RNase E can inhibit the decay of some degradation intermediates: degradation of Desulfovibrio vulgaris cytochrome c3 mRNA in E coli

Biochimie. 1996;78(4):227-35. doi: 10.1016/0300-9084(96)82185-7.

Abstract

In Escherichia coli, ribonuclease E (RNase E) is a key endonuclease in mRNA decay. We have analysed the role of E coli RNase E on the degradation of a heterologous cytochrome c3 (cyc) mRNA from Desulfovibrio vulgaris Hildenborough. The decay of the cyc transcript in wild-type and mutant E coli cells was followed and the degradation intermediates analysed by Northern blotting and S1 protection analysis. The half-life of total cyc mRNA intermediates was increased in the RNase E mutant. A number of degradation intermediates were stabilised, and new species arose. However, some species decayed faster in the met5 mutant at the non-permissive temperature, suggesting that RNase E might inhibit their degradation. The results indicate that RNase E is involved in cyc mRNA degradation, and, interestingly, decay of certain intermediates could be reduced by this enzyme activity. This may suggest a functional interaction between RNase E and exonucleases, like polynucleotide phosphorylase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Northern
  • Cytochrome c Group / genetics*
  • Desulfovibrio vulgaris / enzymology*
  • Endoribonucleases / metabolism*
  • Escherichia coli / metabolism*
  • Half-Life
  • Hydrolysis
  • RNA, Bacterial / genetics
  • RNA, Bacterial / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism*
  • Recombinant Proteins / genetics

Substances

  • Cytochrome c Group
  • RNA, Bacterial
  • RNA, Messenger
  • Recombinant Proteins
  • cytochrome c(3)
  • Endoribonucleases
  • ribonuclease E