Silencing of xenogeneic DNA by H-NS—facilitation of lateral gene transfer in bacteria by a defense system that recognizes foreign DNA

  1. William Wiley Navarre1,
  2. Michael McClelland4,
  3. Stephen J. Libby1, and
  4. Ferric C. Fang1,2,3,5
  1. 1 Department of Laboratory Medicine, University of Washington, Seattle, Washington 98195, USA;
  2. 2 Department of Medicine, University of Washington, Seattle, Washington 98195, USA;
  3. 3 Department of Microbiology, University of Washington, Seattle, Washington 98195, USA;
  4. 4 Sidney Kimmel Cancer Center, San Diego, California 92121, USA

Abstract

Lateral gene transfer has played a prominent role in bacterial evolution, but the mechanisms allowing bacteria to tolerate the acquisition of foreign DNA have been incompletely defined. Recent studies show that H-NS, an abundant nucleoid-associated protein in enteric bacteria and related species, can recognize and selectively silence the expression of foreign DNA with higher adenine and thymine content relative to the resident genome, a property that has made this molecule an almost universal regulator of virulence determinants in enteric bacteria. These and other recent findings challenge the ideas that curvature is the primary determinant recognized by H-NS and that activation of H-NS-silenced genes in response to environmental conditions occurs through a change in the structure of H-NS itself. Derepression of H-NS-silenced genes can occur at specific promoters by several mechanisms including competition with sequence-specific DNA-binding proteins, thereby enabling the regulated expression of foreign genes. The possibility that microorganisms maintain and exploit their characteristic genomic GC ratios for the purpose of self/non-self-discrimination is discussed.

Keywords

Footnotes

| Table of Contents

Life Science Alliance