Pevsner J, Hsu S C, Scheller R H
Department of Molecular and Cellular Physiology, Howard Hughes Medical Institute, Stanford University Medical Center, CA 94305.
Proc Natl Acad Sci U S A. 1994 Feb 15;91(4):1445-9. doi: 10.1073/pnas.91.4.1445.
We have identified n-Sec1, a rat brain homolog of the yeast Sec1p protein that participates in the constitutive secretory pathway between the Golgi apparatus and the plasma membrane. The rat brain cDNA is predicted to encode a 68-kDa protein with 65% amino acid identity to Drosophila rop, 59% identity to Caenorhabditis elegans unc-18, and 27% identity to Saccharomyces cerevisiae Sec1p. By RNA blot analysis, n-Sec1 mRNA expression is neural-specific. An anti-peptide antiserum directed against the n-Sec1 carboxyl terminus detects a 68-kDa protein in rat brain cytosol and membranes, but not in peripheral tissues. In the presence of syntaxin 1a, a plasma membrane protein implicated in synaptic vesicle docking, n-Sec1 becomes membrane-associated. n-Sec1 binds to syntaxin 1a, 2, and 3 fusion proteins coupled to agarose beads, but not to syntaxin 4 fusion protein or beads coupled to a variety of other proteins. These findings indicate that n-Sec1 is a neural-specific, syntaxin-binding protein that may participate in the regulation of synaptic vesicle docking and fusion.
我们已鉴定出n-Sec1,它是酵母Sec1p蛋白在大鼠脑中的同源物,参与高尔基体与质膜之间的组成型分泌途径。预测大鼠脑cDNA编码一种68 kDa的蛋白质,与果蝇rop的氨基酸同一性为65%,与秀丽隐杆线虫unc-18的同一性为59%,与酿酒酵母Sec1p的同一性为27%。通过RNA印迹分析,n-Sec1 mRNA的表达具有神经特异性。针对n-Sec1羧基末端的抗肽抗血清可在大鼠脑细胞质和膜中检测到一种68 kDa的蛋白质,但在外周组织中未检测到。在与突触小泡对接有关的质膜蛋白 syntaxin 1a存在的情况下,n-Sec1与膜结合。n-Sec1与偶联到琼脂糖珠上的syntaxin 1a、2和3融合蛋白结合,但不与syntaxin 4融合蛋白或偶联到多种其他蛋白的珠子结合。这些发现表明,n-Sec1是一种神经特异性的、与syntaxin结合的蛋白,可能参与突触小泡对接和融合的调节。