Genetics, Vol 129, 991-1005, Copyright © 1991


INVESTIGATIONS

On the Deletion of Inverted Repeated DNA in Escherichia coli: Effects of Length, Thermal Stability, and Cruciform Formation in Vivo

R. R. Sinden, G. Zheng, R. G. Brankamp and K. N. Allen
Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati College of Medicine, Cincinnati, Ohio 45267-0524

We have studied the deletion of inverted repeats cloned into the EcoRI site within the CAT gene of plasmid pBR325. A cloned inverted repeat constitutes a palindrome that includes both EcoRI sites flanking the insert. In addition, the two EcoRI sites represent direct repeats flanking a region of palindromic symmetry. A current model for deletion between direct repeats involves the formation of DNA secondary structure which may stabilize the misalignment between the direct repeats during DNA replication. Our results are consistent with this model. We have analyzed deletion frequencies for several series of inverted repeats, ranging from 42 to 106 bp, that were designed to form cruciforms at low temperatures and at low superhelical densities. We demonstrate that length, thermal stability of base pairing in the hairpin stem, and ease of cruciform formation affect the frequency of deletion. In general, longer palindromes are less stable than shorter ones. The deletion frequency may be dependent on the thermal stability of base pairing involving approximately 16-20 bp from the base of the hairpin stem. The formation of cruciforms in vivo leads to a significant increase in the deletion frequency. A kinetic model is presented to describe the relationship between the physical-chemical properties of DNA structure and the deletion of inverted repeats in living cells.


This article has been cited by other articles:


Home page
Nucleic Acids ResHome page
C. P. Lu, J. E. Posey, and D. B. Roth
Understanding how the V(D)J recombinase catalyzes transesterification: distinctions between DNA cleavage and transposition
Nucleic Acids Res., May 1, 2008; 36(9): 2864 - 2873.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
V. I. Hashem, M. J. Pytlos, E. A. Klysik, K. Tsuji, M. Khajav, T. Ashizawa, and R. R. Sinden
Chemotherapeutic deletion of CTG repeats in lymphoblast cells from DM1 patients
Nucleic Acids Res., December 1, 2004; 32(21): 6334 - 6346.
[Abstract] [Full Text] [PDF]


Home page
Eukaryot CellHome page
N. F. Wilson and P. A. Lefebvre
Regulation of Flagellar Assembly by Glycogen Synthase Kinase 3 in Chlamydomonas reinhardtii
Eukaryot. Cell, October 1, 2004; 3(5): 1307 - 1319.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
M. Bzymek and S. T. Lovett
Instability of repetitive DNA sequences: The role of replication in multiple mechanisms
PNAS, July 17, 2001; 98(15): 8319 - 8325.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
M. Bzymek and S. T. Lovett
Evidence for Two Mechanisms of Palindrome-Stimulated Deletion in Escherichia coli: Single-Strand Annealing and Replication Slipped Mispairing
Genetics, June 1, 2001; 158(2): 527 - 540.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
F. Nasar, C. Jankowski, and D. K. Nag
Long Palindromic Sequences Induce Double-Strand Breaks during Meiosis in Yeast
Mol. Cell. Biol., May 15, 2000; 20(10): 3449 - 3458.
[Abstract] [Full Text]


Home page
GeneticsHome page
D. M. DeMarini, M. L. Shelton, A. Abu-Shakra, A. Szakmary, and J. G. Levine
Spectra of Spontaneous Frameshift Mutations at the hisD3052 Allele of Salmonella typhimurium in Four DNA Repair Backgrounds
Genetics, May 1, 1998; 149(1): 17 - 36.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
K. S. Lobachev, B. M. Shor, H. T. Tran, W. Taylor, J. D. Keen, M. A. Resnick, and D. A. Gordenin
Factors Affecting Inverted Repeat Stimulation of Recombination and Deletion in Saccharomyces cerevisiae
Genetics, April 1, 1998; 148(4): 1507 - 1524.
[Abstract] [Full Text] [PDF]