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HOXA9 regulates miR-155 in hematopoietic cells
被引:36
|作者:
Hu, Yu-Long
Fong, Stephen
Largman, Corey
Shen, Wei-Fang
[1
]
机构:
[1] Dept Vet Affairs Med Ctr, Dept Med, San Francisco, CA 94143 USA
基金:
美国国家卫生研究院;
关键词:
STEM-CELLS;
DNA-BINDING;
HOMEODOMAIN PROTEINS;
MYELOID LEUKEMIAS;
B-CELL;
EXPRESSION;
MICRORNAS;
GENE;
HOMEOBOX;
DIFFERENTIATION;
D O I:
10.1093/nar/gkq337
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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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页码:5472 / 5478
页数:7
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