentiation. 2011 Jul;82(1):18-27. doi: 10.1016/j.diff.2011.04.007. Epub 2011 May 17.

Abstract

SRY on the Y-chromosome acts as a transcription factor to initiate testicular differentiation in mammals. Sox9 is a SRY target gene, upregulated immediately after Sry expression, and plays a key role in testicular differentiation. In the present study, we examined the expression of SRY and SOX9 proteins in the B6.Y(TIR) gonad, which undergoes partial or complete sex reversal. The results show that the ontogeny of SRY expression in the B6.Y(TIR) gonad was comparable with that in the B6.XY gonad. On the other hand, while SOX9 expression immediately followed SRY expression in the B6.XY gonad, it was considerably delayed compared to SRY expression in the B6.Y(TIR) gonad or SOX9 expression in the B6.XY gonad. Although SOX9 expression reached the entire gonad at a time point, it was downregulated and became restricted to the central area in which testis cords were organized. MIS, a marker of Sertoli cells, appeared only in well-organized testis cords. We speculate that the SRY protein from the Y(TIR)-chromosome is inefficient in upregulating the Sox9 gene on the B6 background, allowing the initiation of ovarian differentiation.

摘要

Y 染色体上的 SRY 作为转录因子,启动哺乳动物的睾丸分化。Sox9 是 SRY 的靶基因,在 Sry 表达后立即上调,在睾丸分化中发挥关键作用。在本研究中,我们检查了 B6.Y(TIR)性腺中 SRY 和 SOX9 蛋白的表达,B6.Y(TIR)性腺经历部分或完全性别反转。结果表明,B6.Y(TIR)性腺中 SRY 的发育与 B6.XY 性腺中 SRY 的发育相当。另一方面,虽然 SOX9 在 B6.XY 性腺中紧随 SRY 表达,但与 B6.Y(TIR)性腺中的 SRY 表达或 B6.XY 性腺中的 SOX9 表达相比,它明显延迟。尽管 SOX9 表达在一个时间点达到整个性腺,但它被下调并仅限于组织睾丸索的中央区域。MIS 是支持细胞的标志物,仅出现在组织良好的睾丸索中。我们推测来自 Y(TIR)染色体的 SRY 蛋白在 B6 背景下上调 Sox9 基因的效率较低,从而允许卵巢分化的启动。

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