- THIS ARTICLE
- Full Text (PDF)
- Alert me when this article is cited
- Alert me if a correction is posted
- SERVICES
- Similar articles in this journal
- Similar articles in PubMed
- Alert me to new issues of the journal
- Download to citation manager
- Reprints & Permissions
- CITING ARTICLES
- Citing Articles via HighWire
- Citing Articles via Google Scholar
- GOOGLE SCHOLAR
- Articles by Sawyer, S. A.
- Articles by Hartl, D. L.
- Search for Related Content
- PUBMED
- PubMed Citation
- Articles by Sawyer, S. A.
- Articles by Hartl, D. L.
Distribution and Abundance of Insertion Sequences Among Natural Isolates of Escherichia coli
Stanley A. Sawyer 1, Daniel E. Dykhuizen 2, Robert F. DuBose 2, Louis Green 2, T. Mutangadura-Mhlanga 3, David F. Wolczyk 4, and Daniel L. Hartl 2
1 Department of Genetics, Washington University School of Medicine,
St. Louis, Missouri 63110, Department of Mathematics, Washington University,
St. Louis, Missouri 63130
2 Department of Genetics, Washington University School of Medicine,
St. Louis, Missouri 63110
3 Department of Biological Sciences, University of Zimbabwe,
Mount Pleasant, Harare, Zimbabwe
4 Department of Biology, Reed College, Portland, Oregon 97202
A reference collection of 71 natural isolates of Escherichia coli (the ECOR collection) has been studied with respect to the distribution and abundance of transposable insertion sequences using DNA hybridization. The data include 1173 occurrences of six unrelated insertion sequences (IS 1, IS2, IS3, IS4, IS5 and IS 30). The number of insertion elements per strain, and the sizes of DNA restriction fragments containing them, is highly variable and can be used to discriminate even among closely related strains. The occurrence and abundance of pairs of unrelated insertion sequences are apparently statistically independent, but significant correlations result from stratifications in the reference collection. However, there is a highly significant positive association among the insertion sequences considered in the aggregate. Nine branching process models, which differ in assumptions regarding the regulation of transposition and the effect of copy number on fitness, have been evaluated with regard to their fit of the observed distributions. No single model fits all copy number distributions. The best models incorporate no regulation of transposition and a moderate to strong decrease in fitness with increasing copy number for IS1 and IS5, strong regulation of transposition and a negligible to weak decrease in fitness with increasing copy number for IS3, and less than strong regulation of transposition for IS2, IS 4 and IS30.
Submitted on July 7, 1986Accepted on October 11, 1986
This article has been cited by other articles:
![]() |
A. Golomidova, E. Kulikov, A. Isaeva, A. Manykin, and A. Letarov The Diversity of Coliphages and Coliforms in Horse Feces Reveals a Complex Pattern of Ecological Interactions Appl. Envir. Microbiol., October 1, 2007; 73(19): 5975 - 5981. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Wagner, C. Lewis, and M. Bichsel A survey of bacterial insertion sequences using IScan Nucleic Acids Res., August 13, 2007; 35(16): 5284 - 5293. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. H. M. Mes and M. Doeleman Positive Selection on Transposase Genes of Insertion Sequences in the Crocosphaera watsonii Genome. J. Bacteriol., October 1, 2006; 188(20): 7176 - 7185. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. L. Rouzic and P. Capy Population Genetics Models of Competition Between Transposable Element Subfamilies Genetics, October 1, 2006; 174(2): 785 - 793. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. S. Dolgin and B. Charlesworth The Fate of Transposable Elements in Asexual Populations Genetics, October 1, 2006; 174(2): 817 - 827. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Wagner Periodic Extinctions of Transposable Elements in Bacterial Lineages: Evidence from Intragenomic Variation in Multiple Genomes Mol. Biol. Evol., April 1, 2006; 23(4): 723 - 733. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Hery-Arnaud, G. Bruant, P. Lanotte, S. Brun, A. Rosenau, N. van der Mee-Marquet, R. Quentin, and L. Mereghetti Acquisition of Insertion Sequences and the GBSi1 Intron by Streptococcus agalactiae Isolates Correlates with the Evolution of the Species J. Bacteriol., September 1, 2005; 187(17): 6248 - 6252. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. M. Tanaka, N. A. Rosenberg, and P. M. Small The Control of Copy Number of IS6110 in Mycobacterium tuberculosis Mol. Biol. Evol., December 1, 2004; 21(12): 2195 - 2201. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. S. Barker, B. M. Pruss, and P. Matsumura Increased Motility of Escherichia coli by Insertion Sequence Element Integration into the Regulatory Region of the flhD Operon J. Bacteriol., November 15, 2004; 186(22): 7529 - 7537. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Zhong, A. Khodursky, D. E. Dykhuizen, and A. M. Dean Evolutionary genomics of ecological specialization PNAS, August 10, 2004; 101(32): 11719 - 11724. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Ohta, K. Tsuchida, S. Choi, Y. Sekine, Y. Shiga, and E. Ohtsubo Presence of a Characteristic D-D-E Motif in IS1 Transposase J. Bacteriol., November 15, 2002; 184(22): 6146 - 6154. [Abstract] [Full Text] [PDF] |
||||
![]() |
D.C. OLD, P.B. CRICHTON, A. TAYLOR, and H. MATHER An attempt to identify the evolutionary origin of a novel serotype of Salmonella enterica isolated from harbour porpoises J. Med. Microbiol., May 1, 2001; 50(5): 415 - 420. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Kersulyte, A. K. Mukhopadhyay, M. Shirai, T. Nakazawa, and D. E. Berg Functional Organization and Insertion Specificity of IS607, a Chimeric Element of Helicobacter pylori J. Bacteriol., October 1, 2000; 182(19): 5300 - 5308. [Abstract] [Full Text] |
||||
![]() |
D. Mazel, B. Dychinco, V. A. Webb, and J. Davies Antibiotic Resistance in the ECOR Collection: Integrons and Identification of a Novel aad Gene Antimicrob. Agents Chemother., June 1, 2000; 44(6): 1568 - 1574. [Abstract] [Full Text] |
||||
![]() |
A. Wada, R. Mikkola, C. G. Kurland, and A. Ishihama Growth Phase-Coupled Changes of the Ribosome Profile in Natural Isolates and Laboratory Strains of Escherichia coli J. Bacteriol., May 15, 2000; 182(10): 2893 - 2899. [Abstract] [Full Text] |
||||
![]() |
D. Papadopoulos, D. Schneider, J. Meier-Eiss, W. Arber, R. E. Lenski, and M. Blot Genomic evolution during a 10,000-generation experiment with bacteria PNAS, March 30, 1999; 96(7): 3807 - 3812. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Minamisawa, T. Isawa, Y. Nakatsuka, and N. Ichikawa New Bradyrhizobium japonicum Strains That Possess High Copy Numbers of the Repeated Sequence RSalpha Appl. Envir. Microbiol., May 1, 1998; 64(5): 1845 - 1851. [Abstract] [Full Text] |
||||
![]() |
C. J. Thompson, C. Daly, T. J. Barrett, J. P. Getchell, M. J. R. Gilchrist, and M. J. Loeffelholz Insertion Element IS3-Based PCR Method for Subtyping Escherichia coli O157:H7 J. Clin. Microbiol., May 1, 1998; 36(5): 1180 - 1184. [Abstract] [Full Text] |
||||








