Branch migration

Diagram illustrating the movement of a branch point between two homologous pieces of DNA. Migration travels to the left and stops when it reaches the end of the homologous region. The second branch point on the right is free to move in either direction as well.

Branch migration is the process by which base pairs on homologous DNA strands are consecutively exchanged at a Holliday junction, moving the branch point up or down the DNA sequence.[1] Branch migration is the second step of genetic recombination, following the exchange of two single strands of DNA between two homologous chromosomes.[2] The process is random, and the branch point can be displaced in either direction on the strand, influencing the degree of which the genetic material is exchanged.[1] Branch migration can also be seen in DNA repair and replication, when filling in gaps in the sequence. It can also be seen when a foreign piece of DNA invades the strand.[2]

Mechanism

The mechanism for branch migration differs between prokaryotes and eukaryotes.[2]

Prokaryotes

Open X structure of a Holliday junction. RuvA binds to the DNA and fits in between the double strands on all four sides. RuvA also has a domain that fits inside the centre of the junction.

The mechanism for prokaryotic branch migration has been studied many times in Escherichia coli.[2] In E. coli, the proteins RuvA and RuvB come together and form a complex that facilitates the process in a number of ways. RuvA is a tetramer and binds to the DNA at the Holliday junction when it is in the open X form. The protein binds in a way that the DNA entering/departing the junction is still free to rotate and slide through. RuvA has a domain with acidic amino acid residues that interfere with the base pairs in the centre of the junction. This forces the base pairs apart so that they can re-anneal with base pairs on the homologous strands.[3]

In order for migration to occur, RuvA must be associated with RuvB and ATP. RuvB has the ability to hydrolyze ATP, driving the movement of the branch point. RuvB is a hexamer with helicase activity, and also binds the DNA. As ATP is hydrolyzed, RuvB rotates the recombined strands while pulling them out of the junction, but does not separate the strands as helicase would.[3]

The final step in branch migration is called resolution and requires the protein RuvC. The protein is a dimer, and will bind to the Holliday junction when it takes on the stacked X form. The protein has endonuclease activity, and cleaves the strands at exactly the same time. The cleavage is symmetrical, and gives two recombined DNA molecules with single stranded breaks.[4] The breaks are then ligated together to complete the process.[2]

Eukaryotes

The eukaryotic mechanism is much more complex involving different and additional proteins, but follows the same general path.[2]

Control

The Holliday junction converts between the open X structure (top) and the stacked X structure (bottom) depending on the Mg2+ concentration.

The rate of branch migration is dependent on the amount of divalent ions, specifically magnesium ions (Mg2+), present during recombination.[1] The ions determine which structure the Holliday junction will adopt, as they play a stabilizing role. When the ions are absent, the backbones repel each other and the junction takes on the open X structure.[5] In this condition, migration is optimal and the junction will be free to move up and down the strands.[3] When the ions are present, they neutralize the negatively charged backbone. This allows the strands to move closer together and the junction adopts the stacked X structure.[5] It is during this state that resolution will be optimal, allowing RuvC to bind to the junction.[3]

References

  1. 1 2 3 Lilley, David M. J. (2000-05-01). "Structures of helical junctions in nucleic acids". Quarterly Reviews of Biophysics. 33 (02): 109–159. doi:10.1017/s0033583500003590. ISSN 1469-8994.
  2. 1 2 3 4 5 6 "Genetic Recombination | Learn Science at Scitable". www.nature.com. Retrieved 2015-11-13.
  3. 1 2 3 4 Yamada, Kazuhiro; Ariyoshi, Mariko; Morikawa, Kosuke (2004-04-01). "Three-dimensional structural views of branch migration and resolution in DNA homologous recombination". Current Opinion in Structural Biology. 14 (2): 130–137. doi:10.1016/j.sbi.2004.03.005.
  4. ↑ Górecka, Karolina M.; Komorowska, Weronika; Nowotny, Marcin (2013-11-01). "Crystal structure of RuvC resolvase in complex with Holliday junction substrate". Nucleic Acids Research. 41 (21): 9945–9955. doi:10.1093/nar/gkt769. ISSN 0305-1048. PMC 3834835Freely accessible. PMID 23980027.
  5. 1 2 Clegg, R. M. (1993-01-01). "The Structure of the Four-Way Junction in DNA". Annual Review of Biophysics and Biomolecular Structure. 22 (1): 299–328. doi:10.1146/annurev.bb.22.060193.001503. PMID 8347993.
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