Evidence map›Paper›PMID 22580161›Full record

ArticleDevelopmental biology2012

The Drosophila BCL6 homolog Ken and Barbie promotes somatic stem cell self-renewal in the testis niche.

Melanie Issigonis, Erika Matunis

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2012. 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
2.3field-weighted citation impact, top 12% 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, 35 citations in OpenAlex.

  1. B Cell Lymphoma 6 (BCL6): A Conserved Regulator of Immunity and Beyond.International journal of molecular sciences · 2024
    Review
  2. PTP61F Mediates Cell Competition and Mitigates Tumorigenesis.International journal of molecular sciences · 2021
    Article
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  15. Stem cells supporting other stem cells.Frontiers in genetics · 2013
    Review
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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

2 authors at 1 institution in 1 country.

Melanie IssigonisDepartment of Cell Biology, Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA.
Erika Matunis
Johns Hopkins University · US

Funding

CONTROL OF STEM CELL FATE IN DROSOPHILA SPERMATOGENESISR01HD040307 · NICHD · JOHNS HOPKINS UNIVERSITY · PI MATUNIS, ERIKA L · 2001 to 2014
$4.1M
Cellular plasticity in the Drosophila spermatogonial stem cell nicheR01HD052937 · NICHD · JOHNS HOPKINS UNIVERSITY · PI MATUNIS, ERIKA L · 2007 to 2020
$3.8M
Request for Zeiss LSM 510 MP Multiphoton Imaging SystemS10RR024550 · NCRR · JOHNS HOPKINS UNIVERSITY · PI KUO, SCOT CHARLES · 2008 to 2008
$500k
NCRR NIH HHS S10 RR024550NICHD NIH HHS R01 HD040307NICHD NIH HHS R01 HD052937NICHD NIH HHS R01HD40307
6 · The paper itself

Abstract

Stem cells sustain tissue regeneration by their remarkable ability to replenish the stem cell pool and to generate differentiating progeny. Signals from local microenvironments, or niches, control stem cell behavior. In the Drosophila testis, a group of somatic support cells called the hub creates a stem cell niche by locally activating the Janus Kinase-Signal Transducer and Activator of Transcription (JAK-STAT) pathway in two adjacent types of stem cells: germline stem cells (GSCs) and somatic cyst stem cells (CySCs). Here, we find that ken and barbie (ken) is autonomously required for the self-renewal of CySCs but not GSCs. Furthermore, Ken misexpression in the CySC lineage induces the cell-autonomous self-renewal of somatic cells as well as the nonautonomous self-renewal of germ cells outside the niche. Thus, Ken, like Stat92E and its targets ZFH1 (Leatherman and Dinardo, 2008) and Chinmo (Flaherty et al., 2010), is necessary and sufficient for CySC renewal. However, ken is not a JAK-STAT target in the testis, but instead acts in parallel to Stat92E to ensure CySC self-renewal. Ken represses a subset of Stat92E targets in the embryo (Arbouzova et al., 2006) suggesting that Ken maintains CySCs by repressing differentiation factors. In support of this hypothesis, we find that the global JAK-STAT inhibitor Protein tyrosine phosphatase 61F (Ptp61F) is a JAK-STAT target in the testis that is repressed by Ken. Together, our work demonstrates that Ken has an important role in the inhibition of CySC differentiation. Studies of ken may inform our understanding of its vertebrate orthologue B-Cell Lymphoma 6 (BCL6) and how misregulation of this oncogene leads to human lymphomas.

Indexed as

AnimalsAnimals, Genetically ModifiedBlotting, WesternCell DifferentiationCell ProliferationDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsFemaleGene Expression Regulation, DevelopmentalGreen Fluorescent ProteinsIn Situ HybridizationMaleMicroscopy, ConfocalMutationProtein Tyrosine Phosphatases, Non-ReceptorDNA-Binding ProteinsDrosophila ProteinsGreen Fluorescent ProteinsKen protein, DrosophilaProtein Tyrosine Phosphatases, Non-ReceptorPtp61F protein, DrosophilaSocs36E protein, DrosophilaStat92E protein, DrosophilaSTAT Transcription FactorsSuppressor of Cytokine Signaling Proteins

Identifiers

PMID22580161
PMCPMC3402624
OpenAlexW1980197453

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.