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Identification and functional characterization of two Bcl-2 family proteins in swimming crab, Portunus trituberculatus.

Authors :
Zhang, Yunbin
Wang, Lei
Xu, Yao
Ren, Xianyun
Liu, Ping
Source :
Aquaculture. May2022, Vol. 553, pN.PAG-N.PAG. 1p.
Publication Year :
2022

Abstract

Bcl-2 family proteins are regulatory factors of the mitochondrial apoptosis pathway that are vital to immune defenses and many other biological processes. However, the effects of Bcl-2 family proteins on apoptosis and immunity in crustaceans is poorly studied. In the study, two novel genes including Bax gene (PtBax) and Bcl-2 (PtBcl-2) from Portunus trituberculatus were identified and characterized. The deduced amino acid sequences showed that PtBax and PtBcl-2 possess domains of typical Bcl-2-related proteins. Both genes were widely expressed in all tested tissues, with highest expression levels in the hepatopancreas. Fluorescence in situ hybridization revealed that PtBax and PtBcl-2 were mainly expressed in the cytoplasm, where they play an important role in pathogen infection. Both PtBax and PtBcl-2 were significantly upregulated in the hepatopancreas at both mRNA and protein levels following challenge with Vibrio parahaemolyticus or white spot syndrome virus (WSSV). Moreover, double-stranded RNA-mediated silencing of both genes altered apoptosis levels in the hepatopancreas and WSSV copy number in muscles. Interactions between PtBax and PtBcl-2 were analyzed at transcriptional and protein levels. Yeast two-hybrid system analysis showed that PtBcl-2 could interact with PtBax directly. These results suggest that PtBax and PtBcl-2 may participate in pathogen infection by regulating apoptosis. • PtBax and PtBcl-2 from P. trituberculatus were identified and characterized. • WSSV and Vibrio parahaemolyticus challenge upregulated PtBax and PtBcl-2 in hepatopancreas at mRNA and protein levels. • The immune and apoptotic functions of two Bcl-2 family proteins were demonstrated by RNAi silencing experiments. • Yeast two-hybrid analysis revealed a direct interaction between the two proteins. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00448486
Volume :
553
Database :
Academic Search Index
Journal :
Aquaculture
Publication Type :
Academic Journal
Accession number :
155940323
Full Text :
https://doi.org/10.1016/j.aquaculture.2022.738086