The chloramphenicol (Cm)-inducible cat and cmlA genes are regulated by
translation attenuation, a regulatory device that modulates mRNA tran
slation. In this form of gene regulation, translation of the Cm-R codi
ng sequence is prevented by mRNA secondary structure that sequesters i
ts ribosome-binding site (RES). A translated leader of nine codons pre
cedes the secondary structure, and induction results when a ribosome b
ecomes stalled at a specific site in the leader. Here we demonstrate t
hat the site of ribosome stalling in the leader is selected by a cis e
ffect of the nascent leader peptide on its translating ribosome.