The transcriptomic responses of blunt snout bream (Megalobrama amblycephala) to acute hypoxia stress alone, and in combination with bortezomib

Blunt snout bream (Megalobrama amblycephala) is sensitive to hypoxia. A new blunt snout bream strain, "Pujiang No.2", was developed to overcome this shortcoming. As a proteasome inhibitor, bortezomib (PS-341) has been shown to affect the adaptation of cells to a hypoxic environment. In the...

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Veröffentlicht in:BMC genomics 2022-02, Vol.23 (1), p.162-162, Article 162
Hauptverfasser: Zhao, Shan-Shan, Su, Xiao-Lei, Pan, Rong-Jia, Lu, Li-Qun, Zheng, Guo-Dong, Zou, Shu-Ming
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Sprache:eng
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Zusammenfassung:Blunt snout bream (Megalobrama amblycephala) is sensitive to hypoxia. A new blunt snout bream strain, "Pujiang No.2", was developed to overcome this shortcoming. As a proteasome inhibitor, bortezomib (PS-341) has been shown to affect the adaptation of cells to a hypoxic environment. In the present study, bortezomib was used to explore the hypoxia adaptation mechanism of "Pujiang No.2". We examined how acute hypoxia alone (hypoxia-treated, HN: 1.0 mg·L ), and in combination with bortezomib (hypoxia-bortezomib-treated, HB: Use 1 mg bortezomib for 1 kg fish), impacted the hepatic ultrastructure and transcriptome expression compared to control fish (normoxia-treated, NN). Hypoxia tolerance was significantly decreased in the bortezomib-treated group (LOE , loss of equilibrium, 1.11 mg·L and 1.32 mg·L ) compared to the control group (LOE , 0.73 mg·L and 0.85 mg·L ). The HB group had more severe liver injury than the HN group. Specifically, the activities of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) in the HB group (52.16 U/gprot, 32 U/gprot) were significantly (p 
ISSN:1471-2164
1471-2164
DOI:10.1186/s12864-022-08399-7