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Journal of Zhejiang University-SCIENCE B (Biomedicine & Biotechnology)  2008, Vol. 9 Issue (10): 802-810    DOI: 10.1631/jzus.B0860001
Articles     
Fluorescent co-localization of PTS1 and PTS2 and its application in analysis of the gene function and the peroxisomal dynamic in Magnaporthe oryzae
Jiao-yu WANG, Xiao-yan WU, Zhen ZHANG, Xin-fa DU, Rong-yao CHAI, Xiao-hong LIU, Xue-qin MAO, Hai-ping QIU, Yan-li WANG, Fu-cheng LIN, Guo-chang SUN
Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, China; College of Plant Protection, Northwest Agriculture and Forest University, Yangling 712100, China; State Key Laboratory for Rice Biology, College of Agriculture and Biotechnology, Zhejiang University, Hangzhou 310029, China
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Abstract  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 Δmgpex6 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.

Key wordsPeroxisomal targeting signal (PTS)      Peroxisomal localization      MGPEX6 gene      Magnaporthe oryzae     
Received: 24 July 2008     
CLC:  Q36  
  S43  
Cite this article:

Jiao-yu WANG, Xiao-yan WU, Zhen ZHANG, Xin-fa DU, Rong-yao CHAI, Xiao-hong LIU, Xue-qin MAO, Hai-ping QIU, Yan-li WANG, Fu-cheng LIN, Guo-chang SUN. Fluorescent co-localization of PTS1 and PTS2 and its application in analysis of the gene function and the peroxisomal dynamic in Magnaporthe oryzae. Journal of Zhejiang University-SCIENCE B (Biomedicine & Biotechnology), 2008, 9(10): 802-810.

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http://www.zjujournals.com/xueshu/zjus-b/10.1631/jzus.B0860001     OR     http://www.zjujournals.com/xueshu/zjus-b/Y2008/V9/I10/802

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