Cloning, Characterization and Functional Analysis of Caspase 8-like Gene in Apoptosis of Crassostrea hongkongensis Response to Hyper-Salinity Stress

Author:

Lin Jinji12,Yu Ziqi2,Leng Yang3,Zhu Jiexiong12,Yu Feifei124,Lu Yishan124,Chen Jiayu12,He Wenhao12,Zhang Yixin12,Wen Yaoshen2

Affiliation:

1. Shenzhen Institute of Guangdong Ocean University, Shenzhen 518120, China

2. Fishery College of Guangdong Ocean University, Zhanjiang 524088, China

3. Experiment Animal Center, Guangdong Medical University, Zhanjiang 524023, China

4. Academician Joint Laboratory of Germplasm Resource Exploitation, Utilization and Health Assessment for Aquatic Animal, Guangdong Ocean University, Zhanjiang 524088, China

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.

Funder

Natural Science Foundation of Guangdong Province

Science and Technology Development Project of Zhanjiang

Undergraduate Innovation Team Project of Guangdong Ocean University

Shenzhen Science and Technology Program

Projects of Innovation Team of Colleges and Universities in Guangdong Province

Publisher

MDPI AG

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