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Developmental Acquisition of Functions.

机构信息

National Institute of Child Health and Human Development, Bethesda, MD 20892, USA.

National Human Genome Research Institute, Bethesda, MD 20892, USA.

出版信息

Genes (Basel). 2021 Oct 23;12(11):1675. doi: 10.3390/genes12111675.

Abstract

Remarkably, the transcription factor, referred to as "the guardian of the genome", is not essential for mammalian development. Moreover, efforts to identify -dependent developmental events have produced contradictory conclusions. Given the importance of pluripotent stem cells as models of mammalian development, and their applications in regenerative medicine and disease, resolving these conflicts is essential. Here we attempt to reconcile disparate data into justifiable conclusions predicated on reports that -dependent transcription is first detected in late mouse blastocysts, that activity first becomes potentially lethal during gastrulation, and that apoptosis does not depend on . Furthermore, does not regulate expression of genes required for pluripotency in embryonic stem cells (ESCs); it contributes to ESC genomic stability and differentiation. Depending on conditions, accelerates initiation of apoptosis in ESCs in response to DNA damage, but cell cycle arrest as well as the rate and extent of apoptosis in ESCs are -independent. In embryonic fibroblasts, induces cell cycle arrest to allow repair of DNA damage, and cell senescence to prevent proliferation of cells with extensive damage.

摘要

值得注意的是,这种转录因子被称为“基因组的守护者”,对于哺乳动物的发育并非必不可少。此外,试图鉴定与 -dependent 相关的发育事件产生了相互矛盾的结论。鉴于多能干细胞作为哺乳动物发育模型的重要性,及其在再生医学和疾病中的应用,解决这些冲突至关重要。在这里,我们试图将不同的数据协调为合理的结论,依据的是这样的报告:在晚期小鼠胚泡中首次检测到依赖的转录,在原肠胚形成过程中,的活性首次变得潜在致命,凋亡不依赖于。此外,并不调节胚胎干细胞(ESCs)中多能性所需基因的表达;它有助于 ESC 的基因组稳定性和分化。根据条件的不同,在 ESCs 中,在响应 DNA 损伤时加速凋亡的起始,但细胞周期停滞以及 ESCs 中的细胞凋亡的速度和程度都是 -dependent 无关的。在胚胎成纤维细胞中,诱导细胞周期停滞以允许修复 DNA 损伤,并诱导衰老以防止具有广泛损伤的细胞增殖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1278/8622856/5e082d11894f/genes-12-01675-g001.jpg

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