Tead4和Tfap2c在全能胚胎中产生双能和双能开关,以促进强大的血统多样化
Meng Zhu1,2,3, Maciej Meglicki1, Adiyant Lamba1
1Mammalian Embryo and Stem Cell Group, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.
Nature structural & molecular biology
|May 24, 2024
概括
转录因子TFAP2C和TEAD4通过促进全能性丧失和血统多样化,加速早期胚胎发育. 它们调节河马信号传递和细胞命运决策,建立一个可视化的开关,以实现强大的发育.
科学领域:
- 发展生物学 发展生物学
- 细胞生物学 细胞生物学
- 遗传学 遗传学 是一个
背景情况:
- 早期的哺乳动物胚胎失去了全能性,分化为内细胞质 (ICM) 和体 (TE).
- 已知转录因子TFAP2C和TEAD4,以及激活的RHOA,可以加速胚胎极化.
研究的目的:
- 调查TFAP2C和TEAD4在加速全能性损失和血统多样化中的作用.
- 阐明TFAP2C和TEAD4调节Hippo信号和细胞命运规范的机制.
主要方法:
- 在早期小鼠和人类胚胎中分析转录因子活性.
- 研究TFAP2C和TEAD4对Hippo信号通路组件的影响.
- 检查血统特定基因 (ICM和TE) 的激活.
主要成果:
- 在发育中的胚胎中,TFAP2C和TEAD4加速了全能性丧失.
- 这些因素表现出Hippo信号的矛盾调节,促进调节者,同时诱导角域形成,使Hippo失活.
- TFAP2C和TEAD4激活了TE指标,而TFAP2C也激活了ICM指标.
结论:
- 不对称的顶点域隔离调和了对立的Hippo信号调节,导致TE命运 (Hippo OFF) 或ICM命运 (Hippo ON).
- TFAP2C和TEAD4建立了一个双稳定开关机制,推动发育胚胎中强大的血统多样化.
相关概念视频
Lineage Commitment
3.0K
Commitment is the process whereby stem cells:
3.0K
Somatic to iPS Cell Reprogramming
2.2K
Reprogramming alters the gene expression in somatic cells, transforming them into induced pluripotent stem (iPS) cells over several generations. Scientists can reprogram cells by introducing genes for four transcription factors—Oct4, Sox2, Klf4, and c-Myc (OSKM) by viral or non-viral methods. These factors are also known as Yamanaka factors after Shinya Yamanaka, who first generated iPS cells using mouse skin cells. Yamanaka was awarded the Nobel Prize in Physiology or Medicine in 2012...
2.2K
Combinatorial Gene Control
8.3K
Combinatorial gene control is the synergistic action of several transcriptional factors to regulate the expression of a single gene. The absence of one or more of these factors may lead to a significant difference in the level of gene expression or repression.
The expression of more than 30,000 genes is controlled by approximately 2000-3000 transcription factors. This is possible because a single transcription factor can recognize more than one regulatory sequence. The specificity in gene...
The expression of more than 30,000 genes is controlled by approximately 2000-3000 transcription factors. This is possible because a single transcription factor can recognize more than one regulatory sequence. The specificity in gene...
8.3K
Methods of Nuclear Reprogramming
1.8K
Nuclear reprogramming is a process of transforming one cell type into an unrelated cell type by epigenetic changes that alter the cell’s original gene expression pattern. Such epigenetic changes force cells to express a different set of genes, which play a significant role in inducing transformation into other cell types. Nuclear reprogramming offers applications in reproductive cloning for livestock propagation and regenerative medicine — developing patient-specific cells for...
1.8K
Forced Transdifferentiation
1.9K
Transdifferentiation, also known as lineage reprogramming, was first discovered by Selman and Kafatos in 1974 in silkmoths. They observed that the moths’ cuticle-producing cells transformed into salt-producing cells. Many such cases of natural transdifferentiation occur in organisms. In humans, pancreatic alpha cells can become beta cells. In newts, the loss of the eye’s lens causes the pigmented epithelial cells to transdifferentiate into the lens cells.
Artificial...
Artificial...
1.9K
General Transcription Factors
5.2K
Tissue-specific transcription factors contribute to diverse cellular functions in mammals. For example, the gene for beta globin, a major component of hemoglobin, is present in all cells of the body. However, it is only expressed in red blood cells because the transcription factors that can bind to the promoter sequences of the beta globin gene are only expressed in these cells. Tissue-specific transcription factors also ensure that mutations in these factors may impair only the function of...
5.2K


