Mitotic recombination is a type of genetic recombination that may occur in somatic cells during mitosis in both sexual and asexual organisms. In asexual organisms, the study of mitotic recombination is one way to understand genetic linkage because it is the only source of recombination within an individual.[1] Additionally, mitotic recombination can result in the expression of recessive genes in an otherwise heterozygous individual. This expression has important implications for the study of tumorigenesis and lethal recessive genes.[1][2]
Contents
- 1 Discovery
- 2 Occurrence
- 3 Mechanisms
- 4 Method
- 5 Advantages and Disadvantages
- 6 References
Discovery
The discovery of mitotic recombination came from the observation of twin spotting in Drosophila melanogaster. This twin spotting, or mosaic spotting, was observed in D. melanogaster as early as 1925, but it was only in 1936 that Curt Stern explained it as a result of mitotic recombination. Prior to Stern's work, it was hypothesized that twin spotting happened because certain genes had the ability to eliminate the chromosome on which they were located.[3] Later experiments uncovered when mitotic recombination occurs in the cell cycle and the mechanisms behind recombination.
Mitotic recombination can result in homozygous expression in a heterozygous individual
Occurrence
Mitotic recombination can happen at any locus but is observable in individuals that are heterozygous at a given locus. If a crossover event affects that locus, then both homologous chromosomes will have one chromatid containing each genotype. The resulting phenotype of the daughter cells depends on how the chromosomes line up on the metaphase plate. If the chromatids containing different alleles line up on the same side of the plate, then the resulting daughter cells will appear heterozygous and be undetectable, despite the crossover event. However, if chromatids containing the same alleles line up on the same side, the daughter cells will be homozygous at that locus. This results in twin spotting, where one cell presents the homozygous recessive phenotype and the other cell has the homozygous wild type phenotype. If those daughter cells go on to replicate and divide, the twin spots will continue to grow and reflect the differential phenotype.
Mitotic recombination takes place during interphase. It has been suggested that recombination takes place during G1, when the DNA is in its 2-strand phase, and replicated during DNA synthesis.[4] It is also possible to have the DNA break leading to mitotic recombination happen during G1, but for the repair to happen after replication.[5][6]
Mechanisms
The mechanisms behind mitotic recombination are similar to those behind meiotic recombination. These include sister chromatid exchange and mechanisms related to DNA double strand break repair by homologous recombination such as single-strand annealing, synthesis-dependent strand annealing (SDSA), and gene conversion through a double-Holliday Junction intermediate or SDSA. In addition, non-homologous mitotic recombination is a possibility and can often be attributed to non-homologous end joining.[5][6][7][8]
Method
There are several theories on how mitotic crossover occurs. In the simple crossover model, the two homologous chromosomes overlap on or near a common Chromosomal fragile site (CFS). This leads to a double-strand break,[9] which is then repaired using one of the two strands. This can lead to the two chromatids switching places. In another model, two overlapping sister chromosomes form a double holiday junction at a common repeat site and are later sheared in such a way that they switch places. In either model, the chromosomes are not guaranteed to trade evenly, or even to rejoin on opposite sides thus most patterns of cleavage do not result in any crossover event. Uneven trading introduces many of the deleterious effects of mitotic crossover.
Alternatively, a crossover can occur during DNA repair[10] if, due to extensive damage, the homologous chromosome is chosen to be the template over the sister chromatid. This leads to gene synthesis since one copy of the allele is copied across from the homologous chromosome and then synthesized into the breach on the damaged chromosome. The net effect of this would be one heterozygous chromosome and one homozygous chromosome.
Advantages and Disadvantages
Mitotic crossover is known to occur in D. melanogaster, some asexually reproducing fungi and in normal human cells, where the event may allow normally recessive cancer-causing genes to be expressed and thus predispose the cell in which it occurs to the development of cancer. Alternately, a cell may become a homozygous mutant for a tumor-suppressing gene, leading to the same result.[2] For example, Bloom's syndrome is caused by a mutation in RecQ helicase, which plays a role in DNA replication and repair. This mutation leads to high rates of mitotic recombination in mice, and this recombination rate is in turn responsible for causing tumor susceptibility in those mice.[11] At the same time, mitotic recombination may be beneficial: it may play an important role in repairing double stranded breaks, and it may be beneficial to the organism if having homozygous dominant alleles is more functional than the heterozygous state.[2] For use in experimentation with genomes in model organisms such as Drosophila melanogaster, mitotic recombination can be induced via X-ray and the FLP-FRT recombination system.[12]
References
- ^ a b Hartl, Daniel L. and Maryellen Ruvolo (2012). Genetics: Analysis of Genetics and Genomes. Burlington: Jones & Bartlett.
- ^ a b c Tischfield, Jay A. (November 1997). "Loss of Heterozygosity, or: How I learned to Stop Worrying and Love Mitotic Recombination". American Journal of Human Genetics 61 (5): 995–999. doi:10.1086/301617.
- ^ Stern, Curt (1936). "Somatic Crossing Over and Segregation in Drosophila Melanogaster". Genetics 21 (6): 625–730.
- ^ Esposito, Michael S (September 1978). "Evidence that Spontaneous Mitotic Recombination Occurs at the Two-Strand Stage". Proceedings of the National Academy of Sciences of the USA 75 (9): 4436–4440. doi:10.1073/pnas.75.9.4436.
- ^ a b Lee, Phoebe S.; Greenwell, Patricia W.; Dominska, Margaret; Gawel, Malgorzata; Hamilton, Monica; Petes, Thomas D. (2009). "A Fine-Structure Map of Spontaneous Mitotic Crossovers in the Yeast Saccharomyces cerevisiae". PLoS Genet 5 (3): e1000410. doi:10.1371/journal.pgen.1000410. PMID 19282969.
- ^ a b LaFave, MC; J Sekelsky (2009). "Mitotic Recombination: Why? When? How? Where?". PLoS Genet 5 (3). doi:10.1371/journal.pgen.1000411.
- ^ Helleday, Thomas (2003). "Pathways for Mitotic Homologous Recombination in Mammalian Cells". Mutation Research 532 (1-2): 103–115. doi:10.1016/j.mrfmmm.2003.08.013.
- ^ Pâques, Frédéric; James E. Haber (1999). "Multiple Pathways of Recombination Induced by Double-Strand Breaks in Saccharomyces cerevisiae". Microbiology and Molecular Biology Reviews 63 (2): 349–404.
- ^ Helleday, T. "Double-Strand Break Repair via Double Holliday Junctions (Szostak Model)". Animation. MIT.
- ^ Helleday, Thomas (27 November 2003). "Pathways for mitotic homologous recombination in mammalian cells". Mutation research 532 (1-2): 103–115. doi:10.1016/j.mrfmmm.2003.08.013. Retrieved 2012-12-26.
- ^ Luo, Guangbin; et al. (2000). "Cancer predisposition caused by elevated mitotic recombination in Bloom mice". Nature Genetics 26: 424–429. doi:10.1038/82548. PMID 11101838.
- ^ Xu, T; GM Rubin (April 1993). "Analysis of genetic mosaics in developing and adult Drosophila tissues". Development 117 (4): 1223–12237.
- Griffiths et al. 1999. Modern Genetic Analysis. W. H. Freeman and Company.
