TY - JOUR
T1 - Muscle-specific microRNA miR-206 promotes muscle differentiation
AU - Hak, Kyun Kim
AU - Yong, Sun Lee
AU - Sivaprasad, Umasundari
AU - Malhotra, Ankit
AU - Dutta, Anindya
PY - 2006/8/28
Y1 - 2006/8/28
N2 - Three muscle-specific microRNAs, miR-206, -1, and -133, are induced during differentiation of C2C12 myoblasts in vitro. Transfection of miR-206 promotes differentiation despite the presence of serum, whereas inhibition of the microRNA by antisense oligonucleotide inhibits cell cycle withdrawal and differentiation, which are normally induced by serum deprivation. Among the many mRNAs that are down-regulated by miR-206, the p180 subunit of DNA polymerase a and three other genes are shown to be direct targets. Down-regulation of the polymerase inhibits DNA synthesis, an important component of the differentiation program. The direct targets are decreased by mRNA cleavage that is dependent on predicted microRNA target sites. Unlike small interfering RNA-directed cleavage, however, the 5′ ends of the cleavage fragments are distributed and not confined to the target sites, suggesting involvement of exonucleases in the degradation process. In addition, inhibitors of myogenic transcription factors, Id1-3 and MyoR, are decreased upon miR-206 introduction, suggesting the presence of additional mechanisms by which microRNAs enforce the differentiation program.
AB - Three muscle-specific microRNAs, miR-206, -1, and -133, are induced during differentiation of C2C12 myoblasts in vitro. Transfection of miR-206 promotes differentiation despite the presence of serum, whereas inhibition of the microRNA by antisense oligonucleotide inhibits cell cycle withdrawal and differentiation, which are normally induced by serum deprivation. Among the many mRNAs that are down-regulated by miR-206, the p180 subunit of DNA polymerase a and three other genes are shown to be direct targets. Down-regulation of the polymerase inhibits DNA synthesis, an important component of the differentiation program. The direct targets are decreased by mRNA cleavage that is dependent on predicted microRNA target sites. Unlike small interfering RNA-directed cleavage, however, the 5′ ends of the cleavage fragments are distributed and not confined to the target sites, suggesting involvement of exonucleases in the degradation process. In addition, inhibitors of myogenic transcription factors, Id1-3 and MyoR, are decreased upon miR-206 introduction, suggesting the presence of additional mechanisms by which microRNAs enforce the differentiation program.
UR - http://www.scopus.com/inward/record.url?scp=33748102321&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33748102321&partnerID=8YFLogxK
U2 - 10.1083/jcb.200603008
DO - 10.1083/jcb.200603008
M3 - Article
C2 - 16923828
AN - SCOPUS:33748102321
SN - 0021-9525
VL - 174
SP - 677
EP - 687
JO - Journal of Cell Biology
JF - Journal of Cell Biology
IS - 5
ER -