A method comprising treating an RNA composition with a buffered aqueous solution containing a dsRNA-specific endoribonuclease III protein, magnesium cations at a concentration of about 1-4 mM, and a salt providing an ionic strength equivalent to at least about 50 mM potassium acetate or potassium glutamate, wherein the RNA composition comprises either mRNA or a ssRNA precursor to said mRNA prior to it being capped and/or polyadenylated so that the amount of dsRNA that is greater than about 40 basepairs in length following said treating is less than 0.01% of the mass of RNA in said treated RNA composition.