Cloning, Characterization and Functional Analysis of Caspase 8-like Gene in Apoptosis of Crassostrea hongkongensis Response to Hyper-Salinity Stress(类似 Caspase 8 基因在香港鲫鱼高盐度应激凋亡中的克隆、特征和功能分析

Fishes Pub Date : 2024-05-09 DOI:10.3390/fishes9050172
Jinji Lin, Ziqi Yu, Yang Leng, Jiexiong Zhu, Feifei Yu, Yishan Lu, Jiayu Chen, Wenhao He, Yixin Zhang, Yaoshen Wen
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引用次数: 0

摘要

Caspase-8是caspase家族的成员之一,是一种启动caspase,在细胞凋亡中起着至关重要的作用。本研究通过 RACE-PCR 技术从香港鲫(Crassostrea hongkongensis)中分离出了 Caspase8-like (CASP8-like)的全长 cDNA。ChCASP8-like包含一个1599-bp的开放阅读框(ORF),编码533个氨基酸,其中有两个保守的死亡效应结构域(DED)和一个半胱氨酸天冬酶半胱氨酸结构域(CASc)。氨基酸序列比较显示,ChCASP8-like与C. angulata的CASP8-like具有最高的同一性(85.4%)。组织表达谱显示,ChCASP8-like在鳃、肝胰腺、套膜、内收肌、血细胞和性腺中组成型表达,在高盐度胁迫下,血细胞、肝胰腺和鳃显著上调。ATR、CHK1、BCL-XL、CASP8-like、CASP9和CASP3等凋亡相关基因在高盐度胁迫下被显著激活,但在ChCASP8-like沉默后被明显抑制。超盐胁迫后,Caspase 8 的活性增加了 1.7 倍,而 ChCASP8-like 沉默则抑制了 9.4%。此外,ChCASP8-like 沉默明显缓解了超盐胁迫导致的细胞凋亡。这些结果共同表明,ChCASP8-like 在诱导细胞凋亡以对抗超盐胁迫中发挥了关键作用。
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Cloning, Characterization and Functional Analysis of Caspase 8-like Gene in Apoptosis of Crassostrea hongkongensis Response to Hyper-Salinity Stress
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.
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