Evidence map›Paper›PMID 20460684›Full record

ArticleThe Journal of biological chemistry2010

Requiem protein links RelB/p52 and the Brm-type SWI/SNF complex in a noncanonical NF-kappaB pathway.

Toshio Tando, Aya Ishizaka, Hirotaka Watanabe, Taiji Ito, Shun Iida, Takeshi Haraguchi, Taketoshi Mizutani, Tomonori Izumi, Toshiaki Isobe, Taishin Akiyama and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

36 citing papers in PubMed, 55 citations in OpenAlex.

  1. Review
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  3. TheInternational journal of molecular sciences · 2024
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  12. AnBio-protocol · 2022
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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

12 authors at 3 institutions in 3 countries.

Toshio TandoDivision of Host-Parasite Interaction, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.
Aya Ishizaka
Hirotaka Watanabe
Taiji Ito
Shun Iida
Takeshi Haraguchi
Taketoshi Mizutani
Tomonori Izumi
Toshiaki Isobe
Taishin Akiyama
Jun-ichiro Inoue
Hideo Iba
The University of Tokyo · JPInteraction Design (United Kingdom) · GBTokyo University of Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The SWI/SNF chromatin remodeling complex plays pivotal roles in mammalian transcriptional regulation. In this study, we identify the human requiem protein (REQ/DPF2) as an adaptor molecule that links the NF-kappaB and SWI/SNF chromatin remodeling factor. Through in vitro binding experiments, REQ was found to bind to several SWI/SNF complex subunits and also to the p52 NF-kappaB subunit through its nuclear localization signal containing the N-terminal region. REQ, together with Brm, a catalytic subunit of the SWI/SNF complex, enhances the NF-kappaB-dependent transcriptional activation that principally involves the RelB/p52 dimer. Both REQ and Brm were further found to be required for the induction of the endogenous BLC (CXCL13) gene in response to lymphotoxin stimulation, an inducer of the noncanonical NF-kappaB pathway. Upon lymphotoxin treatment, REQ and Brm form a larger complex with RelB/p52 and are recruited to the BLC promoter in a ligand-dependent manner. Moreover, a REQ knockdown efficiently suppresses anchorage-independent growth in several cell lines in which the noncanonical NF-kappaB pathway was constitutively activated. From these results, we conclude that REQ functions as an efficient adaptor protein between the SWI/SNF complex and RelB/p52 and plays important roles in noncanonical NF-kappaB transcriptional activation and its associated oncogenic activity.

Indexed as

Signal TransductionCell LineChemokine CXCL13Chromosomal Proteins, Non-HistoneDNA-Binding ProteinsDNA HelicasesGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansLymphotoxin-alphaNeoplasmsNuclear ProteinsProtein BindingProtein SubunitsTranscriptional ActivationTranscription Factor RelBChemokine CXCL13Chromosomal Proteins, Non-HistoneCXCL13 protein, humanDNA-Binding ProteinsDNA HelicasesDPF2 protein, humanLymphotoxin-alphaNuclear ProteinsProtein SubunitsSMARCA2 protein, humanSMARCA4 protein, humanSWI-SNF-B chromatin-remodeling complexTranscription Factor RelBTranscription Factors

Identifiers

PMID20460684
PMCPMC2903353
OpenAlexW2003483601

What OpenQuestion holds

Textmetadata
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.