Maroteaux L, Scheller R H
Howard Hughes Medical Institute, Department of Molecular and Cellular Physiology, Stanford University, CA 94305.
Brain Res Mol Brain Res. 1991 Oct;11(3-4):335-43. doi: 10.1016/0169-328x(91)90043-w.
The synuclein cDNA was previously cloned from Torpedo califonica using an antiserum against purified synaptic vesicles. Here we show that this gene hybridizes to several clones in a rat brain cDNA library. These clones represent cDNAs coding for different proteins, thus determining a family. These proteins display similar organization to the Torpedo protein. The homology resides within the repetition of 7 amino acids. The diversity is generated by alternative splicing as suggested by Southern analysis, as well as by sequence analysis. These proteins are specifically expressed in the rat brain. In situ hybridization shows expression of synuclein mRNAs in discrete areas of the brain, the hippocampus is the most intensely stained area. This localization is reminiscent of those molecules involved in phosphoinositols second messenger pathways. Synuclein proteins are present in rat brain in dual form--a small form which is soluble and a large form which is associated with synaptosomal membranes in a regulated fashion.
突触核蛋白cDNA先前是利用针对纯化突触小泡的抗血清从加州电鳐中克隆出来的。在此我们表明,该基因与大鼠脑cDNA文库中的几个克隆杂交。这些克隆代表编码不同蛋白质的cDNA,从而确定了一个家族。这些蛋白质与电鳐蛋白具有相似的结构。同源性存在于7个氨基酸的重复序列中。如Southern分析以及序列分析所表明的,多样性是由可变剪接产生的。这些蛋白质在大鼠脑中特异性表达。原位杂交显示突触核蛋白mRNA在脑的离散区域表达,海马是染色最深的区域。这种定位让人联想到那些参与磷酸肌醇第二信使途径的分子。突触核蛋白在大鼠脑中以两种形式存在——一种是可溶的小形式,另一种是与突触体膜以一种受调控的方式相关联的大形式。