Evidence map›Paper›PMID 31607649›Full record

ArticleDevelopmental cell2019

Characterization of Button Loci that Promote Homologous Chromosome Pairing and Cell-Type-Specific Interchromosomal Gene Regulation.

Kayla Viets, Michael E G Sauria, Chaim Chernoff, Rebecca Rodriguez Viales, Max Echterling, Caitlin Anderson, Sang Tran, Abigail Dove, Raghav Goyal, Lukas Voortman and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

44 citing papers in PubMed, 63 citations in OpenAlex.

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  10. ThebioRxiv : the preprint server for biology · 2025
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  15. Building Haplotype-Resolved 3D Genome Maps of Chicken Skeletal Muscle.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  16. Modeling homologous chromosome recognition via nonspecific interactions.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  17. Transcriptional priming and chromatin regulation during stochastic cell fate specification.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Review
  18. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 2 countries.

Kayla VietsDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
Michael E G SauriaDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
Chaim ChernoffDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
Rebecca Rodriguez VialesEuropean Molecular Biology Laboratory, Department of Genome Biology, Heidelberg 69117, Germany.
Max EchterlingDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
Caitlin AndersonDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
Sang TranDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
Abigail DoveDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
Raghav GoyalDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
Lukas VoortmanDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
Andrew GordusDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
Eileen E M FurlongEuropean Molecular Biology Laboratory, Department of Genome Biology, Heidelberg 69117, Germany.
James TaylorDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
Robert J JohnstonDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218, USA. Electronic address: robertjohnston@jhu.edu.
Johns Hopkins University · USEuropean Molecular Biology Laboratory · DE

Funding

Mechanisms controlling stochastic gene expression during eye developmentR01EY025598 · NEI · JOHNS HOPKINS UNIVERSITY · PI Robert John Johnston · 2015 to 2026
$4.9M
Determining the role of 3D nuclear architecture in stochastic gene expressionF31EY026786 · NEI · JOHNS HOPKINS UNIVERSITY · PI VIETS, KAYLA CHELSEA · 2016 to 2018
$88k
NEI NIH HHS F31 EY026786NEI NIH HHS R01 EY025598
6 · The paper itself

Abstract

Homologous chromosomes colocalize to regulate gene expression in processes including genomic imprinting, X-inactivation, and transvection. In Drosophila, homologous chromosomes pair throughout development, promoting transvection. The "button" model of pairing proposes that specific regions along chromosomes pair with high affinity. Here, we identify buttons interspersed across the fly genome that pair with their homologous sequences, even when relocated to multiple positions in the genome. A majority of transgenes that span a full topologically associating domain (TAD) function as buttons, but not all buttons contain TADs. Additionally, buttons are enriched for insulator protein clusters. Fragments of buttons do not pair, suggesting that combinations of elements within a button are required for pairing. Pairing is necessary but not sufficient for transvection. Additionally, pairing and transvection are stronger in some cell types than in others, suggesting that pairing strength regulates transvection efficiency between cell types. Thus, buttons pair homologous chromosomes to facilitate cell-type-specific interchromosomal gene regulation.

Indexed as

Gene Expression RegulationGenetic LociAnimalsChromatinChromosome PairingChromosomesDrosophila melanogasterInsulator ElementsTransgenesChromatinfly eye developmentgene regulationhomologous chromosome pairingnuclear architecturetransvection

Identifiers

PMID31607649
PMCPMC6934266
OpenAlexW2979365992

What OpenQuestion holds

Textmetadata
LicenceTDM
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.