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RNA-Mediated Gene Silencing in Hematopoietic Cells

In the past few years, the discovery of RNA-mediated gene silencing mechanisms, like RNA interference (RNAi), has revolutionized our understanding of eukaryotic gene expression. These mechanisms are activated by double-stranded RNA (dsRNA) and mediate gene silencing either by inducing the sequence-s...

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Detalles Bibliográficos
Autores principales: Venturini, Letizia, Eder, Matthias, Scherr, Michaela
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1559937/
https://www.ncbi.nlm.nih.gov/pubmed/17057372
http://dx.doi.org/10.1155/JBB/2006/87340
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author Venturini, Letizia
Eder, Matthias
Scherr, Michaela
author_facet Venturini, Letizia
Eder, Matthias
Scherr, Michaela
author_sort Venturini, Letizia
collection PubMed
description In the past few years, the discovery of RNA-mediated gene silencing mechanisms, like RNA interference (RNAi), has revolutionized our understanding of eukaryotic gene expression. These mechanisms are activated by double-stranded RNA (dsRNA) and mediate gene silencing either by inducing the sequence-specific degradation of complementary mRNA or by inhibiting mRNA translation. RNAi now provides a powerful experimental tool to elucidate gene function in vitro and in vivo, thereby opening new exciting perspectives in the fields of molecular analysis and eventually therapy of several diseases such as infections and cancer. In hematology, numerous studies have described the successful application of RNAi to better define the role of oncogenic fusion proteins in leukemogenesis and to explore therapeutic approaches in hematological malignancies. In this review, we highlight recent advances and caveats relating to the application of this powerful new methodology to hematopoiesis.
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spelling pubmed-15599372006-10-10 RNA-Mediated Gene Silencing in Hematopoietic Cells Venturini, Letizia Eder, Matthias Scherr, Michaela J Biomed Biotechnol Review Article In the past few years, the discovery of RNA-mediated gene silencing mechanisms, like RNA interference (RNAi), has revolutionized our understanding of eukaryotic gene expression. These mechanisms are activated by double-stranded RNA (dsRNA) and mediate gene silencing either by inducing the sequence-specific degradation of complementary mRNA or by inhibiting mRNA translation. RNAi now provides a powerful experimental tool to elucidate gene function in vitro and in vivo, thereby opening new exciting perspectives in the fields of molecular analysis and eventually therapy of several diseases such as infections and cancer. In hematology, numerous studies have described the successful application of RNAi to better define the role of oncogenic fusion proteins in leukemogenesis and to explore therapeutic approaches in hematological malignancies. In this review, we highlight recent advances and caveats relating to the application of this powerful new methodology to hematopoiesis. Hindawi Publishing Corporation 2006 2006-05-28 /pmc/articles/PMC1559937/ /pubmed/17057372 http://dx.doi.org/10.1155/JBB/2006/87340 Text en Copyright © 2006 Letizia Venturini et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Venturini, Letizia
Eder, Matthias
Scherr, Michaela
RNA-Mediated Gene Silencing in Hematopoietic Cells
title RNA-Mediated Gene Silencing in Hematopoietic Cells
title_full RNA-Mediated Gene Silencing in Hematopoietic Cells
title_fullStr RNA-Mediated Gene Silencing in Hematopoietic Cells
title_full_unstemmed RNA-Mediated Gene Silencing in Hematopoietic Cells
title_short RNA-Mediated Gene Silencing in Hematopoietic Cells
title_sort rna-mediated gene silencing in hematopoietic cells
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1559937/
https://www.ncbi.nlm.nih.gov/pubmed/17057372
http://dx.doi.org/10.1155/JBB/2006/87340
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