Hostname: page-component-586b7cd67f-l7hp2 Total loading time: 0 Render date: 2024-11-26T14:01:16.925Z Has data issue: false hasContentIssue false

Holliday junctions, heteroduplex DNA and map expansion: a commentary on ‘A mechanism for gene conversion in fungi’ by Robin Holliday

Published online by Cambridge University Press:  29 October 2008

DAVID R. F. LEACH*
Affiliation:
Institute of Cell Biology, School of Biological Sciences, University of Edinburgh, King's Buildings, Edinburgh EH9 3JR, UK
*
*Tel: +44 (131) 650 5373. Fax. +44 (131) 650 8650. e-mail: [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Type
Article Commentary
Copyright
Copyright © 2008 Cambridge University Press

Perhaps there is truth in beauty. Robin Holliday's proposal for the mechanism of recombination (Holliday, Reference Holliday1964) was certainly beautifully elegant and has proved to be essentially correct. At the time of his proposal, all the elements of his model were circulating in the scientific ether: the observations on gene conversion and its association with crossing over (Perkins, Reference Perkins1962; Whitehouse, Reference Whitehouse1963), the association of postmeiotic segregation with recombination (Kitani et al., Reference Kitani, Olive and El-Ani1962; Lissouba et al., Reference Lissouba, Mousseau, Rizet and Rossignol1962; Stadler & Towe, Reference Stadler and Towe1963) and the association of DNA breakage with recombination (Kellenberger et al., Reference Kellenberger, Zichichi and Weigle1961; Meselson & Weigle, Reference Meselson and Weigle1961; Siddiqi, Reference Siddiqi1963), but it was the observation of map expansion that Holliday's paper grappled with in particular. Despite the prominence of the 1964 paper and its association with the ‘Holliday junction’, map expansion remains a poorly appreciated phenomenon even today.

I believe that the first depiction of the Holliday junction appeared in the model of break-induced replication proposed for bacteriophage lambda by Meselson & Weigle (Reference Meselson and Weigle1961), but it was Robin Holliday who explicitly recognized that this four-way junction could be formed and resolved in a way that would explain the patterns of recombination observed in fungal meioses. The old models of gene conversion by copying first one chromosome and then another (copy-choice) were no longer easy to understand, given the semi-conservative mechanism of DNA replication, and models of breakage and reunion that involved annealing of single-stranded DNA ends, such as those proposed by Meselson and Weigle and by Whitehouse, were either incompatible with meiotic recombination (Meselson & Weigle, Reference Meselson and Weigle1961) or inelegant (Whitehouse, Reference Whitehouse1963). A detailed discussion of the history of recombination models had recently been published (Haber, Reference Haber2007).

Robin Holliday's 1964 paper will be remembered rightly for proposing the centrality of the ‘Holliday junction’ (see Fig. 1 A). Holliday junctions have been isolated from bacterial cells (Potter & Dressler, Reference Potter and Dressler1977) (Fig. 1 B) and shown to be intermediates in the meiotic recombination of Saccharomyces cerevisiae (Schwacha & Kleckner, Reference Schwacha and Kleckner1995) and Shizosaccharomyces pombe (Cromie et al., Reference Cromie, Hyppa, Taylor, Zakharyevich, Hunter and Smith2006). It was realized by model building that these junctions could form without any loss of base-pairing at the four-way junction (Sigal & Alberts, Reference Sigal and Alberts1972) and physical studies have demonstrated the beauty of the molecular structures adopted by this form of DNA (Duckett et al., Reference Duckett, Murchie, Diekmann, von Kitzing, Kemper and Lilley1988; Ortiz-Lombardia et al., Reference Ortiz-Lombardia, Gonzalez, Eritja, Aymami, Azorin and Coll1999) (Fig. 1 C). Holliday's prediction that this junction could potentially be resolved by cleavage to produce crossover and non-crossover recombinants was confirmed by the isolation of nucleases, such as RuvC from bacteria that can cleave Holliday junctions in the predicted manner (Connolly et al., Reference Connolly, Parsons, Benson, Dunderdale, Sharples, Lloyd and West1991; Dunderdale et al., Reference Dunderdale, Benson, Parsons, Sharples, Lloyd and West1991; Iwasaki et al., Reference Iwasaki, Takahagi, Shiba, Nakata and Shinagawa1991). The identities of the eukaryotic nuclear Holliday junction resolvases have remained elusive though one complex able to carry out the reaction (Mus81/Eme1) has been identified (Boddy et al., Reference Boddy, Gaillard, McDonald, Shanahan, Yates and Russell2001; Chen et al., Reference Chen, Melchionna, Denis, Gaillard, Blasina, Van de Weyer, Boddy, Russell, Vialard and McGowan2001).

