TEAD4 在小鼠植入前胚胎中调控 KRT8 和 YAP,而在牛中则不然。

IF 3.7 3区 生物学 Q1 DEVELOPMENTAL BIOLOGY Reproduction Pub Date : 2024-02-02 Print Date: 2024-03-01 DOI:10.1530/REP-23-0322
Xiaotong Wu, Yan Shi, Bingjie Hu, Panpan Zhao, Shuang Li, Lieying Xiao, Shaohua Wang, Kun Zhang
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引用次数: 0

摘要

TEAD4是植入前发育过程中表达的一个关键转录因子,对小鼠滋养层外胚层特异性基因的表达至关重要。然而,TEAD4在小鼠胚胎植入前发育过程中的功能机制及其在哺乳动物中的保守性仍不清楚。在这里,我们报告了 Tead4 是小鼠囊胚形成所必需的关键转录因子。通过碱基编辑破坏 Tead4 会导致胚胎发育停滞。此外,RNA-seq 分析显示 Tead4 基因敲除胚胎中有 670 个基因失调。正如预期的那样,Tead4 基因敲除导致滋养层外胚层基因 Cdx2 和 Gata3 减少。有趣的是,我们观察到 Krt8 的减少,这表明 Tead4 影响了小鼠滋养层上皮的完整性。更重要的是,我们注意到 Tead4 缺失的小鼠外细胞核 Yap 显著减少,这表明 Tead4 直接调节 Hippo 信号传导。相比之下,TEAD4 缺失的牛胚胎仍能发育成囊胚,CDX2、GATA3 和 SOX2 表达正常,但细胞总数和 ICM 细胞数减少。总之,我们认为 Tead4 可通过 Krt8 和 Yap 调节小鼠囊胚的形成,而 Krt8 和 Yap 都是小鼠胚胎植入前发育的关键调节因子。
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TEAD4 regulates KRT8 and YAP in preimplantation embryos in mice but not in cattle.

In brief: Lineage specification plays a vital role in preimplantation development. TEAD4 is an essential transcription factor for trophectoderm lineage specification in mice but not in cattle.

Abstract: Tead4, a critical transcription factor expressed during preimplantation development, is essential for the expression of trophectoderm-specific genes in mice. However, the functional mechanism of TEAD4 in mouse preimplantation development and its conservation across mammals remain unclear. Here, we report that Tead4 is a crucial transcription factor necessary for blastocyst formation in mice. Disruption of Tead4 through base editing results in developmental arrest at the morula stage. Additionally, RNA-seq analysis reveals dysregulation of 670 genes in Tead4 knockout embryos. As anticipated, Tead4 knockout led to a decrease in trophectoderm genes Cdx2 and Gata3. Intriguingly, we observed a reduction in Krt8, suggesting that Tead4 influences the integrity of the trophectoderm epithelium in mice. More importantly, we noted a dramatic decrease in nuclear Yap in outside cells for Tead4-deficient morula, indicating that Tead4 directly regulates Hippo signaling. In contrast, bovine embryos with TEAD4 depletion could still develop to blastocysts with normal expression of CDX2, GATA3, and SOX2, albeit with a decrease in total cell number and ICM cell number. In conclusion, we propose that Tead4 regulates mouse blastocyst formation via Krt8 and Yap, both of which are critical regulators of mouse preimplantation development.

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来源期刊
Reproduction
Reproduction 生物-发育生物学
CiteScore
7.40
自引率
2.60%
发文量
199
审稿时长
4-8 weeks
期刊介绍: Reproduction is the official journal of the Society of Reproduction and Fertility (SRF). It was formed in 2001 when the Society merged its two journals, the Journal of Reproduction and Fertility and Reviews of Reproduction. Reproduction publishes original research articles and topical reviews on the subject of reproductive and developmental biology, and reproductive medicine. The journal will consider publication of high-quality meta-analyses; these should be submitted to the research papers category. The journal considers studies in humans and all animal species, and will publish clinical studies if they advance our understanding of the underlying causes and/or mechanisms of disease. Scientific excellence and broad interest to our readership are the most important criteria during the peer review process. The journal publishes articles that make a clear advance in the field, whether of mechanistic, descriptive or technical focus. Articles that substantiate new or controversial reports are welcomed if they are noteworthy and advance the field. Topics include, but are not limited to, reproductive immunology, reproductive toxicology, stem cells, environmental effects on reproductive potential and health (eg obesity), extracellular vesicles, fertility preservation and epigenetic effects on reproductive and developmental processes.
期刊最新文献
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