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mTOR对细胞合成代谢的调控:或者说我是如何学会不再担忧并爱上翻译的。

Regulation of cellular anabolism by mTOR: or how I learned to stop worrying and love translation.

作者信息

Deaver J William, López Sara Mata, Ryan Patrick J, Nghiem Peter P, Riechman Steven E, Fluckey James D

机构信息

Department of Health and Kinesiology, 107 Gilchrist Building, 2929 Research Parkway, Texas A&M University, College Station, TX, USA.

Department of Veterinary Integrative Biosciences, 402 Raymond Stotzer Pkwy Building 2, Texas A&M University, College Station, TX, USA.

出版信息

Sports Med Health Sci. 2020 Nov 30;2(4):195-201. doi: 10.1016/j.smhs.2020.11.003. eCollection 2020 Dec.

Abstract

The process and regulation of cellular metabolism are extremely complex and accomplished through multiple signalling pathways that operate in parallel, and often experience significant overlap in upstream and downstream a signal transduction. Despite this complexity, single pathway or even single protein activations are commonly used to extrapolate broad characterizations of cellular metabolism. Furthermore, multiple routes for peptide-chain translation initiation exist, some of which may be either exclusive or overlapping depending on the state and environment of the cell. While it may be highly impractical to account for every aspect of metabolic regulation and permutation of mRNA translation, it is important to acknowledge that investigations relating to these pathways are often incomplete and not necessarily indicative of the overall metabolic status. This becomes urgent when considering the role that cellular anabolism plays in both healthy cellular functions and the aetiology of several disease's altered metabolisms. This review describes recent advances in the understanding of cellular metabolic regulation, with specific focus given to the complexity of 'downstream' mRNA translation initiation through both mTOR-dependent and mTOR-independent signallings.

摘要

细胞代谢的过程和调控极其复杂,是通过多条并行运作的信号通路来完成的,并且在信号转导的上下游常常存在显著重叠。尽管存在这种复杂性,但通常使用单一通路甚至单一蛋白质激活来推断细胞代谢的广泛特征。此外,存在多种肽链翻译起始途径,其中一些途径可能根据细胞状态和环境而相互排斥或重叠。虽然考虑代谢调控和mRNA翻译的每一个方面可能非常不切实际,但重要的是要认识到与这些途径相关的研究往往不完整,不一定能代表整体代谢状态。当考虑细胞合成代谢在健康细胞功能和几种疾病代谢改变的病因学中所起的作用时,这一点变得尤为迫切。本综述描述了在细胞代谢调控理解方面的最新进展,特别关注通过mTOR依赖性和mTOR非依赖性信号传导的“下游”mRNA翻译起始的复杂性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/984d/9219308/b0c08c3465e9/gr1.jpg

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