Li Xueyi, Sapp Ellen, Valencia Antonio, Kegel Kimberly B, Qin Zheng-Hong, Alexander Jonathan, Masso Nicholas, Reeves Patrick, Ritch James J, Zeitlin Scott, Aronin Neil, Difiglia Marian
Laboratory of Cellular Neurobiology and Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, Massachusetts, USA.
Neuroreport. 2008 Oct 29;19(16):1643-7. doi: 10.1097/WNR.0b013e328315cd4c.
Huntingtin is ubiquitously expressed and enriched in the brain. Deletion of the huntingtin gene in mice is lethal during early embryonic development. The function of huntingtin is, however, not clear. Here, we report that huntingtin is important for the function of Rab11, a critical GTPase in regulating membrane traffic from recycling endosomes to the plasma membrane. In huntingtin-null embryonic stem cells, the levels of Rab11 on membranes and nucleotide exchange activity on Rab11 were significantly reduced compared with normal embryonic stem cells. In brain membranes, an antibody against huntingtin immunoprecipitated a nucleotide exchange activity on Rab11 and huntingtin was coprecipitated with Rab11 in the presence of guanosine diphosphate. These data suggest a role for huntingtin in a complex that activates Rab11.
亨廷顿蛋白在全身广泛表达,且在大脑中含量丰富。小鼠中亨廷顿蛋白基因的缺失在胚胎发育早期是致死性的。然而,亨廷顿蛋白的功能尚不清楚。在此,我们报告亨廷顿蛋白对于Rab11的功能很重要,Rab11是一种关键的GTP酶,在调节从循环内体到质膜的膜运输中起作用。在缺乏亨廷顿蛋白的胚胎干细胞中,与正常胚胎干细胞相比,膜上Rab11的水平以及Rab11上的核苷酸交换活性显著降低。在脑膜中,一种抗亨廷顿蛋白的抗体免疫沉淀了Rab11上的核苷酸交换活性,并且在存在二磷酸鸟苷的情况下,亨廷顿蛋白与Rab11共沉淀。这些数据表明亨廷顿蛋白在激活Rab11的复合物中发挥作用。