Evidence map›Paper›PMID 31618265›Full record

ArticlePLoS computational biology2019

Computational design and interpretation of single-RNA translation experiments.

Luis U Aguilera, William Raymond, Zachary R Fox, Michael May, Elliot Djokic, Tatsuya Morisaki, Timothy J Stasevich, Brian Munsky

Abstract read
In one paragraph

Article in PLoS computational biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Translation Dynamics of Single mRNAs in Live Cells.Annual review of biophysics · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Lighting up single-mRNA translation dynamics in living cells.Current opinion in genetics & development · 2020
    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

8 authors.

Luis U AguileraDepartment of Chemical and Biological Engineering, Colorado State University Fort Collins, Colorado, United States of America.ORCID 0000-0003-0609-539X
William RaymondDepartment of Chemical and Biological Engineering, Colorado State University Fort Collins, Colorado, United States of America.ORCID 0000-0002-3155-7499
Zachary R FoxSchool of Biomedical Engineering, Colorado State University Fort Collins, Colorado, United States of America.ORCID 0000-0003-0138-2867
Michael MaySchool of Biomedical Engineering, Colorado State University Fort Collins, Colorado, United States of America.
Elliot DjokicSchool of Biomedical Engineering, Colorado State University Fort Collins, Colorado, United States of America.ORCID 0000-0002-6775-9041
Tatsuya MorisakiDepartment of Biochemistry and Molecular Biology and Institute for Genome Architecture and Function, Colorado State University, Fort Collins, Colorado, United States of America.
Timothy J StasevichDepartment of Biochemistry and Molecular Biology and Institute for Genome Architecture and Function, Colorado State University, Fort Collins, Colorado, United States of America.
Brian MunskyDepartment of Chemical and Biological Engineering, Colorado State University Fort Collins, Colorado, United States of America.ORCID 0000-0001-6147-7329

Funding

Using cellular fluctuations and computational analyses to probe biological mechanismsR35GM124747 · NIGMS · COLORADO STATE UNIVERSITY · PI Brian Munsky · 2017 to 2026
$3.3M
NIGMS NIH HHS R35 GM124747
6 · The paper itself

Abstract

Advances in fluorescence microscopy have introduced new assays to quantify live-cell translation dynamics at single-RNA resolution. We introduce a detailed, yet efficient sequence-based stochastic model that generates realistic synthetic data for several such assays, including Fluorescence Correlation Spectroscopy (FCS), ribosome Run-Off Assays (ROA) after Harringtonine application, and Fluorescence Recovery After Photobleaching (FRAP). We simulate these experiments under multiple imaging conditions and for thousands of human genes, and we evaluate through simulations which experiments are most likely to provide accurate estimates of elongation kinetics. Finding that FCS analyses are optimal for both short and long length genes, we integrate our model with experimental FCS data to capture the nascent protein statistics and temporal dynamics for three human genes: KDM5B, β-actin, and H2B. Finally, we introduce a new open-source software package, RNA Sequence to NAscent Protein Simulator (rSNAPsim), to easily simulate the single-molecule translation dynamics of any gene sequence for any of these assays and for different assumptions regarding synonymous codon usage, tRNA level modifications, or ribosome pauses. rSNAPsim is implemented in Python and is available at: https://github.com/MunskyGroup/rSNAPsim.git.

Indexed as

Computational BiologyComputer SimulationFluorescence Recovery After PhotobleachingHumansKineticsMicroscopy, FluorescenceProtein BiosynthesisProteinsRibosomesRNARNA, MessengerSpectrometry, FluorescenceProteinsRNARNA, Messenger

Identifiers

PMID31618265
PMCPMC6816579

What OpenQuestion holds

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LicenceCC BY
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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.