Transcriptional analysis of the fix ABCXORF1 region of Azorhizobium caulinodans suggests post-transcriptional processing of the fix ABCXORF1 mRNA

Mol Gen Genet. 1992 Nov;235(2-3):422-31. doi: 10.1007/BF00279389.

Abstract

We report here the transcriptional analysis of the fixABCXORF1 region of Azorhizobium caulinodans. This led to the identification of a 0.9 kb transcript covering fixX and ORF1, which was synthesized only under conditions of nitrogen fixation. The 5' end of this transcript was mapped by primer extension and S1 nuclease protection analyses and shown to be located 70 +/- 1 nucleotides upstream of the fixX start codon. By means of transcriptional fixX- and ORF1-lacZ fusions, it was shown that fixX and ORF1 were most probably transcribed from the fixA promoter and that expression of fixX and ORF1 was dependent on NifA activation. This suggests that the 0.9 kb mRNA results from post-transcriptional processing of a large mRNA covering fixA,B,C,X and ORF1. In addition, ORF1 mutants were constructed and were shown not to be impaired in nitrogenase activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Blotting, Northern
  • Chromosomes, Bacterial
  • Escherichia coli / genetics
  • Genes, Bacterial*
  • Genetic Vectors
  • Molecular Sequence Data
  • Nitrogen Fixation / genetics*
  • Open Reading Frames*
  • Plasmids
  • RNA Processing, Post-Transcriptional*
  • RNA, Bacterial / genetics
  • RNA, Bacterial / isolation & purification
  • RNA, Messenger / genetics*
  • RNA, Messenger / metabolism
  • Recombinant Fusion Proteins / metabolism
  • Replicon
  • Restriction Mapping
  • Rhizobiaceae / genetics*
  • Transcription, Genetic*
  • beta-Galactosidase / genetics
  • beta-Galactosidase / metabolism

Substances

  • RNA, Bacterial
  • RNA, Messenger
  • Recombinant Fusion Proteins
  • beta-Galactosidase