Parnas D, Haghighi A P, Fetter R D, Kim S W, Goodman C S
Howard Hughes Medical Institute, Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720, USA.
Neuron. 2001 Nov 8;32(3):415-24. doi: 10.1016/s0896-6273(01)00485-8.
Mutations in dpix were recovered from a large-scale screen in Drosophila for genes that control synaptic structure. dpix encodes dPix, a Rho-type guanine nucleotide exchange factor (RtGEF) homologous to mammalian Pix. Here we show that dPix plays a major role in regulating postsynaptic structure and protein localization at the Drosophila glutamatergic neuromuscular junction. dpix mutations lead to decreased synaptic levels of the PDZ protein Dlg, the cell adhesion molecule Fas II, and the glutamate receptor subunit GluRIIA, and to a complete reduction of the serine/threonine kinase Pak and the subsynaptic reticulum. The electrophysiology of these mutant synapses is nearly normal. Many, but not all, dpix defects are mediated through dPak, a member of the family of Cdc42/Rac1-activated kinases. Thus, a Rho-type GEF and Rho-type effector kinase regulate postsynaptic structure.
dpix突变是在果蝇中进行的一项大规模基因筛选中发现的,该筛选旨在寻找控制突触结构的基因。dpix编码dPix,一种与哺乳动物Pix同源的Rho型鸟嘌呤核苷酸交换因子(RtGEF)。在此我们表明,dPix在调节果蝇谷氨酸能神经肌肉接头处的突触后结构和蛋白质定位中起主要作用。dpix突变导致PDZ蛋白Dlg、细胞粘附分子Fas II和谷氨酸受体亚基GluRIIA的突触水平降低,并导致丝氨酸/苏氨酸激酶Pak和突触下网状结构完全减少。这些突变突触的电生理学几乎正常。许多(但不是全部)dpix缺陷是通过dPak介导的,dPak是Cdc42/Rac1激活激酶家族的成员。因此,一种Rho型GEF和Rho型效应激酶调节突触后结构。