Fig. 1. (A) The model as drawn by Robin Holliday (Holliday, Reference Holliday1964). (B) Electron micrograph of a plasmid DNA molecule containing a Holliday junction (taken from Potter & Dressler, Reference Potter and Dressler1977, with permission from the Proceedings of the National Academy of Sciences of the USA). (C) Crystal structure of a Holliday junction (taken from Ortiz-Lombardia et al., Reference Ortiz-Lombardia, Gonzalez, Eritja, Aymami, Azorin and Coll1999, with permission from the Nature Publishing Group).

The strength of Holliday's paper lies not just in proposing a mechanism for the formation and resolution of ‘Holliday junctions’ but the association of these junctions with mismatches in heteroduplex DNA and the prediction that such mismatches could be corrected in such a way as to generate the patterns of recombination observed in tetrads and map expansion. Holliday's model predicts that 6:2 and 2:6 tetrads can be generated by correction of two symmetrically placed mismatches in heteroduplex DNA; 5:3 and 3:5 tetrads can be explained by one such mismatch remaining uncorrected, resulting in postmeiotic segregation; aberrant 4:4 tetrads can be generated in the absence of correction at both mismatches. Any of these patterns can be associated or not with crossing over according to the plane of cleavage of the junction. This is a remarkable set of divergent predictions to come from such a simple model.

Largely unknown to those who have not read it, the bulk of Holliday's paper is devoted to a discussion of map expansion. So, what is map expansion? Map expansion is a phenomenon where, given three close (e.g. intragenic) markers A, B and C, the recombinant frequency between A and C (R AC) is greater than the sum of the recombinant frequencies between A and B (R AB), and between B and C (R BC).

How can this come about? Holliday realized that this was likely to be an effect of the markers used in the cross and their behaviour in heteroduplex DNA. He proposed that the mutant sites were themselves interfering with intragenic recombination. In particular, he proposed an early version of heteroduplex rejection. He states: ‘If there is an inhibiting effect by mutant sites on the opportunity for pairing, conversion or crossing-over, then the degree of inhibition might be inversely proportional to the distance apart of such sites.’ In a later paper with John Fincham, he proposed a model based on the lengths of correction tracts (Fincham & Holliday, Reference Fincham and Holliday1970). If two markers lie closer together than the length of correction tracts, they will tend to be co-corrected, thus reducing recombinant frequencies for very close markers. Fujitani and Kobayashi have returned to the idea of heteroduplex rejection (Fujitani & Kobayashi, Reference Fujitani and Kobayashi1997). In 1979, Stahl questioned the existence of map expansion (Stahl, Reference Stahl1979), but recent evidence using a sequenced region of the S. pombe genome has confirmed its existence (Baur et al., Reference Baur, Hartsuiker, Lehmann, Ludin, Munz and Kohli2005). Map expansion is in apparent contradiction with high negative interference also observed for close markers. However, Holliday argued that the two may be in harmony if the high negative interference involves markers in the heteroduplex DNA and markers flanking the site of initiation of recombination and/or resolution of the Holliday junction. Other influences on high negative interference may be system-specific (e.g. the nature of the mutations leading to independent correction or the effects of mating pools in the case of bacteriophage crosses).

Holliday's paper is remarkable for its pre-science. It anticipates the central importance of four-way junctions in recombination. It anticipates the importance of the behaviour of mismatches and of mismatch correction in recombination between close markers. Holliday was aware when he wrote his paper that the details of individual systems would vary from the exact format he drew in his figure (Fig. 1 A) and he wrote: ‘… there are strong indications that whatever basic mechanism is operating, the details of this mechanism may not be the same in different organisms; therefore it does not seem profitable at the present time to attempt to make a model more specific by very detailed analysis of particular data from one organism or another.’ The details of how recombination is initiated (e.g. at double-strand breaks, single-strand nicks or single-strand gaps), the extent of DNA degradation at the site of initiation, the extent and symmetry of heteroduplex DNA, the migration distance of Holliday junctions and the rejection and repair of mismatches will all contribute to the precise mechanism of recombination in any given system, but the general proposal put forward for the mechanism of recombination by Robin Holliday has stood the test of time.

