A Holliday junction is a four-way DNA branch in which strands exchange pairing partners between homologous duplexes. It can occur as an intermediate in homologous recombination. The molecular configuration is distinct from a final chromosomal crossover, which is classified by the exchange of flanking chromosome arms. Robin Holliday's 1964 model connected strand exchange, hybrid DNA and gene conversion.[ref]
A mechanism for gene conversion in fungi by Robin Holliday. Section1, pages284–286 and Figure1
For a schematic example, label homologous regions by distant markers and . Alternative strand-pair cleavage and rejoining routes at a junction can preserve the parental combinations , , or produce the exchanged combinations , . Local mismatches and their repair can change an allele independently of that distant-marker outcome. The historical diagram illustrates possibilities; it does not establish equal frequencies for these outcomes in every cell.[ref]
A mechanism for gene conversion in fungi by Robin Holliday. Figure1, alternatives4a/4b and accompanying outside-marker discussion
Later work sought physical evidence. H. Potter and D. Dressler isolated colicinE1 plasmid DNA, linearized it with the restriction enzyme EcoRI, and examined it by electron microscopy. They found crossed structures containing two genome lengths, joined at homologous regions. Such forms occurred in wild-type and tested RecB-C hosts but were absent in their recombination-deficient RecA hosts. They interpreted these controlled observations as intermediates of the Holliday model.[ref]
On the mechanism of genetic recombination: electron microscopic observation of recombination intermediates by H. Potter and D. Dressler. Abstract and original micrographs, pages3000–3004
The combination of shape, DNA content and a genetic control is stronger evidence than an X-shaped image alone. A Holliday junction also need not be an obligatory step in every noncrossover recombination pathway; the outcome and the route producing it remain separate questions.
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