Evidence map›Paper›PMID 24121441›Full record

ArticleNature2013

MX2 is an interferon-induced inhibitor of HIV-1 infection.

Melissa Kane, Shalini S Yadav, Julia Bitzegeio, Sebla B Kutluay, Trinity Zang, Sam J Wilson, John W Schoggins, Charles M Rice, Masahiro Yamashita, Theodora Hatziioannou and 1 more

Open access · greenAbstract read
In one paragraph

Article in Nature, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 335 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
335citing papers in PubMed, 1 pooled it
21.0field-weighted citation impact, top 1% 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

335 citing papers in PubMed, 1 synthesis or guideline pooled it, 497 citations in OpenAlex.

  1. Pooled it
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  7. Review
  8. MX2 Mediates Collapse of the HIV-1 Capsid.bioRxiv : the preprint server for biology · 2026
    Article
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275 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Melissa Kane1] Aaron Diamond AIDS Research Center, New York, New York 10016, USA [2] Laboratory of Retrovirology, The Rockefeller University, New York, New York 10065, USA.
Shalini S Yadav
Julia Bitzegeio
Sebla B Kutluay
Trinity Zang
Sam J Wilson
John W Schoggins
Charles M Rice
Masahiro Yamashita
Theodora Hatziioannou
Paul D Bieniasz
Aaron Diamond AIDS Research Center · USHoward Hughes Medical Institute · USRockefeller University · US

Funding

Viral Pathogenesis and TherapeuticsU54AI057158 · NIAID · WADSWORTH CENTER · PI LEVY, DAVID E · 2003 to 2014
$100.8M
Overcoming Host Restriction Factors to Develop Better Animal Models for HIV/AIDS.R01AI078788 · NIAID · ROCKEFELLER UNIVERSITY · PI HATZIIOANNOU, THEODORA · 2008 to 2021
$9.3M
Mechanism and role of nuclear entry in HIV-1 replicationR01AI100720 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Masahiro Yamashita · 2012 to 2026
$6.5M
Type I interferon-stimulated genes and the antiviral immune responseR01AI091707 · NIAID · ROCKEFELLER UNIVERSITY · PI RICE, CHARLES M · 2011 to 2020
$5.5M
Discovery and Mechanism of Antiretroviral FactorsR37AI064003 · NIAID · ROCKEFELLER UNIVERSITY · PI BIENIASZ, PAUL D. · 2011 to 2020
$4.9M
Interactions between type I and III interferon during resolution of HCV infectionK01DK095031 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI SCHOGGINS, JOHN W. · 2012 to 2016
$629k
Howard Hughes Medical InstituteMedical Research Council G0801822Medical Research Council MR/K024752/1NIAID NIH HHS AI057158NIAID NIH HHS AI091707NIAID NIH HHS R01 AI078788NIAID NIH HHS R01AI078788NIAID NIH HHS R01 AI091707NIAID NIH HHS R01 AI100720NIAID NIH HHS R01AI100720NIAID NIH HHS R37 AI064003NIAID NIH HHS R37AI64003NIAID NIH HHS U54 AI057158NIDDK NIH HHS DK095031NIDDK NIH HHS K01 DK095031
6 · The paper itself

Abstract

HIV-1 replication can be inhibited by type I interferon (IFN), and the expression of a number of gene products with anti-HIV-1 activity is induced by type I IFN. However, none of the known antiretroviral proteins can account for the ability of type I IFN to inhibit early, preintegration phases of the HIV-1 replication cycle in human cells. Here, by comparing gene expression profiles in cell lines that differ in their ability to support the inhibitory action of IFN-α at early steps of the HIV-1 replication cycle, we identify myxovirus resistance 2 (MX2) as an interferon-induced inhibitor of HIV-1 infection. Expression of MX2 reduces permissiveness to a variety of lentiviruses, whereas depletion of MX2 using RNA interference reduces the anti-HIV-1 potency of IFN-α. HIV-1 reverse transcription proceeds normally in MX2-expressing cells, but 2-long terminal repeat circular forms of HIV-1 DNA are less abundant, suggesting that MX2 inhibits HIV-1 nuclear import, or destabilizes nuclear HIV-1 DNA. Consistent with this notion, mutations in the HIV-1 capsid protein that are known, or suspected, to alter the nuclear import pathways used by HIV-1 confer resistance to MX2, whereas preventing cell division increases MX2 potency. Overall, these findings indicate that MX2 is an effector of the anti-HIV-1 activity of type-I IFN, and suggest that MX2 inhibits HIV-1 infection by inhibiting capsid-dependent nuclear import of subviral complexes.

Indexed as

Active Transport, Cell NucleusCapsidCell DivisionCell LineCell NucleusCells, CulturedHIV-1HIV InfectionsHumansInterferon-alphaMutant ProteinsMyxovirus Resistance ProteinsReverse TranscriptionRNA InterferenceTranscriptomeVirus ReplicationInterferon-alphaMutant ProteinsMyxovirus Resistance Proteins

Identifiers

PMID24121441
PMCPMC3912734
OpenAlexW1986829091

What OpenQuestion holds

Textmetadata
LicenceTDM
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.