ACTA AGRICULTURAE BOREALI-SINICA ›› 2012, Vol. 27 ›› Issue (6): 38-42. doi: 10.3969/j.issn.1000-7091.2012.06.009

Special Issue: Biotechnology

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Cloning and Bioinformatic Analysis of PGIPGene from Prunus caoyuan

YU Wen-quan1, LIU Hai-rong1, YANG Xiao-hua1, ZHAO Heng-tian2   

  1. 1. Mudanjiang Branch of Heilongjiang Academy of Agriculture Science, Mudanjiang 157041, China;
    2. Northeast Institute of Geography and Agricutural Ecology, Chinese Academy of Sciences, Harbin 150081, China
  • Received:2012-08-21 Published:2012-12-28

Abstract: Disease resistance mechanism was studied by methods of cloning of the PGIPgene in Prunus caoyuan. A DNA fragment about 1 kb was amplified from the genomic DNA of Prunus caoyuanleaves by PCR with a pair of specific primers based on the conserved sequences of the PGIPgenes of genus Prunus. Sequence analysis showed that the fragment contains a full coding region of 1 193 bp( GenBank accession: GU068977). This sequence had a full open reading frame encoding the PGIP,and eontained two exons interrupted by one intron. The total exons were comprised by 990 bp of deoxynucleotide encoding 330 amino acid. A conserved leucine-rich fragmenthad existed in the derived protein sequence. Sequencing analysis showed that it was 95% to 99% identical with the sequences of Prunus PGIPgenes including P. salicina,P. armeniaca,P. persica,P. mahaleb,P. mume. Phylogenic tree showed that genetic relationship within the genus was closer and between the genera was farther. A PGIPgene of Prunus caoyuanwas cloned. As a result,a gene resource was provided for molecular breeding of plants.

Key words: Prunus caoyuan, PGIPgene, Gene cloning, Bioinformatic

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Cite this article

YU Wen-quan, LIU Hai-rong, YANG Xiao-hua, ZHAO Heng-tian. Cloning and Bioinformatic Analysis of PGIPGene from Prunus caoyuan[J]. ACTA AGRICULTURAE BOREALI-SINICA, 2012, 27(6): 38-42. doi: 10.3969/j.issn.1000-7091.2012.06.009.

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