The 2'-OH group in the ribose sugar of RNA is reactive. It can act as a nucleophile and attack the adjacent phosphodiester bond under alkaline conditions, leading to the self-hydrolysis (cleavage) of the RNA strand. DNA, lacking this 2'-OH, is far more chemically stable.
The 2'-OH group in the ribose sugar of RNA is reactive. It can act as a nucleophile and attack the adjacent phosphodiester bond under alkaline conditions, leading to the self-hydrolysis (cleavage) of the RNA strand. DNA, lacking this 2'-OH, is far more chemically stable.