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MicroRNA profiling of the murine hematopoietic system

BACKGROUND: MicroRNAs (miRNAs) are a class of recently discovered noncoding RNA genes that post-transcriptionally regulate gene expression. It is becoming clear that miRNAs play an important role in the regulation of gene expression during development. However, in mammals, expression data are princi...

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Autores principales: Monticelli, Silvia, Ansel, K Mark, Xiao, Changchun, Socci, Nicholas D, Krichevsky, Anna M, Thai, To-Ha, Rajewsky, Nikolaus, Marks, Debora S, Sander, Chris, Rajewsky, Klaus, Rao, Anjana, Kosik, Kenneth S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1273638/
https://www.ncbi.nlm.nih.gov/pubmed/16086853
http://dx.doi.org/10.1186/gb-2005-6-8-r71
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author Monticelli, Silvia
Ansel, K Mark
Xiao, Changchun
Socci, Nicholas D
Krichevsky, Anna M
Thai, To-Ha
Rajewsky, Nikolaus
Marks, Debora S
Sander, Chris
Rajewsky, Klaus
Rao, Anjana
Kosik, Kenneth S
author_facet Monticelli, Silvia
Ansel, K Mark
Xiao, Changchun
Socci, Nicholas D
Krichevsky, Anna M
Thai, To-Ha
Rajewsky, Nikolaus
Marks, Debora S
Sander, Chris
Rajewsky, Klaus
Rao, Anjana
Kosik, Kenneth S
author_sort Monticelli, Silvia
collection PubMed
description BACKGROUND: MicroRNAs (miRNAs) are a class of recently discovered noncoding RNA genes that post-transcriptionally regulate gene expression. It is becoming clear that miRNAs play an important role in the regulation of gene expression during development. However, in mammals, expression data are principally based on whole tissue analysis and are still very incomplete. RESULTS: We used oligonucleotide arrays to analyze miRNA expression in the murine hematopoietic system. Complementary oligonucleotides capable of hybridizing to 181 miRNAs were immobilized on a membrane and probed with radiolabeled RNA derived from low molecular weight fractions of total RNA from several different hematopoietic and neuronal cells. This method allowed us to analyze cell type-specific patterns of miRNA expression and to identify miRNAs that might be important for cell lineage specification and/or cell effector functions. CONCLUSION: This is the first report of systematic miRNA gene profiling in cells of the hematopoietic system. As expected, miRNA expression patterns were very different between hematopoietic and non-hematopoietic cells, with further subtle differences observed within the hematopoietic group. Interestingly, the most pronounced similarities were observed among fully differentiated effector cells (Th1 and Th2 lymphocytes and mast cells) and precursors at comparable stages of differentiation (double negative thymocytes and pro-B cells), suggesting that in addition to regulating the process of commitment to particular cellular lineages, miRNAs might have an important general role in the mechanism of cell differentiation and maintenance of cell identity.
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spelling pubmed-12736382005-10-29 MicroRNA profiling of the murine hematopoietic system Monticelli, Silvia Ansel, K Mark Xiao, Changchun Socci, Nicholas D Krichevsky, Anna M Thai, To-Ha Rajewsky, Nikolaus Marks, Debora S Sander, Chris Rajewsky, Klaus Rao, Anjana Kosik, Kenneth S Genome Biol Research BACKGROUND: MicroRNAs (miRNAs) are a class of recently discovered noncoding RNA genes that post-transcriptionally regulate gene expression. It is becoming clear that miRNAs play an important role in the regulation of gene expression during development. However, in mammals, expression data are principally based on whole tissue analysis and are still very incomplete. RESULTS: We used oligonucleotide arrays to analyze miRNA expression in the murine hematopoietic system. Complementary oligonucleotides capable of hybridizing to 181 miRNAs were immobilized on a membrane and probed with radiolabeled RNA derived from low molecular weight fractions of total RNA from several different hematopoietic and neuronal cells. This method allowed us to analyze cell type-specific patterns of miRNA expression and to identify miRNAs that might be important for cell lineage specification and/or cell effector functions. CONCLUSION: This is the first report of systematic miRNA gene profiling in cells of the hematopoietic system. As expected, miRNA expression patterns were very different between hematopoietic and non-hematopoietic cells, with further subtle differences observed within the hematopoietic group. Interestingly, the most pronounced similarities were observed among fully differentiated effector cells (Th1 and Th2 lymphocytes and mast cells) and precursors at comparable stages of differentiation (double negative thymocytes and pro-B cells), suggesting that in addition to regulating the process of commitment to particular cellular lineages, miRNAs might have an important general role in the mechanism of cell differentiation and maintenance of cell identity. BioMed Central 2005 2005-08-01 /pmc/articles/PMC1273638/ /pubmed/16086853 http://dx.doi.org/10.1186/gb-2005-6-8-r71 Text en Copyright © 2005 Monticelli et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Monticelli, Silvia
Ansel, K Mark
Xiao, Changchun
Socci, Nicholas D
Krichevsky, Anna M
Thai, To-Ha
Rajewsky, Nikolaus
Marks, Debora S
Sander, Chris
Rajewsky, Klaus
Rao, Anjana
Kosik, Kenneth S
MicroRNA profiling of the murine hematopoietic system
title MicroRNA profiling of the murine hematopoietic system
title_full MicroRNA profiling of the murine hematopoietic system
title_fullStr MicroRNA profiling of the murine hematopoietic system
title_full_unstemmed MicroRNA profiling of the murine hematopoietic system
title_short MicroRNA profiling of the murine hematopoietic system
title_sort microrna profiling of the murine hematopoietic system
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1273638/
https://www.ncbi.nlm.nih.gov/pubmed/16086853
http://dx.doi.org/10.1186/gb-2005-6-8-r71
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