The Connecdenn DENN Domain: A GEF for Rab35 Mediating Cargo-Specific Exit from Early Endosomes

被引:155
作者
Allaire, Patrick D. [1 ]
Marat, Andrea L. [1 ]
Dall'Armi, Claudia [2 ]
Di Paolo, Gilbert [2 ]
McPherson, Peter S. [1 ]
Ritter, Brigitte [1 ]
机构
[1] McGill Univ, Montreal Neurol Inst, Dept Neurol & Neurosurg, Montreal, PQ H3A 2B4, Canada
[2] Columbia Univ, Coll Phys & Surg, Dept Pathol & Cell Biol, Taub Inst Res Alzheimers Dis & Aging Brain,Med Ct, New York, NY 10032 USA
基金
加拿大健康研究院;
关键词
ENDOCYTIC PATHWAY; PLASMA-MEMBRANE; EXCHANGE PROTEIN; BINDING PROTEIN; CELL; CLATHRIN; TRANSFERRIN; RAB11; IDENTIFICATION; CYTOKINESIS;
D O I
10.1016/j.molcel.2009.12.037
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The DENN domain is an evolutionarily ancient protein module. Mutations in the DENN domain cause developmental defects in plants and human diseases, yet the function of this common module is unknown. We now demonstrate that the connecdenn/DENND1A DENN domain functions as a guanine nucleotide exchange factor (GEF) for Rab35 to regulate endosomal membrane trafficking. Loss of Rab35 activity causes an enlargement of early endosomes and inhibits MHC class I recycling. Moreover, it prevents early endosomal recruitment of EHD1, a common component of tubules involved in endosomal cargo recycling. Our data reveal an enzymatic activity for a DENN domain and demonstrate that distinct Rab GTPases can recruit a common protein machinery to various sites within the endosomal network to establish cargo-selective recycling pathways.
引用
收藏
页码:370 / 382
页数:13
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