Widespread regulatory activity of vertebrate microRNA* species

被引:270
作者
Yang, Jr-Shiuan [5 ,6 ]
Phillips, Michael D. [4 ]
Betel, Doron [3 ]
Mu, Ping [2 ]
Ventura, Andrea [2 ]
Siepel, Adam C. [4 ]
Chen, Kevin C. [1 ]
Lai, Eric C. [6 ]
机构
[1] Rutgers State Univ, BioMaPS Inst Quantitat Biol, Piscataway, NJ 08854 USA
[2] Sloan Kettering Inst, Canc Biol & Genet Program, New York, NY 10065 USA
[3] Sloan Kettering Inst, Computat Biol Ctr, New York, NY 10065 USA
[4] Cornell Univ, Dept Biol Stat & Computat Biol, Triinst Program Computat Biol & Med, Ithaca, NY 14853 USA
[5] Cornell Univ, Weill Grad Sch Med Sci, Program Mol Biol, New York, NY 10065 USA
[6] Sloan Kettering Inst, Dept Dev Biol, New York, NY 10065 USA
关键词
3 ' UTR; microRNA*; post-transcriptional repression; TARGET PREDICTIONS; TUMOR-SUPPRESSOR; RNA INTERFERENCE; GENE-EXPRESSION; SIRNAS; IDENTIFICATION; RECOGNITION; MIR-34A; PROTEIN; TRANSCRIPTS;
D O I
10.1261/rna.2537911
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
An obligate intermediate during microRNA (miRNA) biogenesis is an similar to 22-nucleotide RNA duplex, from which the mature miRNA is preferentially incorporated into a silencing complex. Its partner miRNA* species is generally regarded as a passenger RNA, whose regulatory capacity has not been systematically examined in vertebrates. Our bioinformatic analyses demonstrate that a substantial fraction of miRNA* species are stringently conserved over vertebrate evolution, collectively exhibit greatest conservation in their seed regions, and define complementary motifs whose conservation across vertebrate 3'-UTR evolution is statistically significant. Functional tests of 22 miRNA expression constructs revealed that a majority could repress both miRNA and miRNA* perfect match reporters, and the ratio of miRNA: miRNA* sensor repression was correlated with the endogenous ratio of miRNA: miRNA* reads. Analysis of microarray data provided transcriptome-wide evidence for the regulation of seed-matched targets for both mature and star strand species of several miRNAs relevant to oncogenesis, including mir-17, mir-34a, and mir-19. Finally, 3'-UTR sensor assays and mutagenesis tests confirmed direct repression of five miR-19* targets via star seed sites. Overall, our data demonstrate that miRNA* species have demonstrable impact on vertebrate regulatory networks and should be taken into account in studies of miRNA functions and their contribution to disease states.
引用
收藏
页码:312 / 326
页数:15
相关论文
共 78 条
[1]   Characterization of endogenous human Argonautes and their miRNA partners in RNA silencing [J].
Azuma-Mukai, Asuka ;
Oguri, Hideo ;
Mituyama, Toutai ;
Qian, Zhi Rong ;
Asai, Kiyoshi ;
Siomi, Haruhiko ;
Siomi, Mikiko C. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (23) :7964-7969
[2]   Mouse ES cells express endogenous shRNAs, siRNAs, and other Microprocessor-independent, Dicer-dependent small RNAs [J].
Babiarz, Joshua E. ;
Ruby, J. Graham ;
Wang, Yangming ;
Bartel, David P. ;
Blelloch, Robert .
GENES & DEVELOPMENT, 2008, 22 (20) :2773-2785
[3]   The impact of microRNAs on protein output [J].
Baek, Daehyun ;
Villen, Judit ;
Shin, Chanseok ;
Camargo, Fernando D. ;
Gygi, Steven P. ;
Bartel, David P. .
NATURE, 2008, 455 (7209) :64-U38
[4]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[5]   Comprehensive modeling of microRNA targets predicts functional non-conserved and non-canonical sites [J].
Betel, Doron ;
Koppal, Anjali ;
Agius, Phaedra ;
Sander, Chris ;
Leslie, Christina .
GENOME BIOLOGY, 2010, 11 (08)
[6]   Principles of MicroRNA-target recognition [J].
Brennecke, J ;
Stark, A ;
Russell, RB ;
Cohen, SM .
PLOS BIOLOGY, 2005, 3 (03) :404-418
[7]   Revisiting the principles of microRNA target recognition and mode of action [J].
Brodersen, Peter ;
Voinnet, Olivier .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2009, 10 (02) :141-148
[8]   RNA sequence analysis defines Dicer's role in mouse embryonic stem cells [J].
Calabrese, J. Mauro ;
Seila, Amy C. ;
Yeo, Gene W. ;
Sharp, Phillip A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (46) :18097-18102
[9]   Transactivation of miR-34a by p53 broadly influences gene expression and promotes apoptosis [J].
Chang, Tsung-Cheng ;
Wentzel, Erik A. ;
Kent, Oliver A. ;
Ramachandran, Kalyani ;
Mullendore, Michael ;
Lee, Kwang Hyuck ;
Feldmann, Georg ;
Yamakuchi, Munekazu ;
Ferlito, Marcella ;
Lowenstein, Charles J. ;
Arking, Dan E. ;
Beer, Michael A. ;
Maitra, Anirban ;
Mendell, Joshua T. .
MOLECULAR CELL, 2007, 26 (05) :745-752
[10]   MicroRNAs modulate hematopoietic lineage differentiation [J].
Chen, CZ ;
Li, L ;
Lodish, HF ;
Bartel, DP .
SCIENCE, 2004, 303 (5654) :83-86