Chen Liyong, Qian Lu, Zhang Zhiyi, Shi Ming, Song Yuhua, Yuan Guogang, Zhang Hao, Hu Meiru, Yu Ming, Zhang Xuemin, Shen Beifen, Guo Ning
Institute of Basic Medical Sciences, Taiping Road 27, Beijing, 100850, People's Republic of China.
Histochem Cell Biol. 2007 Nov;128(5):473-83. doi: 10.1007/s00418-007-0329-z. Epub 2007 Sep 12.
In the present study, the sub-cellular localization of ErbB2 and its mutants expressed as GFP-tagged proteins in MCF-7 cells or endogenous ErbB2 in SKBR3 cells was examined. The data presented here demonstrate that the full-length ErbB2 was localized at the cytoplasmic membrane and ErbB2 ICD localized in the nucleus predominantly. The sequence of ErbB2 ICD contains the information supporting its nuclear translocation and cytoplasmic retention. A region (residues 721-970) harboring an arginine triplet is essential for the cytoplasmic trafficking of ErbB2. The results indicate that differential sub-cellular localization of ErbB2 ICD and the full-length ErbB2 is dependent on their structural determinants. The present results give initial clues for further analysis of the mechanism of ErbB2 intracellular localization.
在本研究中,检测了在MCF-7细胞中以绿色荧光蛋白(GFP)标记形式表达的ErbB2及其突变体的亚细胞定位,以及SKBR3细胞中内源性ErbB2的亚细胞定位。此处呈现的数据表明,全长ErbB2定位于细胞质膜,而ErbB2胞内结构域(ICD)主要定位于细胞核。ErbB2 ICD的序列包含支持其核转位和细胞质保留的信息。一个含有精氨酸三联体的区域(第721 - 970位氨基酸)对于ErbB2的细胞质转运至关重要。结果表明,ErbB2 ICD和全长ErbB2的亚细胞定位差异取决于它们的结构决定因素。目前的结果为进一步分析ErbB2细胞内定位机制提供了初步线索。