Wang Jiao-Yu, Wu Xiao-Yan, Zhang Zhen, Du Xin-Fa, Chai Rong-Yao, Liu Xiao-Hong, Mao Xue-Qin, Qiu Hai-Ping, Wang Yan-Li, Lin Fu-Cheng, Sun Guo-Chang
Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, China.
J Zhejiang Univ Sci B. 2008 Oct;9(10):802-10. doi: 10.1631/jzus.B0860001.
The peroxisomal matrix proteins involved in many important biological metabolism pathways in eukaryotic cells are encoded by nucleal genes, synthesized in the cytoplasm and then transported into the organelles. Targeting and import of these proteins depend on their two peroxisomal targeting signals (PTS1 and PTS2) in sequence as we have known so far. The vectors of the fluorescent fusions with PTS, i.e., green fluorescence protein (GFP)-PTS1, GFP-PTS2 and red fluorescence protein (RFP)-PTS1, were constructed and introduced into Magnaporthe oryzae Guy11 cells. Transformants containing these fusions emitted fluorescence in a punctate pattern, and the locations of the red and green fluorescence overlapped exactly in RFP-PTS1 and GFP-PTS2 co-transformed strains. These data indicated that both PTS1 and PTS2 fusions were imported into peroxisomes. A probable higher efficiency of PTS1 machinery was revealed by comparing the fluorescence backgrounds in GFP-PTS1 and GFP-PTS2 transformants. By introducing both RFP-PTS1 and GFP-PTS2 into Deltamgpex6 mutants, the involvement of MGPEX6 gene in both PTS1 and PTS2 pathways was proved. In addition, using these transformants, the inducement of peroxisomes and the dynamic of peroxisomal number during the pre-penetration processes were investigated as well. In summary, by the localization and co-localization of PTS1 and PTS2, we provided a useful tool to evaluate the biological roles of the peroxisomes and the related genes.
参与真核细胞中许多重要生物代谢途径的过氧化物酶体基质蛋白由核基因编码,在细胞质中合成,然后转运到细胞器中。到目前为止我们所知,这些蛋白质的靶向和导入取决于它们的两个过氧化物酶体靶向信号(PTS1和PTS2)。构建了与PTS的荧光融合载体,即绿色荧光蛋白(GFP)-PTS1、GFP-PTS2和红色荧光蛋白(RFP)-PTS1,并将其导入稻瘟病菌Guy11细胞。含有这些融合体的转化体以点状模式发出荧光,并且在RFP-PTS1和GFP-PTS2共转化菌株中红色和绿色荧光的位置完全重叠。这些数据表明PTS1和PTS2融合体都被导入了过氧化物酶体。通过比较GFP-PTS1和GFP-PTS2转化体中的荧光背景,揭示了PTS1机制可能具有更高的效率。通过将RFP-PTS1和GFP-PTS2都导入Deltamgpex6突变体,证明了MGPEX6基因在PTS1和PTS2途径中的作用。此外,利用这些转化体,还研究了过氧化物酶体的诱导以及穿透前过程中过氧化物酶体数量的动态变化。总之,通过PTS1和PTS2的定位和共定位,我们提供了一个有用的工具来评估过氧化物酶体和相关基因的生物学作用。