Genome-wide identification of Ago2 binding sites from mouse embryonic stem cells with and without mature microRNAs

被引:202
作者
Leung, Anthony K. L. [1 ]
Young, Amanda G. [1 ,2 ]
Bhutkar, Arjun [1 ]
Zheng, Grace X. [1 ]
Bosson, Andrew D. [1 ,2 ]
Nielsen, Cydney B. [2 ]
Sharp, Phillip A. [1 ,2 ]
机构
[1] MIT, Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[2] MIT, Dept Biol, Cambridge, MA USA
基金
美国国家卫生研究院;
关键词
DNA METHYLATION; PROTEIN; RNAS; EXPRESSION; DISCOVERY; CLIP; DETERMINANTS; SPECIFICITY; REPRESSION; TARGETS;
D O I
10.1038/nsmb.1991
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
MicroRNAs (miRNAs) are 19-22-nucleotide noncoding RNAs that post-transcriptionally regulate mRNA targets. We have identified endogenous miRNA binding sites in mouse embryonic stem cells (mESCs), by performing photo-cross-linking immunoprecipitation using antibodies to Argonaute (Ago2) followed by deep sequencing of RNAs (CLIP-seq). We also performed CLIP-seq in Dicer(-/-) mESCs that lack mature miRNAs, allowing us to define whether the association of Ago2 with the identified sites was miRNA dependent. A significantly enriched motif, GCACUU, was identified only in wild-type mESCs in 3' untranslated and coding regions. This motif matches the seed of a miRNA family that constitutes similar to 68% of the mESC miRNA population. Unexpectedly, a G-rich motif was enriched in sequences cross-linked to Ago2 in both the presence and absence of miRNAs. Expression analysis and reporter assays confirmed that the seed-related motif confers miRNA-directed regulation on host mRNAs and that the G-rich motif can modulate this regulation.
引用
收藏
页码:237 / U309
页数:9
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