Expression patterns in soybean resistant to Phakopsora pachyrhizi reveal the importance of peroxidases and lipoxygenases

被引:41
作者
Choi, J. J. [1 ]
Alkharouf, N. W. [2 ]
Schneider, K. T. [1 ]
Matthews, B. F. [3 ]
Frederick, R. D. [1 ]
机构
[1] USDA ARS, Foreign Dis Weed Sci Res Unit, Ft Detrick, MD 21702 USA
[2] Towson Univ, Dept Comp & Informat Sci, Towson, MD 21252 USA
[3] USDA ARS, Soybean Genom & Improvement Lab, Beltsville, MD 20705 USA
关键词
soybean rust; Phakopsora pachyrhizi; resistance; immune reaction; microarray analysis;
D O I
10.1007/s10142-008-0080-0
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Soybean rust caused by Phakopsora pachyrhizi Sydow is a devastating foliar disease that has spread to most soybean growing regions throughout the world, including the USA. Four independent rust resistance genes, Rpp1-Rpp4, have been identified in soybean that recognize specific isolates of P. pachyrhizi. A suppressive subtraction hybridization (SSH) complementary DNA (cDNA) library was constructed from the soybean accession PI200492, which contains Rpp1, after inoculation with two different isolates of P. pachyrhizi that result in susceptible or immune reactions. Both forward and reverse SSH were performed using cDNA from messenger RNA pooled from 1, 6, 12, 24, and 48 h post-inoculation. A total of 1,728 SSH clones were sequenced and compared to sequences in GenBank for similarity. Microarray analyses were conducted on a custom 7883 soybean-cDNA clone array encompassing all of the soybean-rust SSH clones and expressed sequence tags from four other soybean cDNA libraries. Results of the microarray revealed 558 cDNA clones differentially expressed in the immune reaction. The majority of the upregulated cDNA clones fell into the functional category of defense. In particular, cDNA clones with similarity to peroxidases and lipoxygenases were prevalent. Downregulated cDNA clones included those with similarity to cell-wall-associated protein, such as extensins, proline-rich proteins, and xyloglucan endotransglycosylases.
引用
收藏
页码:341 / 359
页数:19
相关论文
共 81 条
[1]  
Alkharouf N, 2004, GENOME, V47, P380, DOI [10.1139/G03-114, 10.1139/g03-114]
[2]   Timecourse microarray analyses reveal global changes in gene expression of susceptible Glycine max (soybean) roots during infection by Heterodera glycines (soybean cyst nematode) [J].
Alkharouf, Nadim W. ;
Klink, Vincent P. ;
Chouikha, Imed B. ;
Beard, Hunter S. ;
MacDonald, Margaret H. ;
Meyer, Susan ;
Knap, Halina T. ;
Khan, Rana ;
Matthews, Benjamin F. .
PLANTA, 2006, 224 (04) :838-852
[3]   Online analytical processing (OLAP): A fast and effective data mining tool for gene expression databases [J].
Alkharouf, NW ;
Jamison, DC ;
Matthews, BF .
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY, 2005, (02) :181-188
[4]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[5]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[6]   A plant gene up-regulated at rust infection sites [J].
Ayliffe, MA ;
Roberts, JK ;
Mitchell, HJ ;
Zhang, R ;
Lawrence, GJ ;
Ellis, JG ;
Pryor, TJ .
PLANT PHYSIOLOGY, 2002, 129 (01) :169-180
[7]  
Bateman A, 2002, NUCLEIC ACIDS RES, V30, P276, DOI [10.1093/nar/gkr1065, 10.1093/nar/gkp985, 10.1093/nar/gkh121]
[8]   Evaluation of virulence of Phakopsora pachyrhizi and P-meibomiae isolates [J].
Bonde, M. R. ;
Nester, S. E. ;
Austin, C. N. ;
Stone, C. L. ;
Frederick, R. D. ;
Hartman, G. L. ;
Miles, M. R. .
PLANT DISEASE, 2006, 90 (06) :708-716
[9]   ELICITOR-INDUCED AND WOUND-INDUCED OXIDATIVE CROSS-LINKING OF A PROLINE-RICH PLANT-CELL WALL PROTEIN - A NOVEL, RAPID DEFENSE RESPONSE [J].
BRADLEY, DJ ;
KJELLBOM, P ;
LAMB, CJ .
CELL, 1992, 70 (01) :21-30
[10]  
BRISSON LF, 1994, PLANT CELL, V6, P1703, DOI 10.1105/tpc.6.12.1703