Smad Proteins Bind a Conserved RNA Sequence to Promote MicroRNA Maturation by Drosha

被引:418
作者
Davis, Brandi N. [1 ,2 ]
Hilyard, Aaron C. [2 ]
Nguyen, Peter H. [2 ]
Lagna, Giorgio [2 ]
Hata, Akiko [1 ,2 ]
机构
[1] Tufts Univ, Sch Med, Dept Biochem, Medford, MA 02155 USA
[2] Tufts Med Ctr, Mol Cardiol Res Inst, Boston, MA 02111 USA
关键词
TRANSCRIPTION FACTORS; COMPLEX; BETA; INHIBITION; BIOGENESIS; MECHANISMS; HELICASE; MIRNAS; LIN28; P53;
D O I
10.1016/j.molcel.2010.07.011
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
The signal transducers of the transforming growth factor beta (TGF beta)/bone morphogenetic protein (BMP), the Smads, promote the expression of a subset of miRNAs by facilitating the cleavage reaction by Drosha. The mechanism that limits Smad-mediated processing to a selective group of miRNAs remained hitherto unexplored. In this study, we expand the number of TGF beta/BMP-regulated miRNAs (T/B-miRs) to 20. Of interest, a majority of T/B-miRs contain a consensus sequence (R-SBE) within the stem region of the primary transcripts of T/B-miRs (pri-T/B-miRs). Here, we demonstrate that Smads directly bind the R-SBE. Mutation of the R-SBE abrogates TGF beta/BMP-induced recruitment of Smads, Drosha, and DGCR8 to pri-T/B-miRs and impairs their processing, whereas introduction of R-SBE to unregulated pri-miRNAs is sufficient to recruit Smads and to allow regulation by TGF beta/BMP. Thus, Smads are multifunctional proteins that modulate gene expression transcriptionally through DNA binding and post-transcriptionally through pri-miRNA binding and regulation of miRNA processing.
引用
收藏
页码:373 / 384
页数:12
相关论文
共 26 条
[1]
Origins and Mechanisms of miRNAs and siRNAs [J].
Carthew, Richard W. ;
Sontheimer, Erik J. .
CELL, 2009, 136 (04) :642-655
[2]
Having it both ways: transcription factors that bind DNA and RNA [J].
Cassiday, LA ;
Maher, LJ .
NUCLEIC ACIDS RESEARCH, 2002, 30 (19) :4118-4126
[3]
SMAD proteins control DROSHA-mediated microRNA maturation [J].
Davis, Brandi N. ;
Hilyard, Aaron C. ;
Lagna, Giorgio ;
Hata, Akiko .
NATURE, 2008, 454 (7200) :56-U2
[4]
Regulation of MicroRNA Biogenesis: A miRiad of mechanisms [J].
Davis, Brandi N. ;
Hata, Akiko .
CELL COMMUNICATION AND SIGNALING, 2009, 7
[5]
Direct binding of Smad3 and Smad4 to critical TGFβ-inducible elements in the promoter of human plasminogen activator inhibitor-type 1 gene [J].
Dennler, S ;
Itoh, S ;
Vivien, D ;
ten Dijke, P ;
Huet, S ;
Gauthier, JM .
EMBO JOURNAL, 1998, 17 (11) :3091-3100
[6]
RETRACTED: DEAD-box RNA helicase subunits of the Drosha complex are required for processing of rRNA and a subset of microRNAs (Retracted article. See vol. 16, pg. 1126, 2014) [J].
Fukuda, Toru ;
Yamagata, Kaoru ;
Fujiyama, Sally ;
Matsumoto, Takahiro ;
Koshida, Iori ;
Yoshimura, Kimihiro ;
Mihara, Masatomo ;
Naitou, Masanori ;
Endoh, Hideki ;
Nakamura, Takashi ;
Akimoto, Chihiro ;
Yamamoto, Yoko ;
Katagiri, Takenobu ;
Foulds, Charles ;
Takezawa, Shinichiro ;
Kitagawa, Hirochika ;
Takeyama, Ken-ichi ;
O'Malley, Bert W. ;
Kato, Shigeaki .
NATURE CELL BIOLOGY, 2007, 9 (05) :604-U221
[7]
The multifunctional RNA-binding protein hnRNP A1 is required for processing of miR-18a [J].
Guil, Sonia ;
Caceres, Javier F. .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2007, 14 (07) :591-596
[8]
Molecular basis for the recognition of primary microRNAs by the Drosha-DGCR8 complex [J].
Han, Jinju ;
Lee, Yoontae ;
Yeom, Kyu-Hyeon ;
Nam, Jin-Wu ;
Heo, Inha ;
Rhee, Je-Keun ;
Sohn, Sun Young ;
Cho, Yunje ;
Zhang, Byoung-Tak ;
Kim, V. Narry .
CELL, 2006, 125 (05) :887-901
[9]
The Drosha-DGCR8 complex in primary microRNA processing [J].
Han, JJ ;
Lee, Y ;
Yeom, KH ;
Kim, YK ;
Jin, H ;
Kim, VN .
GENES & DEVELOPMENT, 2004, 18 (24) :3016-3027
[10]
Biogenesis of small RNAs in animals [J].
Kim, V. Narry ;
Han, Jinju ;
Siomi, Mikiko C. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2009, 10 (02) :126-139