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Lessons from p53 in non-mammalian models.

机译:非哺乳动物模型中p53的教训。

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摘要

p53 is a fundamental determinant of oncogenesis, aging physiology and neurodegenerative pathologies. The complexity of the p53 regulatory network can hinder attempts to fully understand how this oncogenic protein operates within/betweencells to constrain growth potential. Orthologs of p53 in non-mammalian models, such as zebrafish, Drosophila and Caenorhabditis elegans, afford simpler models that illuminate core properties of this ancient network. The existence of p53 in short-lived organisms, where cancers do not occur, argues that tumor suppression per se was not the evolutionary pressure shaping p53. Instead, p53 as a constraint against tumor growth was probably co-opted from more ancestral, nonautonomous functions that are entirely unknown. Describing these functional properties will be essential for a comprehensive picture of the p53 regulatory network in normal and disease states. The tractable systems described here offer sophisticated genetic tools and fundamental insights that will continue tobe indispensable models for achieving this goal.
机译:p53是肿瘤发生,衰老生理和神经退行性病变的基本决定因素。 p53调控网络的复杂性可能会阻碍尝试全面了解这种致癌蛋白如何在细胞内/细胞间运作以限制生长潜能。在非哺乳动物模型(例如斑马鱼,果蝇和秀丽隐杆线虫)中,p53的直系同源基因提供了更简单的模型,阐明了这个古老网络的核心特性。 p53在不发生癌症的短命生物中的存在表明,抑制肿瘤本身并不是形成p53的进化压力。取而代之的是,p53作为对肿瘤生长的限制可能是从更为未知的祖先,非自治功能中选择的。描述这些功能特性对于全面了解正常和疾病状态下的p53调控网络至关重要。此处描述的易处理系统提供了复杂的遗传工具和基本见识,它们将继续成为实现此目标必不可少的模型。

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