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J Cell Biol. 2017 Oct 2;216(10):3307-3321. doi: 10.1083/jcb.201705151. Epub 2017 Aug 31.

WDR91 is a Rab7 effector required for neuronal development.

Liu K1,2, Xing R1,3, Jian Y1, Gao Z1, Ma X3,4, Sun X1, Li Y1, Xu M1, Wang X1,2, Jing Y1, Guo W5, Yang C6,2.

Author information

1  State Key Laboratory of Molecular and Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.

2  State Key Laboratory of Natural Resource Conservation and Utilization in Yunnan and Center for Life Science, School of Life Sciences, Yunnan University, Kunming, China.

3  Graduate University of Chinese Academy of Sciences, Beijing, China.

4  Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.

5  State Key Laboratory of Molecular and Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China wxguo@genetics.ac.cn.

6  State Key Laboratory of Molecular and Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China clyang@genetics.ac.cn.

Abstract

Early-to-late endosome conversion, which is essential for delivery of endosomal cargoes to lysosomes, requires switching of early endosome-specific Rab5 and PtdIns3P to late endosome-specific Rab7 and PtdIns(3,5)P2 In this study, we identify the WD40-repeat protein WDR91 as a Rab7 effector that couples Rab switching with PtdIns3P down-regulation on endosomes. Loss of WDR91 greatly increases endosomal PtdIns3P levels, arresting endosomes at an intermediate stage and blocking endosomal-lysosomal trafficking.WDR91 is recruited to endosomes by interacting with active guanosine triphosophate-Rab7 and inhibits Rab7-associated phosphatidylinositol 3-kinase activity. In mice, global Wdr91 knockout causes neonatal death, whereas brain-specific Wdr91inactivation impairs brain development and causes postnatal death. Mouse neurons lacking Wdr91 accumulate giant intermediate endosomes and exhibit reduced neurite length and complexity. These phenotypes are rescued by WDR91 but not WDR91 mutants that cannot interact with Rab7. Thus, WDR91 serves as a Rab7 effector that is essential for neuronal development by facilitating endosome conversion in the endosome-lysosome pathway.


PMID: 28860274  PMCID: PMC5626554 [Available on 2018-04-02]   DOI:  10.1083/jcb.201705151

 

 

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