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Comparative Proteomic Analyses of Susceptible and Resistant Maize Inbred Lines at the Stage of Enations Forming following Infection by Rice Black-Streaked Dwarf Virus

文献类型: 外文期刊

作者: Wang, Rong 1 ; Du, Kaitong 2 ; Jiang, Tong 2 ; Di, Dianping 4 ; Fan, Zaifeng 2 ; Zhou, Tao 2 ;

作者机构: 1.Chinese Acad Med Sci & Peking Union Med Coll, Inst Med Plant Dev, Beijing 100193, Peoples R China

2.China Agr Univ, State Key Lab Agrobiotechnol, Beijing 100193, Peoples R China

3.China Agr Univ, Dept Plant Pathol, Beijing 100193, Peoples R China

4.Hebei Acad Agr & Forestry Sci, Inst Plant Protect, Baoding 071000, Peoples R China

关键词: rice black-streaked dwarf virus; Zea mays; comparative proteome; enation structure; differentially expressed protein; stress

期刊名称:VIRUSES-BASEL ( 影响因子:5.818; 五年影响因子:5.811 )

ISSN:

年卷期: 2022 年 14 卷 12 期

页码:

收录情况: SCI

摘要: Rice black-streaked dwarf virus (RBSDV) is the main pathogen causing maize rough dwarf disease (MRDD) in China. Typical enation symptoms along the abaxial leaf veins prevail in RBSDV-infected maize inbred line B73 (susceptible to RBSDV), but not in X178 (resistant to RBSDV). Observation of the microstructures of epidermal cells and cross section of enations from RBSDV-infected maize leaves found that the increase of epidermal cell and phloem cell numbers is associated with enation formation. To identify proteins associated with enation formation and candidate proteins against RBSDV infection, comparative proteomics between B73 and X178 plants were conducted using isobaric tags for relative and absolute quantitation (iTRAQ) with leaf samples at the enation forming stage. The proteomics data showed that 260 and 316 differentially expressed proteins (DEPs) were identified in B73 and X178, respectively. We found that the majority of DEPs are located in the chloroplast and cytoplasm. Moreover, RBSDV infection resulted in dramatic changes of DEPs enriched by the metabolic process, response to stress and the biosynthetic process. Strikingly, a cell number regulator 10 was significantly down-regulated in RBSDV-infected B73 plants. Altogether, these data will provide value information for future studies to analyze molecular events during both enation formation and resistance mechanism to RBSDV infection.

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