Use of target protector morpholinos to analyze the physiological roles of specific miRNA-mRNA pairs in vivo

被引:65
作者
Staton, Alison A. [1 ]
Giraldez, Antonio J. [1 ,2 ]
机构
[1] Yale Univ, Sch Med, Dept Genet, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Yale Stem Cell Ctr, New Haven, CT 06510 USA
基金
美国国家卫生研究院;
关键词
SYSTEMATIC IDENTIFICATION; MICRORNA EXPRESSION; CELL-MIGRATION; TRANSGENESIS; DROSOPHILA; ENCODES; SPONGES; DESIGN; FAMILY; SITES;
D O I
10.1038/nprot.2011.423
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs) regulate gene expression by pairing with complementary sequences in the 39 untranslated regions (UTRs) of transcripts. Although the molecular mechanism underlying miRNA biogenesis and activity is becoming better understood, determining the physiological role of the interaction of an miRNA with its target remains a challenge. A number of methods have been developed to inhibit individual miRNAs, but it can be difficult to determine which specific targets are responsible for any observed phenotypes. To address this problem, we use target protector (TPTP) morpholinos that interfere with a single miRNA-mRNA pair by binding specifically to the miRNA target sequence in the 39 UTR. In this protocol, we detail the steps for identifying miRNA targets, validating their regulation and using TPs to interrogate their function in zebrafish. Depending on the biological context, this set of experiments can be completed in 6-8 weeks.
引用
收藏
页码:2035 / 2049
页数:15
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