Argonaute CLIP-Seq reveals miRNA targetome diversity across tissue types

被引:72
作者
Clark, Peter M. [1 ]
Loher, Phillipe [1 ]
Quann, Kevin [1 ]
Brody, Jonathan [2 ]
Londin, Eric R. [1 ]
Rigoutsos, Isidore [1 ]
机构
[1] Thomas Jefferson Univ, Computat Med Ctr, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Dept Surg, Philadelphia, PA 19107 USA
基金
美国国家卫生研究院;
关键词
TRANSCRIPTOME-WIDE IDENTIFICATION; EMBRYONIC STEM-CELLS; RNA-BINDING PROTEIN; MESSENGER-RNA; MICRORNA TARGETS; CODING REGIONS; SITES; GENE; EXPRESSION; MODEL;
D O I
10.1038/srep05947
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
To date, analyses of individual targets have provided evidence of a miRNA targetome that extends beyond the boundaries of messenger RNAs (mRNAs) and can involve non-Watson-Crick base pairing in the miRNA seed region. Here we report our findings from analyzing 34 Argonaute HITS-CLIP datasets from several human and mouse cell types. Investigation of the architectural (i.e. bulge vs. contiguous pairs) and sequence (Watson-Crick vs. G:U pairs) preferences for human and mouse miRNAs revealed that many heteroduplexes are "non-canonical'' i.e. their seed region comprises G:U and bulge combinations. The genomic distribution of miRNA targets differed distinctly across cell types but remained congruent across biological replicates of the same cell type. For some cell types intergenic and intronic targets were more frequent whereas in other cell types mRNA targets prevailed. The findings suggest an expanded model of miRNA targeting that is more frequent than the standard model currently in use. Lastly, our analyses of data from different cell types and laboratories revealed consistent Ago-loaded miRNA profiles across replicates whereas, unexpectedly, the Ago-loaded targets exhibited a much more dynamic behavior across biological replicates.
引用
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页数:11
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