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

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...

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Autores principales: Shin, Jimann, Padmanabhan, Arun, de Groh, Eric D., Lee, Jeong-Soo, Haidar, Sam, Dahlberg, Suzanne, Guo, Feng, He, Shuning, Wolman, Marc A., Granato, Michael, Lawson, Nathan D., Wolfe, Scot A., Kim, Seok-Hyung, Solnica-Krezel, Lilianna, Kanki, John P., Ligon, Keith L., Epstein, Jonathan A., Look, A. Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Limited 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3484870/
https://www.ncbi.nlm.nih.gov/pubmed/22773753
http://dx.doi.org/10.1242/dmm.009779
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author Shin, Jimann
Padmanabhan, Arun
de Groh, Eric D.
Lee, Jeong-Soo
Haidar, Sam
Dahlberg, Suzanne
Guo, Feng
He, Shuning
Wolman, Marc A.
Granato, Michael
Lawson, Nathan D.
Wolfe, Scot A.
Kim, Seok-Hyung
Solnica-Krezel, Lilianna
Kanki, John P.
Ligon, Keith L.
Epstein, Jonathan A.
Look, A. Thomas
author_facet Shin, Jimann
Padmanabhan, Arun
de Groh, Eric D.
Lee, Jeong-Soo
Haidar, Sam
Dahlberg, Suzanne
Guo, Feng
He, Shuning
Wolman, Marc A.
Granato, Michael
Lawson, Nathan D.
Wolfe, Scot A.
Kim, Seok-Hyung
Solnica-Krezel, Lilianna
Kanki, John P.
Ligon, Keith L.
Epstein, Jonathan A.
Look, A. Thomas
author_sort Shin, Jimann
collection PubMed
description 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.
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spelling pubmed-34848702012-11-16 Zebrafish neurofibromatosis type 1 genes have redundant functions in tumorigenesis and embryonic development Shin, Jimann Padmanabhan, Arun de Groh, Eric D. Lee, Jeong-Soo Haidar, Sam Dahlberg, Suzanne Guo, Feng He, Shuning Wolman, Marc A. Granato, Michael Lawson, Nathan D. Wolfe, Scot A. Kim, Seok-Hyung Solnica-Krezel, Lilianna Kanki, John P. Ligon, Keith L. Epstein, Jonathan A. Look, A. Thomas Dis Model Mech Research Article 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. The Company of Biologists Limited 2012-11 2012-07-05 /pmc/articles/PMC3484870/ /pubmed/22773753 http://dx.doi.org/10.1242/dmm.009779 Text en © 2012. Published by The Company of Biologists Ltd This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial Share Alike License (http://creativecommons.org/licenses/by-nc-sa/3.0), which permits unrestricted non-commercial use, distribution and reproduction in any medium provided that the original work is properly cited and all further distributions of the work or adaptation are subject to the same Creative Commons License terms.
spellingShingle Research Article
Shin, Jimann
Padmanabhan, Arun
de Groh, Eric D.
Lee, Jeong-Soo
Haidar, Sam
Dahlberg, Suzanne
Guo, Feng
He, Shuning
Wolman, Marc A.
Granato, Michael
Lawson, Nathan D.
Wolfe, Scot A.
Kim, Seok-Hyung
Solnica-Krezel, Lilianna
Kanki, John P.
Ligon, Keith L.
Epstein, Jonathan A.
Look, A. Thomas
Zebrafish neurofibromatosis type 1 genes have redundant functions in tumorigenesis and embryonic development
title Zebrafish neurofibromatosis type 1 genes have redundant functions in tumorigenesis and embryonic development
title_full Zebrafish neurofibromatosis type 1 genes have redundant functions in tumorigenesis and embryonic development
title_fullStr Zebrafish neurofibromatosis type 1 genes have redundant functions in tumorigenesis and embryonic development
title_full_unstemmed Zebrafish neurofibromatosis type 1 genes have redundant functions in tumorigenesis and embryonic development
title_short Zebrafish neurofibromatosis type 1 genes have redundant functions in tumorigenesis and embryonic development
title_sort zebrafish neurofibromatosis type 1 genes have redundant functions in tumorigenesis and embryonic development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3484870/
https://www.ncbi.nlm.nih.gov/pubmed/22773753
http://dx.doi.org/10.1242/dmm.009779
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