We have used a genetic approach to uncover the functional roles of rRN
A in protein synthesis. Mutations were constructed in a cloned rrn ope
ron by site-directed mutagenesis or isolated by genetic selections fol
lowing random mutagenesis. We have identified mutations that affect ea
ch step in the process of translation. The data are consistent with th
e results of biochemical and phylogenetic analyses but, in addition, h
ave provided novel information on regions of rRNA not previously inves
tigated.