Bosson Andrew D, Zamudio Jesse R, Sharp Phillip A
David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139, USA; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Mol Cell. 2014 Nov 6;56(3):347-359. doi: 10.1016/j.molcel.2014.09.018. Epub 2014 Oct 23.
Target competition (ceRNA crosstalk) within miRNA-regulated gene networks has been proposed to influence biological systems. To assess target competition, we characterize and quantitate miRNA networks in two cell types. Argonaute iCLIP reveals that hierarchical binding of high- to low-affinity miRNA targets is a key characteristic of in vivo activity. Quantification of cellular miRNA and mRNA/ncRNA target pool levels indicates that miRNA:target pool ratios and an affinity partitioned target pool accurately predict in vivo Ago binding profiles and miRNA susceptibility to target competition. Using single-cell reporters, we directly test predictions and estimate that ?3,000 additional high-affinity target sites can affect active miRNA families with low endogenous miRNA:target ratios, such as miR-92/25. In contrast, the highly expressed miR-294 and let-7 families are not susceptible to increases of nearly 10,000 sites. These results show differential susceptibility based on endogenous miRNA:target pool ratios and provide a physiological context for ceRNA competition in vivo.
有人提出,miRNA调控基因网络中的靶标竞争(ceRNA串扰)会影响生物系统。为了评估靶标竞争,我们对两种细胞类型中的miRNA网络进行了表征和定量分析。AGO蛋白免疫交联分析显示,高亲和力miRNA靶标与低亲和力miRNA靶标之间的分级结合是体内活性的关键特征。细胞miRNA和mRNA/ncRNA靶标库水平的定量分析表明,miRNA:靶标库比率以及亲和力划分的靶标库能够准确预测体内AGO蛋白结合谱以及miRNA对靶标竞争的敏感性。使用单细胞报告基因,我们直接检验了这些预测,并估计另外约3000个高亲和力靶位点会影响内源性miRNA:靶标比率较低的活性miRNA家族,如miR-92/25。相比之下,高表达的miR-294和let-7家族对近10000个位点的增加不敏感。这些结果表明,基于内源性miRNA:靶标库比率存在不同的敏感性,并为体内ceRNA竞争提供了生理背景。