Nucleotide sequence of the essential region of bacteriophage P4.
Journal: 1985/January - Nucleic Acids Research
ISSN: 0305-1048
PUBMED: 6095206
Abstract:
Nucleotide sequence of one-third of the genome of coliphage P4 has been obtained and mutations virl, epsilon am104, cI405, sidl, and delta 35 identified. The epsilon gene likely encodes a 10 kd protein with epsilon am104 being located at the beginning of the gene. cI405, a proposed repressor gene mutation, is located in a sequence capable of coding for a 15 kd protein. A new class of P4 mutations, ash, is located in the neighborhood of cI405. Two TATA-like sequences are mapped 5' to this cI (ash) sequence. Virl is possibly a promoter-up mutation and is located near or within the replication origin, which is about 400 bp long and AT rich. A sidl mutation is amber that shortens the sid protein by 9 amino acids. The delta gene may encode a 17 kd protein and appears to be coupled with the sid gene translationally. In the 5' side of the sid gene a sequence of CACAAT is the best TATA-like sequence. Sequences of two possible genes that are previously unrecognized and part of the alpha and psu genes are also identified.
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Nucleic Acids Res 12(22): 8667-8684

Nucleotide sequence of the essential region of bacteriophage P4.

Abstract

Nucleotide sequence of one-third of the genome of coliphage P4 has been obtained and mutations virl, epsilon am104, cI405, sidl, and delta 35 identified. The epsilon gene likely encodes a 10 kd protein with epsilon am104 being located at the beginning of the gene. cI405, a proposed repressor gene mutation, is located in a sequence capable of coding for a 15 kd protein. A new class of P4 mutations, ash, is located in the neighborhood of cI405. Two TATA-like sequences are mapped 5' to this cI (ash) sequence. Virl is possibly a promoter-up mutation and is located near or within the replication origin, which is about 400 bp long and AT rich. A sidl mutation is amber that shortens the sid protein by 9 amino acids. The delta gene may encode a 17 kd protein and appears to be coupled with the sid gene translationally. In the 5' side of the sid gene a sequence of CACAAT is the best TATA-like sequence. Sequences of two possible genes that are previously unrecognized and part of the alpha and psu genes are also identified.

