A cysteine protease (cathepsin Z) from disk abalone, Haliotis discus discus: Genomic characterization and transcriptional profiling during bacterial infections

Cathepsin Z (CTSZ) is lysosomal cysteine protease of the papain superfamily. It participates in the host immune defense via phagocytosis, signal transduction, cell-cell communication, proliferation, and migration of immune cells such as monocytes, macrophages, and dendritic cells. Hence, CTSZ is als...

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Published in:Gene
Main Authors: Godahewa, G.I., Perera, N.C.N., Lee, S., Kim, M.J., Lee, J.
Format: Article in Journal/Newspaper
Language:English
Published: Elsevier 2017
Subjects:
Online Access:http://hdl.handle.net/2440/120797
https://doi.org/10.1016/j.gene.2017.07.007
id ftunivadelaidedl:oai:digital.library.adelaide.edu.au:2440/120797
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spelling ftunivadelaidedl:oai:digital.library.adelaide.edu.au:2440/120797 2023-12-17T10:29:16+01:00 A cysteine protease (cathepsin Z) from disk abalone, Haliotis discus discus: Genomic characterization and transcriptional profiling during bacterial infections Godahewa, G.I. Perera, N.C.N. Lee, S. Kim, M.J. Lee, J. 2017 http://hdl.handle.net/2440/120797 https://doi.org/10.1016/j.gene.2017.07.007 en eng Elsevier Gene, 2017; 627:500-507 0378-1119 1879-0038 http://hdl.handle.net/2440/120797 doi:10.1016/j.gene.2017.07.007 Godahewa, G.I. [0000-0002-7614-1040] © 2017 Elsevier B.V. All rights reserved. http://dx.doi.org/10.1016/j.gene.2017.07.007 Cathepsin Z Disk abalone Abalone early development Genomic organization Immune responsive expression Journal article 2017 ftunivadelaidedl https://doi.org/10.1016/j.gene.2017.07.007 2023-11-20T23:25:44Z Cathepsin Z (CTSZ) is lysosomal cysteine protease of the papain superfamily. It participates in the host immune defense via phagocytosis, signal transduction, cell-cell communication, proliferation, and migration of immune cells such as monocytes, macrophages, and dendritic cells. Hence, CTSZ is also acknowledged as an acute-phase protein in host immunity. In this study, we sought to identify the CTSZ homolog from disk abalone (AbCTSZ) and characterize it at the molecular, genomic, and transcriptional levels. AbCTSZ encodes a protein with 318 amino acids and a molecular mass of 36kDa. The structure of AbCTSZ reveals amino acid sequences that are characteristic of the signal sequence, pro-peptide, peptidase-C1 papain family cysteine protease domain, mini-loop, HIP motif, N-linked glycosylation sites, active sites, and conserved Cys residues. A pairwise comparison revealed that AbCTSZ shared the highest amino acid homology with its molluscan counterpart from Crassostrea gigas. A multiple alignment analysis revealed the conservation of functionally crucial elements of AbCTSZ, and a phylogenetic study further confirmed a proximal evolutionary relationship with its invertebrate counterparts. Further, an analysis of AbCTSZ genomic structure revealed seven exons separated by six introns, which differs from that of its vertebrate counterparts. Quantitative real time PCR (qPCR) detected the transcripts of AbCTSZ in early developmental stages and in eight different tissues. Higher levels of AbCTSZ transcripts were found in trochophore, gill, and hemocytes, highlighting its importance in the early development and immunity of disk abalone. In addition, we found that viable bacteria (Vibrio parahaemolyticus and Listeria monocytogenes) and bacterial lipopolysaccharides significantly modulated AbCTSZ transcription. Collectively, these lines of evidences suggest that AbCTSZ plays an indispensable role in the innate immunity of disk abalone. G. I. Godahewa, N. C. N. Perera, Sukkyoung Lee, Myoung-Jin Kim, Jehee Lee Article in Journal/Newspaper Crassostrea gigas The University of Adelaide: Digital Library Gene 627 500 507
institution Open Polar
collection The University of Adelaide: Digital Library
op_collection_id ftunivadelaidedl
language English
topic Cathepsin Z
Disk abalone
Abalone early development
Genomic organization
Immune responsive expression
spellingShingle Cathepsin Z
Disk abalone
Abalone early development
Genomic organization
Immune responsive expression
Godahewa, G.I.
