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The Transcription Factor SOX18 Regulates the Expression of Matrix Metalloproteinase 7 and Guidance Molecules in Human Endothelial Cells

BACKGROUND: Mutations in the transcription factor SOX18 are responsible for specific cardiovascular defects in humans and mice. In order to gain insight into the molecular basis of its action, we identified target genes of SOX18 and analyzed one, MMP7, in detail. METHODOLOGY/PRINCIPAL FINDINGS: SOX1...

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Autores principales: Hoeth, Martina, Niederleithner, Heide, Hofer-Warbinek, Renate, Bilban, Martin, Mayer, Herbert, Resch, Ulrike, Lemberger, Christof, Wagner, Oswald, Hofer, Erhard, Petzelbauer, Peter, de Martin, Rainer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3264645/
https://www.ncbi.nlm.nih.gov/pubmed/22292085
http://dx.doi.org/10.1371/journal.pone.0030982
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author Hoeth, Martina
Niederleithner, Heide
Hofer-Warbinek, Renate
Bilban, Martin
Mayer, Herbert
Resch, Ulrike
Lemberger, Christof
Wagner, Oswald
Hofer, Erhard
Petzelbauer, Peter
de Martin, Rainer
author_facet Hoeth, Martina
Niederleithner, Heide
Hofer-Warbinek, Renate
Bilban, Martin
Mayer, Herbert
Resch, Ulrike
Lemberger, Christof
Wagner, Oswald
Hofer, Erhard
Petzelbauer, Peter
de Martin, Rainer
author_sort Hoeth, Martina
collection PubMed
description BACKGROUND: Mutations in the transcription factor SOX18 are responsible for specific cardiovascular defects in humans and mice. In order to gain insight into the molecular basis of its action, we identified target genes of SOX18 and analyzed one, MMP7, in detail. METHODOLOGY/PRINCIPAL FINDINGS: SOX18 was expressed in HUVEC using a recombinant adenoviral vector and the altered gene expression profile was analyzed using microarrays. Expression of several regulated candidate SOX18 target genes was verified by real-time PCR. Knock-down of SOX18 using RNA interference was then used to confirm the effect of the transcription factor on selected genes that included the guidance molecules ephrin B2 and semaphorin 3G. One gene, MMP7, was chosen for further analysis, including detailed promoter studies using reporter gene assays, electrophoretic mobility shift analysis and chromatin-immunoprecipitation, revealing that it responds directly to SOX18. Immunohistochemical analysis demonstrated the co-expression of SOX18 and MMP7 in blood vessels of human skin. CONCLUSIONS/SIGNIFICANCE: The identification of MMP7 as a direct SOX18 target gene as well as other potential candidates including guidance molecules provides a molecular basis for the proposed function of this transcription factor in the regulation of vessel formation.
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spelling pubmed-32646452012-01-30 The Transcription Factor SOX18 Regulates the Expression of Matrix Metalloproteinase 7 and Guidance Molecules in Human Endothelial Cells Hoeth, Martina Niederleithner, Heide Hofer-Warbinek, Renate Bilban, Martin Mayer, Herbert Resch, Ulrike Lemberger, Christof Wagner, Oswald Hofer, Erhard Petzelbauer, Peter de Martin, Rainer PLoS One Research Article BACKGROUND: Mutations in the transcription factor SOX18 are responsible for specific cardiovascular defects in humans and mice. In order to gain insight into the molecular basis of its action, we identified target genes of SOX18 and analyzed one, MMP7, in detail. METHODOLOGY/PRINCIPAL FINDINGS: SOX18 was expressed in HUVEC using a recombinant adenoviral vector and the altered gene expression profile was analyzed using microarrays. Expression of several regulated candidate SOX18 target genes was verified by real-time PCR. Knock-down of SOX18 using RNA interference was then used to confirm the effect of the transcription factor on selected genes that included the guidance molecules ephrin B2 and semaphorin 3G. One gene, MMP7, was chosen for further analysis, including detailed promoter studies using reporter gene assays, electrophoretic mobility shift analysis and chromatin-immunoprecipitation, revealing that it responds directly to SOX18. Immunohistochemical analysis demonstrated the co-expression of SOX18 and MMP7 in blood vessels of human skin. CONCLUSIONS/SIGNIFICANCE: The identification of MMP7 as a direct SOX18 target gene as well as other potential candidates including guidance molecules provides a molecular basis for the proposed function of this transcription factor in the regulation of vessel formation. Public Library of Science 2012-01-23 /pmc/articles/PMC3264645/ /pubmed/22292085 http://dx.doi.org/10.1371/journal.pone.0030982 Text en Hoeth et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hoeth, Martina
Niederleithner, Heide
Hofer-Warbinek, Renate
Bilban, Martin
Mayer, Herbert
Resch, Ulrike
Lemberger, Christof
Wagner, Oswald
Hofer, Erhard
Petzelbauer, Peter
de Martin, Rainer
The Transcription Factor SOX18 Regulates the Expression of Matrix Metalloproteinase 7 and Guidance Molecules in Human Endothelial Cells
title The Transcription Factor SOX18 Regulates the Expression of Matrix Metalloproteinase 7 and Guidance Molecules in Human Endothelial Cells
title_full The Transcription Factor SOX18 Regulates the Expression of Matrix Metalloproteinase 7 and Guidance Molecules in Human Endothelial Cells
title_fullStr The Transcription Factor SOX18 Regulates the Expression of Matrix Metalloproteinase 7 and Guidance Molecules in Human Endothelial Cells
title_full_unstemmed The Transcription Factor SOX18 Regulates the Expression of Matrix Metalloproteinase 7 and Guidance Molecules in Human Endothelial Cells
title_short The Transcription Factor SOX18 Regulates the Expression of Matrix Metalloproteinase 7 and Guidance Molecules in Human Endothelial Cells
title_sort transcription factor sox18 regulates the expression of matrix metalloproteinase 7 and guidance molecules in human endothelial cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3264645/
https://www.ncbi.nlm.nih.gov/pubmed/22292085
http://dx.doi.org/10.1371/journal.pone.0030982
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