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Transcriptome analysis of the spalax hypoxia survival response includes suppression of apoptosis and tight control of angiogenesis
BACKGROUND: The development of complex responses to hypoxia has played a key role in the evolution of mammals, as inadequate response to this condition is frequently associated with cardiovascular diseases, developmental disorders, and cancers. Though numerous studies have used mice and rats in orde...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3533650/ https://www.ncbi.nlm.nih.gov/pubmed/23148642 http://dx.doi.org/10.1186/1471-2164-13-615 |
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author | Malik, Assaf Korol, Abraham Weber, Mathias Hankeln, Thomas Avivi, Aaron Band, Mark |
author_facet | Malik, Assaf Korol, Abraham Weber, Mathias Hankeln, Thomas Avivi, Aaron Band, Mark |
author_sort | Malik, Assaf |
collection | PubMed |
description | BACKGROUND: The development of complex responses to hypoxia has played a key role in the evolution of mammals, as inadequate response to this condition is frequently associated with cardiovascular diseases, developmental disorders, and cancers. Though numerous studies have used mice and rats in order to explore mechanisms that contribute to hypoxia tolerance, these studies are limited due to the high sensitivity of most rodents to severe hypoxia. The blind subterranean mole rat Spalax is a hypoxia tolerant rodent, which exhibits unique longevity and therefore has invaluable potential in hypoxia and cancer research. RESULTS: Using microarrays, transcript abundance was measured in brain and muscle tissues from Spalax and rat individuals exposed to acute and chronic hypoxia for varying durations. We found that Spalax global gene expression response to hypoxia differs from that of rat and is characterized by the activation of functional groups of genes that have not been strongly associated with the response to hypoxia in hypoxia sensitive mammals. Using functional enrichment analysis of Spalax hypoxia induced genes we found highly significant overrepresentation of groups of genes involved in anti apoptosis, cancer, embryonic/sexual development, epidermal growth factor receptor binding, coordinated suppression and activation of distinct groups of transcription factors and membrane receptors, in addition to angiogenic related processes. We also detected hypoxia induced increases of different critical Spalax hub gene transcripts, including antiangiogenic genes associated with cancer tolerance in Down syndrome human individuals. CONCLUSIONS: This is the most comprehensive study of Spalax large scale gene expression response to hypoxia to date, and the first to use custom Spalax microarrays. Our work presents novel patterns that may underlie mechanisms with critical importance to the evolution of hypoxia tolerance, with special relevance to medical research. |
format | Online Article Text |
id | pubmed-3533650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35336502013-01-03 Transcriptome analysis of the spalax hypoxia survival response includes suppression of apoptosis and tight control of angiogenesis Malik, Assaf Korol, Abraham Weber, Mathias Hankeln, Thomas Avivi, Aaron Band, Mark BMC Genomics Research Article BACKGROUND: The development of complex responses to hypoxia has played a key role in the evolution of mammals, as inadequate response to this condition is frequently associated with cardiovascular diseases, developmental disorders, and cancers. Though numerous studies have used mice and rats in order to explore mechanisms that contribute to hypoxia tolerance, these studies are limited due to the high sensitivity of most rodents to severe hypoxia. The blind subterranean mole rat Spalax is a hypoxia tolerant rodent, which exhibits unique longevity and therefore has invaluable potential in hypoxia and cancer research. RESULTS: Using microarrays, transcript abundance was measured in brain and muscle tissues from Spalax and rat individuals exposed to acute and chronic hypoxia for varying durations. We found that Spalax global gene expression response to hypoxia differs from that of rat and is characterized by the activation of functional groups of genes that have not been strongly associated with the response to hypoxia in hypoxia sensitive mammals. Using functional enrichment analysis of Spalax hypoxia induced genes we found highly significant overrepresentation of groups of genes involved in anti apoptosis, cancer, embryonic/sexual development, epidermal growth factor receptor binding, coordinated suppression and activation of distinct groups of transcription factors and membrane receptors, in addition to angiogenic related processes. We also detected hypoxia induced increases of different critical Spalax hub gene transcripts, including antiangiogenic genes associated with cancer tolerance in Down syndrome human individuals. CONCLUSIONS: This is the most comprehensive study of Spalax large scale gene expression response to hypoxia to date, and the first to use custom Spalax microarrays. Our work presents novel patterns that may underlie mechanisms with critical importance to the evolution of hypoxia tolerance, with special relevance to medical research. BioMed Central 2012-11-13 /pmc/articles/PMC3533650/ /pubmed/23148642 http://dx.doi.org/10.1186/1471-2164-13-615 Text en Copyright ©2012 Malik et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Malik, Assaf Korol, Abraham Weber, Mathias Hankeln, Thomas Avivi, Aaron Band, Mark Transcriptome analysis of the spalax hypoxia survival response includes suppression of apoptosis and tight control of angiogenesis |
title | Transcriptome analysis of the spalax hypoxia survival response includes suppression of apoptosis and tight control of angiogenesis |
title_full | Transcriptome analysis of the spalax hypoxia survival response includes suppression of apoptosis and tight control of angiogenesis |
title_fullStr | Transcriptome analysis of the spalax hypoxia survival response includes suppression of apoptosis and tight control of angiogenesis |
title_full_unstemmed | Transcriptome analysis of the spalax hypoxia survival response includes suppression of apoptosis and tight control of angiogenesis |
title_short | Transcriptome analysis of the spalax hypoxia survival response includes suppression of apoptosis and tight control of angiogenesis |
title_sort | transcriptome analysis of the spalax hypoxia survival response includes suppression of apoptosis and tight control of angiogenesis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3533650/ https://www.ncbi.nlm.nih.gov/pubmed/23148642 http://dx.doi.org/10.1186/1471-2164-13-615 |
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