Perera, N.C.N.
Lee, S.
Kim, M.J.
Lee, J.
A cysteine protease (cathepsin Z) from disk abalone, Haliotis discus discus: Genomic characterization and transcriptional profiling during bacterial infections
topic_facet Cathepsin Z
Disk abalone
Abalone early development
Genomic organization
Immune responsive expression
description Cathepsin Z (CTSZ) is lysosomal cysteine protease of the papain superfamily. It participates in the host immune defense via phagocytosis, signal transduction, cell-cell communication, proliferation, and migration of immune cells such as monocytes, macrophages, and dendritic cells. Hence, CTSZ is also acknowledged as an acute-phase protein in host immunity. In this study, we sought to identify the CTSZ homolog from disk abalone (AbCTSZ) and characterize it at the molecular, genomic, and transcriptional levels. AbCTSZ encodes a protein with 318 amino acids and a molecular mass of 36kDa. The structure of AbCTSZ reveals amino acid sequences that are characteristic of the signal sequence, pro-peptide, peptidase-C1 papain family cysteine protease domain, mini-loop, HIP motif, N-linked glycosylation sites, active sites, and conserved Cys residues. A pairwise comparison revealed that AbCTSZ shared the highest amino acid homology with its molluscan counterpart from Crassostrea gigas. A multiple alignment analysis revealed the conservation of functionally crucial elements of AbCTSZ, and a phylogenetic study further confirmed a proximal evolutionary relationship with its invertebrate counterparts. Further, an analysis of AbCTSZ genomic structure revealed seven exons separated by six introns, which differs from that of its vertebrate counterparts. Quantitative real time PCR (qPCR) detected the transcripts of AbCTSZ in early developmental stages and in eight different tissues. Higher levels of AbCTSZ transcripts were found in trochophore, gill, and hemocytes, highlighting its importance in the early development and immunity of disk abalone. In addition, we found that viable bacteria (Vibrio parahaemolyticus and Listeria monocytogenes) and bacterial lipopolysaccharides significantly modulated AbCTSZ transcription. Collectively, these lines of evidences suggest that AbCTSZ plays an indispensable role in the innate immunity of disk abalone. G. I. Godahewa, N. C. N. Perera, Sukkyoung Lee, Myoung-Jin Kim, Jehee Lee
format Article in Journal/Newspaper
author Godahewa, G.I.
Perera, N.C.N.
Lee, S.
Kim, M.J.
Lee, J.
author_facet Godahewa, G.I.
Perera, N.C.N.
Lee, S.
Kim, M.J.
Lee, J.
author_sort Godahewa, G.I.
title A cysteine protease (cathepsin Z) from disk abalone, Haliotis discus discus: Genomic characterization and transcriptional profiling during bacterial infections
title_short A cysteine protease (cathepsin Z) from disk abalone, Haliotis discus discus: Genomic characterization and transcriptional profiling during bacterial infections
title_full A cysteine protease (cathepsin Z) from disk abalone, Haliotis discus discus: Genomic characterization and transcriptional profiling during bacterial infections
title_fullStr A cysteine protease (cathepsin Z) from disk abalone, Haliotis discus discus: Genomic characterization and transcriptional profiling during bacterial infections
title_full_unstemmed A cysteine protease (cathepsin Z) from disk abalone, Haliotis discus discus: Genomic characterization and transcriptional profiling during bacterial infections
title_sort cysteine protease (cathepsin z) from disk abalone, haliotis discus discus: genomic characterization and transcriptional profiling during bacterial infections
publisher Elsevier
publishDate 2017
url http://hdl.handle.net/2440/120797
https://doi.org/10.1016/j.gene.2017.07.007
genre Crassostrea gigas
genre_facet Crassostrea gigas
op_source http://dx.doi.org/10.1016/j.gene.2017.07.007
op_relation Gene, 2017; 627:500-507
0378-1119
1879-0038
http://hdl.handle.net/2440/120797
doi:10.1016/j.gene.2017.07.007
Godahewa, G.I. [0000-0002-7614-1040]
op_rights © 2017 Elsevier B.V. All rights reserved.
op_doi https://doi.org/10.1016/j.gene.2017.07.007
container_title Gene
container_volume 627
container_start_page 500
op_container_end_page 507
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