2020
DOI: 10.1016/j.fsi.2019.11.070
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Functional analysis target of rapamycin (TOR) on the Penaeus vannamei in response to acute low temperature stress

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Cited by 22 publications
(7 citation statements)
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“…Previous studies have shown that loss of circulating hemocytes or hemocyte DNA damage would endanger survival (Li et al, 2013;Liang et al, 2019a). Thus, this possibility was observed, and results showed that overexpression of pva-miR-151 significantly elevated THC, while silencing pva-miR-151 significantly reduced the THC in low-temperature challenge (Figures 5D,E).…”
Section: Alters Of Pva-mir-151 Impact Low-temperature Tolerance Of Shrimpmentioning
confidence: 68%
“…Previous studies have shown that loss of circulating hemocytes or hemocyte DNA damage would endanger survival (Li et al, 2013;Liang et al, 2019a). Thus, this possibility was observed, and results showed that overexpression of pva-miR-151 significantly elevated THC, while silencing pva-miR-151 significantly reduced the THC in low-temperature challenge (Figures 5D,E).…”
Section: Alters Of Pva-mir-151 Impact Low-temperature Tolerance Of Shrimpmentioning
confidence: 68%
“…Autophagy is a relatively conservative cell degradation process in evolution, through which cells recycle ineffectual cellular components (such as damaged DNA, damaged organelles, intracellular pathogens, and misfolded proteins) to maintain homeostasis [56]. The autophagy-lysosome system could clean the oxidized, damaged, and misfolded proteins induced by environmental stress in the cell [58,59]. A recent study reported that low temperature-induced autophagy is a strategy to adapt to and cope with stress in Penaeus vannamei [59].…”
Section: Discussionmentioning
confidence: 99%
“…The tissue lysate was mixed with 5× SDS-PAGE buffer (Beyotime) and boiled for 10 min. Then, 30 μg of each sample was subjected to 10% SDS-PAGE and Western blotting, as previously reported [ 24 ]. The primary antibody diluted 1:1000 and secondary antibody diluted 1:2000 in 0.5% BSA-TBST.…”
Section: Methodsmentioning
confidence: 99%
“…The tissue was lysed in RIPA buffer (Beyotime, China), containing 1 mm PMSF for 30 min at 4 • C, and centrifuged at 12,000× g for 15 min at 4 • C. The tissue lysate was mixed with 5× SDS-PAGE buffer (Beyotime) and boiled for 10 min. Then, 30 µg of each sample was subjected to 10% SDS-PAGE and Western blotting, as previously reported [24]. The primary antibody diluted 1:1000 and secondary antibody diluted 1:2000 in 0.5% BSA-TBST.…”
Section: Western Blottingmentioning
confidence: 99%