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Dataset for characterization of thrombospondin family in chum salmon (Oncorhynchus keta)
An extracellular matrix (ECM) is composed of multiprotein networks for stable interactions between cells. Thrombospondins (TSPs) are known to exert extracellular matrix interactions, synapse formation, angiogenesis and immune response in vertebrates. A five TSP gene family is divided into two subfam...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362859/ https://www.ncbi.nlm.nih.gov/pubmed/30766905 http://dx.doi.org/10.1016/j.dib.2019.01.008 |
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author | Lee, Sang Yoon Kim, Yi Kyung |
author_facet | Lee, Sang Yoon Kim, Yi Kyung |
author_sort | Lee, Sang Yoon |
collection | PubMed |
description | An extracellular matrix (ECM) is composed of multiprotein networks for stable interactions between cells. Thrombospondins (TSPs) are known to exert extracellular matrix interactions, synapse formation, angiogenesis and immune response in vertebrates. A five TSP gene family is divided into two subfamilies on basis of their domain architecture. Until recently, exploitation of diverse TSP genes in teleost has been still limitedly exemplified. Therefore, we report the cDNA structures and expression profiles for TSPs-1, 2, 3A, 3B, and 4B of chum salmon, Oncorhynchus keta. In conjunctional with bioinformatics analysis, the diverse domain structures of TSP genes are identified. In addition, the major domain, repeat and motif of TSP isoforms of chum salmon were aligned with those of other salmonid fishes. |
format | Online Article Text |
id | pubmed-6362859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-63628592019-02-14 Dataset for characterization of thrombospondin family in chum salmon (Oncorhynchus keta) Lee, Sang Yoon Kim, Yi Kyung Data Brief Genetics, Genomics and Molecular Biology An extracellular matrix (ECM) is composed of multiprotein networks for stable interactions between cells. Thrombospondins (TSPs) are known to exert extracellular matrix interactions, synapse formation, angiogenesis and immune response in vertebrates. A five TSP gene family is divided into two subfamilies on basis of their domain architecture. Until recently, exploitation of diverse TSP genes in teleost has been still limitedly exemplified. Therefore, we report the cDNA structures and expression profiles for TSPs-1, 2, 3A, 3B, and 4B of chum salmon, Oncorhynchus keta. In conjunctional with bioinformatics analysis, the diverse domain structures of TSP genes are identified. In addition, the major domain, repeat and motif of TSP isoforms of chum salmon were aligned with those of other salmonid fishes. Elsevier 2019-01-09 /pmc/articles/PMC6362859/ /pubmed/30766905 http://dx.doi.org/10.1016/j.dib.2019.01.008 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Genetics, Genomics and Molecular Biology Lee, Sang Yoon Kim, Yi Kyung Dataset for characterization of thrombospondin family in chum salmon (Oncorhynchus keta) |
title | Dataset for characterization of thrombospondin family in chum salmon (Oncorhynchus keta) |
title_full | Dataset for characterization of thrombospondin family in chum salmon (Oncorhynchus keta) |
title_fullStr | Dataset for characterization of thrombospondin family in chum salmon (Oncorhynchus keta) |
title_full_unstemmed | Dataset for characterization of thrombospondin family in chum salmon (Oncorhynchus keta) |
title_short | Dataset for characterization of thrombospondin family in chum salmon (Oncorhynchus keta) |
title_sort | dataset for characterization of thrombospondin family in chum salmon (oncorhynchus keta) |
topic | Genetics, Genomics and Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362859/ https://www.ncbi.nlm.nih.gov/pubmed/30766905 http://dx.doi.org/10.1016/j.dib.2019.01.008 |
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