Evidence map›Paper›PMID 28931413›Full record

ArticleGenome biology2017

Topological organization and dynamic regulation of human tRNA genes during macrophage differentiation.

Kevin Van Bortle, Douglas H Phanstiel, Michael P Snyder

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

30 citing papers in PubMed, 46 citations in OpenAlex.

  1. Multilevel genomic constraints shape nuclear tRNA gene organization in plants.The Plant journal : for cell and molecular biology · 2026
    Article
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  13. tRNA dysregulation and disease.Nature reviews. Genetics · 2022
    Review
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  16. Review
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  20. RNA Polymerase III, Ageing and Longevity.Frontiers in genetics · 2021
    Review
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

3 authors at 2 institutions in 1 country.

Kevin Van BortleDepartment of Genetics, Stanford University, Stanford, CA, 94305, USA.
Douglas H PhanstielDepartment of Cell Biology and Physiology, University of North Carolina, Chapel Hill, NC, 27599, USA.
Michael P SnyderDepartment of Genetics, Stanford University, Stanford, CA, 94305, USA. mpsnyder@stanford.edu.
Stanford University · USUniversity of North Carolina at Chapel Hill · US

Funding

The development and application of tools to characterize the 4D nucleomeR00HG008662 · NHGRI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI PHANSTIEL, DOUGLAS H. · 2017 to 2019
$747k
Integrated Personalized Epigenome Profiling and the Effect of Dietary Exposure on Individuals at Risk for Type-2-DiabetesF32DK107112 · NIDDK · STANFORD UNIVERSITY · PI VAN BORTLE, KEVIN · 2015 to 2017
$162k
The development and application of tools to characterize the 4D nucleomeK99HG008662 · NHGRI · STANFORD UNIVERSITY · PI PHANSTIEL, DOUGLAS H. · 2015 to 2016
$100k
NHGRI NIH HHS K99 HG008662NHGRI NIH HHS R00 HG008662NIDDK NIH HHS F32 DK107112
6 · The paper itself

Abstract

backgroundThe human genome is hierarchically organized into local and long-range structures that help shape cell-type-specific transcription patterns. Transfer RNA (tRNA) genes (tDNAs), which are transcribed by RNA polymerase III (RNAPIII) and encode RNA molecules responsible for translation, are dispersed throughout the genome and, in many cases, linearly organized into genomic clusters with other tDNAs. Whether the location and three-dimensional organization of tDNAs contribute to the activity of these genes has remained difficult to address, due in part to unique challenges related to tRNA sequencing. We therefore devised integrated tDNA expression profiling, a method that combines RNAPIII mapping with biotin-capture of nascent tRNAs. We apply this method to the study of dynamic tRNA gene regulation during macrophage development and further integrate these data with high-resolution maps of 3D chromatin structure.

resultsIntegrated tDNA expression profiling reveals domain-level and loop-based organization of tRNA gene transcription during cellular differentiation. tRNA genes connected by DNA loops, which are proximal to CTCF binding sites and expressed at elevated levels compared to non-loop tDNAs, change coordinately with tDNAs and protein-coding genes at distal ends of interactions mapped by in situ Hi-C. We find that downregulated tRNA genes are specifically marked by enhanced promoter-proximal binding of MAF1, a transcriptional repressor of RNAPIII activity, altogether revealing multiple levels of tDNA regulation during cellular differentiation.

conclusionsWe present evidence of both local and coordinated long-range regulation of human tDNA expression, suggesting the location and organization of tRNA genes contribute to dynamic tDNA activity during macrophage development.

Indexed as

Cell DifferentiationCell LineGene Expression Regulation, DevelopmentalHumansMacrophagesPromoter Regions, GeneticRepressor ProteinsRNA, TransferTranscriptional ActivationMAF1 protein, humanRepressor ProteinsRNA, TransferBiotin-captureCTCFHi-CtDNATFIIICTopologically associating domainstRNAome

Identifiers

PMID28931413
PMCPMC5607496
OpenAlexW2754356065

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.