Department of Biology and Center for Cell and Genome Science, University of Utah, 257 South 1400 East, Salt Lake City, UT 84112, USA.
Curr Opin Cell Biol. 2013 Aug;25(4):489-94. doi: 10.1016/j.ceb.2013.05.003. Epub 2013 Jun 14.
Endosomal sorting complexes required for transport (ESCRTs) execute the biogenesis of late endosomal multivesicular bodies (MVBs). The ESCRT pathway has traditionally been viewed as a means by which transmembrane proteins are degraded in vacuoles/lysosomes. More recent studies aimed at understanding the broader functions of ESCRTs have uncovered unexpected links with pathways that control cellular metabolism. Central to this communication is TORC1, the kinase complex that controls many of the catabolic and anabolic systems. The connection between TORC1 activity and ESCRTs allows cells to quickly adapt to the stress of nutrient limitations until the longer-term autophagic pathway is activated. Increasing evidence also points to ESCRTs regulating RNA interference (RNAi) pathways that control translation.
内体分选复合物需要运输 (ESCRTs) 执行晚期内体多泡体 (MVBs) 的生物发生。ESCRT 途径传统上被视为跨膜蛋白在液泡/溶酶体中降解的一种方式。最近旨在了解 ESCRTs 更广泛功能的研究揭示了与控制细胞代谢途径的意外联系。这种通信的核心是 TORC1,它是控制许多分解代谢和合成代谢系统的激酶复合物。TORC1 活性与 ESCRTs 之间的联系使细胞能够快速适应营养限制的压力,直到长期的自噬途径被激活。越来越多的证据还表明 ESCRTs 调节控制翻译的 RNA 干扰 (RNAi) 途径。