{"lab": {"correspondence": [{"contact_email": "YXNiZWxAaWxsaW5vaXMuZWR1", "@id": "/users/92f90aed-7df1-4bd9-9e74-a472cb50d663/", "display_title": "Andrew Belmont"}], "@id": "/labs/andrew-belmont-lab/", "status": "current", "title": "Andrew Belmont, ILLINOIS", "display_title": "Andrew Belmont, ILLINOIS", "@type": ["Lab", "Item"], "uuid": "b2c2deeb-e883-4ac0-b9e2-906e598884d6", "pi": {"error": "no view permissions"}, "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin", "role.lab_submitter", "submits_for.b2c2deeb-e883-4ac0-b9e2-906e598884d6"]}}, "award": {"project": "4DN", "description": "RT-CDF: The study of gene expression and possible role of condensates in regulating gene expression havelargely ignored known nuclear structures. This proposal is significant because we propose a novel model forthe role of nuclear organization in regulating gene expression: 1) Nuclear speckles and still unknown nuclearcompartments/bodies help organize other phase-separated condensates to modulate gene expression; 2)Nuclear speckles together with surrounding nuclear compartments/bodies and associated phase-separatedcondensates together represent active nuclear niches which may have different functional properties; 3) Smalldistances matter: gene movements of only a few hundred nm between repressive and these different activenuclear niches may differentially regulate gene expression; 4) Action-at-a distance: component flux into andout of these nuclear compartments will have global effects on gene expression; 5) These same nuclearcompartments/bodies may similarly modulate RNA processing and organize nuclear export. Here we propose to: 1) Identify multiple components of known and still unknown nuclear \u201cactiveniches\u201d; 2) Map genome-wide the positions and predicted movements of genes relative to these active nichesduring physiological transitions; 3) Visualize nuclear body/compartment dynamics and fluxes of proteinsbetween nuclear bodies in steady-state and through physiological transitions; 4) Visualize movements ofreporter transgenes, endogenous genes, and rewired chromosome loci relative to these nuclearbodies/compartments and temporally correlate changes in gene expression with their dynamic movements andcompartment associations; 5) Visualize movements of pre-mRNAs and nuclear mRNAs during RNAprocessing and export; 6) Measure fluxes of nuclear body components to and from adjacent transcribingchromatin. Additionally, we propose developing relatively low-cost, novel microscope platforms and softwarespecifically designed to facilitate these live-cell imaging goals in our laboratories as well as others. Our Aims will be to: 1. Map proteins, genes, RNAs relative to active nuclear compartment(s) usingiterative rounds of TSA-MS-Ratio, validation by light microscopy, and TSA-Seq; 2. Measure dynamics ofbodies, components of nuclear bodies using live-cell imaging; 3. Measure temporal correlation betweenchanges in gene expression and gene movement relative to nuclear bodies and visualize the export path ofexpressed transcripts; 4. Design and deliver two novel microscopes designed to facilitate Aims 1-3 at amodest cost. Successful completion of these Aims should significantly change our current understanding of therole of nuclear organization in regulating gene expression with impact across a wide range of research fields.\"", "display_title": "IDENTIFICATION OF THE ACTIVE NUCLEAR NICHE(S) USING NOVEL PROTEOMIC, GENOMIC, TRANSGENIC, AND LIVE-CELL MICROSCOPY TECHNOLOGIES", "name": "1U01DK127422-01", "@id": "/awards/1U01DK127422-01/", "center_title": "Belmont", "uuid": "ef637c2d-7e48-4e26-aad2-eac1f680d4e8", "@type": ["Award", "Item"], "status": "current", "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin"]}, "pi": {"error": "no view permissions"}}, "md5sum": "0605e35721be71ae7663215ab4aca0ca", "status": "released", "aliases": ["belmont-lab:U2OS_THRAP3_2xDTT_Pulldown_bio1_GTGAAACG_L001_R1_001.fastq"], "filename": "U2OS_THRAP3_2xDTT_Pulldown_bio1_GTGAAACG_L001_R1_001.fastq.gz", "accession": "4DNFISEB2T9R", "file_size": 1843001045, "file_type": "reads", "instrument": "NovaSeq6000", "file_format": {"file_format": "fastq", "@type": ["FileFormat", "Item"], "@id": "/file-formats/fastq/", "uuid": "c13d06cf-218e-4f61-aaf0-91f226248b2c", "status": "released", "display_title": "fastq", "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin"]}}, "read_length": 100, "date_created": "2024-12-19T15:40:03.371345+00:00", "submitted_by": {"error": "no view permissions"}, "last_modified": {"modified_by": {"error": "no view permissions"}, "date_modified": "2025-09-05T17:06:19.757847+00:00"}, "content_md5sum": "79e6c98d5593db16eb1b65c69a271075", "public_release": "2025-08-27", "quality_metric": {"url": "https://s3.amazonaws.com/elasticbeanstalk-fourfront-webprod-wfoutput/4DNFISEB2T9R/fastqc_report.html", "uuid": "f520d86b-0b14-4c18-aafe-e56138380904", "status": "released", "display_title": "QualityMetricFastqc from 2024-12-20", "@type": ["QualityMetricFastqc", "QualityMetric", "Item"], "@id": "/quality-metrics-fastqc/f520d86b-0b14-4c18-aafe-e56138380904/", "overall_quality_status": "PASS", "Total Sequences": 39114021, "Sequence length": "100", "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin"]}}, "schema_version": "2", "file_first_line": "@A00419:487:HL25CDRXY:1:2101:1488:1000 1:N:0:GTGAAACG", "project_release": "2025-08-27", "flowcell_details": [{"barcode": "GTGAAACG", "machine": "NovaSeq6000"}], "file_classification": "raw file", "@id": "/files-fastq/4DNFISEB2T9R/", "@type": ["FileFastq", "File", "Item"], "uuid": "938d3c1d-773a-4190-b410-3b1ac251a87f", "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin"]}, "display_title": "4DNFISEB2T9R.fastq.gz", "external_references": [], "experiments": [{"@type": ["ExperimentTsaseq", "Experiment", "Item"], "accession": "4DNEX6Q6KW56", "display_title": "TSA-seq against THRAP3 protein on U2OS (Tier 2) - 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