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The interplay between the master transcription factor PU.1 and miR-424 regulates human monocyte/macrophage differentiation.by: A Rosa, M Ballarino, A Sorrentino, O Sthandier, FG De Angelis, M Marchioni, B Masella, A Guarini, A Fatica, C Peschle, I Bozzoni
Proc Natl Acad Sci U S A, Vol. 104, No. 50. (11 December 2007), pp. 19849-19854.
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AbstractWe describe a pathway by which the master transcription factor PU.1 regulates human monocyte/macrophage differentiation. This includes miR-424 and the transcriptional factor NFI-A. We show that PU.1 and these two components are interlinked in a finely tuned temporal and regulatory circuitry: PU.1 activates the transcription of miR-424, and this up-regulation is involved in stimulating monocyte differentiation through miR-424-dependent translational repression of NFI-A. In turn, the decrease in NFI-A levels is important for the activation of differentiation-specific genes such as M-CSFr. In line with these data, both RNAi against NFI-A and ectopic expression of miR-424 in precursor cells enhance monocytic differentiation, whereas the ectopic expression of NFI-A has an opposite effect. The interplay among these three components was demonstrated in myeloid cell lines as well as in human CD34+ differentiation. These data point to the important role of miR-424 and NFI-A in controlling the monocyte/macrophage differentiation program.
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