Cargando…

Structural Analysis of Drosophila Merlin Reveals Functional Domains Important for Growth Control and Subcellular Localization

Merlin, the product of the Neurofibromatosis type 2 (NF2) tumor-suppressor gene, is a member of the protein 4.1 superfamily that is most closely related to ezrin, radixin, and moesin (ERM). NF2 is a dominantly inherited disease characterized by the formation of bilateral acoustic schwannomas and oth...

Descripción completa

Detalles Bibliográficos
Autores principales: LaJeunesse, Dennis R., McCartney, Brooke M., Fehon, Richard G.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1998
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2133006/
https://www.ncbi.nlm.nih.gov/pubmed/9647651
_version_ 1782142573095157760
author LaJeunesse, Dennis R.
McCartney, Brooke M.
Fehon, Richard G.
author_facet LaJeunesse, Dennis R.
McCartney, Brooke M.
Fehon, Richard G.
author_sort LaJeunesse, Dennis R.
collection PubMed
description Merlin, the product of the Neurofibromatosis type 2 (NF2) tumor-suppressor gene, is a member of the protein 4.1 superfamily that is most closely related to ezrin, radixin, and moesin (ERM). NF2 is a dominantly inherited disease characterized by the formation of bilateral acoustic schwannomas and other benign tumors associated with the central nervous system. To understand its cellular functions, we are studying a Merlin homologue in Drosophila. As is the case for NF2 tumors, Drosophila cells lacking Merlin function overproliferate relative to their neighbors. Using in vitro mutagenesis, we define functional domains within Merlin required for proper subcellular localization and for genetic rescue of lethal Merlin alleles. Remarkably, the results of these experiments demonstrate that all essential genetic functions reside in the plasma membrane– associated NH(2)-terminal 350 amino acids of Merlin. Removal of a seven–amino acid conserved sequence within this domain results in a dominant-negative form of Merlin that is stably associated with the plasma membrane and causes overproliferation when expressed ectopically in the wing. In addition, we provide evidence that the COOH-terminal region of Merlin has a negative regulatory role, as has been shown for ERM proteins. These results provide insights into the functions and functional organization of a novel tumor suppressor gene.
format Text
id pubmed-2133006
institution National Center for Biotechnology Information
language English
publishDate 1998
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-21330062008-05-01 Structural Analysis of Drosophila Merlin Reveals Functional Domains Important for Growth Control and Subcellular Localization LaJeunesse, Dennis R. McCartney, Brooke M. Fehon, Richard G. J Cell Biol Articles Merlin, the product of the Neurofibromatosis type 2 (NF2) tumor-suppressor gene, is a member of the protein 4.1 superfamily that is most closely related to ezrin, radixin, and moesin (ERM). NF2 is a dominantly inherited disease characterized by the formation of bilateral acoustic schwannomas and other benign tumors associated with the central nervous system. To understand its cellular functions, we are studying a Merlin homologue in Drosophila. As is the case for NF2 tumors, Drosophila cells lacking Merlin function overproliferate relative to their neighbors. Using in vitro mutagenesis, we define functional domains within Merlin required for proper subcellular localization and for genetic rescue of lethal Merlin alleles. Remarkably, the results of these experiments demonstrate that all essential genetic functions reside in the plasma membrane– associated NH(2)-terminal 350 amino acids of Merlin. Removal of a seven–amino acid conserved sequence within this domain results in a dominant-negative form of Merlin that is stably associated with the plasma membrane and causes overproliferation when expressed ectopically in the wing. In addition, we provide evidence that the COOH-terminal region of Merlin has a negative regulatory role, as has been shown for ERM proteins. These results provide insights into the functions and functional organization of a novel tumor suppressor gene. The Rockefeller University Press 1998-06-29 /pmc/articles/PMC2133006/ /pubmed/9647651 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
LaJeunesse, Dennis R.
McCartney, Brooke M.
Fehon, Richard G.
Structural Analysis of Drosophila Merlin Reveals Functional Domains Important for Growth Control and Subcellular Localization
title Structural Analysis of Drosophila Merlin Reveals Functional Domains Important for Growth Control and Subcellular Localization
title_full Structural Analysis of Drosophila Merlin Reveals Functional Domains Important for Growth Control and Subcellular Localization
title_fullStr Structural Analysis of Drosophila Merlin Reveals Functional Domains Important for Growth Control and Subcellular Localization
title_full_unstemmed Structural Analysis of Drosophila Merlin Reveals Functional Domains Important for Growth Control and Subcellular Localization
title_short Structural Analysis of Drosophila Merlin Reveals Functional Domains Important for Growth Control and Subcellular Localization
title_sort structural analysis of drosophila merlin reveals functional domains important for growth control and subcellular localization
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2133006/
https://www.ncbi.nlm.nih.gov/pubmed/9647651
work_keys_str_mv AT lajeunessedennisr structuralanalysisofdrosophilamerlinrevealsfunctionaldomainsimportantforgrowthcontrolandsubcellularlocalization
AT mccartneybrookem structuralanalysisofdrosophilamerlinrevealsfunctionaldomainsimportantforgrowthcontrolandsubcellularlocalization
AT fehonrichardg structuralanalysisofdrosophilamerlinrevealsfunctionaldomainsimportantforgrowthcontrolandsubcellularlocalization