Small interfering RNAs (siRNAs) are non-coding RNAs, around 22 nucleotides long, that regulate gene expression. The Dicer and Argonaute proteins are necessary for the processing of siRNAs from longer double-stranded RNA. The presence of
They used a cloning method designed to isolate Dicer cleavage products, and observed that one third of the sequenced clones matched centromeric repeat sequences in the yeast genome. Reinhart and Bartel suggest that these siRNAs, which they call heterochormatic siRNAs, are generated by Dicer-mediated processing of dsRNA generated from both DNA strands of the repeat region. As