Suppr超能文献

Ovo对动物卵巢生殖细胞中piRNA途径的转录调控。

Transcriptional regulation of the piRNA pathway by Ovo in animal ovarian germ cells.

作者信息

Alizada Azad, Hannon Gregory J, Nicholson Benjamin Czech

机构信息

Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge CB2 0RE, United Kingdom.

Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge CB2 0RE, United Kingdom

出版信息

Genes Dev. 2025 Feb 3;39(3-4):221-241. doi: 10.1101/gad.352120.124.

Abstract

The gene-regulatory mechanisms controlling the expression of the germline PIWI-interacting RNA (piRNA) pathway components within the gonads of metazoan species remain largely unexplored. In contrast to the male germline piRNA pathway, which in mice is known to be activated by the testis-specific transcription factor A-MYB, the nature of the ovary-specific gene-regulatory network driving the female germline piRNA pathway remains a mystery. Here, using as a model, we combined multiple genomics approaches to reveal the transcription factor Ovo as regulator of the germline piRNA pathway in ovarian germ cells. Ectopic expression of Ovo in ovarian somatic cells activates germline piRNA pathway components, including the ping-pong factors Aubergine, Argonaute-3, and Vasa, leading to assembly of perinuclear cellular structures resembling nuage bodies of germ cells. We found that in ovarian somatic cells, transcription of is repressed by , thus preventing expression of germline piRNA pathway genes in the soma. Cross-species ChIP-seq and motif analyses demonstrate that Ovo is binding to genomic CCGTTA motifs within the promoters of germline piRNA pathway genes, suggesting a regulation by Ovo in ovaries analogous to that of A-MYB in testes. Our results also show consistent engagement of the Ovo transcription factor family at ovarian piRNA clusters across metazoan species, reflecting a deep evolutionary conservation of this regulatory paradigm from insects to humans.

摘要

控制后生动物性腺中生殖系PIWI相互作用RNA(piRNA)途径组分表达的基因调控机制在很大程度上仍未被探索。与已知在小鼠中由睾丸特异性转录因子A-MYB激活的雄性生殖系piRNA途径不同,驱动雌性生殖系piRNA途径的卵巢特异性基因调控网络的性质仍是个谜。在这里,我们以 为模型,结合多种基因组学方法,揭示转录因子Ovo是卵巢生殖细胞中生殖系piRNA途径的调节因子。Ovo在卵巢体细胞中的异位表达激活了生殖系piRNA途径组分,包括乒乓因子茄子蛋白、AGO3和Vasa,导致形成类似于生殖细胞类核体的核周细胞结构。我们发现,在卵巢体细胞中, 的转录受到 的抑制,从而阻止了生殖系piRNA途径基因在体细胞中的表达。跨物种ChIP-seq和基序分析表明,Ovo与生殖系piRNA途径基因启动子内的基因组CCGTTA基序结合,这表明Ovo在卵巢中的调控类似于A-MYB在睾丸中的调控。我们的结果还显示,Ovo转录因子家族在跨后生动物物种的卵巢piRNA簇中持续参与,这反映了从昆虫到人类这种调控模式的深度进化保守性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/885e/11789646/1228ccbdfcfb/221f01.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验