Evidence map›Paper›PMID 28624615›Full record

ArticleCell systems2017

Cell-Size-Dependent Transcription of FLC and Its Antisense Long Non-coding RNA COOLAIR Explain Cell-to-Cell Expression Variation.

Robert Ietswaart, Stefanie Rosa, Zhe Wu, Caroline Dean, Martin Howard

Abstract read
In one paragraph

Article in Cell systems, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
–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

42 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Cell Growth and Division Shape mRNA-Protein Correlations.bioRxiv : the preprint server for biology · 2026
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  12. Proceedings of the National Academy of Sciences of the United States of America · 2024
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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

5 authors.

Robert IetswaartComputational and Systems Biology, John Innes Centre, Norwich Research Park, Norwich NR4 7UH, UK; Department of Cell and Developmental Biology, John Innes Centre, Norwich Research Park, Norwich NR4 7UH, UK.
Stefanie RosaDepartment of Cell and Developmental Biology, John Innes Centre, Norwich Research Park, Norwich NR4 7UH, UK.
Zhe WuDepartment of Cell and Developmental Biology, John Innes Centre, Norwich Research Park, Norwich NR4 7UH, UK.
Caroline DeanDepartment of Cell and Developmental Biology, John Innes Centre, Norwich Research Park, Norwich NR4 7UH, UK. Electronic address: caroline.dean@jic.ac.uk.
Martin HowardComputational and Systems Biology, John Innes Centre, Norwich Research Park, Norwich NR4 7UH, UK; Department of Cell and Developmental Biology, John Innes Centre, Norwich Research Park, Norwich NR4 7UH, UK. Electronic address: martin.howard@jic.ac.uk.

Funding

Biotechnology and Biological Sciences Research Council BB/J004588/1Biotechnology and Biological Sciences Research Council BB/K007203/1Biotechnology and Biological Sciences Research Council BBS/E/J/000C0637Biotechnology and Biological Sciences Research Council BBS/E/J/000PR9773Biotechnology and Biological Sciences Research Council BBS/E/J/000PR9788
6 · The paper itself

Abstract

Single-cell quantification of transcription kinetics and variability promotes a mechanistic understanding of gene regulation. Here, using single-molecule RNA fluorescence in situ hybridization and mathematical modeling, we dissect cellular RNA dynamics for Arabidopsis FLOWERING LOCUS C (FLC). FLC expression quantitatively determines flowering time and is regulated by antisense (COOLAIR) transcription. In cells without observable COOLAIR expression, we quantify FLC transcription initiation, elongation, intron processing, and lariat degradation, as well as mRNA release from the locus and degradation. In these heterogeneously sized cells, FLC mRNA number increases linearly with cell size, resulting in a large cell-to-cell variability in transcript level. This variation is accounted for by cell-size-dependent, Poissonian FLC mRNA production, but not by large transcriptional bursts. In COOLAIR-expressing cells, however, antisense transcription increases with cell size and contributes to FLC transcription decreasing with cell size. Our analysis therefore reveals an unexpected role for antisense transcription in modulating the scaling of transcription with cell size.

Indexed as

ArabidopsisArabidopsis ProteinsCell SizeFlowersGene Expression Regulation, PlantRNA, AntisenseRNA, Long NoncodingRNA, MessengerTranscription, GeneticArabidopsis ProteinsRNA, AntisenseRNA, Long NoncodingRNA, Messengerantisense transcriptioncell size variationCOOLAIRFLCintrinsic and extrinsic variationmathematical modellingRNA dynamicssingle-molecule fluorescence in situ hybridizationstochasticitytranscriptional regulation

Identifiers

PMID28624615
PMCPMC5493185

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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.