miR-34s keep osteoblasts bone idle

miR-34s keep osteoblasts bone idle T he development of bone-forming osteoblasts is controlled by transcription factors such as Runx2, Osterix, and ATF4, which, in turn, are regulated by a variety of nuclear proteins that inhibit or activate these factors. miRNAs have also been implicated in osteoblast differentiation, though little is known about the effects of individual miRNAs on skeletogenesis in vivo. Wei et al. now identify a family of miRNAs that restrict bone formation by targeting a key regulator of osteoblast differentiation (1). Embryonic mice whose osteoblast progenitors lack the miRNA-processing enzyme DICER have severe defects in skele-togenesis, whereas loss of the enzyme in adulthood causes enhances bone formation (2). Several studies have identifi ed individual miRNAs that regulate the differentiation of cultured osteoblasts in vitro (3, 4), but, says Gerard Karsenty, from Columbia University in New York, " there hasn't been a systematic analysis in vivo for the loss-of-function of a given miRNA. " Karsenty and colleagues, led by Jianwen Wei, therefore looked for miRNAs specifically expressed in differentiating osteoblasts. " We realized that two members of the miR-34 family—miR-34b and miR-34c—were highly enriched in osteoblasts but poorly expressed in many other cell types, " explains Karsenty. Moreover, these miRNAs were predicted to target the mRNA encoding Satb2, a nuclear matrix protein that promotes osteoblast differentiation by increasing the activity of Runx2 and ATF4 (5). " That caught our attention, " Karsenty says. To investigate the miR-34 family's function in bone formation, Wei et al. generated mice whose osteoblasts overexpressed miR-34c. These mice had fewer osteoblasts, slower rates of bone formation, and lower overall bone mass. Knocking out the miRNAs had the opposite effect: mice whose osteoblasts lacked both miR-34b and miR-34c had increased numbers of osteoblasts and enhanced bone formation. Indeed, embryonic mice initiated skeleto-genesis earlier in the absence of the miR-34 family, indicating that the miRNAs usually inhibit osteoblast differentiation. Wei and colleagues confi rmed that miR-34b and-c target a sequence in the 3Ј untranslated region of the Satb2 mRNA, blocking its translation in osteo-blasts. Satb2 protein levels were thus reduced in the bones of mice overexpressing miR-34c and elevated in mice lacking the two miRNAs. To determine whether the targeting of Satb2 explained the miR-34 family's effects on osteo-blast differentiation, the researchers removed one copy of the Satb2 gene from miR-34 knockout mice. Satb2 protein levels returned to normal, and the mice accumulated bone at the …