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  • Six EW, Klug CA. Bacteriophage P4: a satellite virus depending on a helper such as prophage P2. Virology. 1973 Feb;51(2):327–344. [PubMed] [Google Scholar]
  • Six EW. The helper dependence of satellite bacteriophage P4: which gene functions of bacteriophage P2 are needed by P4? Virology. 1975 Sep;67(1):249–263. [PubMed] [Google Scholar]
  • Gibbs W, Goldstein RN, Wiener R, Lindqvist B, Calendar R. Satellite bacteriophage P4: characterization of mutants in two essential genes. Virology. 1973 May;53(1):24–39. [PubMed] [Google Scholar]
  • Six EW, Lindqvist BH. Mutual derepression in the P2-P4 bacteriophage system. Virology. 1978 Jun 15;87(2):217–230. [PubMed] [Google Scholar]
  • Calendar R, Ljungquist E, Deho G, Usher DC, Goldstein R, Youderian P, Sironi G, Six EW. Lysogenization by satellite phage P4. Virology. 1981 Aug;113(1):20–38. [PubMed] [Google Scholar]
  • Geisselsoder J, Youdarian P, Dehò G, Chidambaram M, Goldstein R, Ljungquist E. Mutants of satellite virus P4 that cannot derepress their bacteriophage P2 helper. J Mol Biol. 1981 May 5;148(1):1–19. [PubMed] [Google Scholar]
  • Souza L, Calendar R, Six EW, Lindqvist BH. A transactivation mutant of satellite phage P4. Virology. 1977 Aug;81(1):81–90. [PubMed] [Google Scholar]
  • Sunshine M, Six E. Relief of P2 bacteriophage amber mutant polarity by the satellite bacteriophage P4. J Mol Biol. 1976 Sep 25;106(3):673–682. [PubMed] [Google Scholar]
  • Sauer B, Ow D, Ling L, Calendar R. Mutants of satellite bacteriophage P4 that are defective in the suppression of transcriptional polarity. J Mol Biol. 1981 Jan 5;145(1):29–46. [PubMed] [Google Scholar]
  • Inman RB, Schnös M, Simon LD, Six EW, Walker DH., Jr Some morphological properties of P4 bacteriophage and P4 DNA. Virology. 1971 Apr;44(1):67–72. [PubMed] [Google Scholar]
  • Souza L, Geisselsoder J, Hopkins A, Calender R. Physical mapping of the satellite phage P4 genome. Virology. 1978 Apr;85(2):335–342. [PubMed] [Google Scholar]
  • Kahn M, Ow D, Sauer B, Rabinowitz A, Calendar R. Genetic analysis of bacteriophage P4 using P4-plasmid ColE1 hybrids. Mol Gen Genet. 1980 Feb;177(3):399–412. [PubMed] [Google Scholar]
  • Harris JD, Calendar R. Transcription map of satellite coliphage P4. Virology. 1978 Apr;85(2):343–358. [PubMed] [Google Scholar]
  • Lindqvist BH, Six EW. Replication of bacteriophage P4 DNA in a nonlysogenic host. Virology. 1971 Jan;43(1):1–7. [PubMed] [Google Scholar]
  • Sasaki I, Bertani G. Growth abnormalities in Hfr derivatives of Escherichia coli strain C. J Gen Microbiol. 1965 Sep;40(3):365–376. [PubMed] [Google Scholar]
  • Sunshine MG, Thorn M, Gibbs W, Calendar R, Kelly B. P2 phage amber mutants: characterization by use of a polarity suppressor. Virology. 1971 Dec;46(3):691–702. [PubMed] [Google Scholar]
  • Geisselsoder J, Chidambaram M, Goldstein R. Transcriptional control of capsid size in the P2:P4 bacteriophage system. J Mol Biol. 1978 Dec 15;126(3):447–456. [PubMed] [Google Scholar]
  • Lindqvist BH, Sinsheimer RL. Process of infection with bacteriophage phi-X174. XIV. Studies on macromolecular synthesis during infection with a lysis-defective mutant. J Mol Biol. 1967 Aug 28;28(1):87–94. [PubMed] [Google Scholar]
  • Kleckner N, Roth J, Botstein D. Genetic engineering in vivo using translocatable drug-resistance elements. New methods in bacterial genetics. J Mol Biol. 1977 Oct 15;116(1):125–159. [PubMed] [Google Scholar]
  • Kahn M, Hopkins A. Restriction endonuclease cleavage map of bacteriophage P4 DNA. Virology. 1978 Apr;85(2):359–363. [PubMed] [Google Scholar]
  • Maxam AM, Gilbert W. Sequencing end-labeled DNA with base-specific chemical cleavages. Methods Enzymol. 1980;65(1):499–560. [PubMed] [Google Scholar]
  • Sanger F, Nicklen S, Coulson AR. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467.[PMC free article] [PubMed] [Google Scholar]
  • Messing J, Vieira J. A new pair of M13 vectors for selecting either DNA strand of double-digest restriction fragments. Gene. 1982 Oct;19(3):269–276. [PubMed] [Google Scholar]
  • Sollner-Webb B, Reeder RH. The nucleotide sequence of the initiation and termination sites for ribosomal RNA transcription in X. laevis. Cell. 1979 Oct;18(2):485–499. [PubMed] [Google Scholar]
  • Berk AJ, Sharp PA. Sizing and mapping of early adenovirus mRNAs by gel electrophoresis of S1 endonuclease-digested hybrids. Cell. 1977 Nov;12(3):721–732. [PubMed] [Google Scholar]
  • Green MR, Roeder RG. Definition of a novel promoter for the major adenovirus-associated virus mRNA. Cell. 1980 Nov;22(1 Pt 1):231–242. [PubMed] [Google Scholar]
  • Baker RF, Yanofsky C. The periodicity of RNA polymerase initiations: a new regulatory feature of transcription. Proc Natl Acad Sci U S A. 1968 May;60(1):313–320.[PMC free article] [PubMed] [Google Scholar]
  • Barrett KJ, Marsh ML, Calendar R. Interactions between a satellite bacteriophage and its helper. J Mol Biol. 1976 Sep 25;106(3):683–707. [PubMed] [Google Scholar]
  • Barrett KJ, Blinkova A, Arnold G. The bacteriophage P4 alpha gene is the structural gene for bacteriophage P4-induced RNA polymerase. J Virol. 1983 Oct;48(1):157–169.[PMC free article] [PubMed] [Google Scholar]
  • Barrett KJ, Gibbs W, Calendar R. A transcribing activity induced by satellite phage P4. Proc Natl Acad Sci U S A. 1972 Oct;69(10):2986–2990.[PMC free article] [PubMed] [Google Scholar]
  • Sanger F, Coulson AR, Hong GF, Hill DF, Petersen GB. Nucleotide sequence of bacteriophage lambda DNA. J Mol Biol. 1982 Dec 25;162(4):729–773. [PubMed] [Google Scholar]
  • Oppenheim DS, Yanofsky C. Translational coupling during expression of the tryptophan operon of Escherichia coli. Genetics. 1980 Aug;95(4):785–795.[PMC free article] [PubMed] [Google Scholar]
  • Schümperli D, McKenney K, Sobieski DA, Rosenberg M. Translational coupling at an intercistronic boundary of the Escherichia coli galactose operon. Cell. 1982 Oct;30(3):865–871. [PubMed] [Google Scholar]
Abstract
Nucleotide sequence of one-third of the genome of coliphage P4 has been obtained and mutations virl, epsilon am104, cI405, sidl, and delta 35 identified. The epsilon gene likely encodes a 10 kd protein with epsilon am104 being located at the beginning of the gene. cI405, a proposed repressor gene mutation, is located in a sequence capable of coding for a 15 kd protein. A new class of P4 mutations, ash, is located in the neighborhood of cI405. Two TATA-like sequences are mapped 5' to this cI (ash) sequence. Virl is possibly a promoter-up mutation and is located near or within the replication origin, which is about 400 bp long and AT rich. A sidl mutation is amber that shortens the sid protein by 9 amino acids. The delta gene may encode a 17 kd protein and appears to be coupled with the sid gene translationally. In the 5' side of the sid gene a sequence of CACAAT is the best TATA-like sequence. Sequences of two possible genes that are previously unrecognized and part of the alpha and psu genes are also identified.
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