scholarly journals Global Expression Profiling of Transcription Factor Genes Provides New Insights into Pathogenicity and Stress Responses in the Rice Blast Fungus

2013 ◽  
Vol 9 (6) ◽  
pp. e1003350 ◽  
Author(s):  
Sook-Young Park ◽  
Jaeyoung Choi ◽  
Se-Eun Lim ◽  
Gir-Won Lee ◽  
Jongsun Park ◽  
...  
2013 ◽  
Vol 61 ◽  
pp. 133-141 ◽  
Author(s):  
Hyunjung Chung ◽  
Jaehyuk Choi ◽  
Sook-Young Park ◽  
Junhyun Jeon ◽  
Yong-Hwan Lee

2007 ◽  
Vol 64 (2) ◽  
pp. 293-307 ◽  
Author(s):  
Dominik Odenbach ◽  
Björn Breth ◽  
Eckhard Thines ◽  
Roland W. S. Weber ◽  
Heidrun Anke ◽  
...  

2014 ◽  
Vol 27 (10) ◽  
pp. 1027-1034 ◽  
Author(s):  
Naoki Yokotani ◽  
Tomoko Tsuchida-Mayama ◽  
Hiroaki Ichikawa ◽  
Nobutaka Mitsuda ◽  
Masaru Ohme-Takagi ◽  
...  

Plants respond to pathogen attack by transcriptionally regulating defense-related genes via various types of transcription factors. We identified a transcription factor in rice, OsNAC111, belonging to the TERN subgroup of the NAC family that was transcriptionally upregulated after rice blast fungus (Magnaporthe oryzae) inoculation. OsNAC111 was localized in the nucleus of rice cells and had transcriptional activation activity in yeast and rice cells. Transgenic rice plants overexpressing OsNAC111 showed increased resistance to the rice blast fungus. In OsNAC111-overexpressing plants, the expression of several defense-related genes, including pathogenesis-related (PR) genes, was constitutively high compared with the control. These genes all showed blast disease-responsive expression in leaves. Among them, two chitinase genes and one β-1,3-glucanase gene showed reduced expression in transgenic rice plants in which OsNAC111 function was suppressed by a chimeric repressor (OsNAC111-SRDX). OsNAC111 activated transcription from the promoters of the chitinase and β-1,3-glucanase genes in rice cells. In addition, brown pigmentation at the infection sites, a defense response of rice cells to the blast fungus, was lowered in OsNAC111-SRDX plants at the early infection stage. These results indicate that OsNAC111 positively regulates the expression of a specific set of PR genes in the disease response and contributes to disease resistance.


2002 ◽  
Vol 15 (3) ◽  
pp. 183-192 ◽  
Author(s):  
Gyungsoon Park ◽  
Chaoyang Xue ◽  
Li Zheng ◽  
Stephen Lam ◽  
Jin-Rong Xu

In the rice blast fungus Magnaporthe grisea, a mitogen-activated protein kinase gene, PMK1, is known to regulate ap-pressorium formation and infectious hyphae growth. Since PMK1 is homologous to the FUS3 and KSS1 genes that regulate the transcription factor STE12 in yeast, we functionally characterized the STE12 homologue in M. grisea (MST12). A polymerase chain reaction-based approach was used to isolate the MST12 gene that is homologous to yeast STE12. Four mst12 deletion mutants were isolated by gene replacement. No obvious defect in vegetative growth, conidiation, or conidia germination was observed in mst12 mutants. However, mst12 mutants were nonpathogenic on rice and barley leaves. In contrast to pmk1 mutants that did not form appressoria, mst12 mutants produced typical dome-shaped and melanized appressoria. However, the ap-pressoria formed by mst12 mutants failed to penetrate onion epidermal cells. When inoculated through wound sites, mst12 mutants failed to cause spreading lesions and appeared to be defective in infectious growth. These data indicate that MST12 may function downstream of PMK1 to regulate genes involved in infectious hyphae growth. A transcription factor or factors other than MST12 must exist in M. grisea and function downstream from PMK1 for ap-pressorium formation.


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