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Published on: May 21, 2020
Functional analysis target of rapamycin (TOR) on the Penaeus vannamei in response to acute low temperature stress
QingJian Liang1, Mufei Ou1, ZhongHua Li1
1Guangzhou Key Laboratory of Subtropical Biodiversity and Biomonitoring, Guangdong Provincial Key Laboratory for Healthy and Safe Aquaculture, Key Laboratory of Ecology and Environmental Science in Guangdong Higher Education, College of Life Science, South China Normal University, Guangzhou, 510631, PR China.
Abstract:
Target of rapamycin (TOR) is an atypical of Ser/Thr protein kinase that plays an important role in many aspects such as cell growth, reproduction, differentiation, cell cycle regulation, autophagy and apoptosis. However, little information is known about the enzyme in crustaceans. Here, a novel TOR was identified from shrimp Penaeus vannamei (PvTOR) and its biological functions were investigated in response low temperature stress. The PvTOR gene encoded a polypeptide of 2464 amino acids with an estimated molecular mass of 279.4 kD and a predicted isoelectronic point (pI) of 7.30. Phylogenetic analysis revealed that PvTOR shared high similarity with other known species. PvTOR mRNA was detected in all the tested tissues and highest transcription in muscle and hepatopancreas. PvTOR transcriptional level was up-regulated significantly at 1.5 h and 3 h, and down-regulated at 12 h and 24 h after low temperature stress. TEM and autophagy indicator system GFP-PvLC3 suggested that low temperature induced autophagy generation. ROS, Ca2+ concentration and apoptosis rate were increased significantly in TOR-knockdown shrimp after low temperature stress. The autophagy associated gene ATG8II/I, PvBeclin-1, PvATG14, apoptosis gene PvPARP, Pvcasp-3, PvBAX and Pvp53 transcripts, and casp-3/8 activity in hemocyte were increased significantly in TOR-knockdown group shrimp at 3 h after low temperature stress. Additionally, THC counts of TOR-knockdown group were significantly higher than the dsGFP group. In summary, these results suggested that PvTOR plays an important role in the adaptation mechanisms of shrimp at low temperature by regulating autophagy and apoptosis.
Insights
The target of rapamycin (TOR) protein in shrimp is crucial for adapting to low temperatures by controlling autophagy and apoptosis. This study identifies and analyzes the function of shrimp PvTOR under cold stress.
Area of Science:
- Molecular Biology
- Crustacean Physiology
- Stress Response Mechanisms
Background:
- Target of rapamycin (TOR) is a key kinase regulating fundamental cellular processes like growth and apoptosis.
- Limited information exists regarding TOR function in crustaceans, particularly concerning environmental stress responses.
Purpose of the Study:
- To identify and characterize a novel TOR from shrimp (Penaeus vannamei), named PvTOR.
- To investigate the role of PvTOR in the shrimp's adaptation to low-temperature stress.
Main Methods:
- Gene identification and sequencing of PvTOR.
- Phylogenetic analysis of PvTOR.
- Quantitative analysis of PvTOR mRNA expression in various tissues and under cold stress.
- Investigation of autophagy, reactive oxygen species (ROS), calcium ion (Ca2+) concentration, and apoptosis rates in TOR-knockdown shrimp under cold stress.
- Analysis of autophagy and apoptosis-related gene expression and enzyme activity.
Main Results:
- PvTOR gene encodes a 2464-amino acid protein with high similarity to known TOR proteins.
- PvTOR mRNA is highly expressed in muscle and hepatopancreas and its transcription is significantly altered by low temperature.
- Low temperature induces autophagy, and TOR knockdown exacerbates ROS, Ca2+ levels, and apoptosis under cold stress.
- Knockdown of PvTOR leads to increased expression of autophagy and apoptosis-related genes and elevated caspase activity.
Conclusions:
- PvTOR plays a significant role in the low-temperature stress adaptation of shrimp.
- PvTOR regulates cellular responses to cold by modulating autophagy and apoptosis pathways.
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