Genomic and genetic analysis of oral stem cells

口腔干细胞的基因组和遗传分析

• 批准号: 9527934
• 负责人: Rose-Anne Romano
• 金额: $ 15.89万
• 依托单位: STATE UNIVERSITY OF NEW YORK AT BUFFALO
• 依托单位国家: 美国
• 财政年份: 2018
• 资助国家: 美国
• 起止时间: 2018-09-01 至 2020-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9527934
• 关键词: ATAC-seq; Address; Affect; Animals; Architecture; Area; Automobile Driving; Biological Assay; Biological Models; Cell Cycle Arrest; Cell Lineage; Cell physiology; Cells; Cellular biology; Chromatin; Critical Pathways; Cues; Development; Disease; Embryo; Environment; Epigenetic Process; Epithelial; Epithelial Cells; Equilibrium; Expression Profiling; Foundations; Future; Gene Expression; Gene Expression Profile; Genes; Genetic; Genetic Transcription; Genome; Genomics; Goals; Homeostasis; Injury; Knowledge; Light; Mediating; Molecular; Molecular Conformation; Morphogenesis; Mus; Natural regeneration; Normal tissue morphology; Oral; Oral cavity; Organ; Pathway interactions; Play; Population; Process; Property; Protein Isoforms; Regulation; Regulator Genes; Regulatory Element; Role; Shapes; Signal Pathway; Signal Transduction; Small Interfering RNA; Stem cells; Stratification; Techniques; Technology; Time; Tissue Engineering; Tissue-Specific Gene Expression; Tissues; Transcriptional Regulation; Transgenic Mice; Work; base; cell type; epigenomics; experimental study; genetic analysis; genome-wide; improved; in vivo; in vivo Model; innovation; insight; interest; keratinocyte; knock-down; mouse model; next generation sequencing; novel; novel therapeutic intervention; oral cavity epithelium; oral tissue; progenitor; prospective; regenerative; repaired; self-renewal; stem; stem cell division; tissue regeneration; tool; transcription factor; transcriptome; transcriptome sequencing; transcriptomics

PROJECT SUMMARY The tightly regulated balance between proliferation and differentiation of basal stem/progenitor cells of the oral epithelium is critical for proper tissue development, repair, renewal, and to maintain homeostasis. Therefore, the development of new tools and strategies directed at identifying transcriptional and signaling networks underlying stem/progenitor cell function of the oral epithelium are critical. Hence, our goal is to examine the molecular mechanisms of the transcriptional and gene-regulatory mechanisms that control stem/progenitor cell function of the oral epithelium with the ultimate goal for using the knowledge gained from such studies towards stem cell regenerative-based therapies and tissue engineering approaches. It is well established that ΔNp63 plays a critical role in epithelial regenerative function as ΔNp63-null animals fail to develop several epithelial-rich organs including those of the oral cavity. However, our current knowledge of how Np63 interacts with and shapes the chromatin and transcriptional regulatory environment of the stem/progenitor cells of the oral epithelium, is lacking. To address these knowledge gaps, we will utilize an enriched population of oral epithelial stem/progenitor cells obtained from novel ΔNp63-GFP transgenic mice to study two major areas of interest. First, we will perform both clonogenic and functional assays to compare the abilities of ΔNp63-GFPhi, ΔNp63-GFPlow, ΔNp63neg and ΔNp63-GFPhi-KD (ΔNp63 specific inducible knockdown in ΔNp63-GFPhi cells using siRNA mediated strategies) oral epithelial cells to retain their progenitor capabilities in organospheres (Aim1A). Furthermore, we will perform transcriptomic profiling (RNA-seq) to generate global gene expression profiles of ΔNp63-GFPhi, ΔNp63-GFPlow, ΔNp63neg and ΔNp63-GFPhi-KD to better understand the Np63-dependent gene regulatory mechanisms that are important for oral epithelial stem/progenitor cell biology (Aim1B). Such studies are important, since they will identify for the first time the gene expression profile of oral epithelial stem/progenitor cells on a broad and dynamic scale. Second, to examine the global status of the chromatin architecture of oral epithelia cells, we will perform ATAC-seq experiments with ΔNp63- GFPhi, ΔNp63-GFPlow, ΔNp63neg and ΔNp63-GFPhi-KD cells to identify the ΔNp63 dependent and independent regulatory chromatin environment that are important for stem/progenitor cell function (Aim 2). Collectively, our approach using a genetically-defined model system and cutting-edge next generation sequencing technology will better elucidate the transcriptomic and epigenomic landscape of oral stem/progenitor cells and shed light on the ΔNp63-governed transcriptional regulatory network and signaling pathways. This work is highly innovative and significant because our proposed use of sophisticated genetic tools, in vivo models and genome-wide profiling assays to examine fundamental transcriptional control mechanisms will lead to new discoveries important for oral epithelial stem cell based regenerative strategies used to treat and regenerate oral tissues following injury, damage or in diseased states.

项目总结