Abstract
We have characterized two rearrangements consisting of inverted repeats of the argE gene. The promoters (p) of argE and of argCBH face each other over an internal operator. The rearrangements were obained as reactivations of argE in a strain harboring an argEp deletion on a λdarg prophage. In both cases the repeat included argE and argCBHp on either side of a unique sequence; the result is a divergent operon in which each copy of argCBHp reads into the adjacent argE repeat. In one case, the pair of repeats adjoins the silent parental gene, forming a triplication (← → ←). The other rearrangement consists of a single argE palindrome, but the whole prophage is rearranged into an inverted repeat, analogous to certain λdv's. Both structures could be explained by breakage of a replication fork passing argE and by inaccurate rejoining of strands. The λdv-like rearrangement would result from breakage at both replication forks of a phage or prophage replicating during transient release of immunity. The triplication would imply breaking of a chromosomal replication fork, formation of a cyclic intermediate by recombination between the daughter duplex molecules and reinsertion into the parental argE gene. Formation of a triplication by replication errors involving appropriate strand switchings and branch migrations can not be excluded however.
Full Text
The Full Text of this article is available as a PDF (1.8 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Beeftinck F., Cunin R., Glansdorff N. Arginine gene duplications in recombination proficient and deficient strains of Escherichia coli K 12. Mol Gen Genet. 1974;132(3):241–253. doi: 10.1007/BF00269397. [DOI] [PubMed] [Google Scholar]
- Besemer J., Görtz G., Charlier D. Deletions and DNA rearrangements within the transposable DNA element IS2. A model for the creation of palindromic DNA by DNA repair synthesis. Nucleic Acids Res. 1980 Dec 11;8(23):5825–5833. doi: 10.1093/nar/8.23.5825. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bolivar F., Betlach M. C., Heyneker H. L., Shine J., Rodriguez R. L., Boyer H. W. Origin of replication of pBR345 plasmid DNA. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5265–5269. doi: 10.1073/pnas.74.12.5265. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Boyen A., Charlier D., Crabeel M., Cunin R., Palchaudhuri S., Glansdorff N. Studies on the control region of the bipolar argECBH operon of Escherichia coli. I. Effect of regulatory mutations and IS2 insertions. Mol Gen Genet. 1978 May 3;161(2):185–196. doi: 10.1007/BF00274187. [DOI] [PubMed] [Google Scholar]
- Charlier D., Crabeel M., Cunin R., Glansdorff N. Tandem and inverted repeats of arginine genes in Escherichia coli: structural and evolutionary considerations. Mol Gen Genet. 1979 Jul 2;174(1):75–88. doi: 10.1007/BF00433308. [DOI] [PubMed] [Google Scholar]
- Charlier D., Piette J., Glansdorff N. IS3 can function as a mobile promoter in E. coli. Nucleic Acids Res. 1982 Oct 11;10(19):5935–5948. doi: 10.1093/nar/10.19.5935. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Elseviers D., Cunin R., Glansdorff N. Control regions within the argECBH gene cluster of Escherichia coli K12. Mol Gen Genet. 1972;117(4):349–366. doi: 10.1007/BF00333028. [DOI] [PubMed] [Google Scholar]
- Emmons S. W. Bacteriophage lambda derivatives carrying two copies of the cohesive end site. J Mol Biol. 1974 Mar 15;83(4):511–525. doi: 10.1016/0022-2836(74)90511-7. [DOI] [PubMed] [Google Scholar]
- GLANSDORFF N. TOPOGRAPHY OF COTRANSDUCIBLE ARGININE MUTATIONS IN ESCHERICHIA COLI K-12. Genetics. 1965 Feb;51:167–179. doi: 10.1093/genetics/51.2.167. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Glansdorff N., Charlier D., Zafarullah M. Activation of gene expression by IS2 and IS3. Cold Spring Harb Symp Quant Biol. 1981;45(Pt 1):153–156. doi: 10.1101/sqb.1981.045.01.024. [DOI] [PubMed] [Google Scholar]
- Hershfield V., Boyer H. W., Yanofsky C., Lovett M. A., Helinski D. R. Plasmid ColEl as a molecular vehicle for cloning and amplification of DNA. Proc Natl Acad Sci U S A. 1974 Sep;71(9):3455–3459. doi: 10.1073/pnas.71.9.3455. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hinton D. M., Musso R. E. Transcription initiation sites within an IS2 insertion in a Gal-constitutive mutant of Escherichia coli. Nucleic Acids Res. 1982 Aug 25;10(16):5015–5031. doi: 10.1093/nar/10.16.5015. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mazaitis A. J., Palchaudhuri S., Glansdorff N., Maas W. K. Isolation and characterization of lambdadargECBH transducing phages and heteroduplex analysis of the argECBH cluster. Mol Gen Genet. 1976 Jan 16;143(2):185–196. doi: 10.1007/BF00266921. [DOI] [PubMed] [Google Scholar]
- Nevers P., Saedler H. Transposable genetic elements as agents of gene instability and chromosomal rearrangements. Nature. 1977 Jul 14;268(5616):109–115. doi: 10.1038/268109a0. [DOI] [PubMed] [Google Scholar]
- Rigby P. W., Dieckmann M., Rhodes C., Berg P. Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I. J Mol Biol. 1977 Jun 15;113(1):237–251. doi: 10.1016/0022-2836(77)90052-3. [DOI] [PubMed] [Google Scholar]
- Ripley L. S. Model for the participation of quasi-palindromic DNA sequences in frameshift mutation. Proc Natl Acad Sci U S A. 1982 Jul;79(13):4128–4132. doi: 10.1073/pnas.79.13.4128. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zafarullah M., Charlier D., Glansdorff N. Insertion of IS3 can "turn-on" a silent gene in Escherichia coli. J Bacteriol. 1981 Apr;146(1):415–417. doi: 10.1128/jb.146.1.415-417.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]