Popovic Doris, Dikic Ivan
Buchmann Institute for Molecular Life Sciences (BMLS) and Institute of Biochemistry II Goethe University School of Medicine, Frankfurt, Germany.
EMBO Rep. 2014 Apr;15(4):392-401. doi: 10.1002/embr.201337995. Epub 2014 Mar 6.
The RabGAP protein TBC1D5 controls cellular endomembrane trafficking processes and binds the retromer subunit VPS29 and the ubiquitin-like protein ATG8 (LC3). Here, we describe that TBC1D5 also associates with ATG9 and the active ULK1 complex during autophagy. Moreover, ATG9 and TBC1D5 interact with clathrin and the AP2 complex. Depletion of TBC1D5 leads to missorting of ATG9 to late endosomes upon activation of autophagy, whereas inhibition of clathrin-mediated endocytosis or AP2 depletion alters ATG9 trafficking and its association with TBC1D5. Taken together, our data show that TBC1D5 and the AP2 complex are important novel regulators of the rerouting of ATG9-containing vesicular carriers toward sites of autophagosome formation.
RabGAP蛋白TBC1D5控制细胞内膜运输过程,并与逆向转运蛋白亚基VPS29以及泛素样蛋白ATG8(LC3)结合。在此,我们描述了TBC1D5在自噬过程中还与ATG9和活性ULK1复合物相关联。此外,ATG9和TBC1D5与网格蛋白和AP2复合物相互作用。TBC1D5的缺失会导致自噬激活后ATG9错误分选至晚期内体,而抑制网格蛋白介导的内吞作用或AP2缺失会改变ATG9的运输及其与TBC1D5的关联。综上所述,我们的数据表明TBC1D5和AP2复合物是含ATG9的囊泡载体重新定向至自噬体形成位点的重要新型调节因子。