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Sox9 表达在性腺中的调控。

The regulation of Sox9 expression in the gonad.

机构信息

The Francis Crick Institute, London, United Kingdom.

出版信息

Curr Top Dev Biol. 2019;134:223-252. doi: 10.1016/bs.ctdb.2019.01.004. Epub 2019 Feb 13.

DOI:10.1016/bs.ctdb.2019.01.004
PMID:30999977
Abstract

The bipotential nature of cell types in the early developing gonad and the process of sex determination leading to either testis or ovary differentiation makes this an interesting system in which to study transcriptional regulation of gene expression and cell fate decisions. SOX9 is a transcription factor with multiple roles during development, including being a key player in mediating testis differentiation and therefore subsequent male development. Loss of Sox9 expression in both humans and mice results in XY female development, whereas its inappropriate activation in XX embryonic gonads can give male development. Multiple cases of Disorders of Sex Development in human patients or sex reversal in mice and other vertebrates can be explained by mutations affecting upstream regulators of Sox9 expression, such as the product of the Y chromosome gene Sry that triggers testis differentiation. Other cases are due to mutations in the Sox9 gene itself, including its own regulatory region. Indeed, rearrangements in and around the Sox9 genomic locus indicate the presence of multiple critical enhancers and the complex nature of its regulation. Here we summarize what is known about the role of Sox9 and its regulation during gonad development, including recently discovered critical enhancers. We also discuss higher order chromatin organization and how this might be involved. We end with some interesting future directions that have the potential to further enrich our understanding on the complex, multi-layered regulation controlling Sox9 expression in the gonads.

摘要

细胞类型在早期发育性腺中的双潜能性以及导致睾丸或卵巢分化的性别决定过程,使得这成为研究基因表达和细胞命运决定的转录调控的有趣系统。SOX9 是一种具有多种作用的转录因子,包括在介导睾丸分化和随后的男性发育中发挥关键作用。在人和小鼠中 Sox9 表达的缺失导致 XY 女性发育,而其在 XX 胚胎性腺中的不当激活可导致男性发育。人类患者的性别发育障碍或小鼠和其他脊椎动物的性别反转的多种情况可以通过影响 Sox9 表达的上游调节剂的突变来解释,例如触发睾丸分化的 Y 染色体基因 Sry 的产物。其他情况是由于 Sox9 基因本身的突变,包括其自身的调节区。事实上,Sox9 基因座内和周围的重排表明存在多个关键增强子,其调控的复杂性。在这里,我们总结了 Sox9 的作用及其在性腺发育过程中的调节作用,包括最近发现的关键增强子。我们还讨论了高级染色质组织,以及它如何参与其中。最后,我们提出了一些有趣的未来方向,有可能进一步丰富我们对控制性腺中 Sox9 表达的复杂、多层次调控的理解。

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