Evidence map›Paper›PMID 30154186›Full record

ArticleThe Journal of cell biology2018

Mapping 3D genome organization relative to nuclear compartments using TSA-Seq as a cytological ruler.

Yu Chen, Yang Zhang, Yuchuan Wang, Liguo Zhang, Eva K Brinkman, Stephen A Adam, Robert Goldman, Bas van Steensel, Jian Ma, Andrew S Belmont

Abstract read
In one paragraph

Article in The Journal of cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 261 papers.

0numbers the graph read from it
0cells of the map it votes in
261citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

261 citing papers in PubMed.

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201 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Yu ChenDepartment of Cell and Developmental Biology, University of Illinois at Urbana-Champaign, Urbana, IL.ORCID 0000-0001-7856-4648
Yang ZhangDepartment of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, IL.
Yuchuan WangComputational Biology Department, School of Computer Science, Carnegie Mellon University, Pittsburgh, PA.ORCID 0000-0001-7082-2884
Liguo ZhangDepartment of Cell and Developmental Biology, University of Illinois at Urbana-Champaign, Urbana, IL.
Eva K BrinkmanDivision of Gene Regulation, Netherlands Cancer Institute, Amsterdam, Netherlands.
Stephen A AdamDepartment of Cell and Molecular Biology, Northwestern University Feinberg School of Medicine, Chicago, IL.
Robert GoldmanDepartment of Cell and Molecular Biology, Northwestern University Feinberg School of Medicine, Chicago, IL.
Bas van SteenselDivision of Gene Regulation, Netherlands Cancer Institute, Amsterdam, Netherlands.
Jian MaComputational Biology Department, School of Computer Science, Carnegie Mellon University, Pittsburgh, PA.
Andrew S BelmontDepartment of Cell and Developmental Biology, University of Illinois at Urbana-Champaign, Urbana, IL asbel@illinois.edu.ORCID 0000-0002-6540-0801

Funding

Mapping Technology DevelopmentU54DK107965 · NIDDK · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI BELMONT, ANDREW STEVEN · 2015 to 2019
$8.6M
CHROMATIN DOMAIN STRUCTURE/FUNCTIONR01GM058460 · NIGMS · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI BELMONT, ANDREW STEVEN · 1999 to 2025
$8.0M
Computational Methods for Next-Generation Comparative GenomicsR01HG007352 · NHGRI · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI MA, JIAN · 2014 to 2023
$2.8M
NHGRI NIH HHS R01 HG007352NIDDK NIH HHS U54 DK107965NIGMS NIH HHS R01 GM058460
6 · The paper itself

Abstract

While nuclear compartmentalization is an essential feature of three-dimensional genome organization, no genomic method exists for measuring chromosome distances to defined nuclear structures. In this study, we describe TSA-Seq, a new mapping method capable of providing a "cytological ruler" for estimating mean chromosomal distances from nuclear speckles genome-wide and for predicting several Mbp chromosome trajectories between nuclear compartments without sophisticated computational modeling. Ensemble-averaged results in K562 cells reveal a clear nuclear lamina to speckle axis correlated with a striking spatial gradient in genome activity. This gradient represents a convolution of multiple spatially separated nuclear domains including two types of transcription "hot zones." Transcription hot zones protruding furthest into the nuclear interior and positioning deterministically very close to nuclear speckles have higher numbers of total genes, the most highly expressed genes, housekeeping genes, genes with low transcriptional pausing, and super-enhancers. Our results demonstrate the capability of TSA-Seq for genome-wide mapping of nuclear structure and suggest a new model for spatial organization of transcription and gene expression.

Indexed as

Chromosome MappingComputer SimulationGenome, HumanGene Expression RegulationGenome-Wide Association StudyHumansK562 CellsNuclear LaminaTranscription, Genetic

Identifiers

PMID30154186
PMCPMC6219710

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.