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A Cellular Function for the RNA-Interference Enzyme Dicer in the Maturation of the let-7 Small Temporal RNA
György Hutvágner,1*Juanita McLachlan,1*Amy E. Pasquinelli,3Éva Bálint,2Thomas Tuschl,4Phillip D. Zamore1
The 21-nucleotide small temporal RNA (stRNA) let-7
regulates developmental timing in Caenorhabditis elegans and
probably inother bilateral animals. We present in vivo and in vitro
evidencethat in Drosophila melanogaster a developmentally
regulated precursorRNA is cleaved by an RNA interference-like
mechanism to producemature let-7 stRNA. Targeted
destruction in cultured human cellsof the messenger RNA encoding the
enzyme Dicer, which acts inthe RNA interference pathway, leads to
accumulation of the let-7precursor. Thus, the RNA
interference and stRNA pathways intersect.Both pathways require the
RNA-processing enzyme Dicer to producethe active small-RNA component
that represses gene expression.
1 Department of Biochemistry and Molecular
Pharmacology;
2 Department of Cell Biology,
University of Massachusetts Medical School, Worcester, MA 01655, USA.
3 Department of Molecular Biology, Massachusetts
General Hospital and Department of Genetics, Harvard Medical School,
Boston, MA 02114, USA.
4 Department of Cellular
Biochemistry, Max-Planck-Institute for Biophysical Chemistry, Am
Fassberg 11, D-37077 Göttingen, Germany.
*
These authors contributed equally to this work.
To whom correspondence should be addressed. E-mail:
phillip.zamore{at}umassmed.edu
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