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Predicted Trans-Acting siRNAs in the Human Brain
Endogenous small non-coding RNAs play pivotal roles in regulating gene expression in eukaryotes. Many studies have investigated the function and molecular mechanism of microRNAs in the development and disease of various organisms via mRNA repression of protein-coding genes. Recent findings indicate...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4346901/ https://www.ncbi.nlm.nih.gov/pubmed/25654231 http://dx.doi.org/10.3390/ijms16023377 |
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author | Liu, Xiaoshuang Zhang, Guangxin Zhang, Changqing Wang, Jin |
author_facet | Liu, Xiaoshuang Zhang, Guangxin Zhang, Changqing Wang, Jin |
author_sort | Liu, Xiaoshuang |
collection | PubMed |
description | Endogenous small non-coding RNAs play pivotal roles in regulating gene expression in eukaryotes. Many studies have investigated the function and molecular mechanism of microRNAs in the development and disease of various organisms via mRNA repression of protein-coding genes. Recent findings indicate microRNAs might trigger the generation of trans-acting small interfering RNAs (ta-siRNAs). The interaction among different types of small RNA molecules reveals an even more complicated and elaborate pattern of RNA regulation during gene expression than previously thought. We developed a method for mining ta-siRNA sequences and evaluated the performance of our novel method using data from Arabidopsis thaliana. Additionally, using small RNA and degradome data for the human brain, we identified 155 small RNAs that satisfied ta-siRNA characteristics. The DRAXIN and ATCAY genes, which are preferentially expressed in the human brain, were predicted to be the targets of 12 potential ta-siRNAs. |
format | Online Article Text |
id | pubmed-4346901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-43469012015-04-03 Predicted Trans-Acting siRNAs in the Human Brain Liu, Xiaoshuang Zhang, Guangxin Zhang, Changqing Wang, Jin Int J Mol Sci Article Endogenous small non-coding RNAs play pivotal roles in regulating gene expression in eukaryotes. Many studies have investigated the function and molecular mechanism of microRNAs in the development and disease of various organisms via mRNA repression of protein-coding genes. Recent findings indicate microRNAs might trigger the generation of trans-acting small interfering RNAs (ta-siRNAs). The interaction among different types of small RNA molecules reveals an even more complicated and elaborate pattern of RNA regulation during gene expression than previously thought. We developed a method for mining ta-siRNA sequences and evaluated the performance of our novel method using data from Arabidopsis thaliana. Additionally, using small RNA and degradome data for the human brain, we identified 155 small RNAs that satisfied ta-siRNA characteristics. The DRAXIN and ATCAY genes, which are preferentially expressed in the human brain, were predicted to be the targets of 12 potential ta-siRNAs. MDPI 2015-02-03 /pmc/articles/PMC4346901/ /pubmed/25654231 http://dx.doi.org/10.3390/ijms16023377 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Liu, Xiaoshuang Zhang, Guangxin Zhang, Changqing Wang, Jin Predicted Trans-Acting siRNAs in the Human Brain |
title | Predicted Trans-Acting siRNAs in the Human Brain |
title_full | Predicted Trans-Acting siRNAs in the Human Brain |
title_fullStr | Predicted Trans-Acting siRNAs in the Human Brain |
title_full_unstemmed | Predicted Trans-Acting siRNAs in the Human Brain |
title_short | Predicted Trans-Acting siRNAs in the Human Brain |
title_sort | predicted trans-acting sirnas in the human brain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4346901/ https://www.ncbi.nlm.nih.gov/pubmed/25654231 http://dx.doi.org/10.3390/ijms16023377 |
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