Peroxidation due to cryoprotectant treatment is a vital factor for cell survival in Arabidopsis cryopreservation
Copyright © 2013 Elsevier Ireland Ltd. All rights reserved.
Veröffentlicht in: | Plant science : an international journal of experimental plant biology. - 1985. - 212(2013) vom: 07. Nov., Seite 37-47 |
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Format: | Online-Aufsatz |
Sprache: | English |
Veröffentlicht: |
2013
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Zugriff auf das übergeordnete Werk: | Plant science : an international journal of experimental plant biology |
Schlagworte: | Journal Article Research Support, Non-U.S. Gov't AFLPa Arabidopsis thaliana BLAST Cryopreservation EST FDA LN MDA mehr... |
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245 | 1 | 0 | |a Peroxidation due to cryoprotectant treatment is a vital factor for cell survival in Arabidopsis cryopreservation |
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500 | |a Citation Status MEDLINE | ||
520 | |a Copyright © 2013 Elsevier Ireland Ltd. All rights reserved. | ||
520 | |a Cryopreservation can be a safe and cost-effective tool for the long-term storage of plant germplasm. In Arabidopsis, the ability to recover from cryogenic treatment was lost as growth progressed. Growth could be restored in 48-h seedlings, whereas 72-h seedlings died after cryogenic treatment. Why seedling age and survival are negatively correlated is an interesting issue. A comparative transcriptomics was performed to screen differentially expressed genes between 48- and 72-h seedlings after exposure to cryoprotectant. Among differentially expressed genes, oxidative stress response genes played important roles in cryoprotectant treatment, and peroxidation was a key factor related to cell survival. Seedlings underwent more peroxidation at 72-h than at 48-h. A comprehensive analysis indicated that peroxidation injured membrane systems leading to photophosphorylation and oxidative phosphorylation damage. Furthermore, the apoptosis-like events were found in cryogenic treatment of Arabidopsis seedlings. 48- and 72-h seedlings underwent different degrees of membrane lipid peroxidation during cryoprotectant treatment, and reducing the injury of oxidative stress was an important factor to successful cryopreservation. This study provided a novel insight of genetic regulatory mechanisms in cryopreservation, and established an excellent model to test and evaluate the effect of exogenous antioxidants and conventional cryoprotectants in plant cryopreservation | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a AFLPa | |
650 | 4 | |a Arabidopsis thaliana | |
650 | 4 | |a BLAST | |
650 | 4 | |a Cryopreservation | |
650 | 4 | |a EST | |
650 | 4 | |a FDA | |
650 | 4 | |a LN | |
650 | 4 | |a MDA | |
650 | 4 | |a MS | |
650 | 4 | |a Murashige and Skoog [1] | |
650 | 4 | |a NCBI | |
650 | 4 | |a National Center for Biotechnology Information | |
650 | 4 | |a Oxidative stress | |
650 | 4 | |a PVS | |
650 | 4 | |a Peroxidation | |
650 | 4 | |a ROS | |
650 | 4 | |a TBA | |
650 | 4 | |a TCA | |
650 | 4 | |a TDFs | |
650 | 4 | |a basic local alignment search tool | |
650 | 4 | |a cDNA-AFLP | |
650 | 4 | |a expressed sequence tag | |
650 | 4 | |a fluorescein diacetate | |
650 | 4 | |a liquid nitrogen | |
650 | 4 | |a malondialdehyde | |
650 | 4 | |a mplified fragment length polymorphism | |
650 | 4 | |a plant vitrification solution | |
650 | 4 | |a qRT-PCR | |
650 | 4 | |a quantitative real time-PCR | |
650 | 4 | |a reactive oxygen species | |
650 | 4 | |a thiobarbituric acid | |
650 | 4 | |a transcript-derived fragments | |
650 | 4 | |a trichloroacetic acid | |
650 | 7 | |a Antioxidants |2 NLM | |
650 | 7 | |a Cryoprotective Agents |2 NLM | |
650 | 7 | |a Plant Proteins |2 NLM | |
650 | 7 | |a RNA, Messenger |2 NLM | |
700 | 1 | |a Zhang, Di |e verfasserin |4 aut | |
700 | 1 | |a Jiang, Xiang-Ning |e verfasserin |4 aut | |
700 | 1 | |a Gai, Ying |e verfasserin |4 aut | |
700 | 1 | |a Wang, Wei-Ming |e verfasserin |4 aut | |
700 | 1 | |a Reed, Barbara M |e verfasserin |4 aut | |
700 | 1 | |a Shen, Xiao-Hui |e verfasserin |4 aut | |
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