Effects of mutations on gene expression noise and cellular memory
Effects of mutations on gene expression noise and cellular memory
批准号:
7431787
负责人:
Scott Rifkin
金额:
$5.13万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-05-01 至 2009-12-31
关键词:
AllelesBiochemicalBiochemical ReactionBiological ModelsBuffersCell physiologyCellsComplexComputer ArchitecturesConditionDiseaseEquilibriumEvolutionExhibitsFaceFeedbackFellowshipGalactoseGene ExpressionGenesGeneticGenetic TranscriptionGenomeLeadLinkMalignant NeoplasmsMeasuresMemoryModelingMoldsMolecularMolecular ProbesMonitorMutationNational Research Service AwardsNatural SelectionsNoiseNumbersPaperPhenotypePlayPopulation GrowthProcessProductionProteinsRateRoleSaccharomyces cerevisiaeSystemTATA BoxTestingTranscriptional ActivationTranslationsVariantYeastsin vivomutantpromotersimulationtheoriestraittranscription factor
中文摘要
描述(由申请人提供):噪声是遗传网络不可避免的特征,即使在相同的环境条件下,也会导致基因相同的细胞之间的变异。由于表达是一个涉及许多生化反应的多步骤过程,许多最近的研究推测,自然选择可以调节噪音水平,以避免可能损害细胞功能的波动。在选择测试中一个重要的参数是一个性状的新变异由突变产生的速率。本研究旨在(1)利用已被充分研究的酿酒酵母半乳糖网络作为模型系统,估计噪声及其对网络活动的影响仅因突变而进化的速率;(2)测量该网络的关键正反馈回路对调控突变的鲁棒性;(3)利用理论和模拟分析突变和选择下基本调控网络的进化。目标(1)和(2)将通过在体内监测暴露于不同水平的半乳糖的细胞中的基因和网络活性来实现,这些细胞在基因组中随机携带突变(1),或针对特定的网络成分(2)。突变等位基因在先天性疾病中起着重要作用,突变的积累是细胞向癌症发展的特征之一。在这两种情况下,突变等位基因可能会破坏正常的遗传网络功能,因此了解遗传网络如何缓冲突变的影响以及网络功能如何容易受到损害是很重要的。
英文摘要
DESCRIPTION (provided by applicant): Noise is an inescapable feature of genetic networks, causing variation among genetically identical cells even under identical environmental conditions. Because expression is a multistep process involving many biochemical reactions, many recent studies have conjectured that natural selection can tune levels of noise to avoid fluctuations which could impair cellular function. One important parameter in tests for selection is the rate at which new variation in a trait is generated by mutation. This proposal aims to (1) estimate the rate at which noise and its effects on network activity evolve solely due to mutation, using the well-studied galactose network of Saccharomyces cerevisiae as a model system, (2) measure how robust the key positive feedback loop of this network is to regulatory mutations, and (3) use theory and simulation to analyze the evolution of a basic regulatory network under mutation and selection. Aims (1) and (2) will be pursued through in vivo monitoring of gene and network activity in cells exposed to varying levels of galactose carrying mutations randomly throughout the genome (1), or targeted to a particular network component (2). Mutant alleles play an important role in congenital diseases, and the accumulation of mutations is one of the features of cellular progression to cancer. In both of these cases, mutant alleles probably disrupt normal genetic network functioning, and so it is important to understand how genetic networks buffer the effects of mutations and how easily network function can be compromised.
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会议论文
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依托单位:
海外基金