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CALCOCO2/NDP52 initiates selective autophagy through recruitment of ULK and TBK1 kinase complexes

机译:Calcoco2 / NDP52通过募集ULK和TBK1激酶复合物来启动选择性自噬

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摘要

The selective macroautophagy of prospective cargo necessitates activity of the autophagy machinery at cargo-determined locations. Whether phagophore membranes are recruited to, or are generated de novo at, the cargo is unknown. In our recent study we show that damaged Salmonella-containing vacuoles, marked by LGALS8/galectin-8, engage the cargo receptor CALCOCO2/NDP52 to recruit the autophagy-initiating ULK and TBK1 complexes and cause the formation of WIPI2-positive phagophore membranes. CALCOCO2 functions in the induction of autophagy by forming a trimer with RB1CC1/FIP200 and TBKBP1/SINTBAD-AZI2/NAP1, components of the ULK and TBK1 kinase complexes, respectively. Such recruitment of the upstream autophagy machinery to prospective cargo reveals how in complex eukaryotes detection of cargo-associated 'eat me' signals, induction of autophagy, and juxtaposition of cargo and phagophores are integrated.
机译:前瞻性货物的选择性宏观摄像性需要在货物确定的地点进行自噬机械的活动。 植物膜是否被招募到,或者在诺维中被生成,货物未知。 在我们最近的研究中,我们展示了含有Lgals8 / Galectin-8标记的含沙门氏菌的含有损伤的液压液,从而接受货物受体Calcoco2 / NDP52募集自噬引发ULK和TBK1复合物,并导致形成Wipi2阳性噬菌体膜。 Calcoco2通过形成具有RB1CC1 / FIP200和TBKBP1 / Sintbad-AZI2 / NAP1的三聚体,分别用ULK和TBK1激酶复合物的组分来诱导自噬。 这种招聘上游自噬机械到潜在货物,揭示了复杂的真核生物检测如何检测货物相关的“吃我”信号,诱导自噬,货物和吞噬细胞的并置。

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