dc.contributor.author |
Premachandra, H. K. A. |
|
dc.contributor.author |
Wan, Q. |
|
dc.contributor.author |
Elvitigala, D. A. S |
|
dc.contributor.author |
De Zoysa, M. |
|
dc.contributor.author |
Choi, C. Y. |
|
dc.contributor.author |
Whang, I. |
|
dc.contributor.author |
Lee, J. |
|
dc.date.accessioned |
2021-06-06T17:19:24Z |
|
dc.date.available |
2021-06-06T17:19:24Z |
|
dc.date.issued |
2012 |
|
dc.identifier.citation |
Premachandra, H. K. A., Wan, Q., Elvitigala, D. A. S., De Zoysa, M., Choi, C. Y., Whang, I., & Lee, J. (2012). Genomic characterization and expression profiles upon bacterial infection of a novel cystatin B homologue from disk abalone (Haliotis discus discus). Developmental & Comparative Immunology, 38(4), 495-504. |
en_US |
dc.identifier.uri |
http://archive.cmb.ac.lk:8080/xmlui/handle/70130/5334 |
|
dc.description.abstract |
Cystatins are a large family of cysteine proteinase inhibitors which are involved in diverse biological and
pathological processes. In the present study, we identified a gene related to cystatin superfamily, AbCyt B,
from disk abalone Haliotis discus discus by expressed sequence tag (EST) analysis and BAC library
screening. The complete cDNA sequence of AbCyt B is comprised of 1967 nucleotides with a 306 bp open
reading frame (ORF) encoding for 101 amino acids. The amino acid sequence consists of a single cystatinlike domain, which has a cysteine proteinase inhibitor signature, a conserved Gly in N-terminal region,
QVVAG motif and a variant of PW motif. No signal peptide, disulfide bonds or carbohydrate side chains
were identified. Analysis of deduced amino acid sequence revealed that AbCyt B shares up to 44.7% identity and 65.7% similarity with the cystatin B genes from other organisms. The genomic sequence of AbCyt
B is approximately 8.4 Kb, consisting of three exons and two introns. Phylogenetic tree analysis showed
that AbCyt B was closely related to the cystatin B from pacific oyster (Crassostrea gigas) under the family
1.Functional analysis of recombinant AbCyt B protein exhibited inhibitory activity against the papain,
with almost 84% inhibition at a concentration of 3.5 lmol/L. In tissue expression analysis, AbCyt B
transcripts were expressed abundantly in the hemocyte, gill, mantle, and digestive tract, while weakly
in muscle, testis, and hepatopancreas. After the immune challenge with Vibrio parahemolyticus, the AbCyt
B showed significant (P < 0.05) up-regulation of relative mRNA expression in gill and hemocytes at 24 and
6 h of post infection, respectively. These results collectively suggest that AbCyst B is a potent inhibitor of
cysteine proteinases and is also potentially involved in immune responses against invading bacterial
pathogens in abalone. |
|
dc.language.iso |
en |
en_US |
dc.publisher |
Elsevier |
en_US |
dc.subject |
Cysteine protease inhibitors |
en_US |
dc.subject |
Cystatin B |
en_US |
dc.subject |
Disk abalone |
en_US |
dc.subject |
Bacterial challenge |
en_US |
dc.subject |
Papain inhibition Transcriptional analysis |
en_US |
dc.title |
Genomic characterization and expression profiles upon bacterial infection of a novel cystatin B homologue from disk abalone ( Haliotis discus discus) |
en_US |
dc.type |
Article |
en_US |