Evidence map›Paper›PMID 32816370›Full record

ArticleMolecular systems biology2020

Exploring the virulence gene interactome with CRISPR/dCas9 in the human malaria parasite.

Jessica M Bryant, Sebastian Baumgarten, Florent Dingli, Damarys Loew, Ameya Sinha, Aurélie Claës, Peter R Preiser, Peter C Dedon, Artur Scherf

Open access · goldAbstract read
In one paragraph

Article in Molecular systems biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
6.7field-weighted citation impact, top 3% of its field
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

31 citing papers in PubMed, 59 citations in OpenAlex.

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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

9 authors at 4 institutions in 3 countries.

Jessica M BryantBiology of Host-Parasite Interactions Unit, Institut Pasteur, Paris, France.ORCID 0000-0002-2349-8353
Sebastian BaumgartenBiology of Host-Parasite Interactions Unit, Institut Pasteur, Paris, France.ORCID 0000-0003-2646-7699
Florent DingliInstitut Curie, PSL Research University, Centre de Recherche, Mass Spectrometry and Proteomics Facility, Paris, France.ORCID 0000-0002-7715-2446
Damarys LoewInstitut Curie, PSL Research University, Centre de Recherche, Mass Spectrometry and Proteomics Facility, Paris, France.ORCID 0000-0002-9111-8842
Ameya SinhaSchool of Biological Sciences, Nanyang Technological University, Singapore, Singapore.ORCID 0000-0001-7959-075X
Aurélie ClaësBiology of Host-Parasite Interactions Unit, Institut Pasteur, Paris, France.
Peter R PreiserSchool of Biological Sciences, Nanyang Technological University, Singapore, Singapore.ORCID 0000-0003-4331-7000
Peter C DedonAntimicrobial Resistance Interdisciplinary Research Group, Singapore-MIT Alliance for Research and Technology, Singapore, Singapore.ORCID 0000-0003-0011-3067
Artur ScherfBiology of Host-Parasite Interactions Unit, Institut Pasteur, Paris, France.ORCID 0000-0003-2411-3328
Centre National de la Recherche Scientifique · FRNanyang Technological University · SGUniversité Paris Sciences et Lettres · FRSingapore-MIT Alliance for Research and Technology · SG

Funding

TOXICOLOGY CORE UNITP30ES002109 · NIEHS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI NILES, JACQUIN C · 1985 to 2020
$25.6M
NIEHS NIH HHS P30 ES002109
6 · The paper itself

Abstract

Mutually exclusive expression of the var multigene family is key to immune evasion and pathogenesis in Plasmodium falciparum, but few factors have been shown to play a direct role. We adapted a CRISPR-based proteomics approach to identify novel factors associated with var genes in their natural chromatin context. Catalytically inactive Cas9 ("dCas9") was targeted to var gene regulatory elements, immunoprecipitated, and analyzed with mass spectrometry. Known and novel factors were enriched including structural proteins, DNA helicases, and chromatin remodelers. Functional characterization of PfISWI, an evolutionarily divergent putative chromatin remodeler enriched at the var gene promoter, revealed a role in transcriptional activation. Proteomics of PfISWI identified several proteins enriched at the var gene promoter such as acetyl-CoA synthetase, a putative MORC protein, and an ApiAP2 transcription factor. These findings validate the CRISPR/dCas9 proteomics method and define a new var gene-associated chromatin complex. This study establishes a tool for targeted chromatin purification of unaltered genomic loci and identifies novel chromatin-associated factors potentially involved in transcriptional control and/or chromatin organization of virulence genes in the human malaria parasite.

Indexed as

Adenosine TriphosphatasesAnimalsAntigens, ProtozoanChromatin Immunoprecipitation SequencingCRISPR-Cas SystemsHumansIntronsMass SpectrometryPlasmodium falciparumPromoter Regions, GeneticProtein Interaction MapsProteomicsTranscription FactorsVirulence FactorsAdenosine TriphosphatasesAntigens, ProtozoanISWI proteinTranscription FactorsVirulence FactorschromatinCRISPRepigeneticsPlasmodium falciparumvar genes

Identifiers

PMID32816370
PMCPMC7440042
OpenAlexW3056632053

What Socratic 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 Socratic graph.