Regulation of DNA methylation by TETs and QSER1

TET 和 QSER1 对 DNA 甲基化的调节

基本信息

批准号：
10585325
负责人：
Todd R Evans
金额：
$ 68.84万
依托单位：
WEILL MEDICAL COLL OF CORNELL UNIV
依托单位国家：
美国
项目类别：
财政年份：
2022
资助国家：
美国
起止时间：
2022-09-22 至 2027-08-31
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/10585325
关键词：
ATAC-seq Aberrant DNA Methylation Aging Animal Model Binding Binding Proteins Biochemical Biochemical Genetics Biological Assay Biological Models CRISPR screen Cell Differentiation process Cells Chromatin Chromatin Structure Collaborations Complex Congenital Abnormality Coronary Arteriosclerosis DNA DNA Methylation DNA Methylation Regulation DNA methylation profiling Data Development Developmental Gene Disease Embryonic Development Endoderm Enhancers Enzymes Epiblast Epigenetic Process Excision Family Family member Fragile X Syndrome Gene Expression Genes Genetic Genetic Transcription Germ Layers Goals Histones Human Hydroxylation In Situ Hybridization Knowledge Larva Link Malignant Neoplasms Mesoderm Methylation Modeling Mus Mutation Nerve Degeneration Neuroectoderm Nucleic Acid Regulatory Sequences Oncogene Deregulation Organogenesis Pathway interactions Pattern Phenotype Play Productivity Proteins Proteomics Publishing Reader Regulation Regulator Genes Regulatory Element Reporter Research Personnel Role Science Seckel syndrome Site Structural Congenital Anomalies Structure Syndrome Testing Validation Vertebrates Zebrafish base chromatin modification demethylation directed differentiation epigenomics experimental study genetic analysis genetic variant genome-wide human embryonic stem cell immunodeficiency-centromeric instability-facial anomalies syndrome member methylome mutant novel paralogous gene progenitor programs promoter protein complex single-cell RNA sequencing stem cell fate specification stem cell model stem cells tool

项目摘要

The goal of this project is to discover fundamental epigenomic regulatory mechanisms that commit cells to defined fates during early stages of embryogenesis. Early in development, commitment of the epiblast to germ layers is followed by activation of key regulatory genes that drive lineage fate. These genes control normal development and underlie the genetic basis for a broad range of human structural birth defects. We have studied members of the TET family of hydroxylation enzymes, which regulate the demethylation of DNA, or block active methylation of DNA, to control gene expression. We discovered requirements for TET enzymes during early development in the zebrafish model, and for progenitor specification from human embryonic stem cells (hESCs). Major gaps in understanding include: i) whether common or distinct mechanisms control demethylation for progenitors from different germ layers, ii) whether different TET family members distinguish developmental programs, and iii) how TETs are targeted to regulatory regions such as bivalent promoters. Suspecting that additional proteins beyond TETs are needed to target DNA demethylation, we carried out a genome-wide CRISPR screen and discovered QSER1, a previously uncharacterized chromatin-binding protein. We showed that QSER1 is a key guardian of bivalent promoters and poised enhancers of developmental genes, especially those residing in DNA methylation valleys, broadly across different cell fates. We found biochemical and genetic interactions between QSER1 and TETs, suggesting that they cooperate to safeguard transcriptional and developmental programs from methylation. QSER1 variant alleles were recently linked to coronary artery disease, while haploinsufficiency of a QSER1 paralog, PRR12, is associated with multi-organ developmental birth defect syndromes. We propose to fully explore the genetic relationships and downstream networks of TET/QSER1 (TQ) family members, including how they function to control methylation and impact chromatin structure in the context of two complementary model systems, zebrafish and hESCs. The zebrafish model allows full genetic analysis of potentially compensatory or cooperating family members (including tet1, tet2, tet3, qser1, and prr12), in an animal model with highly conserved developmental programs. The hESC model provides outstanding biochemical and “omics” capacity, and validation in developing human progenitor and differentiated cells. The multi-PI project represents a continued collaboration among investigators with complementary and overlapping expertise, with a strong record of productivity. Specific Aims are proposed to determine the relative contribution of these genes for directing early progenitor fate, discover the regulatory networks in which they function, and to test interacting factors as candidates for linking TQ methylation control to chromatin modification. Because regulation of methylation is a fundamental step of progenitor fate determination, our results will be broadly relevant to organogenesis and structural birth defects.

该项目的目标是发现基本的表观基因组调控机制，使细胞在胚胎发生的早期阶段确定了外胚层对胚芽的命运。随后激活驱动谱系命运的关键调控基因。我们研究了多种人类结构性出生缺陷的遗传基础。羟基化酶 TET 家族的成员，可调节 DNA 的去甲基化，或阻断活性 DNA 甲基化，以控制基因表达，我们在早期就发现了 TET 酶的需求。斑马鱼模型的发育以及人类胚胎干细胞（hESC）的祖细胞规范。理解上的主要差距包括：i) 控制去甲基化的机制是共同的还是不同的来自不同胚层的祖细胞，ii) 不同的 TET 家族成员是否区分发育计划，以及 iii) TET 如何针对二价启动子等调控区域。需要除 TET 之外的其他蛋白质来靶向 DNA 去甲基化，我们进行了全基因组范围的研究我们展示了 CRISPR 筛选并发现了 QSER1，这是一种以前未表征的染色质结合蛋白。 QSER1 是发育基因的二价启动子和增强子的关键守护者，尤其是我们发现，这些存在于DNA甲基化谷中的细胞广泛地跨越了不同的细胞命运。 QSER1 和 TET 之间的相互作用，表明它们合作保护转录和 QSER1 变异等位基因的发育程序最近与冠状动脉有关。疾病，而 QSER1 旁系同源物 PRR12 的单倍体不足与多器官发育相关我们建议充分探索出生缺陷综合症的遗传关系和下游网络。 TET/QSER1 (TQ) 家族成员，包括它们如何发挥控制甲基化和影响染色质的作用斑马鱼和 hESC 两个互补模型系统的结构。对潜在补偿或合作家庭成员（包括 tet1、tet2、tet3、qser1、和 prr12），在具有高度保守的发育程序的动物模型中，hESC 模型提供了。杰出的生化和“组学”能力，以及在开发人类祖细胞和分化细胞方面的验证多 PI 项目代表了研究人员之间的持续合作，具有互补性和互补性。重叠的专业知识，具有良好的生产力记录，建议确定相对的具体目标。这些基因对指导早期祖细胞命运的贡献，发现它们所在的调控网络功能，并测试相互作用的因素作为将 TQ 甲基化控制与染色质修饰联系起来的候选因素。因为甲基化的调节是祖细胞命运决定的基本步骤，所以我们的结果将是与器官发生和结构性出生缺陷广泛相关。