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The transcriptional landscape of dorsal root ganglia after sciatic nerve transection
Following peripheral nerve injury, transcriptional responses are orchestrated to regulate the expression of numerous genes in the lesioned nerve, thus activating the intrinsic regeneration program. To better understand the molecular regulation of peripheral nerve regeneration, we aimed at investigat...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4649668/ https://www.ncbi.nlm.nih.gov/pubmed/26576491 http://dx.doi.org/10.1038/srep16888 |
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author | Li, Shiying Xue, Chengbin Yuan, Ying Zhang, Ruirui Wang, Yaxian Wang, Yongjun Yu, Bin Liu, Jie Ding, Fei Yang, Yuming Gu, Xiaosong |
author_facet | Li, Shiying Xue, Chengbin Yuan, Ying Zhang, Ruirui Wang, Yaxian Wang, Yongjun Yu, Bin Liu, Jie Ding, Fei Yang, Yuming Gu, Xiaosong |
author_sort | Li, Shiying |
collection | PubMed |
description | Following peripheral nerve injury, transcriptional responses are orchestrated to regulate the expression of numerous genes in the lesioned nerve, thus activating the intrinsic regeneration program. To better understand the molecular regulation of peripheral nerve regeneration, we aimed at investigating the transcriptional landscape of dorsal root ganglia (DRGs) after sciatic nerve transection in rats. The cDNA microarray analysis was used to identify thousands of genes that were differentially expressed at different time points post nerve injury (PNI). The results from Euclidean distance matrix, principal component analysis, and hierarchical clustering indicated that 2 nodal transitions in temporal gene expressions could segregate 3 distinct transcriptional phases within the period of 14 d PNI. The 3 phases were designated as “a stress response phase”, “a pre-regeneration phase”, and “a regeneration phase”, respectively, by referring to morphological observation of post-nerve-injury changes. The gene ontology (GO) analysis revealed the distinct features of biological process, cellular component, and molecular function at each transcriptional phase. Moreover, Ingenuity Pathway Analysis suggested that differentially expressed genes, mainly transcription factors and genes associated with neurite/axon growth, might be integrated into regulatory networks to mediate the regulation of peripheral nerve regeneration in a highly cooperative manner. |
format | Online Article Text |
id | pubmed-4649668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46496682015-11-23 The transcriptional landscape of dorsal root ganglia after sciatic nerve transection Li, Shiying Xue, Chengbin Yuan, Ying Zhang, Ruirui Wang, Yaxian Wang, Yongjun Yu, Bin Liu, Jie Ding, Fei Yang, Yuming Gu, Xiaosong Sci Rep Article Following peripheral nerve injury, transcriptional responses are orchestrated to regulate the expression of numerous genes in the lesioned nerve, thus activating the intrinsic regeneration program. To better understand the molecular regulation of peripheral nerve regeneration, we aimed at investigating the transcriptional landscape of dorsal root ganglia (DRGs) after sciatic nerve transection in rats. The cDNA microarray analysis was used to identify thousands of genes that were differentially expressed at different time points post nerve injury (PNI). The results from Euclidean distance matrix, principal component analysis, and hierarchical clustering indicated that 2 nodal transitions in temporal gene expressions could segregate 3 distinct transcriptional phases within the period of 14 d PNI. The 3 phases were designated as “a stress response phase”, “a pre-regeneration phase”, and “a regeneration phase”, respectively, by referring to morphological observation of post-nerve-injury changes. The gene ontology (GO) analysis revealed the distinct features of biological process, cellular component, and molecular function at each transcriptional phase. Moreover, Ingenuity Pathway Analysis suggested that differentially expressed genes, mainly transcription factors and genes associated with neurite/axon growth, might be integrated into regulatory networks to mediate the regulation of peripheral nerve regeneration in a highly cooperative manner. Nature Publishing Group 2015-11-18 /pmc/articles/PMC4649668/ /pubmed/26576491 http://dx.doi.org/10.1038/srep16888 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Li, Shiying Xue, Chengbin Yuan, Ying Zhang, Ruirui Wang, Yaxian Wang, Yongjun Yu, Bin Liu, Jie Ding, Fei Yang, Yuming Gu, Xiaosong The transcriptional landscape of dorsal root ganglia after sciatic nerve transection |
title | The transcriptional landscape of dorsal root ganglia after sciatic nerve transection |
title_full | The transcriptional landscape of dorsal root ganglia after sciatic nerve transection |
title_fullStr | The transcriptional landscape of dorsal root ganglia after sciatic nerve transection |
title_full_unstemmed | The transcriptional landscape of dorsal root ganglia after sciatic nerve transection |
title_short | The transcriptional landscape of dorsal root ganglia after sciatic nerve transection |
title_sort | transcriptional landscape of dorsal root ganglia after sciatic nerve transection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4649668/ https://www.ncbi.nlm.nih.gov/pubmed/26576491 http://dx.doi.org/10.1038/srep16888 |
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