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An evolutionary view of human recombination
Abstract
Recombination has essential functions in mammalian meiosis, which impose several constraints on the recombination process. However, recent studies have shown that, in spite of these roles, recombination rates vary tremendously among humans, and show marked differences between humans and closely related species. These findings provide important insights into the determinants of recombination rates and raise new questions about the selective pressures that affect recombination over different genomic scales, with implications for human genetics and evolutionary biology.
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“because short chromosomes have a higher recombination rate 67”
From Genome analysis of the platypus reveals unique signatures of evolution (2008) · cites this paper as [67]
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“Specifically, selection for a recombination driver allele may be favored when it is tightly linked to two or more genes with alleles under selection (61).”
From Comparative analysis of the domestic cat genome reveals genetic signatures underlying feline biology and domestication (2014) · cites this paper as [61]
Citations
Cites
Pleiotropy, natural selection, and the evolution of senescence.
Williams, G. C. (1957) · Evolution · doi:10.1111/j.1558-5646.1957.tb02911.x · Cited by 4,279
To err (meiotically) is human: the genesis of human aneuploidy
Hassold, T. J., & Hunt, P. A. (2001) · Nature Reviews Genetics · doi:10.1038/35066065 · Cited by 2,456
The effect of linkage on limits to artificial selection
Hill, W. G., & Robertson, A. (1966) · Genetical Research · doi:10.1017/s0016672300010156 · Cited by 1,823
Sex ratio and unisexual sterility in hybrid animals
Haldane, J. B. S. (1922) · Journal of Genetics · doi:10.1007/bf02983075 · Cited by 1,820
A high-resolution recombination map of the human genome
Kong, A., Gudbjartsson, D. F., Sainz, J., Jonsdottir, G. M., Gudjonsson, S. A., Richardsson, B., Sigurdardottir, S. L., Barnard, J., Hallbeck, B., Másson, G., et al. (2002) · Nature Genetics · doi:10.1038/ng917 · Cited by 1,750
THE EVOLUTIONARY ADVANTAGE OF RECOMBINATION
Felsenstein, J. (1974) · Genetics · doi:10.1093/genetics/78.2.737 · Cited by 1,711
The effect of linkage on limits to artificial selection
Hill, W. G., & Robertson, A. (2007) · Genetics Research · doi:10.1017/s001667230800949x · Cited by 1,562
(1991) · Choice Reviews Online · doi:10.5860/choice.28-5664 · Cited by 1,306
Meiotic Chromosomes: Integrating Structure and Function
Zickler, D., & Kleckner, N. E. (1999) · Annual Review of Genetics · doi:10.1146/annurev.genet.33.1.603 · Cited by 1,256
A Fine-Scale Map of Recombination Rates and Hotspots Across the Human Genome
Myers, S., Bottolo, L., Freeman, C., McVean, G., & Donnelly, P. (2005) · Science · doi:10.1126/science.1117196 · Cited by 1,134
Flagged first, then by citations
Research works printed but not linked: 3
- Li, W. -H. Molecular Evolution (Sinauer Associates, Sunderland, 1997).
- Sturtevant, A. H. The genetics of Drosophila simulans. Carnegie Inst. Washington Publ. 399, 1–62. (1929).
- Trivers, R. L. in The Evolution Of Sex (eds Michod, R. E. & Levin, B. R.) 270–286 (Sinauer Associates, Sunderland, 1988).
