Each of the Conserved Sequence Elements Flanking the Cleavage Site of Mammalian Histone Pre-mRNAs Has a Distinct Role in the 3′-End Processing Reaction

Abstract

To study the substrate requirements for the histone 3′-end processing reaction of mammalian histone pre-mRNAs, we created a set of mutations in the sequences flanking the processing site of a mouse H3 gene. We found that deletion of the downstream purine-rich element hypothesized to interact with U7 small nuclear RNA abolishes in vitro 3′-end processing. Somewhat surprisingly, however, mutations in the hairpin loop element which destabilize or destroy the secondary structure reduce but do not abolish 3′-end processing. This is in apparent contrast to results obtained for the sea urchin system, where both sequence elements appear to be absolutely required for 3′-end formation.