"The development of genetics and genomics for analysis of quantitative traits"

“用于数量性状分析的遗传学和基因组学的发展”

基本信息

  • 批准号:
    7894574
  • 负责人:
  • 金额:
    $ 35.18万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2008
  • 资助国家:
    美国
  • 起止时间:
    2008-08-01 至 2012-07-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): The objective of this grant proposal is to develop and make available to the community tools to identify genes responsible for any phenotype that can be measured in the model filamentous fungus, Neurospora crassa. We propose to develop as a community resource two large mapping populations, which will enable the identification of quantitative trait loci (QTLs) controlling naturally varying complex phenotypes. One of our populations comprises 500 wild isolates from a single phylogenetic clade of N. crassa, to be used for association mapping, the method of choice for identification of loci of small effect. The other population is an advanced intercross between two divergent N. crassa strains, to allow linkage mapping of rare alleles at high genetic resolution. For each population, we will measure genotype and gene expression via massively parallel signature sequencing using the Solexa platform. These resources will enable any research lab to score the strains for a trait of interest and map the underlying QTLs. As a proof of principle, we will characterize the wild and advanced intercross strains with respect to phenotypes that have broad interest to the Neurospora research community: asexual spore reproduction, sexual reproduction, vegetative growth, hyphal architecture and cooperative behavior during spore germination. We will pioneer the use of the mRNA expression data from our Solexa experiment to identify the molecular players underlying these macroscopic traits, as the expression of genes is shown to co-vary with traits across individuals. In addition, the expression measurements will be used to detail the N. crassa regulatory network, as we analyze covariation between expression levels and genetically map their controlling regulators. Our specific aims are (i) to construct the advanced intercross and characterize phenotypes that vary among these strains and the wild isolates; (ii) to perform short-read sequencing on cDNAs using the Solexa platform from each individual in each mapping population, to generate dense genotyping data and measure gene expression; and (iii) to conduct linkage and association mapping of mRNA expression and our proof-of-principle organismal traits. We believe that the mapping between genotypes, phenotypes, and gene expression levels that we propose would propel N. crassa to the forefront as a model for the study of natural variation in all eukaryotic species. Relevance to Public Health: Using N. crassa, we propose to study genetic differences between individuals that control traits like growth, organism shape, and sensitivity to drugs. N. crassa is a model for pathogenic fungi, and we aim to understand many aspects of its biology that are important for disease and treatment. Also, since so little is known about the 'principles of -genetic differences between individuals, our work will provide hypotheses about the genetics of other species, like humans.
描述(由申请人提供):本拨款提案的目的是开发并向社区提供工具,以识别与可在模型丝状真菌粗糙脉孢菌中测量的任何表型有关的基因。我们建议开发两个大型绘图群体作为社区资源,这将能够识别控制自然变化的复杂表型的数量性状基因座(QTL)。我们的种群之一包含来自粗糙脉孢菌单个系统发育分支的 500 个野生分离株,用于关联作图,这是识别小效应基因座的首选方法。另一个群体是两个不同的粗糙脉孢菌菌株之间的高级杂交,以允许以高遗传分辨率对稀有等位基因进行连锁图谱。对于每个群体,我们将使用 Solexa 平台通过大规模并行特征测序来测量基因型和基因表达。这些资源将使任何研究实验室能够对菌株的感兴趣性状进行评分并绘制潜在的 QTL。作为原理证明,我们将根据脉孢菌研究界广泛感兴趣的表型来描述野生和高级杂交菌株的特征:无性孢子繁殖、有性繁殖、营养生长、菌丝结构和孢子萌发期间的合作行为。我们将率先使用 Solexa 实验中的 mRNA 表达数据来识别这些宏观特征背后的分子因素,因为基因的表达被证明与个体的特征共同变化。此外,当我们分析表达水平之间的协变并从基因上绘制其控制调节因子时,表达测量将用于详细说明粗糙脉孢菌调节网络。我们的具体目标是(i)构建先进的杂交并表征这些菌株和野生分离株之间不同的表型; (ii) 使用 Solexa 平台对每个作图群体中每个个体的 cDNA 进行短读长测序,以生成密集的基因分型数据并测量基因表达; (iii) 进行 mRNA 表达和我们的原理验证生物性状的连锁和关联图谱。我们相信,我们提出的基因型、表型和基因表达水平之间的映射将推动粗糙猪笼草成为研究所有真核物种自然变异的模型的前沿。 与公共卫生的相关性:我们建议利用粗糙猪笼草来研究控制生长、生物体形状和对药物敏感性等特征的个体之间的遗传差异。粗糙脉孢菌是病原真菌的模型,我们的目标是了解其生物学的许多方面,这些方面对于疾病和治疗很重要。此外,由于人们对个体之间遗传差异的原理知之甚少,我们的工作将提供有关其他物种(如人类)遗传学的假设。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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JOHN W. TAYLOR其他文献

JOHN W. TAYLOR的其他文献

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{{ truncateString('JOHN W. TAYLOR', 18)}}的其他基金

2010 Cell and Molecular Fungal Biology; Gordon Research Conference
2010 细胞与分子真菌生物学;
  • 批准号:
    7905513
  • 财政年份:
    2010
  • 资助金额:
    $ 35.18万
  • 项目类别:
Illumina Sequencer to Facilitate Functional Genomics at Berkeley
Illumina 测序仪促进伯克利功能基因组学的发展
  • 批准号:
    7795092
  • 财政年份:
    2010
  • 资助金额:
    $ 35.18万
  • 项目类别:
"The development of genetics and genomics for analysis of quantitative traits"
“用于数量性状分析的遗传学和基因组学的发展”
  • 批准号:
    7508956
  • 财政年份:
    2008
  • 资助金额:
    $ 35.18万
  • 项目类别:
"The development of genetics and genomics for analysis of quantitative traits"
“用于数量性状分析的遗传学和基因组学的发展”
  • 批准号:
    8109212
  • 财政年份:
    2008
  • 资助金额:
    $ 35.18万
  • 项目类别:
Coccidioidomycosis:Genome Comparison, Selection and Transcription.
球孢子菌病:基因组比较、选择和转录。
  • 批准号:
    7800260
  • 财政年份:
    2007
  • 资助金额:
    $ 35.18万
  • 项目类别:
Coccidioidomycosis:Genome Comparison, Selection and Transcription.
球孢子菌病:基因组比较、选择和转录。
  • 批准号:
    7264463
  • 财政年份:
    2007
  • 资助金额:
    $ 35.18万
  • 项目类别:
Coccidioidomycosis:Genome Comparison, Selection and Transcription.
球孢子菌病:基因组比较、选择和转录。
  • 批准号:
    7608670
  • 财政年份:
    2007
  • 资助金额:
    $ 35.18万
  • 项目类别:
Coccidioidomycosis:Genome Comparison, Selection and Transcription.
球孢子菌病:基因组比较、选择和转录。
  • 批准号:
    7417795
  • 财政年份:
    2007
  • 资助金额:
    $ 35.18万
  • 项目类别:
Coccidioidomycosis:Genome Comparison, Selection and Transcription.
球孢子菌病:基因组比较、选择和转录。
  • 批准号:
    8059647
  • 财政年份:
    2007
  • 资助金额:
    $ 35.18万
  • 项目类别:
COCCIDIOIDES IMMITIS EVOLUTION AND VACCINE PRODUCTION
球孢子菌的进化和疫苗生产
  • 批准号:
    6657471
  • 财政年份:
    2002
  • 资助金额:
    $ 35.18万
  • 项目类别:
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