RIG/CAA: Demolition of Ceramide Synthesis Genes in Magnaporthe grisea with Putative Roles in Pathogenicity
RIG/CAA: Demolition of Ceramide Synthesis Genes in Magnaporthe grisea with Putative Roles in Pathogenicity
批准号:
0641823
负责人:
Sherrice Allen
金额:
$0.0万
依托单位国家:
美国
项目类别:
Continuing grant
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-07-01 至 2010-06-30
中文摘要
稻瘟病是由稻瘟病菌引起的稻瘟病,对世界上最重要的粮食作物造成严重威胁,每年损失10-30%。这种病原体可以感染植物的所有部位,最具破坏性的情况是在穗下的颈部定植。真菌通过感染结构附着胞渗透需要多种因素,如物理和生化信号。附着胞是一种高度黑化的细胞,它产生足够的膨胀压力,迫使刺穿钉穿过植物角质层,进入下层组织。神经酰胺单己糖(CMHs)是假设在这种形态转变中起作用的化合物。该项目将有助于了解CMHs如何影响稻瘟病菌的生物学,以及确定它们在附着胞形成和感染中的作用。此外,人们认为芳基磺化酶有助于维持神经酰胺单己糖的细胞池。我将通过在编码这种酶的基因中制造破坏突变体来验证这一假设。特异性目标II将集中于确定每个基因在附着胞形成和真菌毒力中的作用。产生缺乏参与CMHs生物合成的关键酶活性的突变体是研究真菌发育和分化的基础应用。该项目的具体目标将利用分子和遗传技术进行,这些技术可以由本科生和研究生研究人员执行。这个项目更广泛的影响将是为少数民族研究生和本科生提供微生物植物发病机理的研究经验,这是一个传统上没有被少数民族所追求的领域。此外,拟议的研究将增加费耶特维尔州立大学(一所历史悠久的黑人大学)不断增长的研究社区,允许与北卡罗来纳州立大学真菌基因组学实验室发展合作关系。
英文摘要
Sherrice Vallette AllenProposal # 0641823Demolition of Ceramide Synthesis Gene in Magnaporthe grisea with Putative Roles in PathogenicityRice blast, caused by the fungus Magnaporthe grisea, poses a serious threat to the world's most important food crop with losses between 10-30% of annual harvest. The pathogen can infect all parts of the plant, with the most devastating situation being colonization of the neck just below the panicle. Fungal penetration via an infection structure, the appressorium, requires a variety of factors such as physical and biochemical signals. The appressorium is a highly melanized cell that builds up sufficient turgor pressure to force a penetration peg through the plant cuticle to gain access to the underlying tissues. Ceramide monohexosides (CMHs) are compounds hypothesized to have a role in this morphological transition. This project will aid in understanding how CMHs influence the biology of M. grisea, as well as establishing their role in appressorium formation and infection. In addition, it is thought that the enzyme arylsulfatase assists in maintaining the cellular pool of ceramide monohexosides. Specific Aim I will test this hypothesis by creating disruption mutants in genes that encode this enzyme . Specific Aim II will concentrate on determining the role of each gene in appressorium formation and fungal virulence. The generation of mutants lacking key enzymatic activities involved in CMHs biosynthesis is a fundamental application to study fungal development and differentiation. The specific aims of this project will be carried out utilizing molecular and genetic techniques that can be performed by undergraduate and graduate student researchers. The broader impacts of this project will be to provide research experiences for underrepresented minority graduate and undergraduate students in microbial-plant pathogenesis, an area not traditionally pursued by underrepresented minorities. Also, the proposed research will add to a growing research community at Fayetteville State University, a historically black university, allowing for the development of partnerships with the North Carolina State University Fungal Genomics laboratory.
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