Discriminating between causes of age-related variegated gene expression

区分与年龄相关的杂色基因表达的原因

• 批准号: 10558669
• 负责人: Nikolay Burnaevskiy
• 金额: $ 24.9万
• 依托单位: ALTIUS INSTITUTE FOR BIOMEDICAL SCIENCES
• 依托单位国家: 美国
• 财政年份: 2022
• 资助国家: 美国
• 起止时间: 2022-02-01 至 2025-01-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10558669
• 关键词: Address; Adult; Age; Aging; Alleles; Animals; Biological Models; Caenorhabditis elegans; Cell Communication; Cell Culture Techniques; Cells; Chromosomes; Coculture Techniques; Communication; Controlled Environment; Deterioration; Diploidy; Event; Fibroblasts; Gene Expression; Gene Proteins; Genes; Genetic Transcription; Genome; Genome engineering; Gerontology; Global Change; Health; Homeostasis; Human; Individual; Intestines; Knowledge; Lead; Learning; Longevity; Mammalian Cell; Mammals; Measures; Messenger RNA; Methods; Muscle; Organ; Organism; Pathway interactions; Pattern; Phase; Physiological; Polyploidy; Population; Prevalence; Production; Proteins; Quantitative Microscopy; RNA; Reporter; Reporter Genes; Reproducibility; Resistance; Sister; Somatic Mutation; Stress; Techniques; Testing; Tissues; Training; Variant; age related; autosome; cell type; cohort; deviant; dosage; experimental study; gene expression variation; human tissue; in vivo; individual response; juvenile animal; large datasets; promoter; response; senescence; single cell analysis; single-cell RNA sequencing; skills; stoichiometry; tissue culture; young adult

Project Summary: Cells in the same tissue can express the exact same gene at different levels, and this cell-to-cell variation tends to increase with age. Cells in tissues need to coordinate gene expression to maintain homeostasis. Thus, dysregulated variation may be related to, or causative of, the loss of physiological capacities with age. However, the causes and consequences of this increased gene expression variation are not known. In this project I propose to use C. elegans and human tissue culture as model systems to study age-related variation in gene expression between homologous cells in controlled environments. In our prior study, we found strong, cell-specific expression patterns for many reporter genes in young C. elegans animals; that is, for many genes in young animals, the ratio of gene A to gene B expression was fixed in cell type X, and different than in cell type Y. We found that this fixed expression pattern deteriorates with age; in a given cell type genes become expressed at variable stoichiometry in individual animals. Similarly, in mammals, cell-to-cell variation in gene expression observed during aging or senescence is also uncorrelated. Thus, I propose that growing dissimilarity between homologous cells with age may be a conserved phenomenon of aging. I refer to increase of uncorrelated gene expression variation with age as age-related variegated gene expression (VGE). In the proposed project, I will harness both the power of C. elegans and human cell culture to investigate how homologous cells become more dissimilar with age. In the K99 phase of the project I will learn techniques for quantitative microscopy, single cell RNAseq and aging-focused human cell culture methods. Throughout the K99 and R00, I will be investigating potential causes that contribute to age-related VGE. K99-Aim1: I will determine if changes of allele access with age contribute into VGE in C. elegans by analyzing expression from of identical promoters integrated at the identical loci on sister chromosomes. K99-Aim2: I will learn and use single-cell RNA-seq to determine if prevalence of allele bias/monoallelism rises in human fibroblasts with age. R00-Aim3: I will determine what genes and pathways become highly variably expressed with age. I will examine if variable expression of these genes is stochastic or adaptive by determining if expression levels of reporters of these genes predict stress resistance, health or lifespan. These experiments will address the hypothesis that adaptive physiological responses of individual cells to age-related stress contribute to VGE. R00-Aim 4: Using human cell culture, I will determine if cell-to-cell communications propagate VGE among cells with youthful expression patterns – that is, cells without VGE.

项目概要： 同一组织中的细胞可以在不同水平上表达完全相同的基因，这种细胞间的变异 随着年龄的增长而增加。组织中的细胞需要协调基因表达以维持稳态。 因此，失调的变异可能与生理能力随年龄的丧失有关，或引起生理能力随年龄的丧失。 然而，这种增加的基因表达变异的原因和后果尚不清楚。在这 项目我建议使用C.线虫和人类组织培养作为研究年龄相关变异的模型系统 在受控环境中同源细胞之间的基因表达。在我们之前的研究中，我们发现， 细胞特异性表达模式的许多报告基因在年轻的C。elegans动物;也就是说，对于许多基因， 在幼年动物中，基因A与基因B表达的比率在X型细胞中是固定的，并且与在细胞中不同。 Y型血我们发现，这种固定的表达模式随着年龄的增长而恶化;在给定的细胞类型中， 在个体动物中以可变的化学计量表示。类似地，在哺乳动物中， 在老化或衰老期间观察到的表达也是不相关的。因此，我建议， 随着年龄的增长，同源细胞之间的相异性可能是老化的保守现象。我指的是增加 年龄相关的杂色基因表达（VGE）。在 建议的项目，我将利用这两个权力的C。线虫和人类细胞培养来研究 随着年龄的增长，同源细胞变得越来越不相似。在项目的K99阶段，我将学习以下技术 定量显微术、单细胞RNAseq和聚焦衰老的人细胞培养方法。在整个 K99和R 00，我将调查导致年龄相关VGE的潜在原因。K99-Aim 1：我会的 确定等位基因接近随年龄的变化是否对C. elegans通过分析表达， 在姐妹染色体上的相同位点整合的相同启动子。K99-Aim 2：我会学习和使用 单细胞RNA-seq，以确定等位基因偏倚/单等位基因现象的患病率是否随着年龄的增长而在人成纤维细胞中上升。 R 00-Aim 3：我将确定哪些基因和途径随着年龄的增长而高度表达。我会 通过确定这些基因的表达水平来检查这些基因的可变表达是随机的还是适应性的。 这些基因的报告者可以预测压力抵抗力、健康或寿命。这些实验将解决 假设个体细胞对年龄相关应激的适应性生理反应有助于VGE。 R 00-目的4：使用人类细胞培养，我将确定细胞间的通信是否会在 具有年轻表达模式的细胞-即没有VGE的细胞。