References

Baur, M., Hartsuiker, E., Lehmann, E., Ludin, K., Munz, P. & Kohli, J. (2005). The meiotic recombination hot spot ura4A in Schizosaccharomyces pombe. Genetics 169, 551561.CrossRefGoogle ScholarPubMed
Boddy, M. N., Gaillard, P. H., McDonald, W. H., Shanahan, P., Yates, J. R. III & Russell, P. (2001). Mus81--Eme1 are essential components of a Holliday junction resolvase. Cell 107, 537548.CrossRefGoogle ScholarPubMed
Chen, X. B., Melchionna, R., Denis, C. M., Gaillard, P. H., Blasina, A., Van de Weyer, I., Boddy, M. N., Russell, P., Vialard, J. & McGowan, C. H. (2001). Human Mus81-associated endonuclease cleaves Holliday junctions in vitro. Molecular Cell 8, 11171127.Google Scholar
Connolly, B., Parsons, C. A., Benson, F. E., Dunderdale, H. J., Sharples, G. J., Lloyd, R. G. & West, S. C. (1991). Resolution of Holliday junctions in vitro requires the Escherichia coli ruvC gene product. Proceedings of the National Academy of Sciences of the USA 88, 60636067.Google Scholar
Cromie, G. A., Hyppa, R. W., Taylor, A. F., Zakharyevich, K., Hunter, N. & Smith, G. R. (2006). Single Holliday junctions are intermediates of meiotic recombination. Cell 127, 11671178.CrossRefGoogle ScholarPubMed
Duckett, D. R., Murchie, A. I., Diekmann, S., von Kitzing, E., Kemper, B. & Lilley, D. M. (1988). The structure of the Holliday junction, and its resolution. Cell 55, 7989.CrossRefGoogle ScholarPubMed
Dunderdale, H. J., Benson, F. E., Parsons, C. A., Sharples, G. J., Lloyd, R. G. & West, S. C. (1991). Formation and resolution of recombination intermediates by E. coli RecA and RuvC proteins. Nature 354, 506510.CrossRefGoogle Scholar
Fincham, J. R. & Holliday, R. (1970). An explanation of fine structure map expansion in terms of excision repair. Molecular and General Genetics 109, 309322.Google Scholar
Fujitani, Y. & Kobayashi, I. (1997). Mismatch-stimulated destruction of intermediates as an explanation for map expansion in genetic recombination. Journal of Theoretical Biology 189, 443447.Google Scholar
Haber, J. (2007). Evolution of models of homologous recombination. In Genome Dynamics and Stability. Berlin: Springer Vol 3 Ed. Egel.Google Scholar
Holliday, R. (1964). A mechanism for gene conversion in fungi. Genetical Research 5, 283304.CrossRefGoogle Scholar
Iwasaki, H., Takahagi, M., Shiba, T., Nakata, A. & Shinagawa, H. (1991). Escherichia coli RuvC protein is an endonuclease that resolves the Holliday structure. EMBO Journal 10, 43814389.CrossRefGoogle ScholarPubMed
Kellenberger, G., Zichichi, M. L. & Weigle, J. J. (1961). Exchange of DNA in the recombination of bacteriophage lambda. Proceedings of the National Academy of Sciences of the USA 47, 869878.Google Scholar
Kitani, Y., Olive, L. S. & El-Ani, A. S. (1962). Genetics of Sordaria fumicola. V. Aberrant segregation at the g locus. American Journal of Botany 49, 697706.Google Scholar
Lissouba, P., Mousseau, J., Rizet, G. & Rossignol, J. L. (1962). Fine structure of genes in the ascomycete Ascobolus immersus. Advances in Genetics 11, 343380.Google Scholar
Meselson, M. & Weigle, J. J. (1961). Chromosome breakage accompanying genetic recombination in bacteriophage. Proceedings of the National Academy of Sciences of the USA 47, 857868.CrossRefGoogle Scholar
Ortiz-Lombardia, M., Gonzalez, A., Eritja, R., Aymami, J., Azorin, F. & Coll, M. (1999). Crystal structure of a DNA Holliday junction. Nature Structural Biology 6, 913917.Google ScholarPubMed
Perkins, D. D. (1962). The frequency in Neurospora tetrads of multiple exchanges within short intervals. Genetical Research 3, 315327.CrossRefGoogle Scholar
Potter, H. & Dressler, D. (1977). On the mechanism of genetic recombination: the maturation of recombination intermediates. Proceedings of the National Academy of Sciences of the USA 74, 41684172.Google Scholar
Schwacha, A. & Kleckner, N. (1995). Identification of double Holliday junctions as intermediates in meiotic recombination. Cell 83, 783791.Google Scholar
Siddiqi, O. H. (1963). Incorporation of parental DNA into genetic recombinants of E. coli. Proceedings of the National Academy of Sciences of the USA 49, 589592.Google Scholar
Sigal, N. & Alberts, B. (1972). Genetic recombination: the nature of a crossed strand-exchange between two homologous DNA molecules. Journal of Molecular Biology 71, 789793.CrossRefGoogle ScholarPubMed
Stadler, D. R. & Towe, A. M. (1963). Recombination of allelic cysteine mutants in Neurospora. Genetica 30, 293311.Google Scholar
Stahl, F. W. (1979). Genetic Recombination: Thinking About It in Phage and Fungi. San Francisco, CA: W. H. Freeman and Company. IBSN 0-7167-1037-4.Google Scholar
Whitehouse, H. L. (1963). A theory of crossing-over by means of hybrid deoxyribonucleic acid. Nature 199, 10341040.CrossRefGoogle ScholarPubMed
Figure 0

Fig. 1. (A) The model as drawn by Robin Holliday (Holliday, 1964). (B) Electron micrograph of a plasmid DNA molecule containing a Holliday junction (taken from Potter & Dressler, 1977, with permission from the Proceedings of the National Academy of Sciences of the USA). (C) Crystal structure of a Holliday junction (taken from Ortiz-Lombardia et al., 1999, with permission from the Nature Publishing Group).