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      A cellular function for the RNA-interference enzyme Dicer in the maturation of the let-7 small temporal RNA.

      Science (New York, N.Y.)
      Animals, Blotting, Northern, Drosophila melanogaster, Endoribonucleases, genetics, metabolism, Gene Expression Regulation, Developmental, HeLa Cells, Humans, Nucleic Acid Conformation, Protein Structure, Tertiary, RNA Precursors, RNA Processing, Post-Transcriptional, RNA, Double-Stranded, RNA, Helminth, chemistry, RNA, Messenger, Ribonuclease III, Transcription, Genetic, Transfection

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          Abstract

          The 21-nucleotide small temporal RNA (stRNA) let-7 regulates developmental timing in Caenorhabditis elegans and probably in other bilateral animals. We present in vivo and in vitro evidence that in Drosophila melanogaster a developmentally regulated precursor RNA is cleaved by an RNA interference-like mechanism to produce mature let-7 stRNA. Targeted destruction in cultured human cells of the messenger RNA encoding the enzyme Dicer, which acts in the RNA interference pathway, leads to accumulation of the let-7 precursor. Thus, the RNA interference and stRNA pathways intersect. Both pathways require the RNA-processing enzyme Dicer to produce the active small-RNA component that represses gene expression.

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