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TSC1/TSC2-TOR 信号通路的演变。

Evolution of the TSC1/TSC2-TOR signaling pathway.

机构信息

Cambridgeshire and Peterborough NHS Foundation Trust, Addenbrooke's Hospital, Hills Road, Cambridge CB2 0QQ, UK.

出版信息

Sci Signal. 2010 Jun 29;3(128):ra49. doi: 10.1126/scisignal.2000803.

Abstract

The TSC1/TSC2-TOR signaling pathway [the signaling pathway that includes the heterodimeric TSC1 (tuberous sclerosis 1 protein)-TSC2 (tuberous sclerosis 2 protein) complex and TOR (target of rapamycin)] regulates various cellular processes, including protein synthesis, in response to growth factors and nutrient availability. Homologs of some pathway components have been reported from animals, fungi, plants, and protozoa. These observations led to the perception that the whole pathway is evolutionarily conserved throughout eukaryotes. Using complete genome sequences, we show that, contrary to this view, the pathway was built up from a simpler one, present in the ancestral eukaryote, coupling cell growth to energy supplies. Additional elements, such as TSC1 and TSC2, were "bolted on" in particular eukaryotic lineages. Our results also suggest that unikonts [Opisthokonta (including animals and fungi) and Amoebozoa] form a monophyletic group with the Excavata and Chromalveolata. A previous proposal, that the root of the eukaryotic "tree of life" lies between the unikonts and other organisms, should therefore be reevaluated.

摘要

TSC1/TSC2-TOR 信号通路[包括异二聚体 TSC1(结节性硬化症蛋白 1)-TSC2(结节性硬化症蛋白 2)复合物和 TOR(雷帕霉素的靶标)]调节各种细胞过程,包括蛋白质合成,以响应生长因子和营养物质的可用性。该通路的一些途径成分的同源物已在动物、真菌、植物和原生动物中报道过。这些观察结果使人们认为整个通路在真核生物中是进化保守的。我们使用完整的基因组序列表明,与这种观点相反,该通路是由祖先真核生物中存在的一种更简单的通路构建而成的,它将细胞生长与能量供应联系起来。在特定的真核生物谱系中,还添加了其他元件,如 TSC1 和 TSC2。我们的研究结果还表明,后生动物(包括动物和真菌)和变形虫与吞噬生物和叶绿体形成一个单系群。因此,应该重新评估之前提出的真核生物“生命之树”的根位于后生动物和其他生物之间的观点。

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