Advanced computational predictive models of miRNA-mRNA interaction efficiency

被引:0
作者
Bader, Sharon [1 ]
Tuller, Tamir [1 ,2 ]
机构
[1] Tel Aviv Univ, Dept Biomed Engn, Tel Aviv, Israel
[2] Tel Aviv Univ, Segol Sch Neurosci, Tel Aviv, Israel
关键词
MiRNAs; MRNA; Biophysics; Competition; Machine Learning; MICRORNA TARGETS; BIOGENESIS; BINDING; TRANSCRIPTOME; DETERMINANTS; RECOGNITION; SPECIFICITY; EXPRESSION; REPRESSION; STABILITY;
D O I
暂无
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
The modeling of miRNA-mRNA interactions holds significant implications for synthetic biology and human health. However, this research area presents specific challenges due to the multifaceted nature of mRNA downregulation by miRNAs, influenced by numerous factors including competition or synergism among miRNAs and mRNAs. In this study, we present an improved computational model for predicting miRNA-mRNA interactions, addressing aspects not previously modeled. Firstly, we integrated a novel set of features that significantly enhanced the predictor's performance. Secondly, we demonstrated the cell-specific nature of certain aspects of miRNA-mRNA interactions, highlighting the importance of designing models tailored to specific cell types for improved accuracy. Moreover, we introduce a miRNA binding site interaction model (miBSIM) that, for the first time, accounts for both the distribution of miRNA binding sites along the mRNA and their respective strengths in regulating mRNA stability. Our analysis suggests that distant miRNA sites often compete with each other, revealing the intricate interplay of binding site interactions. Overall, our new predictive model shows a significant improvement of up to 6.43% over previous models in the field.
引用
收藏
页码:1740 / 1754
页数:15
相关论文
共 77 条
[1]   Predicting effective microRNA target sites in mammalian mRNAs [J].
Agarwal, Vikram ;
Bell, George W. ;
Nam, Jin-Wu ;
Bartel, David P. .
ELIFE, 2015, 4
[2]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[3]   Molecular basis for target RNA recognition and cleavage by human RISC [J].
Ameres, Stefan Ludwig ;
Martinez, Javier ;
Schroeder, Renee .
CELL, 2007, 130 (01) :101-112
[4]   Target mRNA abundance dilutes microRNA and siRNA activity [J].
Arvey, Aaron ;
Larsson, Erik ;
Sander, Chris ;
Leslie, Christina S. ;
Marks, Debora S. .
MOLECULAR SYSTEMS BIOLOGY, 2010, 6
[5]   Metazoan MicroRNAs [J].
Bartel, David P. .
CELL, 2018, 173 (01) :20-51
[6]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[7]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[8]   New computational model for miRNA-mediated repression reveals novel regulatory roles of miRNA bindings inside the coding region [J].
Bergman, Shaked ;
Diament, Alon ;
Tuller, Tamir .
BIOINFORMATICS, 2020, 36 (22-23) :5398-5404
[9]   Principles of MicroRNA-target recognition [J].
Brennecke, J ;
Stark, A ;
Russell, RB ;
Cohen, SM .
PLOS BIOLOGY, 2005, 3 (03) :404-418
[10]   The biochemical basis for the cooperative action of microRNAs [J].
Briskin, Daniel ;
Wang, Peter Y. ;
Bartel, David P. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2020, 117 (30) :17764-17774