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Identification of human microRNA targets from isolated argonaute protein complexes.
RNA Biol. 4, 76-84 (2007)
Verlagsversion Volltext
DOI
PMC
MicroRNAs (miRNAs) constitute a class of small non-coding RNAs that regulate gene expression on the level of translation and/or mRNA stability. Mammalian miRNAs associate with members of the Argonaute (Ago) protein family and bind to partially complementary sequences in the 3' untranslated region (UTR) of specific target mRNAs. Computer algorithms based on factors such as free binding energy or sequence conservation have been used to predict miRNA target mRNAs. Based on such predictions, up to one third of all mammalian mRNAs seem to be under miRNA regulation. However, due to the low degree of complementarity between the miRNA and its target, such computer programs are often imprecise and therefore not very reliable. Here we report the first biochemical identification approach of miRNA targets from human cells. Using highly specific monoclonal antibodies against members of the Ago protein family, weco-immunoprecipitate Ago-bound mRNAs and identify them by cloning. Interestingly, most of the identified targets are also predicted by different computer programs. Moreover, we randomly analyzed six different target candidates and were able to experimentally validate five as miRNA targets. Our data clearly indicate that miRNA targets can be experimentally identified from Ago complexes and therefore provide a new tool to directly analyze miRNA function.
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Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Schlagwörter
RNAi; RNA interference; microRNAs; Argonaute; gene silencing; non-coding RNAs; translation; gene regulation; TRANSLATION INITIATION; CAENORHABDITIS-ELEGANS; MICROPROCESSOR COMPLEX; CRYSTAL-STRUCTURE; RNA CLEAVAGE; HUMAN-CELLS; BIOGENESIS; MECHANISMS; REPRESS; MIRNAS
ISSN (print) / ISBN
1547-6286
e-ISSN
1555-8584
Zeitschrift
RNA Biology
Quellenangaben
Band: 4,
Heft: 2,
Seiten: 76-84
Verlag
Landes Bioscience
Nichtpatentliteratur
Publikationen
Begutachtungsstatus
Peer reviewed
Institut(e)
Institute of Molecular Immunology (IMI)