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Characterisation of the Drosophila procollagen lysyl hydroxylase, dPlod

The lysyl hydroxylase (LH) family of enzymes has important roles in the biosynthesis of collagen. In this paper we present the first description of Drosophila LH3 (dPlod), the only lysyl hydroxylase encoded in the fly genome. We have characterised in detail the developmental expression patterns of d...

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Detalles Bibliográficos
Autores principales: Bunt, Stephanie, Denholm, Barry, Skaer, Helen
Formato: Texto
Lenguaje:English
Publicado: Elsevier 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3044864/
https://www.ncbi.nlm.nih.gov/pubmed/20888931
http://dx.doi.org/10.1016/j.gep.2010.09.006
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author Bunt, Stephanie
Denholm, Barry
Skaer, Helen
author_facet Bunt, Stephanie
Denholm, Barry
Skaer, Helen
author_sort Bunt, Stephanie
collection PubMed
description The lysyl hydroxylase (LH) family of enzymes has important roles in the biosynthesis of collagen. In this paper we present the first description of Drosophila LH3 (dPlod), the only lysyl hydroxylase encoded in the fly genome. We have characterised in detail the developmental expression patterns of dPlod RNA and protein during embryogenesis. Consistent with its predicted function as a collagen-modifying enzyme, we find that dPlod is highly expressed in type-IV collagen-producing cells, particularly the haemocytes and fat body. Examination of dPlod subcellular localisation reveals that it is an endoplasmic reticulum resident protein, that partially overlaps with intracellular type-IV collagen. Furthermore, we show that dPlod is required for type-IV collagen secretion from haemocytes and fat body, and thus establish that LH3 enzyme function is conserved across widely separated animal phyla. Our findings, and the new tools we describe, establish the fly as an attractive model in which to study this important collagen biosynthesis enzyme.
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spelling pubmed-30448642011-03-14 Characterisation of the Drosophila procollagen lysyl hydroxylase, dPlod Bunt, Stephanie Denholm, Barry Skaer, Helen Gene Expr Patterns Article The lysyl hydroxylase (LH) family of enzymes has important roles in the biosynthesis of collagen. In this paper we present the first description of Drosophila LH3 (dPlod), the only lysyl hydroxylase encoded in the fly genome. We have characterised in detail the developmental expression patterns of dPlod RNA and protein during embryogenesis. Consistent with its predicted function as a collagen-modifying enzyme, we find that dPlod is highly expressed in type-IV collagen-producing cells, particularly the haemocytes and fat body. Examination of dPlod subcellular localisation reveals that it is an endoplasmic reticulum resident protein, that partially overlaps with intracellular type-IV collagen. Furthermore, we show that dPlod is required for type-IV collagen secretion from haemocytes and fat body, and thus establish that LH3 enzyme function is conserved across widely separated animal phyla. Our findings, and the new tools we describe, establish the fly as an attractive model in which to study this important collagen biosynthesis enzyme. Elsevier 2011-01 /pmc/articles/PMC3044864/ /pubmed/20888931 http://dx.doi.org/10.1016/j.gep.2010.09.006 Text en © 2011 Elsevier B.V. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Article
Bunt, Stephanie
Denholm, Barry
Skaer, Helen
Characterisation of the Drosophila procollagen lysyl hydroxylase, dPlod
title Characterisation of the Drosophila procollagen lysyl hydroxylase, dPlod
title_full Characterisation of the Drosophila procollagen lysyl hydroxylase, dPlod
title_fullStr Characterisation of the Drosophila procollagen lysyl hydroxylase, dPlod
title_full_unstemmed Characterisation of the Drosophila procollagen lysyl hydroxylase, dPlod
title_short Characterisation of the Drosophila procollagen lysyl hydroxylase, dPlod
title_sort characterisation of the drosophila procollagen lysyl hydroxylase, dplod
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3044864/
https://www.ncbi.nlm.nih.gov/pubmed/20888931
http://dx.doi.org/10.1016/j.gep.2010.09.006
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