Home LiteratureArticle Details
PMID: 7982573 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Construction of chromosomal rearrangements in Salmonella by transduction: inversions of non-permissive segments are not lethal.

Genetics ·Vol. 137 ·No. 4 ·1994-08-00 ·Pages 919-32

Miesel L, Segall A, Roth JR

Abstract

Homologous sequences placed in inverse order at particular separated sites in the bacterial chromosome (termed "permissive") can recombine to form an inversion of the intervening chromosome segment. When the same repeated sequences flank other chromosome segments ("non-permissive"), recombination occurs but the expected inversion rearrangement is not found among the products. The failure to recover inversions of non-permissive chromosomal segments could be due to lethal effects of the final rearrangement. Alternatively, local chromosomal features might pose barriers to reciprocal exchanges between sequences at particular sites and could thereby prevent formation of inversions of the region between such sites. To distinguish between these two possibilities, we have constructed inversions of two non-permissive intervals by means of phage P22-mediated transduction crosses. These crosses generate inversions by simultaneous incorporation of two transduced fragments, each with a sequence that forms one join-point of the final inversion. We constructed inversions of the non-permissive intervals trp ('34) to his ('42) and his ('42) to cysA ('50). Strains with the constructed inversions are viable and grow normally. These results show that our previous failure to detect formation of these inversions by recombination between chromosomal sequences was not due to lethal effects of the final rearrangement. We infer that the "non-permissive" character of some chromosomal segments reflects the inability of the recombination system to perform the needed exchanges between inverse order sequences at particular sites. Apparently these mechanistic problems were circumvented by the transductional method used here to direct inversion formation.

Related Genes
MeSH Terms
Chromosome Inversion Chromosomes, Bacterial/ultrastructure Recombination, Genetic Repetitive Sequences, Nucleic Acid Salmonella typhimurium/genetics Transduction, Genetic
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Miesel L
Department of Biology, University of Utah, Salt Lake City 84112.
Segall A
Roth J R
References (24)
24 references, click to expand
  1. Ethanolamine utilization in Salmonella typhimurium.
    J Bacteriol. 1988 Sep;170(9):3855-63 PMID: 3045078
  2. Rearrangement of the bacterial chromosome: forbidden inversions.
    Science. 1988 Sep 9;241(4871):1314-8 PMID: 3045970
  3. Conditionally transposition-defective derivative of Mu d1(Amp Lac).
    J Bacteriol. 1984 Jul;159(1):130-7 PMID: 6330026
  4. Involvement of ribosomal ribonucleic acid operons in Salmonella typhimurium chromosomal rearrangements.
    J Bacteriol. 1980 Jul;143(1):492-8 PMID: 6156935
  5. Evidence for two sites for initiation of gene expression in the tryptophan operon of Salmonella typhimurium.
    J Mol Biol. 1967 Jun 28;26(3):423-36 PMID: 5339794
  6. Acetylornithinase of Escherichia coli: partial purification and some properties.
    J Biol Chem. 1956 Jan;218(1):97-106 PMID: 13278318
  7. Linkage map of Salmonella typhimurium, edition VII.
    Microbiol Rev. 1988 Dec;52(4):485-532 PMID: 3070321
  8. Analysis of genetic recombination between two partially deleted lactose operons of Escherichia coli K-12.
    J Bacteriol. 1977 Jul;131(1):123-32 PMID: 326755
  9. Spontaneous tandem genetic duplications in Salmonella typhimurium arise by unequal recombination between rRNA (rrn) cistrons.
    Proc Natl Acad Sci U S A. 1981 May;78(5):3113-7 PMID: 6789329
  10. Internal promoter of the tryptophan operon of Escherichia coli is located in a structural gene.
    J Mol Biol. 1972 Aug 21;69(2):307-13 PMID: 4560950
  11. Salmonella typhimurium synthesizes cobalamin (vitamin B12) de novo under anaerobic growth conditions.
    J Bacteriol. 1984 Jul;159(1):206-13 PMID: 6376471
  12. Preferential unequal recombination in the glyS region of the Escherichia coli chromosome.
    J Mol Biol. 1979 Jan 5;127(1):73-87 PMID: 370413
  13. Hfr formation directed by tn10.
    Genetics. 1979 Apr;91(4):639-55 PMID: 17248903
  14. Tandem genetic duplications in phage and bacteria.
    Annu Rev Microbiol. 1977;31:473-505 PMID: 334045
  15. Genetic methods for analysis and manipulation of inversion mutations in bacteria.
    Genetics. 1983 Nov;105(3):517-37 PMID: 6357943
  16. Directed formation of deletions and duplications using Mud(Ap, lac).
    Genetics. 1985 Feb;109(2):263-82 PMID: 3156064
  17. Role of recBC function in formation of chromosomal rearrangements: a two-step model for recombination.
    Genetics. 1989 Mar;121(3):433-43 PMID: 2714635
  18. A single regulatory gene integrates control of vitamin B12 synthesis and propanediol degradation.
    J Bacteriol. 1992 Apr;174(7):2253-66 PMID: 1312999
  19. Approaches to half-tetrad analysis in bacteria: recombination between repeated, inverse-order chromosomal sequences.
    Genetics. 1994 Jan;136(1):27-39 PMID: 8138164
  20. Recombination between repeated genes in microorganisms.
    Annu Rev Genet. 1988;22:147-68 PMID: 3071247
  21. Recombination between homologies in direct and inverse orientation in the chromosome of Salmonella: intervals which are nonpermissive for inversion formation.
    Genetics. 1989 Aug;122(4):737-47 PMID: 2547692
  22. Lactose genes fused to exogenous promoters in one step using a Mu-lac bacteriophage: in vivo probe for transcriptional control sequences.
    Proc Natl Acad Sci U S A. 1979 Sep;76(9):4530-3 PMID: 159458
  23. Further tests of a recombination model in which chi removes the RecD subunit from the RecBCD enzyme of Escherichia coli.
    Genetics. 1990 Nov;126(3):519-33 PMID: 2249753
  24. Method for the isolation of Escherichia coli mutants with enhanced recombination between chromosomal duplications.
    J Bacteriol. 1977 Apr;130(1):167-72 PMID: 323226
Article Info
Journal
Genetics
Abbr.
Genetics
ISSN
0016-6731
Published
1994-08-00
Pages
919-32
Language
English
Region
United States
NLM ID
0374636
PMCID
PMC1206069
Subset
IM
Grants
NIGMS NIH HHS · GM27068 · United States
NIGMS NIH HHS · T32-GM07464-15 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com