Evidence map›Paper›PMID 38834852›Full record

ArticleThe EMBO journal2024

PARP14 is regulated by the PARP9/DTX3L complex and promotes interferon γ-induced ADP-ribosylation.

Victoria Chaves Ribeiro, Lilian Cristina Russo, Nícolas Carlos Hoch

Abstract read
In one paragraph

Article in The EMBO journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Review
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  5. NovelNeurology. Genetics · 2026
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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

3 authors.

Victoria Chaves Ribeiro *Department of Biochemistry, University of São Paulo, São Paulo, 05508-000, Brazil.ORCID http://orcid.org/0000-0003-4612-3009
Lilian Cristina Russo *Department of Biochemistry, University of São Paulo, São Paulo, 05508-000, Brazil.ORCID http://orcid.org/0000-0002-9846-1352
Nícolas Carlos HochDepartment of Biochemistry, University of São Paulo, São Paulo, 05508-000, Brazil. nicolas@iq.usp.br.ORCID http://orcid.org/0000-0002-7610-1305

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) 2015/02654-3Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) 2018/18007-5Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) 2019/06039-2Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) 2019/25914-1Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) 2020/05317-6Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) 2020/11162-5 and 2022/10947-4
6 · The paper itself

Abstract

Protein ADP-ribosylation plays important but ill-defined roles in antiviral signalling cascades such as the interferon response. Several viruses of clinical interest, including coronaviruses, express hydrolases that reverse ADP-ribosylation catalysed by host enzymes, suggesting an important role for this modification in host-pathogen interactions. However, which ADP-ribosyltransferases mediate host ADP-ribosylation, what proteins and pathways they target and how these modifications affect viral infection and pathogenesis is currently unclear. Here we show that host ADP-ribosyltransferase activity induced by IFNγ signalling depends on PARP14 catalytic activity and that the PARP9/DTX3L complex is required to uphold PARP14 protein levels via post-translational mechanisms. Both the PARP9/DTX3L complex and PARP14 localise to IFNγ-induced cytoplasmic inclusions containing ADP-ribosylated proteins, and both PARP14 itself and DTX3L are likely targets of PARP14 ADP-ribosylation. We provide evidence that these modifications are hydrolysed by the SARS-CoV-2 Nsp3 macrodomain, shedding light on the intricate cross-regulation between IFN-induced ADP-ribosyltransferases and the potential roles of the coronavirus macrodomain in counteracting their activity.

Indexed as

ADP-RibosylationInterferon-gammaPoly(ADP-ribose) PolymerasesADP Ribose TransferasesHEK293 CellsHost-Pathogen InteractionsHumansNeoplasm ProteinsProtein Processing, Post-TranslationalSARS-CoV-2Ubiquitin-Protein LigasesADP Ribose TransferasesDTX3L protein, humanInterferon-gammaNeoplasm ProteinsPARP14 protein, humanPARP9 protein, humanPoly(ADP-ribose) PolymerasesUbiquitin-Protein LigasesADP-RibosylationCoronavirusInnate ImmunityInterferonPARP

Identifiers

PMID38834852
PMCPMC11251048

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.