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Title: | Cloning, Characterization and Functional Analysis of Caspase 8-like Gene in Apoptosis of Crassostrea hongkongensis Response to Hyper-Salinity Stress |
Authors: | Jinji Lin Ziqi Yu Yang Leng Jiexiong Zhu Feifei Yu Yishan Lu Jiayu Chen Wenhao He Yixin Zhang Yaoshen Wen |
Keywords: | Crassostrea hongkongensis caspase8-like apoptosis hyper-salinity stress |
Issue Date: | 2024 |
Publisher: | MDPI |
Abstract: | Caspase-8, a member of the caspase family, is an initiating caspase and plays a crucial role in apoptosis. In this study, the full-length cDNA of caspase8-like (CASP8-like) was isolated from Crassostrea hongkongensis (C. hongkongensis) by RACE-PCR. ChCASP8-like contained a 1599-bp open reading frame (ORF) encoding 533 amino acids with two conserved death effector domains (DEDs) and a cysteine aspartase cysteine structural domain (CASc). Amino acid sequence comparison showed that ChCASP8-like shared the highest identity (85.4%) with CASP8-like of C. angulata. The tissue expression profile showed that ChCASP8-like was constitutively expressed in gills, hepatopancreas, mantle, adductor muscle, hemocytes and gonads, and was significantly upregulated in hemocytes, hepatopancreas and gills under hyper-salinity stress. The apoptosis-related genes, including ATR, CHK1, BCL-XL, CASP8-like, CASP9 and CASP3, were significantly activated by hyper-salinity stress, but were remarkably inhibited by ChCASP8-like silencing. The caspase 8 activity was increased by 1.7-fold after hyper-salinity stress, and was inhibited by 9.4% by ChCASP8-like silencing. Moreover, ChCASP8-like silencing clearly alleviated the apoptosis resulting from hyper-salinity stress. These results collectively demonstrated that ChCASP8-like played a crucial role in inducing apoptosis against hyper-salinity stress. |
URI: | http://umt-ir.umt.edu.my:8080/handle/123456789/22457 |
Appears in Collections: | UMT Niche E-Book |
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File | Description | Size | Format | |
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Cloning, Characterization and Functional.pdf Restricted Access | 1.85 MB | Adobe PDF | View/Open Request a copy |
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