Evidence map›Paper›PMID 39346775›Full record

ReviewFrontiers in genetics2024

Transcriptional bursting dynamics in gene expression.

Qiuyu Zhang, Wenjie Cao, Jiaqi Wang, Yihao Yin, Rui Sun, Zunyi Tian, Yuhan Hu, Yalan Tan, Ben-Gong Zhang

Abstract readReview
In one paragraph

Review in Frontiers in genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. What makes genes burst.Trends in cell biology · 2026
    Review
  6. Review
  7. Review
  8. Article
  9. Article
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

9 authors.

Qiuyu ZhangResearch Center of Nonlinear Sciences, School of Mathematical & Physical Sciences, Wuhan Textile University, Wu Han, China.
Wenjie CaoSchool of Mathematics, Sun Yat-sen University, Guangzhou, China.
Jiaqi WangResearch Center of Nonlinear Sciences, School of Mathematical & Physical Sciences, Wuhan Textile University, Wu Han, China.
Yihao YinResearch Center of Nonlinear Sciences, School of Mathematical & Physical Sciences, Wuhan Textile University, Wu Han, China.
Rui SunResearch Center of Nonlinear Sciences, School of Mathematical & Physical Sciences, Wuhan Textile University, Wu Han, China.
Zunyi TianResearch Center of Nonlinear Sciences, School of Mathematical & Physical Sciences, Wuhan Textile University, Wu Han, China.
Yuhan HuResearch Center of Nonlinear Sciences, School of Mathematical & Physical Sciences, Wuhan Textile University, Wu Han, China.
Yalan TanSchool of Bioengineering & Health, Wuhan Textile University, Wu Han, China.
Ben-Gong ZhangResearch Center of Nonlinear Sciences, School of Mathematical & Physical Sciences, Wuhan Textile University, Wu Han, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gene transcription is a stochastic process that occurs in all organisms. Transcriptional bursting, a critical molecular dynamics mechanism, creates significant heterogeneity in mRNA and protein levels. This heterogeneity drives cellular phenotypic diversity. Currently, the lack of a comprehensive quantitative model limits the research on transcriptional bursting. This review examines various gene expression models and compares their strengths and weaknesses to guide researchers in selecting the most suitable model for their research context. We also provide a detailed summary of the key metrics related to transcriptional bursting. We compared the temporal dynamics of transcriptional bursting across species and the molecular mechanisms influencing these bursts, and highlighted the spatiotemporal patterns of gene expression differences by utilizing metrics such as burst size and burst frequency. We summarized the strategies for modeling gene expression from both biostatistical and biochemical reaction network perspectives. Single-cell sequencing data and integrated multiomics approaches drive our exploration of cutting-edge trends in transcriptional bursting mechanisms. Moreover, we examined classical methods for parameter estimation that help capture dynamic parameters in gene expression data, assessing their merits and limitations to facilitate optimal parameter estimation. Our comprehensive summary and review of the current transcriptional burst dynamics theories provide deeper insights for promoting research on the nature of cell processes, cell fate determination, and cancer diagnosis.

Indexed as

data integrationgene expression modelparameter inferencesingle-cell sequencing datatranscriptional bursting

Identifiers

PMID39346775
PMCPMC11437526

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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.