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Genome-wide microRNA profiling in human fetal nervous tissues by oligonucleotide microarray
OBJECTS: Our objective was to develop an oligonucleotide DNA microarray (OMA) for genome-wide microRNA profiling and use this method to find miRNAs, which control organic development especially for nervous system. MATERIALS AND METHODS: Eighteen organic samples included cerebrum and spinal cord samp...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1705512/ https://www.ncbi.nlm.nih.gov/pubmed/16983573 http://dx.doi.org/10.1007/s00381-006-0173-9 |
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author | Zhao, Jian-Jun Hua, You-Jia Sun, Da-Guang Meng, Xian-Xin Xiao, Hua-Sheng Ma, Xu |
author_facet | Zhao, Jian-Jun Hua, You-Jia Sun, Da-Guang Meng, Xian-Xin Xiao, Hua-Sheng Ma, Xu |
author_sort | Zhao, Jian-Jun |
collection | PubMed |
description | OBJECTS: Our objective was to develop an oligonucleotide DNA microarray (OMA) for genome-wide microRNA profiling and use this method to find miRNAs, which control organic development especially for nervous system. MATERIALS AND METHODS: Eighteen organic samples included cerebrum and spinal cord samples from two aborted human fetuses. One was 12 gestational weeks old (G12w) and the other was 24 gestational weeks old (G24w). Global miRNA expression patterns of different organs were investigated using OMA and Northern blot. CONCLUSION: The OMA revealed that 72–83% of miRNAs were expressed in human fetal organs. A series of microRNAs were found specifically and higher-expressed in the human fetal nervous system and confirmed consistently by Northern blot, which may play a critical role in nervous system development. |
format | Text |
id | pubmed-1705512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-17055122006-12-18 Genome-wide microRNA profiling in human fetal nervous tissues by oligonucleotide microarray Zhao, Jian-Jun Hua, You-Jia Sun, Da-Guang Meng, Xian-Xin Xiao, Hua-Sheng Ma, Xu Childs Nerv Syst Original Paper OBJECTS: Our objective was to develop an oligonucleotide DNA microarray (OMA) for genome-wide microRNA profiling and use this method to find miRNAs, which control organic development especially for nervous system. MATERIALS AND METHODS: Eighteen organic samples included cerebrum and spinal cord samples from two aborted human fetuses. One was 12 gestational weeks old (G12w) and the other was 24 gestational weeks old (G24w). Global miRNA expression patterns of different organs were investigated using OMA and Northern blot. CONCLUSION: The OMA revealed that 72–83% of miRNAs were expressed in human fetal organs. A series of microRNAs were found specifically and higher-expressed in the human fetal nervous system and confirmed consistently by Northern blot, which may play a critical role in nervous system development. Springer-Verlag 2006-09-16 2006-11 /pmc/articles/PMC1705512/ /pubmed/16983573 http://dx.doi.org/10.1007/s00381-006-0173-9 Text en © Springer-Verlag 2006 |
spellingShingle | Original Paper Zhao, Jian-Jun Hua, You-Jia Sun, Da-Guang Meng, Xian-Xin Xiao, Hua-Sheng Ma, Xu Genome-wide microRNA profiling in human fetal nervous tissues by oligonucleotide microarray |
title | Genome-wide microRNA profiling in human fetal nervous tissues by oligonucleotide microarray |
title_full | Genome-wide microRNA profiling in human fetal nervous tissues by oligonucleotide microarray |
title_fullStr | Genome-wide microRNA profiling in human fetal nervous tissues by oligonucleotide microarray |
title_full_unstemmed | Genome-wide microRNA profiling in human fetal nervous tissues by oligonucleotide microarray |
title_short | Genome-wide microRNA profiling in human fetal nervous tissues by oligonucleotide microarray |
title_sort | genome-wide microrna profiling in human fetal nervous tissues by oligonucleotide microarray |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1705512/ https://www.ncbi.nlm.nih.gov/pubmed/16983573 http://dx.doi.org/10.1007/s00381-006-0173-9 |
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