Liver transcriptome changes in zebrafish during acclimation to transport-associated stress.
Liver plays a key role during the stress acclimation, and liver transcriptome analysis of shipped zebrafish could reveal the molecular adjustments that occur in the organ. Transcriptional changes in liver were analyzed with a 44 K oligo array using total RNA from fish prior to transport and during a...
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| Format: | Article |
| Language: | English |
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Public Library of Science (PLoS)
2013-01-01
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| Series: | PLoS ONE |
| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23762281/pdf/?tool=EBI |
| _version_ | 1818459817297051648 |
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| author | Anusha K S Dhanasiri Jorge M O Fernandes Viswanath Kiron |
| author_facet | Anusha K S Dhanasiri Jorge M O Fernandes Viswanath Kiron |
| author_sort | Anusha K S Dhanasiri |
| collection | DOAJ |
| description | Liver plays a key role during the stress acclimation, and liver transcriptome analysis of shipped zebrafish could reveal the molecular adjustments that occur in the organ. Transcriptional changes in liver were analyzed with a 44 K oligo array using total RNA from fish prior to transport and during a mock transport process--immediately after packing (0 h), at 48 and 72 h. Large numbers of genes related to a variety of biological processes and pathways were regulated, mainly during transport (at 48/72 h). Immediately after packing, transcripts of genes related to both gluconeogenesis and glycolysis were induced. During transport, induction of gluconeogenesis-linked genes and reduction of glycolysis-related genes may be supporting the increase in blood glucose levels. Inhibition of genes involved in fatty acid beta-oxidation may be pointing to the poor ability of fish to utilize energy from fatty acids, under transport conditions. Genes involved in some of the mechanisms that regulate body ammonia were also affected. Even though genes associated with certain transaminases were inhibited in liver, sustained glutamate deamination may have led to high ammonia accumulation in liver/body. Enhanced levels of gene transcripts in ubiquitination and MAPK signalling cascade and reduced levels of gene transcripts related to ROS generation via peroxisomal enzymes as well as xenobiotic metabolism may be signifying the importance of such cellular and tissue responses to maintain homeostasis. Furthermore, transcripts connected with stress and thyroid hormones were also regulated. Moreover, suppression of genes related to specific immune components may be denoting the deleterious impact of transport on fish health. Thus, this study has revealed the complex molecular adjustments that occur in zebrafish when they are transported. |
| first_indexed | 2024-12-14T23:20:23Z |
| format | Article |
| id | doaj.art-47af3befa65545558db839138b542aba |
| institution | Directory Open Access Journal |
| issn | 1932-6203 |
| language | English |
| last_indexed | 2024-12-14T23:20:23Z |
| publishDate | 2013-01-01 |
| publisher | Public Library of Science (PLoS) |
| record_format | Article |
| series | PLoS ONE |
| spelling | doaj.art-47af3befa65545558db839138b542aba2022-12-21T22:43:59ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0186e6502810.1371/journal.pone.0065028Liver transcriptome changes in zebrafish during acclimation to transport-associated stress.Anusha K S DhanasiriJorge M O FernandesViswanath KironLiver plays a key role during the stress acclimation, and liver transcriptome analysis of shipped zebrafish could reveal the molecular adjustments that occur in the organ. Transcriptional changes in liver were analyzed with a 44 K oligo array using total RNA from fish prior to transport and during a mock transport process--immediately after packing (0 h), at 48 and 72 h. Large numbers of genes related to a variety of biological processes and pathways were regulated, mainly during transport (at 48/72 h). Immediately after packing, transcripts of genes related to both gluconeogenesis and glycolysis were induced. During transport, induction of gluconeogenesis-linked genes and reduction of glycolysis-related genes may be supporting the increase in blood glucose levels. Inhibition of genes involved in fatty acid beta-oxidation may be pointing to the poor ability of fish to utilize energy from fatty acids, under transport conditions. Genes involved in some of the mechanisms that regulate body ammonia were also affected. Even though genes associated with certain transaminases were inhibited in liver, sustained glutamate deamination may have led to high ammonia accumulation in liver/body. Enhanced levels of gene transcripts in ubiquitination and MAPK signalling cascade and reduced levels of gene transcripts related to ROS generation via peroxisomal enzymes as well as xenobiotic metabolism may be signifying the importance of such cellular and tissue responses to maintain homeostasis. Furthermore, transcripts connected with stress and thyroid hormones were also regulated. Moreover, suppression of genes related to specific immune components may be denoting the deleterious impact of transport on fish health. Thus, this study has revealed the complex molecular adjustments that occur in zebrafish when they are transported.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23762281/pdf/?tool=EBI |
| spellingShingle | Anusha K S Dhanasiri Jorge M O Fernandes Viswanath Kiron Liver transcriptome changes in zebrafish during acclimation to transport-associated stress. PLoS ONE |
| title | Liver transcriptome changes in zebrafish during acclimation to transport-associated stress. |
| title_full | Liver transcriptome changes in zebrafish during acclimation to transport-associated stress. |
| title_fullStr | Liver transcriptome changes in zebrafish during acclimation to transport-associated stress. |
| title_full_unstemmed | Liver transcriptome changes in zebrafish during acclimation to transport-associated stress. |
| title_short | Liver transcriptome changes in zebrafish during acclimation to transport-associated stress. |
| title_sort | liver transcriptome changes in zebrafish during acclimation to transport associated stress |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23762281/pdf/?tool=EBI |
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