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Integrated microRNA-mRNA analyses reveal OPLL specific microRNA regulatory network using high-throughput sequencing
Ossification of the posterior longitudinal ligament (OPLL) is a genetic disorder which involves pathological heterotopic ossification of the spinal ligaments. Although studies have identified several genes that correlated with OPLL, the underlying regulation network is far from clear. Through small...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751494/ https://www.ncbi.nlm.nih.gov/pubmed/26868491 http://dx.doi.org/10.1038/srep21580 |
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author | Xu, Chen Chen, Yu Zhang, Hao Chen, Yuanyuan Shen, Xiaolong Shi, Changgui Liu, Yang Yuan, Wen |
author_facet | Xu, Chen Chen, Yu Zhang, Hao Chen, Yuanyuan Shen, Xiaolong Shi, Changgui Liu, Yang Yuan, Wen |
author_sort | Xu, Chen |
collection | PubMed |
description | Ossification of the posterior longitudinal ligament (OPLL) is a genetic disorder which involves pathological heterotopic ossification of the spinal ligaments. Although studies have identified several genes that correlated with OPLL, the underlying regulation network is far from clear. Through small RNA sequencing, we compared the microRNA expressions of primary posterior longitudinal ligament cells form OPLL patients with normal patients (PLL) and identified 218 dysregulated miRNAs (FDR < 0.01). Furthermore, assessing the miRNA profiling data of multiple cell types, we found these dysregulated miRNAs were mostly OPLL specific. In order to decipher the regulation network of these OPLL specific miRNAs, we integrated mRNA expression profiling data with miRNA sequencing data. Through computational approaches, we showed the pivotal roles of these OPLL specific miRNAs in heterotopic ossification of longitudinal ligament by discovering highly correlated miRNA/mRNA pairs that associated with skeletal system development, collagen fibril organization, and extracellular matrix organization. The results of which provide strong evidence that the miRNA regulatory networks we established may indeed play vital roles in OPLL onset and progression. To date, this is the first systematic analysis of the micronome in OPLL, and thus may provide valuable resources in finding novel treatment and diagnostic targets of OPLL. |
format | Online Article Text |
id | pubmed-4751494 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47514942016-02-22 Integrated microRNA-mRNA analyses reveal OPLL specific microRNA regulatory network using high-throughput sequencing Xu, Chen Chen, Yu Zhang, Hao Chen, Yuanyuan Shen, Xiaolong Shi, Changgui Liu, Yang Yuan, Wen Sci Rep Article Ossification of the posterior longitudinal ligament (OPLL) is a genetic disorder which involves pathological heterotopic ossification of the spinal ligaments. Although studies have identified several genes that correlated with OPLL, the underlying regulation network is far from clear. Through small RNA sequencing, we compared the microRNA expressions of primary posterior longitudinal ligament cells form OPLL patients with normal patients (PLL) and identified 218 dysregulated miRNAs (FDR < 0.01). Furthermore, assessing the miRNA profiling data of multiple cell types, we found these dysregulated miRNAs were mostly OPLL specific. In order to decipher the regulation network of these OPLL specific miRNAs, we integrated mRNA expression profiling data with miRNA sequencing data. Through computational approaches, we showed the pivotal roles of these OPLL specific miRNAs in heterotopic ossification of longitudinal ligament by discovering highly correlated miRNA/mRNA pairs that associated with skeletal system development, collagen fibril organization, and extracellular matrix organization. The results of which provide strong evidence that the miRNA regulatory networks we established may indeed play vital roles in OPLL onset and progression. To date, this is the first systematic analysis of the micronome in OPLL, and thus may provide valuable resources in finding novel treatment and diagnostic targets of OPLL. Nature Publishing Group 2016-02-12 /pmc/articles/PMC4751494/ /pubmed/26868491 http://dx.doi.org/10.1038/srep21580 Text en Copyright © 2016, 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 Xu, Chen Chen, Yu Zhang, Hao Chen, Yuanyuan Shen, Xiaolong Shi, Changgui Liu, Yang Yuan, Wen Integrated microRNA-mRNA analyses reveal OPLL specific microRNA regulatory network using high-throughput sequencing |
title | Integrated microRNA-mRNA analyses reveal OPLL specific microRNA regulatory network using high-throughput sequencing |
title_full | Integrated microRNA-mRNA analyses reveal OPLL specific microRNA regulatory network using high-throughput sequencing |
title_fullStr | Integrated microRNA-mRNA analyses reveal OPLL specific microRNA regulatory network using high-throughput sequencing |
title_full_unstemmed | Integrated microRNA-mRNA analyses reveal OPLL specific microRNA regulatory network using high-throughput sequencing |
title_short | Integrated microRNA-mRNA analyses reveal OPLL specific microRNA regulatory network using high-throughput sequencing |
title_sort | integrated microrna-mrna analyses reveal opll specific microrna regulatory network using high-throughput sequencing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751494/ https://www.ncbi.nlm.nih.gov/pubmed/26868491 http://dx.doi.org/10.1038/srep21580 |
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