Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, Quebec H3A 2B4, Canada.
Mol Cell. 2010 Feb 12;37(3):370-82. doi: 10.1016/j.molcel.2009.12.037.
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.
DENN 结构域是一个进化上古老的蛋白质模块。DENN 结构域中的突变会导致植物发育缺陷和人类疾病,但这个常见模块的功能尚不清楚。我们现在证明 connecdenn/DENND1A 的 DENN 结构域作为 Rab35 的鸟嘌呤核苷酸交换因子(GEF)发挥作用,以调节内体膜运输。Rab35 活性的丧失会导致早期内体增大,并抑制 MHC Ⅰ类的再循环。此外,它还阻止 EHD1 向早期内体的募集,EHD1 是参与内体货物再循环的管状结构的常见成分。我们的数据揭示了 DENN 结构域的酶活性,并证明不同的 Rab GTPases 可以募集共同的蛋白质机器到内体网络的各个部位,以建立货物选择性再循环途径。