Evidence map›Paper›PMID 25770217›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Spatial proximity of homologous alleles and long noncoding RNAs regulate a switch in allelic gene expression.

Kalliopi Stratigi, Manouela Kapsetaki, Michalis Aivaliotis, Terrence Town, Richard A Flavell, Charalampos G Spilianakis

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

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

15 citing papers in PubMed.

  1. A novel SATB1 protein isoform with different biophysical properties.Frontiers in cell and developmental biology · 2023
    Article
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  13. The emerging landscape ofF1000Research · 2017
    Review
  14. Article
  15. Pairing and anti-pairing: a balancing act in the diploid genome.Current opinion in genetics & development · 2016
    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

6 authors.

Kalliopi StratigiInstitute of Molecular Biology and Biotechnology-Foundation for Research and Technology Hellas, GR70013 Heraklion, Greece; Department of Biology, University of Crete, GR70013 Heraklion, Greece;
Manouela KapsetakiInstitute of Molecular Biology and Biotechnology-Foundation for Research and Technology Hellas, GR70013 Heraklion, Greece;
Michalis AivaliotisInstitute of Molecular Biology and Biotechnology-Foundation for Research and Technology Hellas, GR70013 Heraklion, Greece;
Terrence TownDepartment of Physiology and Biophysics, Zilkha Neurogenetic Institute, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90089; and.
Richard A FlavellDepartment of Immunobiology and Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT 06520 spiliana@imbb.forth.gr richard.flavell@yale.edu.
Charalampos G SpilianakisInstitute of Molecular Biology and Biotechnology-Foundation for Research and Technology Hellas, GR70013 Heraklion, Greece; Department of Biology, University of Crete, GR70013 Heraklion, Greece; spiliana@imbb.forth.gr richard.flavell@yale.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Physiological processes rely on the regulation of total mRNA levels in a cell. In diploid organisms, the transcriptional activation of one or both alleles of a gene may involve trans-allelic interactions that provide a tight spatial and temporal level of gene expression regulation. The mechanisms underlying such interactions still remain poorly understood. Here, we demonstrate that lipopolysaccharide stimulation of murine macrophages rapidly resulted in the actin-mediated and transient homologous spatial proximity of Tnfα alleles, which was necessary for the mono- to biallelic switch in gene expression. We identified two new complementary long noncoding RNAs transcribed from the TNFα locus and showed that their knockdown had opposite effects in Tnfα spatial proximity and allelic expression. Moreover, the observed spatial proximity of Tnfα alleles depended on pyruvate kinase muscle isoform 2 (PKM2) and T-helper-inducing POZ-Krüppel-like factor (ThPOK). This study suggests a role for lncRNAs in the regulation of somatic homologous spatial proximity and allelic expression control necessary for fine-tuning mammalian immune responses.

Indexed as

RNA, Long NoncodingTranscriptional ActivationAllelesAnimalsCarrier ProteinsCell LineGene Expression ProfilingGene Expression RegulationIn Situ Hybridization, FluorescenceLipopolysaccharidesLymphotoxin-alphaLymphotoxin-betaMacrophagesMembrane ProteinsMiceMice, Inbred C57BLCarrier ProteinsLipopolysaccharidesLymphotoxin-alphaLymphotoxin-betaMembrane ProteinsRNA, Long NoncodingThyroid Hormone-Binding ProteinsThyroid HormonesTranscription FactorsTumor Necrosis Factor-alphaZbtb7b protein, mousehomologous spatial proximitylncRNAsmacrophagesTnfα

Identifiers

PMID25770217
PMCPMC4386343

What OpenQuestion holds

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Registered trials

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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.