Coordinated Networks of microRNAs and Transcription Factors with Evolutionary Perspectives

被引:15
作者
Iwama, Hisakazu [1 ,2 ]
机构
[1] Kagawa Univ, Life Sci Res Ctr, Miki, Kagawa 7610793, Japan
[2] Kagawa Univ, Fac Med, Miki, Kagawa 7610793, Japan
来源
MICRORNA CANCER REGULATION: ADVANCED CONCEPTS, BIOINFORMATICS AND SYSTEMS BIOLOGY TOOLS | 2013年 / 774卷
关键词
MicroRNA; Transcription factor; Coordinated regulation; regulatory network; Redundancy; Natural selection; OPEN-ACCESS DATABASE; CANONICAL MICRORNAS; GENE-EXPRESSION; PROTEIN; MOTIFS; BINDING; TARGETS; PREDICTION; IDENTIFICATION; IMPACT;
D O I
10.1007/978-94-007-5590-1_10
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) and transcription factors (TFs) are two major classes of trans-regulators in gene regulatory networks. Coordination between miRNAs and TFs has been demonstrated by individual studies on developmental processes and the pathogenesis of various cancers. Systematic computational approaches have an advantage in elucidating global network features of the miRNA-TF coordinated regulation. miRNAs and TFs have distinct molecular and evolutionary properties. In particular, miRNA genes have a rapid turnover of birth-and-death processes during evolution, and their effects are widespread but modest. Therefore, miRNAs and TFs are considered to have different contributions to their coordination. The miRNA-TF coordinated feedforward circuits are considered to cause significant increases in redundancy but drastically reduce the target gene repertoire, which poses the question, to what extent is miRNA-TF coordination beneficial? Evolutionary analyses provide wide perspectives on the features of miRNA-TF coordinated regulatory networks at a systems level.
引用
收藏
页码:169 / 187
页数:19
相关论文
共 116 条
[1]   Drosophila microRNAs exhibit diverse spatial expression patterns during embryonic development [J].
Aboobaker, AA ;
Tomancak, P ;
Patel, N ;
Rubin, GM ;
Lai, EC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (50) :18017-18022
[2]   Evolution of microRNA genes by inverted duplication of target gene sequences in Arabidopsis thaliana [J].
Allen, E ;
Xie, ZX ;
Gustafson, AM ;
Sung, GH ;
Spatafora, JW ;
Carrington, JC .
NATURE GENETICS, 2004, 36 (12) :1282-1290
[3]   Network motifs: theory and experimental approaches [J].
Alon, Uri .
NATURE REVIEWS GENETICS, 2007, 8 (06) :450-461
[4]  
Alon Uri, 2006, An Introduction to Systems Biology: Design Principles of Biological Circuits
[5]   Neuronal subtype-specific genes that control corticospinal motor neuron development in vivo [J].
Arlotta, P ;
Molyneaux, BJ ;
Chen, J ;
Inoue, J ;
Kominami, R ;
Macklis, JD .
NEURON, 2005, 45 (02) :207-221
[6]   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
[7]   MicroRNA expression detected by oligonucleotide microarrays: System establishment and expression profiling in human tissues [J].
Barad, O ;
Meiri, E ;
Avniel, A ;
Aharonov, R ;
Barzilai, A ;
Bentwich, I ;
Einav, U ;
Glad, S ;
Hurban, P ;
Karov, Y ;
Lobenhofer, EK ;
Sharon, E ;
Shiboleth, YM ;
Shtutman, M ;
Bentwich, Z ;
Einat, P .
GENOME RESEARCH, 2004, 14 (12) :2486-2494
[8]   EDGEdb:: a transcription factor-DNA Interaction database for the analysis of C-elegans differential gene expression [J].
Barrasa, M. Inmaculada ;
Vaglio, Philippe ;
Cavasino, Fabien ;
Jacotot, Laurent ;
Walhout, Albertha J. M. .
BMC GENOMICS, 2007, 8 (1)
[9]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[10]   Micromanagers of gene expression: the potentially widespread influence of metazoan microRNAs [J].
Bartel, DP ;
Chen, CZ .
NATURE REVIEWS GENETICS, 2004, 5 (05) :396-400