Thomas U, Phannavong B, Müller B, Garner C C, Gundelfinger E D
Federal Institute for Neurobiology, Department of Neurochemistry and Molecular Biology, Magdeburg, Germany.
Mech Dev. 1997 Mar;62(2):161-74. doi: 10.1016/s0925-4773(97)00658-8.
The synapse-associated proteins SAP97 and SAP102 are mammalian proteins that are structurally related to the Drosophila tumor suppressor protein DlgA. Previous analyses revealed that DlgA is essential for the integrity of epithelia and neuromuscular synapses. Here we show that synaptic bouton structure is severely affected in mutant larvae carrying the dlg-1(XI-2) allele. We have tested SAP97 and SAP102 for functional homology to DlgA by heterologous expression in Drosophila. Both SAP97 and SAP102 can suppress tumor formation in dlg-1 mutant flies and mimic DlgA at larval neuromuscular junctions. Neuronal expression of SAP97 or SAP102 is required for morphological restoration of synaptic boutons, indicating that presynaptic DlgA function is essential for establishing structurally intact motor nerve terminals at larval neuromuscular junctions.
与突触相关的蛋白质SAP97和SAP102是哺乳动物蛋白质,其在结构上与果蝇肿瘤抑制蛋白DlgA相关。先前的分析表明,DlgA对于上皮细胞和神经肌肉突触的完整性至关重要。在这里,我们表明携带dlg - 1(XI - 2)等位基因的突变幼虫的突触小体结构受到严重影响。我们通过在果蝇中的异源表达测试了SAP97和SAP102与DlgA的功能同源性。SAP97和SAP102都可以抑制dlg - 1突变果蝇中的肿瘤形成,并在幼虫神经肌肉接头处模拟DlgA。突触小体形态恢复需要神经元表达SAP97或SAP102,这表明突触前DlgA功能对于在幼虫神经肌肉接头处建立结构完整的运动神经末梢至关重要。