Chromatin-mediated mechanisms of transcription regulation in ES cells

ES 细胞中染色质介导的转录调控机制

• 批准号: 10001562
• 负责人: Sarah Jane Hainer
• 金额: $ 38.33万
• 依托单位: UNIVERSITY OF PITTSBURGH AT PITTSBURGH
• 依托单位国家: 美国
• 财政年份: 2019
• 资助国家: 美国
• 起止时间: 2019-09-01 至 2024-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10001562
• 关键词: Address; Binding; Cells; Chromatin; Chromatin Remodeling Factor; Chromatin Structure; Code; Collection; Complex; Enhancers; Gene Activation; Gene Expression Regulation; Genes; Genetic Transcription; Genome; Goals; Higher Order Chromatin Structure; Individual; Laboratories; Lead; Mediating; Messenger RNA; NURF; Nucleosomes; Positioning Attribute; Proteins; RNA; Regulation; Regulator Genes; Repression; Research; Role; Transcriptional Regulation; Untranslated RNA; base; cell type; embryonic stem cell; interest; mammalian genome; promoter; stem cell fate; targeted treatment

PROJECT SUMMARY/ABSTRACT Our research interests focus on the similarities and differences in chromatin structure among different cell types and how chromatin remodeling factors that modulate these differences regulate cell fate. The long- term goals of our laboratory are to comprehensively understand the functions, targets, regulation, and mechanisms of action of non-coding RNAs (ncRNAs) and chromatin regulatory factors with critical functions in gene regulatory networks. Approximately 75% of the mammalian genome is transcribed. While coding regions account for only ~2% of the genome, the remaining intergenic and intragenic transcription generates a large collection of non- coding RNAs (ncRNAs). Two regions rich with non-coding transcription are active enhancers (where ncRNAs are generated bi-directionally) and promoters (where ncRNAs are generated in the antisense orientation from protein-coding genes). While a few individual ncRNAs have been shown to function in gene activation, their activities in gene regulation have not been systematically addressed. Recently, we showed that esBAF, a nucleosome remodeling complex that binds enhancers and promoters, is necessary for repression of numerous ncRNAs throughout the genome in ES cells. Upon depletion of esBAF, nucleosome occupancy flanking regions of open chromatin was reduced, resulting in elevated ncRNA transcription. Based on these studies, we are in a unique position to build a network of ncRNA regulation by nucleosome remodeling factors in ES cells. Specifically, we will determine (1) how esBAF regulates higher order chromatin structure, (2) the functions of enhancer-specific ncRNAs (eRNAs) in enhancer looping and gene regulation, (3) the mechanisms underlying regulation of mRNAs by ncRNAs, and (4) the network of nucleosome remodeling complexes regulating ncRNA expression. These studies will enhance our understanding of the chromatin-centered regulation of ncRNAs. Over the next five years, our laboratory will identify nucleosome remodelers that regulate ncRNA expression, explore the role of nucleosome remodeling factors in regulating higher order chromatin structure at the level of enhancer-promoter looping, and determine the function of two uncharacterized classes of ncRNAs in ES cells. The proposed research is significant because it will uncover fundamental mechanisms that choreograph the interplay of chromatin dynamics with ncRNA function, consequently providing a crucial step in understanding ES cell fate decisions.

项目总结/文摘