Rosenberg Miriam I, Georges Sara A, Asawachaicharn Amy, Analau Erwin, Tapscott Stephen J
Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
J Cell Biol. 2006 Oct 9;175(1):77-85. doi: 10.1083/jcb.200603039.
Terminal differentiation of distinct cell types requires the transcriptional activation of differentiation-specific genes and the suppression of genes associated with the precursor cell. For example, the expression of utrophin (Utrn) is suppressed during skeletal muscle differentiation, and it is replaced at the sarcolemma by the related dystrophin protein. The MyoD transcription factor directly activates the expression of a large number of skeletal muscle genes, but also suppresses the expression of many genes. To characterize a mechanism of MyoD-mediated suppression of gene expression, we investigated two genes that are suppressed in fibroblasts converted to skeletal muscle by MyoD, follistatin-like 1 (Fstl1) and Utrn. MyoD directly activates the expression of a muscle-specific microRNA (miRNA), miR-206, which targets sequences in the Fstl1 and Utrn RNA, and these sequences are sufficient to suppress gene expression in the presence of miR-206. These findings demonstrate that MyoD, in addition to activating muscle-specific genes, induces miRNAs that repress gene expression during skeletal muscle differentiation.
不同细胞类型的终末分化需要分化特异性基因的转录激活以及与前体细胞相关基因的抑制。例如,在骨骼肌分化过程中,肌养蛋白(Utrn)的表达受到抑制,并且在肌膜处被相关的抗肌萎缩蛋白所取代。MyoD转录因子直接激活大量骨骼肌基因的表达,但也抑制许多基因的表达。为了表征MyoD介导的基因表达抑制机制,我们研究了两个在被MyoD转化为骨骼肌的成纤维细胞中被抑制的基因,卵泡抑素样1(Fstl1)和Utrn。MyoD直接激活一种肌肉特异性微小RNA(miRNA),即miR-206的表达,该miRNA靶向Fstl1和Utrn RNA中的序列,并且这些序列在存在miR-206的情况下足以抑制基因表达。这些发现表明,MyoD除了激活肌肉特异性基因外,还诱导miRNA在骨骼肌分化过程中抑制基因表达。