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HOXA9 regulates miR-155 in hematopoietic cells

HOXA9-mediated up-regulation of miR-155 was noted during an array-based analysis of microRNA expression in Hoxa9(−/−)bone marrow (BM) cells. HOXA9 induction of miR-155 was confirmed in these samples, as well as in wild-type versus Hoxa9-deficient marrow, using northern analysis and qRT–PCR. Infectio...

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Detalles Bibliográficos
Autores principales: Hu, Yu-Long, Fong, Stephen, Largman, Corey, Shen, Wei-Fang
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2938212/
https://www.ncbi.nlm.nih.gov/pubmed/20444872
http://dx.doi.org/10.1093/nar/gkq337
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author Hu, Yu-Long
Fong, Stephen
Largman, Corey
Shen, Wei-Fang
author_facet Hu, Yu-Long
Fong, Stephen
Largman, Corey
Shen, Wei-Fang
author_sort Hu, Yu-Long
collection PubMed
description HOXA9-mediated up-regulation of miR-155 was noted during an array-based analysis of microRNA expression in Hoxa9(−/−)bone marrow (BM) cells. HOXA9 induction of miR-155 was confirmed in these samples, as well as in wild-type versus Hoxa9-deficient marrow, using northern analysis and qRT–PCR. Infection of wild-type BM with HOXA9 expressing or GFP(+) control virus further confirmed HOXA9-mediated regulation of miR-155. miR-155 expression paralleled Hoxa9 mRNA expression in fractionated BM progenitors, being highest in the stem cell enriched pools. HOXA9 capacity to induce myeloid colony formation was blunted in miR-155-deficient BM cells, indicating that miR-155 is a downstream mediator of HOXA9 function in blood cells. Pu.1, an important regulator of myelopoiesis, was identified as a putative down stream target for miR-155. Although miR-155 was shown to down-regulate the Pu.1 protein, HOXA9 did not appear to modulate Pu.1 expression in murine BM cells.
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spelling pubmed-29382122010-09-13 HOXA9 regulates miR-155 in hematopoietic cells Hu, Yu-Long Fong, Stephen Largman, Corey Shen, Wei-Fang Nucleic Acids Res Molecular Biology HOXA9-mediated up-regulation of miR-155 was noted during an array-based analysis of microRNA expression in Hoxa9(−/−)bone marrow (BM) cells. HOXA9 induction of miR-155 was confirmed in these samples, as well as in wild-type versus Hoxa9-deficient marrow, using northern analysis and qRT–PCR. Infection of wild-type BM with HOXA9 expressing or GFP(+) control virus further confirmed HOXA9-mediated regulation of miR-155. miR-155 expression paralleled Hoxa9 mRNA expression in fractionated BM progenitors, being highest in the stem cell enriched pools. HOXA9 capacity to induce myeloid colony formation was blunted in miR-155-deficient BM cells, indicating that miR-155 is a downstream mediator of HOXA9 function in blood cells. Pu.1, an important regulator of myelopoiesis, was identified as a putative down stream target for miR-155. Although miR-155 was shown to down-regulate the Pu.1 protein, HOXA9 did not appear to modulate Pu.1 expression in murine BM cells. Oxford University Press 2010-09 2010-05-05 /pmc/articles/PMC2938212/ /pubmed/20444872 http://dx.doi.org/10.1093/nar/gkq337 Text en © The Author(s) 2010. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Molecular Biology
Hu, Yu-Long
Fong, Stephen
Largman, Corey
Shen, Wei-Fang
HOXA9 regulates miR-155 in hematopoietic cells
title HOXA9 regulates miR-155 in hematopoietic cells
title_full HOXA9 regulates miR-155 in hematopoietic cells
title_fullStr HOXA9 regulates miR-155 in hematopoietic cells
title_full_unstemmed HOXA9 regulates miR-155 in hematopoietic cells
title_short HOXA9 regulates miR-155 in hematopoietic cells
title_sort hoxa9 regulates mir-155 in hematopoietic cells
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2938212/
https://www.ncbi.nlm.nih.gov/pubmed/20444872
http://dx.doi.org/10.1093/nar/gkq337
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