Evidence map›Paper›PMID 26824388›Full record

ArticleeLife2016

Single-cell analysis of transcription kinetics across the cell cycle.

Samuel O Skinner, Heng Xu, Sonal Nagarkar-Jaiswal, Pablo R Freire, Thomas P Zwaka, Ido Golding

Abstract read
In one paragraph

Article in eLife, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing 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

93 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Single-Cell Multiomic Analysis of Circadian Rhythmicity in Mouse Liver.bioRxiv : the preprint server for biology · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Control of cell state transitions by post-transcriptional regulation.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Samuel O SkinnerVerna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, United States.
Heng XuVerna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, United States.
Sonal Nagarkar-JaiswalCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston, United States.
Pablo R FreireDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, United States.
Thomas P ZwakaCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston, United States.
Ido GoldingVerna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, United States.ORCID http://orcid.org/0000-0002-4308-4959

Funding

The Role of p53 in Human Embryonic Stem CellsP01GM081627 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI GOODELL, MARGARET A. · 2007 to 2011
$9.9M
GENE REGULATION IN PHAGE LAMBDA: A REAL-TIME STUDY WITH SINGLE-EVENT RESOLUTIONR01GM082837 · NIGMS · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI GOLDING, IDO · 2008 to 2020
$4.0M
NON-APOPTOTIC ACTION OF CASPASES IN PLURIPOTENT EMBRYONIC STEM CELLSR01GM077442 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI ZWAKA, THOMAS P. · 2008 to 2012
$1.5M
NIGMS NIH HHS P01 GM081627NIGMS NIH HHS P01 GM81627NIGMS NIH HHS R01 GM077442NIGMS NIH HHS R01 GM082837
6 · The paper itself

Abstract

Transcription is a highly stochastic process. To infer transcription kinetics for a gene-of-interest, researchers commonly compare the distribution of mRNA copy-number to the prediction of a theoretical model. However, the reliability of this procedure is limited because the measured mRNA numbers represent integration over the mRNA lifetime, contribution from multiple gene copies, and mixing of cells from different cell-cycle phases. We address these limitations by simultaneously quantifying nascent and mature mRNA in individual cells, and incorporating cell-cycle effects in the analysis of mRNA statistics. We demonstrate our approach on Oct4 and Nanog in mouse embryonic stem cells. Both genes follow similar two-state kinetics. However, Nanog exhibits slower ON/OFF switching, resulting in increased cell-to-cell variability in mRNA levels. Early in the cell cycle, the two copies of each gene exhibit independent activity. After gene replication, the probability of each gene copy to be active diminishes, resulting in dosage compensation.

Indexed as

Cell CycleGene Expression ProfilingSingle-Cell AnalysisTranscription, GeneticAnimalsEmbryonic Stem CellsMiceNanog Homeobox ProteinOctamer Transcription Factor-3RNA, MessengerNanog Homeobox ProteinNanog protein, mouseOctamer Transcription Factor-3Pou5f1 protein, mouseRNA, Messengerchromosomescomputational biologyfluorescence in situgenesmathematical modelingmousesingle cellsingle moleculestochastic gene expressionsystems biologytheory

Identifiers

PMID26824388
PMCPMC4801054

What OpenQuestion holds

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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.