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Sorted by citations
Items 101–200 of 346
Poissant, J., Hogg, J. T., Davis, C. S., Miller, J. M., Maddox, J. F., & Coltman, D. W. (2010) · BMC Genomics · doi:10.1186/1471-2164-11-524 · Cited by 48
Human-macaque comparisons illuminate variation in neutral substitution rates
Tyekucheva, S., Makova, K. D., Karro, J. E., Hardison, R. C., Miller, W., & Chiaromonte, F. (2008) · Genome biology · doi:10.1186/gb-2008-9-4-r76 · Cited by 50
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Muñoz‐Fuentes, V., Marcet-Ortega, M., Alkorta‐Aranburu, G., Forsberg, C. L., Morrell, J. M., Manzano-Piedras, E., Söderberg, A., Daniel, K., Villalba, A., Tóth, A., et al. (2014) · Molecular Biology and Evolution · doi:10.1093/molbev/msu322 · Cited by 47
Andolfatto, P. (2008) · Genetics · doi:10.1534/genetics.108.091850 · Cited by 47
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Basheva, E. A., Bidau, C. J., & Бородин, П. М. (2008) · Chromosome Research · doi:10.1007/s10577-008-1221-y · Cited by 47
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Dapper, A. L., & Payseur, B. A. (2019) · Evolution · doi:10.1111/evo.13850 · Cited by 39
Lim, M., Witt, C. C., Graham, C. H., & Dávalos, L. M. (2019) · Genome Biology and Evolution · doi:10.1093/gbe/evz101 · Cited by 44
Sun, F., Mikhaail-Philips, M., Oliver‐Bonet, M., Ko, E., RADEMAKER, A. W., Turek, P. J., & Martin, R. H. (2008) · Molecular Human Reproduction · doi:10.1093/molehr/gan030 · Cited by 42
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Xu, S., Ackerman, M. S., Long, H., Bright, L. J., Spitze, K., Ramsdell, J. S., Thomas, W. K., & Lynch, M. (2015) · Genetics · doi:10.1534/genetics.115.179028 · Cited by 44
Zhu, L., Fernández‐Jiménez, N., Szymańska-Lejman, M., Pelé, A., Underwood, C. J., Serra, H., Lambing, C., Dluzewska, J., Bieluszewski, T., Pradillo, M., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2021970118 · Cited by 40
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Alves, I., Houle, A. A., Hussin, J., & Awadalla, P. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0465 · Cited by 37
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Kent, C. F., & Zayed, A. (2013) · Communicative & Integrative Biology · doi:10.4161/cib.22919 · Cited by 39
Vaughan, L. K., Divers, J., Padilla, M. A., Redden, D. T., Tiwari, H. K., Pomp, D., & Allison, D. B. (2008) · Computational Statistics & Data Analysis · doi:10.1016/j.csda.2008.02.032 · Cited by 37
High Diversity at PRDM9 in Chimpanzees and Bonobos
Groeneveld, L. F., Atencia, R., Garriga, R. M., & Vigilant, L. (2012) · PLoS ONE · doi:10.1371/journal.pone.0039064 · Cited by 42
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Imai, Y., Biot, M., Clément, J. A. J., Teragaki, M., Urbach, S., Robert, T., Baudat, F., Grey, C., & de Massy, B. (2020) · eLife · doi:10.7554/elife.57117 · Cited by 39
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Clark, A. G., Wang, X., & Matise, T. C. (2010) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-082908-150031 · Cited by 39
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Van Arsdale, A. P. (2019) · Annual Review of Anthropology · doi:10.1146/annurev-anthro-102218-011154 · Cited by 18
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Lawrence, E. J., Griffin, C., & Henderson, I. R. (2017) · Journal of Experimental Botany · doi:10.1093/jxb/erx306 · Cited by 38
Tigano, A., Khan, R., Omer, A. D., Weisz, D., Dudchenko, O., Multani, A. S., Pathak, S., Behringer, R. R., Aiden, E. L., Fisher, H. S., et al. (2022) · Evolution · doi:10.1111/evo.14467 · Cited by 31
Influenza A virus reassortment is strain dependent
Taylor, K. Y., Agu, I., José, I. R., Mäntynen, S., Campbell, A. J., Mattson, C. L., Chou, T.-W., Zhou, B., Gresham, D., Ghedin, E., et al. (2023) · PLoS Pathogens · doi:10.1371/journal.ppat.1011155 · Cited by 35
Extreme Differences in Recombination Rate between the Genomes of a Solitary and a Social Bee
Jones, J. C., Wållberg, A., Christmas, M. J., Kapheim, K. M., & Webster, M. T. (2019) · Molecular Biology and Evolution · doi:10.1093/molbev/msz130 · Cited by 35
Ma, J., Iannuccelli, N., Duan, Y., Huang, W., Guo, B., Riquet, J., Lusheng, H., & Denis Milan, A. (2010) · BMC Genomics · doi:10.1186/1471-2164-11-159 · Cited by 35
