Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G).

<h4>Background</h4>The somatic mutation in the FOXL2 gene c.402C>G (p.Cys134Trp) has recently been identified in the vast majority of adult ovarian granulosa cell tumors (OGCTs) studied. In addition, this mutation seems to be specific to adult OGCTs and is likely to be a driver of mal...

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Autores principales: Bérénice A Benayoun, Sandrine Caburet, Aurélie Dipietromaria, Adrien Georges, Barbara D'Haene, P J Eswari Pandaranayaka, David L'Hôte, Anne-Laure Todeschini, Sankaran Krishnaswamy, Marc Fellous, Elfride De Baere, Reiner A Veitia
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Publicado: Public Library of Science (PLoS) 2010
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spelling oai:doaj.org-article:a9ad7ce6b18146d99665cfccbcd63a622021-11-25T06:26:33ZFunctional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G).1932-620310.1371/journal.pone.0008789https://doaj.org/article/a9ad7ce6b18146d99665cfccbcd63a622010-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20098707/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>The somatic mutation in the FOXL2 gene c.402C>G (p.Cys134Trp) has recently been identified in the vast majority of adult ovarian granulosa cell tumors (OGCTs) studied. In addition, this mutation seems to be specific to adult OGCTs and is likely to be a driver of malignant transformation. However, its pathogenic mechanisms remain elusive.<h4>Methodology/principal findings</h4>We have sequenced the FOXL2 open reading frame in a panel of tumor cell lines (NCI-60, colorectal carcinoma cell lines, JEG-3, and KGN cells). We found the FOXL2 c.402C>G mutation in the adult OGCT-derived KGN cell line. All other cell lines analyzed were negative for the mutation. In order to gain insights into the pathogenic mechanism of the p.Cys134Trp mutation, the subcellular localization and mobility of the mutant protein were studied and found to be no different from those of the wild type (WT). Furthermore, its transactivation ability was in most cases similar to that of the WT protein, including in conditions of oxidative stress. A notable exception was an artificial promoter known to be coregulated by FOXL2 and Smad3, suggesting a potential modification of their interaction. We generated a 3D structural model of the p.Cys134Trp variant and our analysis suggests that homodimer formation might also be disturbed by the mutation.<h4>Conclusions/significance</h4>Here, we confirm the specificity of the FOXL2 c.402C>G mutation in adult OGCTs and begin the exploration of its molecular significance. This is the first study demonstrating that the p.Cys134Trp mutant does not have a strong impact on FOXL2 localization, solubility, and transactivation abilities on a panel of proven target promoters, behaving neither as a dominant-negative nor as a loss-of-function mutation. Further studies are required to understand the specific molecular effects of this outstanding FOXL2 mutation.Bérénice A BenayounSandrine CaburetAurélie DipietromariaAdrien GeorgesBarbara D'HaeneP J Eswari PandaranayakaDavid L'HôteAnne-Laure TodeschiniSankaran KrishnaswamyMarc FellousElfride De BaereReiner A VeitiaPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 5, Iss 1, p e8789 (2010)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Bérénice A Benayoun
Sandrine Caburet
Aurélie Dipietromaria
Adrien Georges
Barbara D'Haene
P J Eswari Pandaranayaka
David L'Hôte
Anne-Laure Todeschini
Sankaran Krishnaswamy
Marc Fellous
Elfride De Baere
Reiner A Veitia
Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G).
description <h4>Background</h4>The somatic mutation in the FOXL2 gene c.402C>G (p.Cys134Trp) has recently been identified in the vast majority of adult ovarian granulosa cell tumors (OGCTs) studied. In addition, this mutation seems to be specific to adult OGCTs and is likely to be a driver of malignant transformation. However, its pathogenic mechanisms remain elusive.<h4>Methodology/principal findings</h4>We have sequenced the FOXL2 open reading frame in a panel of tumor cell lines (NCI-60, colorectal carcinoma cell lines, JEG-3, and KGN cells). We found the FOXL2 c.402C>G mutation in the adult OGCT-derived KGN cell line. All other cell lines analyzed were negative for the mutation. In order to gain insights into the pathogenic mechanism of the p.Cys134Trp mutation, the subcellular localization and mobility of the mutant protein were studied and found to be no different from those of the wild type (WT). Furthermore, its transactivation ability was in most cases similar to that of the WT protein, including in conditions of oxidative stress. A notable exception was an artificial promoter known to be coregulated by FOXL2 and Smad3, suggesting a potential modification of their interaction. We generated a 3D structural model of the p.Cys134Trp variant and our analysis suggests that homodimer formation might also be disturbed by the mutation.<h4>Conclusions/significance</h4>Here, we confirm the specificity of the FOXL2 c.402C>G mutation in adult OGCTs and begin the exploration of its molecular significance. This is the first study demonstrating that the p.Cys134Trp mutant does not have a strong impact on FOXL2 localization, solubility, and transactivation abilities on a panel of proven target promoters, behaving neither as a dominant-negative nor as a loss-of-function mutation. Further studies are required to understand the specific molecular effects of this outstanding FOXL2 mutation.
format article
author Bérénice A Benayoun
Sandrine Caburet
Aurélie Dipietromaria
Adrien Georges
Barbara D'Haene
P J Eswari Pandaranayaka
David L'Hôte
Anne-Laure Todeschini
Sankaran Krishnaswamy
Marc Fellous
Elfride De Baere
Reiner A Veitia
author_facet Bérénice A Benayoun
Sandrine Caburet
Aurélie Dipietromaria
Adrien Georges
Barbara D'Haene
P J Eswari Pandaranayaka
David L'Hôte
Anne-Laure Todeschini
Sankaran Krishnaswamy
Marc Fellous
Elfride De Baere
Reiner A Veitia
author_sort Bérénice A Benayoun
title Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G).
title_short Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G).
title_full Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G).
title_fullStr Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G).
title_full_unstemmed Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G).
title_sort functional exploration of the adult ovarian granulosa cell tumor-associated somatic foxl2 mutation p.cys134trp (c.402c>g).
publisher Public Library of Science (PLoS)
publishDate 2010
url https://doaj.org/article/a9ad7ce6b18146d99665cfccbcd63a62
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