Lee Y J, Kim D H, Kim Y W, Hwang I
Division of Molecular and Life Science, Pohang University of Science and Technology, Pohang 790-784, Korea.
Plant Cell. 2001 Oct;13(10):2175-90. doi: 10.1105/tpc.010232.
Certain small outer envelope membrane proteins of chloroplasts are encoded by the nuclear genome without a cleavable N-terminal transit peptide. We investigated in vivo the targeting mechanism of AtOEP7, an Arabidopsis homolog of the small outer envelope membrane protein. AtOEP7 was expressed as a fusion protein with the green fluorescent protein (GFP) either transiently in protoplasts or stably in transgenic plants. In either case, fluorescence microscopy of transformed cells and protein gel blot analysis of fractionated proteins confirmed that the AtOEP7:GFP fusion protein was targeted to the chloroplast outer envelope membrane. In vivo targeting experiments revealed that two regions, the transmembrane domain (TMD) and its C-terminal neighboring seven-amino acid region, were necessary and sufficient for targeting to the chloroplast outer membrane. Substitution of aspartic acid or lysine residues with glycine residues or scrambling of the amino acid sequence of the seven-amino acid region caused mistargeting to the plasma membrane. Although the amino acid sequence of the TMD is not important for targeting, amino acid residues with large side chains inhibited targeting to the chloroplasts and resulted in the formation of large aggregates in the protoplasts. In addition, introduction of a proline residue within the TMD resulted in inhibition of targeting. Finally, a fusion protein, AtOEP7:NLS:GFP, was targeted efficiently to the chloroplast envelope membranes despite the presence of a nuclear localization signal. On the basis of these results, we conclude that the seven-amino acid region and the TMD are determinants for targeting to the chloroplast outer envelope membrane. The seven-amino acid region plays a critical role in AtOEP7 evading the endomembrane system and entering the chloroplast pathway, and the TMD plays critical roles in migration to the chloroplasts and/or subsequent insertion into the membrane.
叶绿体的某些小外膜蛋白由核基因组编码,没有可切割的N端转运肽。我们在体内研究了小外膜蛋白的拟南芥同源物AtOEP7的靶向机制。AtOEP7与绿色荧光蛋白(GFP)融合表达,在原生质体中瞬时表达或在转基因植物中稳定表达。在这两种情况下,转化细胞的荧光显微镜观察和分级分离蛋白的蛋白质凝胶印迹分析均证实AtOEP7:GFP融合蛋白靶向叶绿体外膜。体内靶向实验表明,跨膜结构域(TMD)及其C端相邻的七个氨基酸区域对于靶向叶绿体外膜是必需且足够的。用甘氨酸残基取代天冬氨酸或赖氨酸残基或打乱七个氨基酸区域的氨基酸序列会导致错误靶向到质膜。虽然TMD的氨基酸序列对靶向不重要,但具有大侧链的氨基酸残基会抑制靶向叶绿体,并导致原生质体中形成大聚集体。此外,在TMD内引入脯氨酸残基会导致靶向抑制。最后,尽管存在核定位信号,融合蛋白AtOEP7:NLS:GFP仍有效地靶向叶绿体包膜膜。基于这些结果,我们得出结论,七个氨基酸区域和TMD是靶向叶绿体外膜的决定因素。七个氨基酸区域在AtOEP7逃避内膜系统并进入叶绿体途径中起关键作用,而TMD在向叶绿体迁移和/或随后插入膜中起关键作用。