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Characterization and regulation of ADAMTS-16

The ADAMTS (a disintegrin and metalloproteinase domain with thrombospondin motifs) family includes 19 secreted proteinases in man. ADAMTS16 is a recently cloned gene expressed at high levels in fetal lung and kidney and adult brain and ovary. The ADAMTS-16 protein currently has no known function. AD...

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Autores principales: Surridge, Alison K, Rodgers, Ursula R, Swingler, Tracey E, Davidson, Rose K, Kevorkian, Lara, Norton, Rosemary, Waters, Jasmine G, Goldring, Mary B, Parker, Andrew E, Clark, Ian M
Formato: Texto
Lenguaje:English
Publicado: Elsevier 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2789966/
https://www.ncbi.nlm.nih.gov/pubmed/19635554
http://dx.doi.org/10.1016/j.matbio.2009.07.001
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author Surridge, Alison K
Rodgers, Ursula R
Swingler, Tracey E
Davidson, Rose K
Kevorkian, Lara
Norton, Rosemary
Waters, Jasmine G
Goldring, Mary B
Parker, Andrew E
Clark, Ian M
author_facet Surridge, Alison K
Rodgers, Ursula R
Swingler, Tracey E
Davidson, Rose K
Kevorkian, Lara
Norton, Rosemary
Waters, Jasmine G
Goldring, Mary B
Parker, Andrew E
Clark, Ian M
author_sort Surridge, Alison K
collection PubMed
description The ADAMTS (a disintegrin and metalloproteinase domain with thrombospondin motifs) family includes 19 secreted proteinases in man. ADAMTS16 is a recently cloned gene expressed at high levels in fetal lung and kidney and adult brain and ovary. The ADAMTS-16 protein currently has no known function. ADAMTS16 is also expressed in human cartilage and synovium where its expression is increased in tissues from osteoarthritis patients compared to normal tissues. In this study, we ascertained that the full length ADAMTS16 mRNA was expressed in chondrocytes and cloned the appropriate cDNA. Stable over-expression of ADAMTS16 in chondrosarcoma cells led to a decrease in cell proliferation and migration, though not adhesion, as well as a decrease in the expression of matrix metalloproteinase-13 (MMP13). The transcription start point of the human ADAMTS16 gene was experimentally identified as 138 bp upstream of the translation start ATG and the basal promoter was mapped out to − 1802 bp. Overexpression of Egr1 induced ADAMTS16 promoter constructs of − 157/+138 or longer whilst Sp1 induced all ADAMTS16 promoter constructs. Transforming growth factor beta (TGFβ) stimulated expression of endogenous ADAMTS16 gene expression in chondrocyte cell lines.
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spelling pubmed-27899662009-12-22 Characterization and regulation of ADAMTS-16 Surridge, Alison K Rodgers, Ursula R Swingler, Tracey E Davidson, Rose K Kevorkian, Lara Norton, Rosemary Waters, Jasmine G Goldring, Mary B Parker, Andrew E Clark, Ian M Matrix Biol Article The ADAMTS (a disintegrin and metalloproteinase domain with thrombospondin motifs) family includes 19 secreted proteinases in man. ADAMTS16 is a recently cloned gene expressed at high levels in fetal lung and kidney and adult brain and ovary. The ADAMTS-16 protein currently has no known function. ADAMTS16 is also expressed in human cartilage and synovium where its expression is increased in tissues from osteoarthritis patients compared to normal tissues. In this study, we ascertained that the full length ADAMTS16 mRNA was expressed in chondrocytes and cloned the appropriate cDNA. Stable over-expression of ADAMTS16 in chondrosarcoma cells led to a decrease in cell proliferation and migration, though not adhesion, as well as a decrease in the expression of matrix metalloproteinase-13 (MMP13). The transcription start point of the human ADAMTS16 gene was experimentally identified as 138 bp upstream of the translation start ATG and the basal promoter was mapped out to − 1802 bp. Overexpression of Egr1 induced ADAMTS16 promoter constructs of − 157/+138 or longer whilst Sp1 induced all ADAMTS16 promoter constructs. Transforming growth factor beta (TGFβ) stimulated expression of endogenous ADAMTS16 gene expression in chondrocyte cell lines. Elsevier 2009-09 /pmc/articles/PMC2789966/ /pubmed/19635554 http://dx.doi.org/10.1016/j.matbio.2009.07.001 Text en © 2009 Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license
spellingShingle Article
Surridge, Alison K
Rodgers, Ursula R
Swingler, Tracey E
Davidson, Rose K
Kevorkian, Lara
Norton, Rosemary
Waters, Jasmine G
Goldring, Mary B
Parker, Andrew E
Clark, Ian M
Characterization and regulation of ADAMTS-16
title Characterization and regulation of ADAMTS-16
title_full Characterization and regulation of ADAMTS-16
title_fullStr Characterization and regulation of ADAMTS-16
title_full_unstemmed Characterization and regulation of ADAMTS-16
title_short Characterization and regulation of ADAMTS-16
title_sort characterization and regulation of adamts-16
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2789966/
https://www.ncbi.nlm.nih.gov/pubmed/19635554
http://dx.doi.org/10.1016/j.matbio.2009.07.001
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