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Non-oncogenic roles of TAp73: from multiciliogenesis to metabolism.

机译:TAP73的非致癌作用:从多硅发生到代谢。

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摘要

The p53 family of transcription factors (p53, p63 and p73) covers a wide range of functions critical for development, homeostasis and health of mammals across their lifespan. Beside the well-established tumor suppressor role, recent evidence has highlighted novel non-oncogenic functions exerted by p73. In particular, p73 is required for multiciliated cell (MCC) differentiation; MCCs have critical roles in brain and airways to move fluids across epithelial surfaces and to transport germ cells in the reproductive tract. This novel function of p73 provides a unifying cellular mechanism for the disparate inflammatory and immunological phenotypes of p73-deficient mice. Indeed, mice with Trp73 deficiency suffer from hydrocephalus, sterility and chronic respiratory tract infections due to profound defects in ciliogenesis and complete loss of mucociliary clearance since MCCs are essential for cleaning airways from inhaled pollutants, pathogens and allergens. Cross-species genomic analyses and functional rescue experiments identify TAp73 as the master transcriptional integrator of ciliogenesis, upstream of previously known central nodes. In addition, TAp73 shows a significant ability to regulate cellular metabolism and energy production through direct transcriptional regulation of several metabolic enzymes, such as glutaminase-2 and glucose-6 phosphate dehydrogenase. This recently uncovered role of TAp73 in the regulation of cellular metabolism strongly affects oxidative balance, thus potentially influencing all the biological aspects associated with p73 function, including development, homeostasis and cancer. Although through different mechanisms, p63 isoforms also contribute to regulation of cellular metabolism, thus indicating a common route used by all family members to control cell fate. At the structural level, the complexity of p73's function is further enhanced by its ability to form heterotetramers with some p63 isoforms, thus indicating the existence of an intrafamily crosstalk that determines the global outcome of p53 family function. In this review, we have tried to summarize all the recent evidence that have emerged on the novel non-oncogenic roles of p73, in an attempt to provide a unified view of the complex function of this gene within its family.
机译:P53系列转录因子(P53,P63和P73)涵盖了在其寿命周围的发育,稳态和哺乳动物的健康至关重要的广泛功能。除了完善的肿瘤抑制作用旁,最近的证据突出显示P73施加的新型非致癌功能。特别地,多型细胞(MCC)分化需要P73; MCCS在大脑和呼吸道中具有关键作用,以将流体移入上皮表面并在生殖道中运送生殖细胞。 P73的这种新功能提供了P73缺陷小鼠的不同炎症和免疫表型的统一细胞机制。实际上,由于MCCS在吸入污染物,病原体和过敏原于清洁气道至关重要跨物种基因组分析和功能救援实验鉴定TaP73作为纤氯的母血症转录积分剂,以前已知的中央节点的上游。此外,TAP73显示了通过直接转录若干代谢酶的直接转录调节来调节细胞代谢和能量产生的显着能力,例如谷氨酰胺酶-2和葡萄糖-6磷酸脱氢酶。这最近发现TAP73在细胞新陈代谢调节中的作用强烈影响氧化平衡,从而可能影响与P73功能相关的所有生物方面,包括发育,稳态和癌症。虽然通过不同的机制,但P63同种型也有助于调节细胞代谢,从而指示所有家庭成员使用的常见途径控制细胞命运。在结构层面,通过其形成具有一些P63同种型的异质蛋白的能力进一步增强了P73功能的复杂性,从而表明存在确定P53家族功能的全球结果的卵巢串扰的存在。在这篇综述中,我们试图总结最近出现在P73的新型非致病作用上的所有证据,以便在其家庭内提供统一的本基因的复杂功能的统一视图。

著录项

  • 来源
    《Cell death and differentiation》 |2018年第1期|共10页
  • 作者单位

    Department of Pathology Stony Brook University;

    Medical Research Council Toxicology Unit Leicester University;

    Institute of Biophysical Chemistry and Center for Biomolecular Magnetic Resonance Goethe;

    Institute of Biophysical Chemistry and Center for Biomolecular Magnetic Resonance Goethe;

    Medical Research Council Toxicology Unit Leicester University;

    Department of Pathology Stony Brook University;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 细胞生物学;
  • 关键词

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