A Computational Approach to Understand Arabidopsis thaliana and Soybean Resistance to Fusarium solani (Fsg)

In this study, we reported the analysis of Arabidopsis thaliana microarray gene expression profile of root tissues after the plant was challenged with fungal pathogen Fusarium solani f. sp. glycines (Fsg). Our microarray analysis showed that the infection caused 130 transcript abundances (TAs) to increase by more than 2 fold and 32 out of 130 TAs were increased by more than 3 fold in the root tissues. However, only nineteen ESTs were observed with a decrease in TAs by more than 2 fold and 13 of them went down more than 3 fold due to the pathogen infection. In addition, the number of the up-regulated genes was nearly seven times more than that of downregulated genes. The coordinate regulation of adjacent genes was detected and the distance distribution of the nearest neighbor genes was less likely to be randomly scattered in genome. The results of this study enabled us to decipher the resistance mechanism to Fsg through an integrated computational approach.

[1]  M. Iqbal,et al.  Root response to Fusarium solani f. sp . glycines: temporal accumulation of transcripts in partially resistant and susceptible soybean , 2005, Theoretical and Applied Genetics.

[2]  C. Pál,et al.  The evolutionary dynamics of eukaryotic gene order , 2004, Nature Reviews Genetics.

[3]  Jian Wang,et al.  A microarray analysis of the rice transcriptome and its comparison to Arabidopsis. , 2005, Genome research.

[4]  J. R. Wood,et al.  Functional homologs of the Arabidopsis RPM1 disease resistance gene in bean and pea. , 1992, The Plant cell.

[5]  S. Somerville,et al.  Coordinated plant defense responses in Arabidopsis revealed by microarray analysis. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[6]  Takayuki Aoki,et al.  Sudden-death syndrome of soybean is caused by two morphologically and phylogenetically distinct species within the Fusarium solani species complex--F. virguliforme in North America and F. tucumaniae in South America. , 2003, Mycologia.

[7]  Sudhir Kumar,et al.  MEGA3: Integrated software for Molecular Evolutionary Genetics Analysis and sequence alignment , 2004, Briefings Bioinform..

[8]  D. Leister,et al.  A PCR–based approach for isolating pathogen resistance genes from potato with potential for wide application in plants , 1996, Nature Genetics.

[9]  G. Martin,et al.  An NB-LRR protein required for HR signalling mediated by both extra- and intracellular resistance proteins. , 2007, The Plant journal : for cell and molecular biology.

[10]  J. Thompson,et al.  The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. , 1997, Nucleic acids research.

[11]  E. Radwanski,et al.  Comparative genetics of disease resistance within the solanaceae. , 2000, Genetics.

[12]  E. Winzeler,et al.  Genomics, gene expression and DNA arrays , 2000, Nature.

[13]  F. Skoog,et al.  A revised medium for the growth and bioassay with tobacco tissue culture , 1962 .

[14]  V. Corces,et al.  Setting the Boundaries of Chromatin Domains and Nuclear Organization , 2002, Cell.

[15]  Justus-Liebig-University Giessen Powdery mildew susceptibility and biotrophic infection strategies , 2005 .

[16]  P Bork,et al.  Inversions and the dynamics of eukaryotic gene order. , 2001, Trends in genetics : TIG.

[17]  M. Dante,et al.  A compilation of soybean ESTs: generation and analysis. , 2002, Genome.

[18]  J. Thompson,et al.  CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. , 1994, Nucleic acids research.

[19]  A. Bent,et al.  Probing plant-pathogen interactions and downstream defense signaling using DNA microarrays , 2002, Functional & Integrative Genomics.

[20]  Andy Greenfield,et al.  Using DNA microarrays. , 2008, Methods in molecular biology.

[21]  Simonich Mt,et al.  A disease resistance gene in Arabidopsis with specificity for the avrPph3 gene of Pseudomonas syringae pv. phaseolicola. , 1995 .

[22]  M. Sawadogo,et al.  SURVEY AND SUMMARY: Spatial organization of RNA polymerase II transcription in the nucleus , 2000 .

[23]  O. Zakhleniuk,et al.  Responses of primary and secondary metabolism to sugar accumulation revealed by microarray expression analysis of the Arabidopsis mutant, pho3. , 2004, Journal of experimental botany.

[24]  T. Ashfield,et al.  Convergent Evolution of Disease Resistance Gene Specificity in Two Flowering Plant Families On-line version contains Web-only data. , 2004, The Plant Cell Online.

[25]  J. Cherry,et al.  Identification of unstable transcripts in Arabidopsis by cDNA microarray analysis: Rapid decay is associated with a group of touch- and specific clock-controlled genes , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[26]  Jonathan Pevsner,et al.  Bioinformatics and functional genomics , 2003 .

[27]  B. Keller,et al.  Map-based isolation of the leaf rust disease resistance gene Lr10 from the hexaploid wheat (Triticum aestivum L.) genome , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[28]  I. Somssich,et al.  The Transcription Factors WRKY11 and WRKY17 Act as Negative Regulators of Basal Resistance in Arabidopsis thaliana[W][OA] , 2006, The Plant Cell Online.