Translation regulation of integrons gene cassette expression by the attC sites

Mol Microbiol. 2009 Jun;72(6):1475-86. doi: 10.1111/j.1365-2958.2009.06736.x. Epub 2009 May 26.

Abstract

Integron are genetic elements able to carry, capture and shuffle the genes embedded in gene cassettes. The attC recombination sites adopt a stable secondary structure when single-stranded that is necessary for their recombination. In this study, we evaluated the impact of the structure of the attC site on expression of the 3' gene in class 1 integrons. This was analysed by substituting the attC of the bla(IMP-8) gene cassette with various mutated attC sites spanning a wide range of sizes and secondary structures, and measuring the integron-dependent translation of the 3'aac(6')-Ib7 gene. In the resulting constructs, the 5'-attC site differentially affected the expression of the aac(6')-Ib7 gene. Contrary to what was expected from their proposed role as Rho-independent transcription terminators, the transcription of the aac(6')-Ib7 gene was not affected by the various attC sites. Mutations of natural sites revealed that destabilization of the potential stem-loop structure of the attC site in the transcript could enhance the expression of the 3' gene. In particular, the presence of a translated open reading frame was shown to increase translation of the 3' gene. These findings might be explained by the capacity of the stem-loop structures to impede ribosome progression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Attachment Sites, Microbiological*
  • Base Sequence
  • Escherichia coli / genetics
  • Gene Expression Regulation, Bacterial
  • Genetic Vectors
  • Integrons*
  • Molecular Sequence Data
  • Mutation
  • Nucleic Acid Conformation
  • Plasmids
  • Protein Biosynthesis*
  • RNA, Bacterial / metabolism
  • RNA, Messenger / metabolism
  • Ribosomes / metabolism

Substances

  • RNA, Bacterial
  • RNA, Messenger