Unknown

Dataset Information

0

Labeled microRNA pull-down assay system: an experimental approach for high-throughput identification of microRNA-target mRNAs.


ABSTRACT: We developed a simple, direct and cost-effective approach to search for the most likely target genes of a known microRNA (miRNA) in vitro. We term this method 'labeled miRNA pull-down (LAMP)' assay system. Briefly, the pre-miRNA is labeled with digoxigenin (DIG), mixed with cell extracts and immunoprecipitated by anti-DIG antiserum. When the DIG-labeled miRNA and bound mRNA complex are obtained, the total cDNAs are then subcloned and sequenced, or RT-PCR-amplified, to search for the putative target genes of a known miRNA. After successfully identifying the known target genes of Caenorhabditis elegans miRNAs lin-4 and let-7 and zebrafish let-7, we applied LAMP to find the unknown target gene of zebrafish miR-1, which resulted in the identification of hand2. We then confirmed hand2 as a novel target gene of miR-1 by whole-mount in situ hybridization and luciferase reporter gene assay. We further validated this target gene by microarray analysis, and the results showed that hand2 is the top-scoring among 302 predicted putative target genes. We concluded that LAMP is an experimental approach for high-throughput identification of the target gene of known miRNAs from both C. elegans and zebrafish, yielding fewer false positive results than those produced by using only the bioinformatics approach.

SUBMITTER: Hsu RJ 

PROVIDER: S-EPMC2691847 | biostudies-literature | 2009 Jun

REPOSITORIES: biostudies-literature

altmetric image

Publications

Labeled microRNA pull-down assay system: an experimental approach for high-throughput identification of microRNA-target mRNAs.

Hsu Ren-Jun RJ   Yang Hsin-Jung HJ   Tsai Huai-Jen HJ  

Nucleic acids research 20090506 10


We developed a simple, direct and cost-effective approach to search for the most likely target genes of a known microRNA (miRNA) in vitro. We term this method 'labeled miRNA pull-down (LAMP)' assay system. Briefly, the pre-miRNA is labeled with digoxigenin (DIG), mixed with cell extracts and immunoprecipitated by anti-DIG antiserum. When the DIG-labeled miRNA and bound mRNA complex are obtained, the total cDNAs are then subcloned and sequenced, or RT-PCR-amplified, to search for the putative tar  ...[more]

Similar Datasets

2020-10-02 | GSE136179 | GEO
2018-08-28 | GSE119019 | GEO
| S-EPMC9238377 | biostudies-literature
| S-EPMC5901726 | biostudies-literature
| S-EPMC9317552 | biostudies-literature
2018-08-21 | PXD007521 | JPOST Repository
| S-EPMC6271496 | biostudies-literature
| S-EPMC4532895 | biostudies-literature
| S-EPMC7918074 | biostudies-literature
2017-07-01 | GSE98218 | GEO