Variation in crossover interference levels on individual chromosomes from human males
Lian, J., Yin, Y. A., Oliver‐Bonet, M., Liehr, T., Ko, E., Turek, P. J., Sun, F., & Martin, R. H. (2008) · Human Molecular Genetics · doi:10.1093/hmg/ddn158 · Cited by 35
Hering, S., Edelmann, J., Augustin, C., Kuhlisch, E., & Szibor, R. (2009) · International Journal of Legal Medicine · doi:10.1007/s00414-009-0387-y · Cited by 34
Sequence imperfections and base triplet recognition by the Rad51/RecA family of recombinases
Lee, J. Y., Steinfeld, J. B., Qi, Z., Kwon, Y., Sung, P., & Greene, E. C. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.787614 · Cited by 32
Cheng, R., Ma, Y., Nie, Y., Qiao, X., Yang, Z., Zeng, R., & Xu, L. (2017) · Reproductive BioMedicine Online · doi:10.1016/j.rbmo.2017.03.022 · Cited by 31
Biochemical attributes of mitotic and meiotic presynaptic complexes
Crickard, J. B., & Greene, E. C. (2018) · DNA repair · doi:10.1016/j.dnarep.2018.08.018 · Cited by 35
Castellano, D., Eyre‐Walker, A., & Munch, K. (2019) · Genome Biology and Evolution · doi:10.1093/gbe/evz215 · Cited by 30
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Liu, H., Maclean, C. J., & Zhang, J. (2018) · Molecular Biology and Evolution · doi:10.1093/molbev/msy233 · Cited by 28
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Lee, I.-W., Kuan, L.-C., Lin, C., Pan, H., Hsu, C., Tsai, Y.-C., Kuo, P., & Teng, Y. (2008) · Asian Journal of Andrology · doi:10.1111/j.1745-7262.2008.00439.x · Cited by 28
Furman, B. L. S., & Evans, B. J. (2018) · Genome Biology and Evolution · doi:10.1093/gbe/evy045 · Cited by 28
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Simonti, C., & Capra, J. A. (2015) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2015.08.005 · Cited by 24
Manzano‐Winkler, B., McGaugh, S. E., & Noor, M. A. F. (2013) · PLoS ONE · doi:10.1371/journal.pone.0071582 · Cited by 25
Lišková, P., Gwilliam, R., Filipec, M., Jirsová, K., Merjava, S. R., Deloukas, P., Webb, T. R., Bhattacharya, S. S., Ebenezer, N. D., Morris, A. G., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0045495 · Cited by 25
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Carrasco, B., Serrano, E., Sánchez, H., Wyman, C., & Alonso, J. C. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkv1546 · Cited by 25
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Initiation of Meiotic Recombination in Mammals
Kumar, R., & de Massy, B. (2010) · Genes · doi:10.3390/genes1030521 · Cited by 30
Reduced meiotic recombination in rhesus macaques and the origin of the human recombination landscape
Xue, C., Rustagi, N., Liu, X., Raveendran, M., Harris, R. A., Venkata, M. G., Rogers, J., & Yu, F. (2020) · PLoS ONE · doi:10.1371/journal.pone.0236285 · Cited by 19
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Boideau, F., Pelé, A., Tanguy, C., Trotoux, G., Eber, F., Maillet, L., Gilet, M.-M., Lodé‐Taburel, M., Huteau, V., Morice, J., et al. (2021) · Biology · doi:10.3390/biology10080771 · Cited by 22
Brekke, C., Berg, P., Gjuvsland, A. B., & Johnston, S. E. (2022) · Genetics Selection Evolution · doi:10.1186/s12711-022-00723-9 · Cited by 22
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Adrian, A. B., Corchado, J. C., & Comeron, J. M. (2016) · Genome Biology and Evolution · doi:10.1093/gbe/evw181 · Cited by 22
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Zhang, J., Kadri, N. K., Mullaart, E., Spelman, R. J., Fritz, S., Boichard, D., Charlier, C., Georges, M., & Druet, T. (2020) · Heredity · doi:10.1038/s41437-020-0341-9 · Cited by 23
Fröhlich, J., Vozdová, M., Kubı́čková, S., Černohorská, H., Sebestova, H., & Rubeš, J. (2015) · Cytogenetic and Genome Research · doi:10.1159/000439452 · Cited by 21
Zhou, Y., Shen, B., Jiang, J., Padhi, A., Park, K., Oswalt, A., Sattler, C. G., Telugu, B. P. V. L., Chen, H., Cole, J. B., et al. (2017) · DNA Research · doi:10.1093/dnares/dsx048 · Cited by 21
Venu, V., Harjunmaa, E., Dréau, A., Brady, S. D., Absher, D., Kingsley, D. M., & Jones, F. C. (2024) · Nature Ecology & Evolution · doi:10.1038/s41559-024-02434-4 · Cited by 22
Versoza, C. J., Weiss, S. A., Johal, R., Rosa, B. L., Jensen, J. D., & Pfeifer, S. P. (2023) · Genome Biology and Evolution · doi:10.1093/gbe/evad223 · Cited by 19
