Asymmetric template function of microbial deoxyribonucleic acids: transcription of ribosomal and soluble ribonucleic acids

J Bacteriol. 1970 Sep;103(3):560-8. doi: 10.1128/jb.103.3.560-568.1970.

Abstract

In Bacillus subtilis and Escherichia coli, 16 and 23S ribosomal ribonucleic acid (rRNA) hybridize exclusively with the heavy (H) strand of methylated albuminkieselguhr (MAK)-fractionated complementary deoxyribonucleic acid (DNA) strands. All the soluble RNA (4S RNA) in B. subtilis and 66 to 75% of the 4S RNA in E. coli also hybridize with the H strand. Interspecific hybridization shows that E. coli 23S rRNA also binds selectively to the DNA H strand of Salmonella typhimurium. The hybridization peak for all three cellular RNA components is specifically located in the late-eluting region of the absorbance profile of the DNA H strand. The early-eluting region of the light (L) strand preferentially inhibits the hybridization between the peak region of the H strand and 23S rRNA. These regions are considered to represent the transcribing sequences and their complements for 23S rRNA in the separated H and L strands of DNA, respectively.

MeSH terms

  • Albumins
  • Bacillus subtilis*
  • Chromatography
  • DNA, Bacterial* / isolation & purification
  • Escherichia coli*
  • Genetic Code
  • Genetics, Microbial
  • Hybridization, Genetic*
  • RNA, Bacterial* / isolation & purification
  • Ribosomes
  • Salmonella typhimurium*
  • Silicon Dioxide
  • Templates, Genetic*
  • Tritium
  • Uracil

Substances

  • Albumins
  • DNA, Bacterial
  • RNA, Bacterial
  • Tritium
  • Uracil
  • Silicon Dioxide