New Chromosomal Location for Structural Genes of Ribosomal Proteins

An Escherichia coli mutant, ts9, previously reported by Flaks et al. (Cold Spring Harbor Symp. Quant. Biol. 31, 623-631, 1966) to have an electrophoretically altered ribosomal protein, has been further characterized and the altered component has been identified as L7/L12. Although mutant ts9 is temp...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 1975-07, Vol.72 (7), p.2765-2769
Hauptverfasser: Watson, Robert J., Parker, Jack, Fiil, Niels P., Flaks, Joel G., Friesen, James D.
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Sprache:eng
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Zusammenfassung:An Escherichia coli mutant, ts9, previously reported by Flaks et al. (Cold Spring Harbor Symp. Quant. Biol. 31, 623-631, 1966) to have an electrophoretically altered ribosomal protein, has been further characterized and the altered component has been identified as L7/L12. Although mutant ts9 is temperature sensitive for growth (rts-), the rts and L7/L12 mutations are genetically separable and are both located between argH and rif. The L7/L12 mutation (rpyL) maps very close to relC, mutants of which have a defect in the 50S ribosomal subunit. The gene order is argH-rts-(rpyL, relC)-rif. Protein synthesis directed by bacteriophage λ cI857S7drifd18 in ultraviolet-irradiated cells indicates that L7/L12, as well as L1, L10, L11, and possibly L8 or L9 are coded by the phage DNA. Our results indicate that rpyL is the structural gene for L7/L12 and that this region of the E. coli chromosome contains a cluster of structural genes for ribosomal proteins.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.72.7.2765