Söderqvist H, Imreh G, Kihlmark M, Linnman C, Ringertz N, Hallberg E
Department of Biochemistry, Stockholm University, Sweden.
Eur J Biochem. 1997 Dec 15;250(3):808-13. doi: 10.1111/j.1432-1033.1997.00808.x.
The 121-kDa pore membrane protein (POM121) is a bitopic integral membrane protein specifically located in the pore membrane domain of the nuclear envelope with its short N-terminal tail exposed on the luminal side and its major C-terminal portion adjoining the nuclear pore complex. In order to locate a signal for targeting of POM121 to the nuclear pores, we overexpressed selected regions of POM121 alone or fused to the green fluorescent protein (GFP) in transiently transfected COS-1 cells or in a stably transfected neuroblastoma cell line. Microscopic analysis of the GFP fluorescence or immunostaining was used to determine the intracellular distribution of the overexpressed proteins. The endofluorescent GFP tag had no effect on the distribution of POM121, since the chimerical POM121-GFP fusion protein was correctly targeted to the nuclear pores of both COS-1 cells and neuroblastoma cells. Based on the differentiated intracellular sorting of the POM121 variants, we conclude that the first 128 amino acids of POM121 contains signals for targeting to the continuous endoplasmic reticulum/nuclear envelope membrane system but not specifically to the nuclear pores and that a specific nuclear pore targeting signal is located between amino acids 129 and 618 in the endoplasmically exposed portion of POM121.
121千道尔顿的孔膜蛋白(POM121)是一种双拓扑整合膜蛋白,特异性定位于核膜的孔膜结构域,其短的N端尾巴暴露在腔侧,主要的C端部分毗邻核孔复合体。为了找到将POM121靶向核孔的信号,我们单独过表达POM121的选定区域,或将其与绿色荧光蛋白(GFP)融合,在瞬时转染的COS-1细胞或稳定转染的神经母细胞瘤细胞系中进行表达。通过对GFP荧光或免疫染色的显微镜分析来确定过表达蛋白在细胞内的分布。由于嵌合的POM121-GFP融合蛋白能正确靶向COS-1细胞和神经母细胞瘤细胞的核孔,所以内荧光GFP标签对POM121的分布没有影响。基于POM121变体在细胞内的不同分选情况,我们得出结论,POM121的前128个氨基酸包含靶向连续内质网/核膜系统的信号,但并非特异性靶向核孔,并且特定的核孔靶向信号位于POM121内质网暴露部分的第129至618个氨基酸之间。