Evidence map›Paper›PMID 31509524›Full record

ArticlePLoS computational biology2019

Predicting gene expression in the human malaria parasite Plasmodium falciparum using histone modification, nucleosome positioning, and 3D localization features.

David F Read, Kate Cook, Yang Y Lu, Karine G Le Roch, William Stafford Noble

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 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
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  4. Article
  5. Review
  6. Article
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  9. Article
  10. Review
  11. Article
  12. Peculiarities ofInternational journal of molecular sciences · 2021
    Review
  13. Article
  14. Article
  15. Review
  16. From Genes to Transcripts, a Tightly Regulated Journey inFrontiers in cellular and infection microbiology · 2020
    Review
  17. 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

5 authors.

David F ReadDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Kate CookDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Yang Y LuDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.ORCID 0000-0003-1686-5917
Karine G Le RochDepartment of Molecular, Cell and Systems Biology, University of California, Riverside, California, United States of America.
William Stafford NobleDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.ORCID 0000-0001-7283-4715

Funding

TrainingP41GM103533 · NIGMS · UNIVERSITY OF WASHINGTON · PI YATES III, JOHN R · 2012 to 2021
$20.7M
Chromatin structure and control of gene expression in the human malaria parasiteR01AI136511 · NIAID · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI LE ROCH, KARINE GAELLE · 2018 to 2022
$3.4M
The spatial organization of the Plasmodium genome throughout its infectious cycleR01AI106775 · NIAID · UNIVERSITY OF WASHINGTON · PI LE ROCH, KARINE GAELLE, NOBLE, WILLIAM STAFFORD · 2013 to 2016
$1.8M
NIAID NIH HHS R01 AI106775NIAID NIH HHS R01 AI136511NIGMS NIH HHS P41 GM103533
6 · The paper itself

Abstract

Empirical evidence suggests that the malaria parasite Plasmodium falciparum employs a broad range of mechanisms to regulate gene transcription throughout the organism's complex life cycle. To better understand this regulatory machinery, we assembled a rich collection of genomic and epigenomic data sets, including information about transcription factor (TF) binding motifs, patterns of covalent histone modifications, nucleosome occupancy, GC content, and global 3D genome architecture. We used these data to train machine learning models to discriminate between high-expression and low-expression genes, focusing on three distinct stages of the red blood cell phase of the Plasmodium life cycle. Our results highlight the importance of histone modifications and 3D chromatin architecture in Plasmodium transcriptional regulation and suggest that AP2 transcription factors may play a limited regulatory role, perhaps operating in conjunction with epigenetic factors.

Indexed as

Models, StatisticalComputational BiologyErythrocytesGene Expression ProfilingGene Expression RegulationGenes, ProtozoanHistone CodeHumansLife Cycle StagesMachine LearningMalaria, FalciparumModels, BiologicalNucleosomesPlasmodium falciparumNucleosomes

Identifiers

PMID31509524
PMCPMC6756558

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.