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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...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Elsevier
2011
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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. |
format | Text |
id | pubmed-3044864 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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