2-D DIGE reveals changes in wheat xylanase inhibitor protein families due to Fusarium graminearum ΔTri5 infection and grain development

被引:23
|
作者
Dornez, Emmie [1 ,2 ]
Croes, Evi [1 ,2 ]
Gebruers, Kurt [1 ,2 ]
Carpentier, Sebastien [3 ]
Swennen, Rony [3 ]
Laukens, Kris [4 ]
Witters, Erwin [4 ,5 ]
Urban, Martin [6 ]
Delcour, Jan A. [1 ,2 ]
Courtin, Christophe M. [1 ,2 ]
机构
[1] Katholieke Univ Leuven, Dept Microbial & Mol Syst, Lab Food Chem & Biochem, B-3001 Louvain, Belgium
[2] Katholieke Univ Leuven, Leuven Food Sci & Nutr Res Ctr, B-3001 Louvain, Belgium
[3] Katholieke Univ Leuven, Div Crop Biotech, B-3001 Louvain, Belgium
[4] Univ Antwerp, Ctr Proteome Anal & Mass Spectrometry, B-2020 Antwerp, Belgium
[5] Flemish Inst Technol Res VITO, Mol, Belgium
[6] Ctr Sustainable Pest & Dis Management, Dept Plant Pathol & Microbiol, Harpenden, Herts, England
关键词
2-D DIGE; Fusarium graminearum Delta Tri5 infection; Plant proteomics; Wheat development; Xylanase inhibitor families; DEFENSE RESPONSE GENES; ENDOXYLANASE INHIBITORS; GLYCOSIDASE INHIBITORS; TRITICUM-AESTIVUM; HEXAPLOID WHEAT; CDNA CLONING; TAXI-I; XIP-I; EXPRESSION; IDENTIFICATION;
D O I
10.1002/pmic.200900493
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Wheat contains three different classes of proteinaceous xylanase inhibitors (XIs), i.e. Triticum aestivum xylanase inhibitors (TAXIs) xylanase-inhibiting proteins (XIPs), and thaumatin-like xylanase inhibitors (TLXIs) which are believed to act as a defensive barrier against phytopathogenic attack. In the absence of relevant data in wheat kernels, we here examined the response of the different members of the XI protein population to infection with a Delta Tri5 mutant of Fusarium graminearum, the wild type of which is one of the most important wheat ear pathogens, in early developing wheat grain. Wheat ears were inoculated at anthesis, analyzed using 2-D DICE and multivariate analysis at 5, 15, and 25 days post anthesis (DPA), and compared with control samples. Distinct abundance patterns could be distinguished for different XI forms in response to infection with F. graminearum Delta Tri5. Some (iso)forms were up-regulated, whereas others were down-regulated. This pathogen-specific regulation of proteins was mostly visible at five DPA and levelled off in the samples situated further from the inoculation point. Furthermore, it was shown that most identified TAXI- and XIP-type XI (iso)forms significantly increased in abundance from the milky (15 DPA) to the soft dough stages (25 DPA) on a per kernel basis, although the extent of increase differed greatly. Non-glycosylated XIP forms increased more strongly than their glycosylated counterparts.
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页码:2303 / 2319
页数:17
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