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Cloning, characterization, and expression analysis of the CHITINASE gene family in Helice tientsinensis

Chitinase is a kind of glycoside hydrolase which is widely distributed in nature and encoded by multiple genes to catalyze the decomposition of chitin, which plays an important role in the molting and pathogen defense of crustaceans. However, the research on chitinase in crustaceans is mainly focuse...

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Autores principales: Chen, Lulu, Hua, Yuyan, Ji, Wenxuan, Wang, Jiayu, Zhao, Hua, Wang, Zhengfei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10022498/
https://www.ncbi.nlm.nih.gov/pubmed/36935907
http://dx.doi.org/10.7717/peerj.15045
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author Chen, Lulu
Hua, Yuyan
Ji, Wenxuan
Wang, Jiayu
Zhao, Hua
Wang, Zhengfei
author_facet Chen, Lulu
Hua, Yuyan
Ji, Wenxuan
Wang, Jiayu
Zhao, Hua
Wang, Zhengfei
author_sort Chen, Lulu
collection PubMed
description Chitinase is a kind of glycoside hydrolase which is widely distributed in nature and encoded by multiple genes to catalyze the decomposition of chitin, which plays an important role in the molting and pathogen defense of crustaceans. However, the research on chitinase in crustaceans is mainly focused on a few species with economic value. In this study, full-length cDNA sequences of the HtCHT1, HtCHT3 and HtCHT4 genes were cloned from the mudflat crab Helice tientsinensis by RACE, and the sequences were analyzed. The results showed that the full-length 2,229 bp of HtCHT1 gene encoded 627 amino acids, while the full-length 2,191 bp of HtCHT3 gene produced 489 amino acids, and the full-length 3,312 bp of HtCHT4 gene encoded 664 amino acids. Bioinformatics analysis showed that all the obtained chitinase proteins had the glycosyl hydrolase family 18 (GH18) catalytic domain and chitin-binding domain (ChtBD2), furthermore, HtCHT1 and HtCHT4 proteins had signal peptide domains at N-terminal. Phylogenetic analysis showed that different types of chitinase were clustered, and HtCHTs were closely related to chitinases in the Eriocheir sinensis. Expression profile analysis showed that the HtCHT1, HtCHT3 and HtCHT4 were significantly expressed in hepatopancreas. Furthermore, the expression of three genes was significantly up-regulated in hepatopancreas after the Vibrio parahaemolyticus challenge. These results suggested that HtCHT1, HtCHT3 and HtCHT4 were belonged to the CHITINASE gene family in H. tientsinensis and were potentially involved in the antibacterial immune response. This study provides essential information for further research of chitinase in H. tientsinensis and even crustaceans.
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spelling pubmed-100224982023-03-18 Cloning, characterization, and expression analysis of the CHITINASE gene family in Helice tientsinensis Chen, Lulu Hua, Yuyan Ji, Wenxuan Wang, Jiayu Zhao, Hua Wang, Zhengfei PeerJ Marine Biology Chitinase is a kind of glycoside hydrolase which is widely distributed in nature and encoded by multiple genes to catalyze the decomposition of chitin, which plays an important role in the molting and pathogen defense of crustaceans. However, the research on chitinase in crustaceans is mainly focused on a few species with economic value. In this study, full-length cDNA sequences of the HtCHT1, HtCHT3 and HtCHT4 genes were cloned from the mudflat crab Helice tientsinensis by RACE, and the sequences were analyzed. The results showed that the full-length 2,229 bp of HtCHT1 gene encoded 627 amino acids, while the full-length 2,191 bp of HtCHT3 gene produced 489 amino acids, and the full-length 3,312 bp of HtCHT4 gene encoded 664 amino acids. Bioinformatics analysis showed that all the obtained chitinase proteins had the glycosyl hydrolase family 18 (GH18) catalytic domain and chitin-binding domain (ChtBD2), furthermore, HtCHT1 and HtCHT4 proteins had signal peptide domains at N-terminal. Phylogenetic analysis showed that different types of chitinase were clustered, and HtCHTs were closely related to chitinases in the Eriocheir sinensis. Expression profile analysis showed that the HtCHT1, HtCHT3 and HtCHT4 were significantly expressed in hepatopancreas. Furthermore, the expression of three genes was significantly up-regulated in hepatopancreas after the Vibrio parahaemolyticus challenge. These results suggested that HtCHT1, HtCHT3 and HtCHT4 were belonged to the CHITINASE gene family in H. tientsinensis and were potentially involved in the antibacterial immune response. This study provides essential information for further research of chitinase in H. tientsinensis and even crustaceans. PeerJ Inc. 2023-03-14 /pmc/articles/PMC10022498/ /pubmed/36935907 http://dx.doi.org/10.7717/peerj.15045 Text en ©2023 Chen et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Marine Biology
Chen, Lulu
Hua, Yuyan
Ji, Wenxuan
Wang, Jiayu
Zhao, Hua
Wang, Zhengfei
Cloning, characterization, and expression analysis of the CHITINASE gene family in Helice tientsinensis
title Cloning, characterization, and expression analysis of the CHITINASE gene family in Helice tientsinensis
title_full Cloning, characterization, and expression analysis of the CHITINASE gene family in Helice tientsinensis
title_fullStr Cloning, characterization, and expression analysis of the CHITINASE gene family in Helice tientsinensis
title_full_unstemmed Cloning, characterization, and expression analysis of the CHITINASE gene family in Helice tientsinensis
title_short Cloning, characterization, and expression analysis of the CHITINASE gene family in Helice tientsinensis
title_sort cloning, characterization, and expression analysis of the chitinase gene family in helice tientsinensis
topic Marine Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10022498/
https://www.ncbi.nlm.nih.gov/pubmed/36935907
http://dx.doi.org/10.7717/peerj.15045
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