Differential Gene Expression of Soybean[Glycine max(L.) Merr.] in Response to Xanthomonas axonopodis pv. glycines by Using Oligonulceotide Macroarray

  • Van, Kyujung (Department of Plant Science, Seoul National University) ;
  • Lestari, Puji (Department of Plant Science, Seoul National University) ;
  • Park, Yong-Jin (Genetic Resource Division, National Institute of Agricultural Science and Technology) ;
  • Gwag, Jae-Gyun (Genetic Resource Division, National Institute of Agricultural Science and Technology) ;
  • Kim, Moon-Young (Department of Plant Science, Seoul National University) ;
  • Kim, Dong-Hyun (Department of Plant Science, Seoul National University) ;
  • Heu, Sung-Gi (Plant Pathology Division, National Institute of Agricultural Science and Technology) ;
  • Lee, Suk-Ha (Department of Plant Science, Seoul National University)
  • Published : 2007.09.30

Abstract

Xanthomonas axonopodis pv. glycines(Xag) is a pathogen that causes bacterial leaf pustule(BLP) disease in soybeans grown in Korea and the southern United States. Typical and early symptoms of the disease are small, yellow to brown lesions with raised pustules that develop into large necrotic lesions leading to a substantial loss in yield due to premature defoliation. After Xag infects PI 96188, only pustules without chlorotic haloes were observed, indicating the different response to Xag. To identify differentially expressed genes prior to and 24 hr after Xag inoculation to PI 96188 and BLP-resistant SS2-2, an oligonucleotide macroarray was constructed with 100 genes related to disease resistance and metabolism from soybean and Arabidopsis. After cDNAs from each genotype were applied on the oligonucleotide macroarrays with three replicates and dye swapping, 36 and 81 genes were expressed as significantly different between 0 hr and 24 hr in PI 96188 and SS2-2, respectively. Six UniGenes, such as the leucine-rich repeat protein precursor or 14-3-3-like protein, were selected because they down-regulated in PI 96188 and up-regulated in SS2-2 after Xag infection, simultaneously. Using tubulin and cDNA of Jangyeobkong(BLP-susceptible) as controls, the oligonucleotide macroarray data concurred with quantitative real-time RT-PCR(QRT RT-PCR) results in most cases, supporting the accuracy of the oligonucleotide macroarray experiments. Also, QRT RT-PCR data suggested six candidate genes that might be involved in a necrotic response to Xag in PI 96188.

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