The RuvA Recombination Protein of
Escherichia coli

David Marcey
© 2006

I. Introduction
II. RuvA Structure
III. RuvA Tetramer-Holliday Junction DNA

IV. References

Directions

This exhibit displays molecules in the left part of the screen, and text that addresses structure-function relationships of the molecules in the right part (below). Use the scrollbar to the right to scroll through the text of this exhibit.

To evoke renderings of the molecule that illustrate particular points, click the radio buttons:

Please click the load PDB buttons, , when present.

To reset the molecule, use the reset buttons:

If you resize your browser window, simply refresh the page in order to restore proper viewing.



I. Introduction

Homologous recombination is essential for the generation of genetic diversity and for DNA repair in all organisms. A crucial step in recombination is the resolution of Holliday junctions, DNA intermediates which form as a result of strand exchange between two homologous DNA helices:

After the formation of Holliday intermediates, the length of heteroduplex DNA is extended through the process of branch migration. Heteroduplex double helical DNA contains two strands that were originally paired with other strands in the original double helices. Branch migration involves the sequential disruption of DNA base pairs in the two parental DNA helices, and the formation of new base pairs in the hybrid helices. Branch migration results in a region with two heteroduplexes and two original duplexes. To visualize this, it is useful to rotate the Holliday junction (the region near the arrow in the above figure) so that it has no crossing DNA strands and is in a square-planer configuration:

In Escherichia coli, branch migration and resolution of Holliday junctions to produce two, separate, intact DNA helices is accomplished by a suite of proteins: RuvA, RuvB, and RuvC.

RuvA binds as a tetramer to the Holliday junction; this binding allows loading of RuvB, which acts as a molecular motor to drive branch migration. RuvC then cleaves the junction and resolves the two DNA molecules into mature recombination products.

At left is shown an RuvA tetramer bound to DNA oligonucleotides representing a square-planer configuration of a Holliday junction. The regions of heteroduplex DNA (the top and bottom arms of the square planar DNA) correspond to the figures, above.


return to beginning



II. RuvA Structure

The RuvA monomer has an "L" shape, composed of three domains: I, II, III. The loop connecting domain II and domain III is not shown.

Domain I is a six-stranded, anti-parallel beta barrel, whereas both domains II and III consist entirely of alpha helices.


 

return to beginning



III. RuvA Tetramer-Holliday Junction DNA

In tetrameric RuvA, each monomer is a lobe of the symmetrical tetramer. The domain I beta barrels of each monomer are positioned centrally, and domains II and III are located peripherally.

Examining the charge distribution of atoms over the surface of the RuvA tetramer, it is clear that the DNA binding surface is largely positively charged (basic), whereas the opposite surface is largely negatively charged (acidic). The yellow, orange, and red colors represent relatively negatively charged atoms and the green and blue colors represent more positively charged atoms (red and blue indicate acidic or basic residues). The relative positive charge of the DNA binding surface attracts the negatively charged DNA backbone.

An exception to the mostly basic surface of the DNA binding side of the RuvA tetramer is an eight residue acidic "central pin" containing glutamate55 and aspartate56 from each monomer. This negatively charged center may repel the negatively charged oxygens of the DNA backbone, driving the DNA away from the center of the Holliday junction.

A number of residues that interact directly or indirectly (via water molecules) with the DNA backbone line the channels in which Holliday junction DNA is bound.


 

return to beginning



IV. References

Ariyoshi, M., Nishino, T., Iwasaki, H., Shinagawa, H., Morikawa, K.: Crystal Structure of the Holliday Junction DNA in Complex with a Single Ruva Tetramer. Proc.Nat.Acad.Sci. 97: 8257-8262 (2000).

Hargreaves, D., Rice, D. W., Sedelnikova, S. E., Artymiuk, P. J., Lloyd, R. G., Rafferty, J. B.: Crystal structure of E.coli RuvA with bound DNA Holliday junction at 6 A resolution. Nat. Struct. Biol. 5: 441-446 (1998).

Roe, S. M., Barlow, T., Brown, T., Oram, M., Keeley, A., Tsaneva, I. R., Pearl, L. H.: Crystal structure of an octameric RuvA-Holliday junction complex. Mol. Cell 2: 361-372 (1998).

return to beginning