Cargando…
A novel microarray approach reveals new tissue-specific signatures of known and predicted mammalian microRNAs
Microarrays to examine the global expression levels of microRNAs (miRNAs) in a systematic in-parallel manner have become important tools to help unravel the functions of miRNAs and to understand their roles in RNA-based regulation and their implications in human diseases. We have established a novel...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1874652/ https://www.ncbi.nlm.nih.gov/pubmed/17355992 http://dx.doi.org/10.1093/nar/gkl1118 |
_version_ | 1782133496561532928 |
---|---|
author | Beuvink, Iwan Kolb, Fabrice A. Budach, Wolfgang Garnier, Arlette Lange, Joerg Natt, Francois Dengler, Uwe Hall, Jonathan Filipowicz, Witold Weiler, Jan |
author_facet | Beuvink, Iwan Kolb, Fabrice A. Budach, Wolfgang Garnier, Arlette Lange, Joerg Natt, Francois Dengler, Uwe Hall, Jonathan Filipowicz, Witold Weiler, Jan |
author_sort | Beuvink, Iwan |
collection | PubMed |
description | Microarrays to examine the global expression levels of microRNAs (miRNAs) in a systematic in-parallel manner have become important tools to help unravel the functions of miRNAs and to understand their roles in RNA-based regulation and their implications in human diseases. We have established a novel miRNA-specific microarray platform that enables the simultaneous expression analysis of both known and predicted miRNAs obtained from human or mouse origin. Chemically modified 2′-O-(2-methoxyethyl)-(MOE) oligoribonucleotide probes were arrayed onto Evanescent Resonance (ER) microchips by robotic spotting. Supplementing the complementary probes against miRNAs with carefully designed mismatch controls allowed for accurate sequence-specific determination of miRNA expression profiles obtained from a panel of mouse tissues. This revealed new expression signatures of known miRNAs as well as of novel miRNAs previously predicted using bioinformatic methods. Systematic confirmation of the array data with northern blotting and, in particular, real-time PCR suggests that the described microarray platform is a powerful tool to analyze miRNA expression patterns with rapid throughput and high fidelity. |
format | Text |
id | pubmed-1874652 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-18746522007-05-25 A novel microarray approach reveals new tissue-specific signatures of known and predicted mammalian microRNAs Beuvink, Iwan Kolb, Fabrice A. Budach, Wolfgang Garnier, Arlette Lange, Joerg Natt, Francois Dengler, Uwe Hall, Jonathan Filipowicz, Witold Weiler, Jan Nucleic Acids Res Methods Online Microarrays to examine the global expression levels of microRNAs (miRNAs) in a systematic in-parallel manner have become important tools to help unravel the functions of miRNAs and to understand their roles in RNA-based regulation and their implications in human diseases. We have established a novel miRNA-specific microarray platform that enables the simultaneous expression analysis of both known and predicted miRNAs obtained from human or mouse origin. Chemically modified 2′-O-(2-methoxyethyl)-(MOE) oligoribonucleotide probes were arrayed onto Evanescent Resonance (ER) microchips by robotic spotting. Supplementing the complementary probes against miRNAs with carefully designed mismatch controls allowed for accurate sequence-specific determination of miRNA expression profiles obtained from a panel of mouse tissues. This revealed new expression signatures of known miRNAs as well as of novel miRNAs previously predicted using bioinformatic methods. Systematic confirmation of the array data with northern blotting and, in particular, real-time PCR suggests that the described microarray platform is a powerful tool to analyze miRNA expression patterns with rapid throughput and high fidelity. Oxford University Press 2007-04 2007-03-13 /pmc/articles/PMC1874652/ /pubmed/17355992 http://dx.doi.org/10.1093/nar/gkl1118 Text en © 2007 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methods Online Beuvink, Iwan Kolb, Fabrice A. Budach, Wolfgang Garnier, Arlette Lange, Joerg Natt, Francois Dengler, Uwe Hall, Jonathan Filipowicz, Witold Weiler, Jan A novel microarray approach reveals new tissue-specific signatures of known and predicted mammalian microRNAs |
title | A novel microarray approach reveals new tissue-specific signatures of known and predicted mammalian microRNAs |
title_full | A novel microarray approach reveals new tissue-specific signatures of known and predicted mammalian microRNAs |
title_fullStr | A novel microarray approach reveals new tissue-specific signatures of known and predicted mammalian microRNAs |
title_full_unstemmed | A novel microarray approach reveals new tissue-specific signatures of known and predicted mammalian microRNAs |
title_short | A novel microarray approach reveals new tissue-specific signatures of known and predicted mammalian microRNAs |
title_sort | novel microarray approach reveals new tissue-specific signatures of known and predicted mammalian micrornas |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1874652/ https://www.ncbi.nlm.nih.gov/pubmed/17355992 http://dx.doi.org/10.1093/nar/gkl1118 |
work_keys_str_mv | AT beuvinkiwan anovelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas AT kolbfabricea anovelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas AT budachwolfgang anovelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas AT garnierarlette anovelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas AT langejoerg anovelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas AT nattfrancois anovelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas AT dengleruwe anovelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas AT halljonathan anovelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas AT filipowiczwitold anovelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas AT weilerjan anovelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas AT beuvinkiwan novelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas AT kolbfabricea novelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas AT budachwolfgang novelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas AT garnierarlette novelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas AT langejoerg novelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas AT nattfrancois novelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas AT dengleruwe novelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas AT halljonathan novelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas AT filipowiczwitold novelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas AT weilerjan novelmicroarrayapproachrevealsnewtissuespecificsignaturesofknownandpredictedmammalianmicrornas |