Evidence map›Paper›PMID 24682156›Full record

ArticleGenome biology and evolution2014

Ancient and recent selective pressures shaped genetic diversity at AIM2-like nucleic acid sensors.

Rachele Cagliani, Diego Forni, Mara Biasin, Manuel Comabella, Franca R Guerini, Stefania Riva, Uberto Pozzoli, Cristina Agliardi, Domenico Caputo, Sunny Malhotra and 4 more

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

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  16. Inflammasome control of viral infection.Current opinion in virology · 2015
    Review
  17. cGAS-mediated stabilization of IFI16 promotes innate signaling during herpes simplex virus infection.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  18. Review
  19. OASes and STING: adaptive evolution in concert.Genome biology and evolution · 2015
    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

14 authors at 6 institutions in 2 countries.

Rachele CaglianiBioinformatics Laboratory, Scientific Institute IRCCS E. Medea, Bosisio Parini (LC), Italy.
Diego Forni
Mara Biasin
Manuel Comabella
Franca R Guerini
Stefania Riva
Uberto Pozzoli
Cristina Agliardi
Domenico Caputo
Sunny Malhotra
Xavier Montalban
Nereo Bresolin
Mario Clerici
Manuela Sironi
IRCCS Eugenio Medea · ITDon Carlo Gnocchi Foundation · ITUniversity of Milan · ITVall d'Hebron Hospital Universitari · ESCentre d'Esclerosi Múltiple de CatalunyaFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

AIM2-like receptors (ALRs) are a family of nucleic acid sensors essential for innate immune responses against viruses and bacteria. We performed an evolutionary analysis of ALR genes (MNDA, PYHIN1, IFI16, and AIM2) by analyzing inter- and intraspecies diversity. Maximum-likelihood analyses indicated that IFI16 and AIM2 evolved adaptively in primates, with branch-specific selection at the catarrhini lineage for IFI16. Application of a population genetics-phylogenetics approach also allowed identification of positive selection events in the human lineage. Positive selection in primates targeted sites located at the DNA-binding interface in both IFI16 and AIM2. In IFI16, several sites positively selected in primates and in the human lineage were located in the PYD domain, which is involved in protein-protein interaction and is bound by a human cytomegalovirus immune evasion protein. Finally, positive selection was found to target nuclear localization signals in IFI16 and the spacer region separating the two HIN domains. Population genetic analysis in humans revealed that an IFI16 genic region has been a target of long-standing balancing selection, possibly acting on two nonsynonymous polymorphisms located in the spacer region. Data herein indicate that ALRs have been repeatedly targeted by natural selection. The balancing selection region in IFI16 carries a variant with opposite risk effect for distinct autoimmune diseases, suggesting antagonistic pleiotropy. We propose that the underlying scenario is the result of an ancestral and still ongoing host-pathogen arms race and that the maintenance of susceptibility alleles for autoimmune diseases at IFI16 represents an evolutionary trade-off.

Indexed as

Evolution, MolecularGenetic VariationPhylogenySelection, GeneticAnimalsBase SequenceChlorocebus aethiopsCOS CellsDNA-Binding ProteinsGorilla gorillaHumansMacaca fascicularisMolecular Sequence DataPan troglodytesPongo pygmaeusDNA-Binding ProteinsAIM2-like receptorsIFI16long-standing balancing selectionpositive selection

Identifiers

PMID24682156
PMCPMC4007548
OpenAlexW2109735258

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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.