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Physical mapping of the transfer RNA genes on lambda-h80dglytsu+36
Authors:M Wu  N Davidson  J Carbon
Institution:Department of Chemistry California Institute of Technology Pasadena, Calif. 91109, U.S.A.;Section of Biochemistry and Molecular Biology Department of Biological Sciences University of California Santa Barbara, Calif. 93106, U.S.A.
Abstract:The three Escherichia coli transfer RNA genes of the DNA of the transducing phage λ80cI857S?t68dglyTsu+36tyrTthrT (abbreviated λh80T), which specify the structures of tRNAGly2(su+36), tRNATyr2 and tRNAThr3, have been mapped by hybridizing ferritin-labeled E. coli tRNA to heteroduplexes of λh80T DNA with the DNA of the parental phage (λh80cI857S?t68) and examining the product in the electron microscope. The DNA of λh80T contains a piece of bacterial DNA of length 0·43 λ unit3 that replaces a piece of phage DNA of length 0·46 λ unit, proceeding left from B · P′ (the junction of bacterial DNA and phage DNA) (i.e. att80). A cluster of three ferritin binding sites, and thus of tRNA genes, is seen at a position of 0·24 λ unit (1·1 × 104 nucleotides) to the left of B· P′. The three tRNA genes of the cluster are separated by the unequal spacings of 260 (±30) and 140 (± 30) nucleotides, proceeding left from B·P′. The specific map positions have been identified by hybridization competition between ferritin-labeled whole E. coli tRNA with unlabeled purified tRNATyr2 and with unlabeled partially purified tRNAGly2. The central gene of the cluster is tRNATyr2. The tRNAGly2gene is probably the one furthest from B·P′. Thus, the gene order and spacings, proceeding left from B·P′, are: tRNAThr3, 260 nucleotides, tRNATry2, 140 nucleotides, tRNAGly2.
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