Mechanistic target of rapamycin inhibition with rapamycin induces autophagy and correlative regulation in white shrimp (Litopenaeus vannamei). (17th April 2018)

• Record Type: Journal Article
• Authors: Liu, Xinwei; Wang, Mengqiang; Sun, Guoqiong; Wang, Baojie; Jiang, Keyong; Shao, Jianchun; Qi, Cancan; Zhao, Wei; Han, Siyin; Liu, Mei; Wang, Lei
• Is Part Of: Aquaculture nutrition. Volume 24:Number 5(2018)
• Page Start: 1509
• Page End: 1520
• Publication Date: 2018-04-17
• Subjects: autophagy -- Litopenaeus vannamei -- mTOR -- rapamycin -- transcriptome; Aquaculture -- Periodicals; Aquatic animals -- Feeding and feeds -- Periodicals; Fishes -- Feeding and feeds -- Periodicals; 639.3
• DOI: 10.1111/anu.12688
• Languages: English
• ISSNs: 1353-5773

Abstract

Abstract: Mechanistic target of rapamycin (mTOR) is a central regulator of cell growth and metabolism including autophagy. The mTORC1 signalling pathway is a major regulator of autophagy in response to nutrient levels. The drug rapamycin induces autophagy in various cell types and species by specifically inhibiting the activity of mTOR. To identify the genes and correlative regulatory pathways involved in cell metabolism and autophagy of Litopenaeus vannamei, we analysed the transcriptome of shrimps treated with rapamycin. We found that the expression of some genes related to autophagy was significantly changed. To further explore the autophagy regulatory mechanism, the concentration and phosphorylation of related proteins were analysed by Western blot. We found that treatment with the rapamycin can depress phosphorylating of ATG1 and promote dephosphorylating of ATG13. There are some heat‐shock protein genes and genes involving apoptosis, function of lysosome and feedback regulation of mTOR signalling path differently expressed. The relationship between them and autophagy induced by inhibiting mTOR is also discussed. Evidences show the complicated positive and negative feedback loops controlling autophagy crustaceans are scarce. Our study verifies and contributes to the current understanding of autophagy induced by mTOR in crustacean, providing an abundant source for the identification of novel genes.