Search

A hallmark of RNA silencing is a class of approximately 22-nucleotide RNAs that are processed from double-stranded RNA precursors by Dicer. Accurate processing by Dicer is crucial for the functionality of microRNAs (miRNAs). The current model posits that Dicer selects cleavage sites by measuring a set distance from the 3? overhang of the double-stranded RNA terminus. Here we report that human Dicer anchors not only the 3? end but also the 5? end, with the cleavage site determined mainly by the distance (?22 nucleotides) from the 5? end (5? counting rule). This cleavage requires a 5?-terminal phosphate group. Further, we identify a novel basic motif (5? pocket) in human Dicer that recognizes the 5?-phosphorylated end. The 5? counting rule and the 5? anchoring residues are conserved in Drosophila Dicer-1, but not in Giardia Dicer. Mutations in the 5? pocket reduce processing efficiency and alter cleavage sites in vitro. Consistently, miRNA biogenesis is perturbed in vivo when Dicer-null embryonic stem cells are replenished with the 5?-pocket mutant. Thus, 5?-end recognition by Dicer is important for precise and effective biogenesis of miRNAs. Insights from this study should also afford practical benefits to the design of small hairpin RNAs. [ABSTRACT FROM AUTHOR]

Culturing intestinal stem cells into 3D organoids results in heterogeneous cell populations, reflecting the in vivo cell type diversity. In a recent paper published in Nature, Wang et al. established a culture condition for a highly homogeneous population of intestinal stem cells. [ABSTRACT FROM AUTHOR]