Molecular cloning, characterization and expression analysis of p53 from turbot Scophthalmus maximus and its response to thermal stress.

The tumor suppressor protein, p53 plays a crucial role in protecting genetic integrity. Once activated by diverse cell stresses, p53 reversibly activates downstream target genes to regulate cell cycle and apoptosis. However, few studies have investigated the effects of thermal stress in turbot, specifically the p53 signaling pathway. In this study, the rapid amplification of cDNA ends was used to obtain a full-length cDNA of the turbot p53 gene (Sm -p53) and perform bioinformatics analysis. The results showed that the cDNA of the Sm -p53 gene was 2928 bp in length, encoded a 381 amino acid protein, with a theoretical isoelectric point of 6.73. It was composed of a DNA binding and a tetramerization domain. Expression of Sm -p53 in different tissues was detected and quantified by qRT-PCR, and was highest in the liver. We also investigated the expression profiles of Sm -p53 in different tissue and TK cells after thermal stress. These result suggested that Sm -p53 plays a key role, and provides a theoretical basis for Sm -p53 changes in environmental stress responses in the turbot. • A full-length cDNA encoding Sm-p53 from turbot was cloned for the first time. • This is the first time to report the expression level of Sm-p53 in vivo and in kidney cell after thermal stress in turbot. • Our study has confirmed that Sm-p53 is a critical regulator of thermal stress in fish. • Sm-p53 could be used as potential representative biomarkers as an early heat stress bioindicator. [ABSTRACT FROM AUTHOR]