| Literature DB >> 31809835 |
Pin-Hong Li1, Yu-Lin Liang1, Yu-Ling Su1, Yu-Feng Jiang2, Biao Chen2, Shu-Yin Chen1, You-Hua Huang1, Jing-Guang Wei1, Xiao-Hong Huang1, Qi-Wei Qin3, Hong-Yan Sun4.
Abstract
Heat shock protein 22 (Hsp22) is an important regulatory factor response to various stresses in mammals. In this study, the full length cDNA of Epinephelus coioides Hsp22, which was 1680bp in length, with a 289 bp 5' UTR, a 725 bp 3'UTR, and a 666 bp open reading frame encoding 221 amino acids, was obtained. E. coioides Hsp22 contains a highly conserved α-crystallin domain. E. coioides Hsp22 mRNA was detected in all tissues examined by quantitative real-time PCR, with the highest expression in blood, followed by the spleen, skin, gill, head kidney, muscle, heart, liver, trunk kidney, stomach, pyloric caeca, intestine, brain and thymus. The expression patterns of E. coioides Hsp22 response to infection with Singapore grouper iridovirus (SGIV) and Vribro alginolyticus, the important pathogens of E. coioides, were studied. The expression levels of the gene were up-regulated in the tissues examined. Subcellular localization analysis demonstrated that E. coioides Hsp22 was distributed in both the cytoplasm and nucleus. In addition, E. coioides Hsp22 significantly inhibited the SGIV-induced cell apoptosis. In summary, the E. coioides Hsp22 might play a critical role in pathogenic stimulation.Entities:
Keywords: Apoptosis; Epinephelus coioides; Hsp22; SGIV; Vibrio alginolyticus
Year: 2019 PMID: 31809835 DOI: 10.1016/j.fsi.2019.11.069
Source DB: PubMed Journal: Fish Shellfish Immunol ISSN: 1050-4648 Impact factor: 4.581