DNA rearrangement permits bacteria to regulate gene content and expression. In Helicobacter pylori, cagY, which contains an extraordinary number of direct DNA repeats, encodes a surface-exposed subunit of a (type IV) bacterial secretory system. Examining potential DNA rearrangements involving the cagY repeats indicated that recombination events invariably yield in-frame open reading frames, producing alternatively expressed genes. In individual hosts, H. pylori cell populations include strains that produce CagY proteins that differ in size, due to the predicted in-frame deletions or duplications, and elicit minimal or no host antibody recognition. Using repetitive DNA, H. pylori rearrangements in a host-exposed subunit of a conserved bacterial secretion system may permit a novel form of antigenic evasion.
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3 November 2003
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October 27 2003
Plasticity of Repetitive DNA Sequences within a Bacterial (Type IV) Secretion System Component
Rahul A. Aras,
Rahul A. Aras
1Department of Medicine and Department of Microbiology, New York University School of Medicine, and VA Medical Center, New York, NY 10016
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Wolfgang Fischer,
Wolfgang Fischer
2Max von Pettenkofer-Institut fur Hygiene und Medizinische Mikrobiologie, Ludwig-Maximilians-Universitat, 80336 Munich, Germany
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Guillermo I. Perez-Perez,
Guillermo I. Perez-Perez
1Department of Medicine and Department of Microbiology, New York University School of Medicine, and VA Medical Center, New York, NY 10016
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MariaLuisa Crosatti,
MariaLuisa Crosatti
1Department of Medicine and Department of Microbiology, New York University School of Medicine, and VA Medical Center, New York, NY 10016
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Takafumi Ando,
Takafumi Ando
3First Department of Internal Medicine, Nagoya University School of Medicine, 466-8550 Nagoya, Japan
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Rainer Haas,
Rainer Haas
2Max von Pettenkofer-Institut fur Hygiene und Medizinische Mikrobiologie, Ludwig-Maximilians-Universitat, 80336 Munich, Germany
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Martin J. Blaser
Martin J. Blaser
1Department of Medicine and Department of Microbiology, New York University School of Medicine, and VA Medical Center, New York, NY 10016
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Rahul A. Aras
1Department of Medicine and Department of Microbiology, New York University School of Medicine, and VA Medical Center, New York, NY 10016
Wolfgang Fischer
2Max von Pettenkofer-Institut fur Hygiene und Medizinische Mikrobiologie, Ludwig-Maximilians-Universitat, 80336 Munich, Germany
Guillermo I. Perez-Perez
1Department of Medicine and Department of Microbiology, New York University School of Medicine, and VA Medical Center, New York, NY 10016
MariaLuisa Crosatti
1Department of Medicine and Department of Microbiology, New York University School of Medicine, and VA Medical Center, New York, NY 10016
Takafumi Ando
3First Department of Internal Medicine, Nagoya University School of Medicine, 466-8550 Nagoya, Japan
Rainer Haas
2Max von Pettenkofer-Institut fur Hygiene und Medizinische Mikrobiologie, Ludwig-Maximilians-Universitat, 80336 Munich, Germany
Martin J. Blaser
1Department of Medicine and Department of Microbiology, New York University School of Medicine, and VA Medical Center, New York, NY 10016
Address correspondence to Rahul A. Aras, Cold Spring Harbor Laboratory, P.O. Box 100, Cold Spring Harbor, NY 11724. Phone: (516) 367-6885; Fax: (516) 367-8435; email: [email protected]
Abbreviations used in this paper: FCR, 5′ conserved region; FRR, 5′ repeat region; MRR, middle repeat region; ORF, open reading frame; RFLP, restriction fragment length polymorphism; RAPD, random amplification of polymorphic DNA; TCR, 3′ conserved region; VHR, VirB10 homology region.
Received:
March 11 2003
Revision Received:
July 23 2003
Accepted:
September 22 2003
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2003
J Exp Med (2003) 198 (9): 1349–1360.
Article history
Received:
March 11 2003
Revision Received:
July 23 2003
Accepted:
September 22 2003
Citation
Rahul A. Aras, Wolfgang Fischer, Guillermo I. Perez-Perez, MariaLuisa Crosatti, Takafumi Ando, Rainer Haas, Martin J. Blaser; Plasticity of Repetitive DNA Sequences within a Bacterial (Type IV) Secretion System Component . J Exp Med 3 November 2003; 198 (9): 1349–1360. doi: https://doi.org/10.1084/jem.20030381
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