Genetic analysis of the Shine-Dalgarno interaction: Selection of alternative functional mRNA-rRNA combinations

RNA

Volumn 2, Issue 12, 1996, Pages 1270-1285

  Lee, Kangseok ^a   Holland Staley, Carol A ^a   Cunningham, Philip R ^a  

^a WAYNE STATE UNIVERSITY   (United States)

Author keywords

Initiation; message binding sequence; mutation; protein synthesis; ribosome binding sequence

Indexed keywords

MESSENGER RNA; RIBOSOME RNA;

ARTICLE; GENETIC ANALYSIS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN SYNTHESIS; RNA BINDING; RNA TRANSLATION; TRANSLATION INITIATION;

BASE COMPOSITION; BINDING SITES; CHLORAMPHENICOL; CHLORAMPHENICOL O-ACETYLTRANSFERASE; DRUG RESISTANCE; ESCHERICHIA COLI; GENES, DOMINANT; GENES, LETHAL; MUTAGENESIS; NUCLEOTIDES; PROTEIN BIOSYNTHESIS; RNA, BACTERIAL; RNA, MESSENGER; RNA, RIBOSOMAL, 16S; SEQUENCE ALIGNMENT; THERMODYNAMICS;

BACTERIA (MICROORGANISMS); ESCHERICHIA COLI; FELIS CATUS;

EID: 0029905958     PISSN: 13558382     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (8)

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7. Chen H, Bjerknes M, Kumar R, Jay E. 1994. Determination of the optimal aligned spacing between the Shine-Dalgarno sequence and the translation initiation codon of Escherichia coli mRNAs. Nucleic Acids Res 22(23):4953-4957.
8. Clarke L, Carbon J. 1976. A colony bank containing synthetic Col E1 hybrid plasmids representative of the entire E. coli genome. Cell 9:91-99.