2020
DOI: 10.7717/peerj.8868
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Characterization of calcineurin A and B genes in the abalone, Haliotis diversicolor, and their immune response role during bacterial infection

Abstract: Calcineurin (CN) is known to be involved in many biological processes, particularly, the immune response mechanism in many invertebrates. In this study, we characterized both HcCNA and HcCNB genes in Haliotis diversicolor, documented their expression in many tissues, and discerned their function as immune responsive genes against Vibrio parahaemolyticus infection. Similar to other mollusk CNs, the HcCNA gene lacked a proline-rich domain and comprised only one isoform of its catalytic unit, in contrast to CNs f… Show more

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Cited by 3 publications
(4 citation statements)
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“…Adult abalone H. diversicolor, about 2 years of age, 55.0 mm in size and 10.0 g in weight, were reared in polyethylene tanks at 23−25 °C with a salinity of 28–30 ppt at Phuket Abalone Farm, Phuket, Thailand and fed daily with fresh kelp as previously described ( Buddawong et al, 2020 ). Animal handling followed the guideline of Animal Care and Use Committee (SCMU-ACUC, Protocol Number MUSC60-040-390), Faculty of Science, Mahidol University.…”
Section: Methodsmentioning
confidence: 99%
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“…Adult abalone H. diversicolor, about 2 years of age, 55.0 mm in size and 10.0 g in weight, were reared in polyethylene tanks at 23−25 °C with a salinity of 28–30 ppt at Phuket Abalone Farm, Phuket, Thailand and fed daily with fresh kelp as previously described ( Buddawong et al, 2020 ). Animal handling followed the guideline of Animal Care and Use Committee (SCMU-ACUC, Protocol Number MUSC60-040-390), Faculty of Science, Mahidol University.…”
Section: Methodsmentioning
confidence: 99%
“…qPCR was used to quantify the expression levels of HcCNA and HcCNB . As described previously ( Buddawong et al, 2020 ), 1 µg of the total RNA from mantle was reverse transcribed into cDNA and qPCR was performed in triplicate using a Bio-Rad CFX96 Touch Real-Time PCR Detection System (Bio-Rad Laboratories, Inc., Hercules, CA, USA) with Luna Universal qPCR Master Mix (New England Biolabs, Ipswich, MA, USA). The 20 µl reaction mixture contained 0.5 µl (20 ng) of cDNA, 10 µl of Luna Universal qPCR mix with Hot Start Taq DNA Polymerase, 0.5 µl of 10 µM of each primer (for primer details see Table 1 ), and 8.5 µl of PCR grade water.…”
Section: Methodsmentioning
confidence: 99%
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