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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...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Limited
2012
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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. |
format | Online Article Text |
id | pubmed-3484870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Company of Biologists Limited |
record_format | MEDLINE/PubMed |
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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