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Monitoring the Expression of Maize Genes in Developing Kernels under Droug ht Stress usingOligo-microarray 被引量:5

Monitoring the Expression of Maize Genes in Developing Kernels under Drought Stress using Oligo-microarray
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摘要 Preharvest aflatoxin contamination of grain grown on the US southeastern Coast Plain is provoked and aggravated by abiotic stress. The primary abiotic stress is drought along with high temperatures. The objectives of the present study were to monitor gene expression in developing kernels in response to drought stress and to identify drought-responsive genes for possible use in germplasm assessment. The maize breeding line Tex6 was used, and gene expression profiles were analyzed in developing kernels under drought stress verses well-watered conditions at the stages of 25, 30, 35, 40, 45 d after pollination (DAP) using the 70 mer maize oligo-arrays. A total of 9 573 positive array spots were detected with unique gene IDs, and 7 988 were common in both stressed and well-watered samples. Expression patterns of some genes in several stress response-associated pathways, including abscisic acid, jasmonic acid and phenylalanine ammonia-lyase, were examined, and these specific genes were responsive to drought stress positively. Real-time quantitative polymerase chain reaction validated microarray expression data. The comparison between Tex6 and B73 revealed that there were significant differences in specific gene expression, patterns and levels. Several defense-related genes had been downregulated, even though some defense-related or drought responsive genes were upregulated at the later stages. Preharvest aflatoxin contamination of grain grown on the US southeastern Coast Plain is provoked and aggravated by abiotic stress. The primary abiotic stress is drought along with high temperatures. The objectives of the present study were to monitor gene expression in developing kernels in response to drought stress and to identify drought-responsive genes for possible use in germplasm assessment. The maize breeding line Tex6 was used, and gene expression profiles were analyzed in developing kernels under drought stress verses well-watered conditions at the stages of 25, 30, 35, 40, 45 d after pollination (DAP) using the 70 mer maize oligo-arrays. A total of 9 573 positive array spots were detected with unique gene IDs, and 7 988 were common in both stressed and well-watered samples. Expression patterns of some genes in several stress response-associated pathways, including abscisic acid, jasmonic acid and phenylalanine ammonia-lyase, were examined, and these specific genes were responsive to drought stress positively. Real-time quantitative polymerase chain reaction validated microarray expression data. The comparison between Tex6 and B73 revealed that there were significant differences in specific gene expression, patterns and levels. Several defense-related genes had been downregulated, even though some defense-related or drought responsive genes were upregulated at the later stages.
出处 《Journal of Integrative Plant Biology》 SCIE CAS CSCD 2010年第12期1059-1074,共16页 植物学报(英文版)
基金 supported by USDA Specific Cooperative Agreements 58-6602-1-213 and 58-6602-6-121 with the University of Georgia supported by funds provided by the USDA Agricultural Research Service the Georgia Agricultural Commodity Commission for Corn
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  • 1Krishnamachari KA, Bhat RV, Nagarajan V, Tilak TB (1975). Hepatitis due to aflatoxicosis: an outbreak of hepatitis in parts of western India. Lancet 1, 1061-1063.
  • 2Lewis L, Onsongo M, Njapau H, Schurz-Rogers H, Luber G, Kieszak S et al. (2005). Aflatoxin contamination of commercial maize products during an outbreak of acute aflatoxicosis in eastern and central Kenya. Environ. Health Perspect. 113, 1763-1767.
  • 3Llu Q, Kasuga M, Sakuma Y, Abe H, Miura S, Yamaguchi-Shinozaki K et al. (1998). Two transcription factors, DREB1 and DREB2, with an EREBP/AP2 DNA binding domain separate two cellular signal transduction pathways in drought- and low temperature responsive gene expression, respectively, in Arabidopsis. Plant Cell 10, 1391- 1406.
  • 4Luo M, Dang P, Guo BZ, He G, Holbrook CC, Bausher MG et al. (2005a). Generation of expressed sequence tags (ESTs) for gene discovery and marker development in cultivated peanut. Crop Sci. 45, 346-353.
  • 5Luo M, Dang P, Holbrook CC, Bausher MG, Lynch RE, Lee RD et al. (2005b). Identification of transcripts involved in resistance responses to leaf spot disease caused by Cercosporidium personatum in peanut (Arachis hypogaea L.). Phytopathology 95, 381-387.
  • 6Luo M, Liang X, Dang P, Holbrook CC, Bausher MG, Lee RD et al. (2005c). Microarray-based screening of differentially expressed genes in peanut in response to Aspergillus parasiticus infection and drought stress. Plant Sci. 169, 695-703.
  • 7Maggio-Hall LA, Wilson RA, Keller NP (2005). Fundamental contribution of beta-oxidation to polyketide mycotoxin production in planta. MoL Plant Microb Interact. 18, 783-793.
  • 8McMillian WW, Wldstrom NW, Wilson DM (1993). Registration of GTMAS:gk maize germplasm. Crop Sci. 33, 882.
  • 9McMilllan WW, Wilson DM, Widstrom NW (1985). Aflatoxin contamination of preharvest corn in Georgia: a six-year study of insect damage and visible Aspergillus flavus. J. Environ. Qual. 14, 200-202.
  • 10Menklr A, Brown RL, Bandyopadhyay R, Chen ZY, Cleveland TE (2006). A U.S.A.-Africa collaborative strategy for identifying, charactedzing, and developing maize germptasm with resistance to aflatoxin contamination. Mycopathologia 162,225-232.

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