Pu Jing, Schindler Christina, Jia Rui, Jarnik Michal, Backlund Peter, Bonifacino Juan S
Cell Biology and Metabolism Program, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
Biomedical Mass Spectrometry Facility, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
Dev Cell. 2015 Apr 20;33(2):176-88. doi: 10.1016/j.devcel.2015.02.011.
The positioning of lysosomes within the cytoplasm is emerging as a critical determinant of many lysosomal functions. Here we report the identification of a multisubunit complex named BORC that regulates lysosome positioning. BORC comprises eight subunits, some of which are shared with the BLOC-1 complex involved in the biogenesis of lysosome-related organelles, and the others of which are products of previously uncharacterized open reading frames. BORC associates peripherally with the lysosomal membrane, where it functions to recruit the small GTPase Arl8. This initiates a chain of interactions that promotes the kinesin-dependent movement of lysosomes toward the plus ends of microtubules in the peripheral cytoplasm. Interference with BORC or other components of this pathway results in collapse of the lysosomal population into the pericentriolar region. In turn, this causes reduced cell spreading and migration, highlighting the importance of BORC-dependent centrifugal transport for non-degradative functions of lysosomes.
溶酶体在细胞质中的定位正逐渐成为许多溶酶体功能的关键决定因素。在此,我们报告了一种名为BORC的多亚基复合物的鉴定,该复合物调节溶酶体定位。BORC由八个亚基组成,其中一些与参与溶酶体相关细胞器生物发生的BLOC-1复合物共享,其他亚基则是先前未表征的开放阅读框的产物。BORC在外周与溶酶体膜结合,在那里它起到招募小GTP酶Arl8的作用。这引发了一系列相互作用,促进了溶酶体在周围细胞质中沿着微管正端的驱动蛋白依赖性运动。干扰BORC或该途径的其他成分会导致溶酶体群体坍塌到中心粒周围区域。反过来,这会导致细胞铺展和迁移减少,突出了BORC依赖性离心运输对溶酶体非降解功能的重要性。