Evidence map›Paper›PMID 22773753›Full record

ArticleDisease models & mechanisms2012

Zebrafish neurofibromatosis type 1 genes have redundant functions in tumorigenesis and embryonic development.

Jimann Shin, Arun Padmanabhan, Eric D de Groh, Jeong-Soo Lee, Sam Haidar, Suzanne Dahlberg, Feng Guo, Shuning He, Marc A Wolman, Michael Granato and 8 more

Open access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

67 citing papers in PubMed, 92 citations in OpenAlex.

  1. Review
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  8. Engineering precision zebrafish alleles of human disease.bioRxiv : the preprint server for biology · 2025
    Article
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  14. Cells · 2024
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7 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

18 authors at 7 institutions in 1 country.

Jimann ShinDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, and Children's Hospital Boston, Harvard Medical School, Boston, MA 02115, USA.
Arun Padmanabhan
Eric D de Groh
Jeong-Soo Lee
Sam Haidar
Suzanne Dahlberg
Feng Guo
Shuning He
Marc A Wolman
Michael Granato
Nathan D Lawson
Scot A Wolfe
Seok-Hyung Kim
Lilianna Solnica-Krezel
John P Kanki
Keith L Ligon
Jonathan A Epstein
A Thomas Look
Harvard University · USUniversity of Pennsylvania · USUniversity of Massachusetts Chan Medical School · USCalifornia University of Pennsylvania · USDana-Farber Cancer Institute · USVanderbilt University · USWashington University in St. Louis · US

Funding

Training Program in Cardiovascular Biology and MedicineT32HL007843 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI THOMAS P. CAPPOLA, Sharlene M Day · 1996 to 2026
$11.0M
Using zinc finger nucleases to manipulate the zebrafish genomeR01HL093766 · NHLBI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LAWSON, NATHAN D, WOLFE, SCOT A · 2008 to 2017
$4.1M
NEUROFIBROMIN, NEURAL CREST AND CARDIAC DEVELOPMENTR01HL062974 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI EPSTEIN, JONATHAN A. · 1999 to 2012
$4.0M
TILLING the Zebrafish Genome: A Reverse Genetic ApproachR01HG002995 · NHGRI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MOENS, CECILIA B, POSTLETHWAIT, JOHN H. · 2003 to 2010
$3.5M
Genetic analysis of simple learning behaviorsR01MH092257 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI GRANATO, MICHAEL · 2010 to 2014
$2.0M
TILLING the Zebrafish Genome: A Reverse Genetics ApproachR01HD076585 · NICHD · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MOENS, CECILIA B, SOLNICAKREZEL, LILIANNA · 2012 to 2014
$1.9M
NHGRI NIH HHS R01 HG002995NHLBI NIH HHS R01 HL062974NHLBI NIH HHS R01 HL093766NHLBI NIH HHS T32 HL007843NHLBI NIH HHS T32 HL007843-15NICHD NIH HHS R01 HD076585NIMH NIH HHS R01 MH092257
6 · The paper itself

Abstract

Neurofibromatosis type 1 (NF1) is a common, dominantly inherited genetic disorder that results from mutations in the neurofibromin 1 (NF1) gene. Affected individuals demonstrate abnormalities in neural-crest-derived tissues that include hyperpigmented skin lesions and benign peripheral nerve sheath tumors. NF1 patients also have a predisposition to malignancies including juvenile myelomonocytic leukemia (JMML), optic glioma, glioblastoma, schwannoma and malignant peripheral nerve sheath tumors (MPNSTs). In an effort to better define the molecular and cellular determinants of NF1 disease pathogenesis in vivo, we employed targeted mutagenesis strategies to generate zebrafish harboring stable germline mutations in nf1a and nf1b, orthologues of NF1. Animals homozygous for loss-of-function alleles of nf1a or nf1b alone are phenotypically normal and viable. Homozygous loss of both alleles in combination generates larval phenotypes that resemble aspects of the human disease and results in larval lethality between 7 and 10 days post fertilization. nf1-null larvae demonstrate significant central and peripheral nervous system defects. These include aberrant proliferation and differentiation of oligodendrocyte progenitor cells (OPCs), dysmorphic myelin sheaths and hyperplasia of Schwann cells. Loss of nf1 contributes to tumorigenesis as demonstrated by an accelerated onset and increased penetrance of high-grade gliomas and MPNSTs in adult nf1a(+/-); nf1b(-/-); p53(e7/e7) animals. nf1-null larvae also demonstrate significant motor and learning defects. Importantly, we identify and quantitatively analyze a novel melanophore phenotype in nf1-null larvae, providing the first animal model of the pathognomonic pigmentation lesions of NF1. Together, these findings support a role for nf1a and nf1b as potent tumor suppressor genes that also function in the development of both central and peripheral glial cells as well as melanophores in zebrafish.

Indexed as

Genes, Neurofibromatosis 1Amino Acid SequenceAnimalsBase SequenceCell ProliferationCell Transformation, NeoplasticEmbryonic DevelopmentHyperplasiaLarvaLearningMelanophoresMolecular Sequence DataMotor ActivityMutationMyelin SheathNeurofibromatosis 1Neurofibromin 1ras ProteinsTumor Suppressor Protein p53Zebrafish Proteins

Identifiers

PMID22773753
PMCPMC3484870
OpenAlexW2163173059

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.