共 33 条
Bone morphogenetic protein-2 down-regulates miR-206 expression by blocking its maturation process
被引:69
作者:
Sato, Mari M.
[1
]
Nashimoto, Masayuki
[2
]
Katagiri, Takenobu
[3
]
Yawaka, Yasutaka
Tamura, Masato
[1
]
机构:
[1] Hokkaido Univ, Grad Sch Dent Med, Dept Biochem & Mol Biol, Sapporo, Hokkaido 0608586, Japan
[2] Niigata Univ Pharm & Appl Life Sci, Dept Appl Life Sci, Niigata, Japan
[3] Saitama Med Univ, Res Ctr Genom Med, Div Pathophysiol, Hidaka, Japan
基金:
日本学术振兴会;
关键词:
miR-206;
miRNA processing;
Bone morphogenetic protein;
Smad;
Myoblasts;
POSTTRANSCRIPTIONAL REGULATION;
DIFFERENTIATION PATHWAY;
FUNCTIONAL INTERACTION;
MICRORNA EXPRESSION;
C2C12;
MYOBLASTS;
RNA HELICASE;
SMAD;
MECHANISMS;
SKELETAL;
TRANSCRIPTION;
D O I:
10.1016/j.bbrc.2009.03.142
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
070307 [化学生物学];
071010 [生物化学与分子生物学];
摘要:
MicroRNAs (miRNAs) are small non-coding RNAs that are emerging as important post-transcriptional gene regulators. miR-206 is unique in that it is expressed only in skeletal muscle, including the myoblastic C2C12 cell line. In C2C12 cells, miR-206 expression was reduced dramatically after bone morphogenetic protein (BMP)-2 treatment. The down-regulation of miR-206 expression was also observed after co-transfection with constitutively-active Smad1 and Smad4, which are the intracellular signaling molecules of the BMP pathway. BMP-2 also reduced miR-206 expression in the presence of alpha-amanitin in a similar manner to that in the absence of alpha-amanitin. Moreover, the expression of pri-miR-206 was increased upon BMP-2 treatment for 6 h compared to that in the absence of BMP-2. These results suggested that BMP-2 down-regulates miR-206 expression at the post-transcriptional level, by inhibiting the processing of pri-miR-206 into mature miR-206, and that BMP-2 Could regulate miRNA biogenesis by a novel mechanism. Crown Copyright (C) 2009 Published by Elsevier Inc. All rights reserved.
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页码:125 / 129
页数:5
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