Evidence map›Paper›PMID 21813606›Full record

ArticleJournal of virology2011

A Kaposi's sarcoma-associated herpesvirus-encoded ortholog of microRNA miR-155 induces human splenic B-cell expansion in NOD/LtSz-scid IL2Rγnull mice.

Isaac W Boss, Peter E Nadeau, Jeffrey R Abbott, Yajie Yang, Ayalew Mergia, Rolf Renne

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
6.5field-weighted citation impact, top 2% 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

83 citing papers in PubMed, 118 citations in OpenAlex.

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  7. Viral miRNA regulation of host gene expression.Seminars in cell & developmental biology · 2023
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23 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

Isaac W BossDepartment of Molecular Genetics and Microbiology, University of Florida,Gainesville, FL, USA.
Peter E Nadeau
Jeffrey R Abbott
Yajie Yang
Ayalew Mergia
Rolf Renne
University of Florida · USUniversity of Florida Health · US

Funding

BASIC MICROBIOLOGY &INFECTIOUS DISEASEST32AI007110 · NIAID · UNIVERSITY OF FLORIDA · PI Stephanie M Karst · 1985 to 2026
$4.3M
Studying the role of KSHV-encoded miRNAsR01CA119917 · NCI · UNIVERSITY OF FLORIDA · PI RENNE, ROLF F · 2008 to 2017
$3.2M
LANA AND CELLULAR GENE EXPRESSION IN KAPOSIS SARCOMAR01CA088763 · NCI · UNIVERSITY OF FLORIDA · PI RENNE, ROLF F · 2000 to 2015
$3.2M
Early life factors, gene-environment interaction and eosinophilic esophagitisR01AI139126 · NIAID · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI JENSEN, ELIZABETH T · 2018 to 2023
$1.7M
Biodefense and Emerging Infectious Diseases (BEID)T32AI060527 · NIAID · UNIVERSITY OF FLORIDA · PI RENNE, ROLF F · 2005 to 2009
$357k
NCI NIH HHS CA119917NCI NIH HHS CA88763NCI NIH HHS R01 CA088763NCI NIH HHS R01 CA119917NIAID NIH HHS AI139126NIAID NIH HHS R01 AI139126NIAID NIH HHS T32 AI007110NIAID NIH HHS T32AI007110NIAID NIH HHS T32 AI060527NIAID NIH HHS T32AI060527
6 · The paper itself

Abstract

MicroRNAs (miRNAs) are small noncoding RNA molecules that function as posttranscriptional regulators of gene expression. Kaposi's sarcoma (KS)-associated herpesvirus (KSHV), a B-cell-tropic virus associated with KS and B-cell lymphomas, encodes 12 miRNA genes that are highly expressed in these tumor cells. One viral miRNA, miR-K12-11, shares 100% seed sequence homology with hsa-miR-155, an oncogenic human miRNA that functions as a key regulator of hematopoiesis and B-cell differentiation. So far, in vitro studies have shown that both miRNAs can regulate a common set of cellular target genes, suggesting that miR-K12-11 may mimic miR-155 function. To comparatively study miR-K12-11 and miR-155 function in vivo, we used a foamy virus vector to express the miRNAs in human hematopoietic progenitors and performed immune reconstitutions in NOD/LtSz-scid IL2Rγ(null) mice. We found that ectopic expression of miR-K12-11 or miR-155 leads to a significant expansion of the CD19(+) B-cell population in the spleen. Subsequent quantitative PCR analyses of these splenic B cells revealed that C/EBPβ, a transcriptional regulator of interleukin-6 that is linked to B-cell lymphoproliferative disorders, is downregulated when either miR-K12-11 or miR-155 is ectopically expressed. In addition, inhibition of miR-K12-11 function using antagomirs in KSHV-infected human primary effusion lymphoma B cells resulted in derepression of C/EBPβ transcript levels. This in vivo study validates miR-K12-11 as a functional ortholog of miR-155 in the context of hematopoiesis and suggests a novel mechanism by which KSHV miR-K12-11 induces splenic B-cell expansion and potentially KSHV-associated lymphomagenesis by targeting C/EBPβ.

Indexed as

Cell ProliferationAnimalsAntigens, CD19B-LymphocytesCCAAT-Enhancer-Binding Protein-betaDown-RegulationHerpesvirus 8, HumanHumansMaleMiceMice, KnockoutMice, SCIDMicroRNAsRNA, ViralSpleenAntigens, CD19CCAAT-Enhancer-Binding Protein-betaCEBPB protein, humanMicroRNAsMIRN155 microRNA, humanRNA, Viral

Identifiers

PMID21813606
PMCPMC3196388
OpenAlexW2169294034

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.