Back to Search Start Over

Identification and function of an evolutionarily conserved signaling intermediate in Toll pathways (ECSIT) from Crassostrea hongkongensis.

Authors :
Qu, Fufa
Xiang, Zhiming
Wang, Fuxuan
Zhang, Yang
Li, Jun
Zhang, Yuehuan
Xiao, Shu
Yu, Ziniu
Source :
Developmental & Comparative Immunology. Nov2015, Vol. 53 Issue 1, p244-252. 9p.
Publication Year :
2015

Abstract

Evolutionarily conserved signaling intermediate in Toll pathways (ECSIT) is a multifunctional adaptor protein that plays a key role in the regulation of the oxidative phosphorylation (OXPHOS) system, bone morphogenetic protein (BMP) pathway and Toll-like receptor (TLR) signaling pathway in mammals. However, the function of ECSIT homologs in mollusks, the second most diverse group of animals, is not well understood. In this study, we identified an ECSIT homolog in the Hong Kong oyster Crassostrea hongkongensis ( Ch ECSIT) and investigated its biological functions. The full-length cDNA of Ch ECSIT is 1734 bp and includes an open reading frame (ORF) of 1074 bp that encodes a polypeptide of 451 amino acids. The predicted Ch ECSIT protein shares similar structural characteristics with other known ECSIT family proteins. Quantitative real-time PCR analysis revealed that Ch ECSIT mRNA is broadly expressed in all of the examined tissues and at different stages of embryonic development; its transcript level could be significantly up-regulated by challenge with microorganisms ( Vibrio alginolyticus , Staphylococcus haemolyticus and Saccharomyces cerevisiae ). In addition, Ch ECSIT was found to be located primarily in the cytoplasm, and its overexpression stimulated the transcriptional activity of an NF-κB reporter gene in HEK293T cells. These findings suggest that Ch ECSIT might be involved in embryogenesis processes and immune responses in C. hongkongensis . [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0145305X
Volume :
53
Issue :
1
Database :
Academic Search Index
Journal :
Developmental & Comparative Immunology
Publication Type :
Academic Journal
Accession number :
108809464
Full Text :
https://doi.org/10.1016/j.dci.2015.07.015