Microarray analysis of developing Arabidopsis seeds

被引:268
作者
Girke, T
Todd, J
Ruuska, S
White, J
Benning, C
Ohlrogge, J [1 ]
机构
[1] Michigan State Univ, Dept Bot & Plant Pathol, E Lansing, MI 48824 USA
[2] Michigan State Univ, Dept Biochem, E Lansing, MI 48824 USA
关键词
D O I
10.1104/pp.124.4.1570
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
To provide a broad analysis of gene expression in developing Arabidopsis seeds, microarrays have been produced that display approximately 2,600 seed-expressed genes. DNA for genes spotted on the arrays were selected from >10,000 clones partially sequenced from a cDNA library of developing seeds. Based on a series of controls, sensitivity of the arrays was estimated at one to two copies of mRNA per cell and cross hybridization was estimated to occur if closely related genes have >70% to 80% sequence identity. These arrays have been hybridized in a series of experiments with probes derived from seeds, leaves, and roots of Arabidopsis. Analysis of expression ratios between the different tissues has allowed the tissue-specific expression patterns of many hundreds of genes to be described for the first time. Approximately 25% of the 2,600 genes were expressed at ratios greater than or equal to 2-fold higher in seeds than leaves or roots and 10% at ratios greater than or equal to 10. Included in this list are a large number of proteins of unknown function, and potential regulatory factors such as protein kinases, phosphatases, and transcription factors. The Arabidopsis arrays were also found to be useful for transcriptional profiling of mRNA isolated from developing oilseed rape (Brassica napus) seeds and expression patterns correlated well between the two species.
引用
收藏
页码:1570 / 1581
页数:12
相关论文
共 32 条
  • [1] Role of the proline knot motif in oleosin endoplasmic reticulum topology and oil body targeting
    Abell, BM
    Holbrook, LA
    Abenes, M
    Murphy, DJ
    Hills, MJ
    Moloney, MM
    [J]. PLANT CELL, 1997, 9 (08) : 1481 - 1493
  • [2] Direct evidence for rapid degradation of Bacillus thuringiensis toxin mRNA as a cause of poor expression in plants
    De Rocher, EJ
    Vargo-Gogola, TC
    Diehn, SH
    Green, PJ
    [J]. PLANT PHYSIOLOGY, 1998, 117 (04) : 1445 - 1461
  • [3] Exploring the metabolic and genetic control of gene expression on a genomic scale
    DeRisi, JL
    Iyer, VR
    Brown, PO
    [J]. SCIENCE, 1997, 278 (5338) : 680 - 686
  • [4] Differential gene expression in Arabidopsis monitored using cDNA arrays
    Desprez, T
    Amselem, J
    Caboche, M
    Höfte, H
    [J]. PLANT JOURNAL, 1998, 14 (05) : 643 - 652
  • [5] DILLON PJ, 1990, BIOTECHNIQUES, V9, P298
  • [6] DEVELOPMENTAL BIOCHEMISTRY OF COTTONSEED EMBRYOGENESIS AND GERMINATION - CHANGING MESSENGER RIBONUCLEIC-ACID POPULATIONS AS SHOWN BY INVITRO AND INVIVO PROTEIN-SYNTHESIS .14.
    DURE, L
    GREENWAY, SC
    GALAU, GA
    [J]. BIOCHEMISTRY, 1981, 20 (14) : 4162 - 4168
  • [7] Coordinate changes in carbon partitioning and plastidial metabolism during the development of oilseed rape embryo
    Eastmond, PJ
    Rawsthorne, S
    [J]. PLANT PHYSIOLOGY, 2000, 122 (03) : 767 - 774
  • [8] Eccleston VS, 1998, PLANT CELL, V10, P613, DOI 10.1105/tpc.10.4.613
  • [9] ASSESSMENT OF LIPOXYGENASE ACTIVITY IN SEED EXTRACTS FROM 35 PLANT-SPECIES
    FAUCONNIER, ML
    VANZEVEREN, E
    MARLIER, M
    LOGNAY, G
    WATHELET, JP
    SEVERIN, M
    [J]. GRASAS Y ACEITES, 1995, 46 (01) : 6 - 10
  • [10] wrinkled1:: A novel, low-seed-oil mutant of Arabidopsis with a deficiency in the seed-specific regulation of carbohydrate metabolism
    Focks, N
    Benning, C
    [J]. PLANT PHYSIOLOGY, 1998, 118 (01) : 91 - 101