Synapsis and Meiotic Recombination in Male Chinese Muntjac (Muntiacus reevesi)
Yang, Q., Zhang, D., Leng, M., Yang, L., Zhong, L., Cooke, H. J., & Shi, Q. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019255 · Cited by 20
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Bessoltane, N., Toffano‐Nioche, C., Solignac, M., & Mougel, F. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036229 · Cited by 19
Rueppell, O., Kuster, R. D., Miller, K., Fouks, B., Correa, S. Y., Collazo, J., Phaincharoen, M., Tingek, S., & Koeniger, N. (2016) · Genome Biology and Evolution · doi:10.1093/gbe/evw269 · Cited by 19
Schmid‐Hempel, P. (2021) · Oxford University Press eBooks · doi:10.1093/oso/9780198832140.003.0005 · Cited by 19
Long, X., & Xue, H. (2021) · Human Genomics · doi:10.1186/s40246-021-00318-3 · Cited by 21
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Ahlawat, S., Sharma, P., Sharma, R., Arora, R., Verma, N. K., Brahma, B., Mishra, P., & De, S. (2016) · Animal Genetics · doi:10.1111/age.12487 · Cited by 20
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Liu, G., Xing, Y., & Cai, L. (2015) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2015.06.030 · Cited by 16
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Mouresan, E. F., González‐Rodríguez, A., Álvarez, J. J. C., Munilla, S., Altarriba, J., Díaz, C., de la Fuente, J. Á. B., Molina, A., López‐Buesa, P., Piedrafita, J., et al. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.01170 · Cited by 15
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Řeboun, M., Sikora, J., Magner, M., Wiederlechnerová, H., Černá, A., Poupětová, H., Štorkánová, G., Mušálková, D., Dostálová, G., Goláň, L., et al. (2022) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.62728 · Cited by 15
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Wang, R. J., Predrag Radivojac, A., & Hahn, M. W. (2020) · Genetics · doi:10.1093/genetics/iyaa014 · Cited by 11
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McGaugh, S. E., Heil, C. S., Manzano‐Winkler, B., Himmel, T. L., & Noor, M. A. F. (2012) · Nature Precedings · doi:10.1038/npre.2012.7005.1 · Cited by 13
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Dumont, B. L., Devlin, A. A., Truempy, D. M., Miller, J. C., & Singh, N. D. (2015) · PLoS ONE · doi:10.1371/journal.pone.0142266 · Cited by 12
del Priore, L., & Pigozzi, M. I. (2020) · PLoS ONE · doi:10.1371/journal.pone.0240245 · Cited by 11
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Self-citationGenome-wide recombination map construction from single sperm sequencing in cattle
Yang, L., Gao, Y., Li, M., Park, K., Liu, S., Kang, X., Liu, M., Oswalt, A., Fang, L., Telugu, B. P. V. L., et al. (2022) · BMC Genomics · doi:10.1186/s12864-022-08415-w · Cited by 11
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Single-crossover recombination and ancestral recombination trees
Baake, E., & von Wangenheim, U. (2011) · PUB – Publications at Bielefeld University (Bielefeld University) · Cited by 11
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Topaloudis, A., Cumer, T., Lavanchy, E., Ducrest, A., Simon, C., Machado, A. P., Paposhvili, N., Roulin, A., & Goudet, J. (2024) · Genetics · doi:10.1093/genetics/iyae190 · Cited by 10
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Pettie, N., Llopart, A., & Comeron, J. M. (2022) · PLoS Genetics · doi:10.1371/journal.pgen.1010087 · Cited by 10
Evidence of Site-Specific and Male-Biased Germline Mutation Rate in a Wild Songbird
Zhang, H., Lundberg, M., Tarka, M., Hasselquist, D., & Hansson, B. (2023) · Genome Biology and Evolution · doi:10.1093/gbe/evad180 · Cited by 12
MRLR: unraveling high-resolution meiotic recombination by linked reads
Xu, P., Kennell, T., Gao, M., Kimberly, R. P., & Chong, Z. (2019) · Bioinformatics · doi:10.1093/bioinformatics/btz503 · Cited by 9
Variation in Patterns of Human Meiotic Recombination
Khil, P. P., & Camerini‐Otero, R. D. (2008) · Genome dynamics · doi:10.1159/000166623 · Cited by 10
BARRIERS TO THE SPREAD OF NEUTRAL ALLELES IN THE CYTONUCLEAR SYSTEM
Hu, X. (2008) · Evolution · doi:10.1111/j.1558-5646.2008.00439.x · Cited by 10
Accounting for haplotype phase uncertainty in linkage disequilibrium estimation
Kulle, B., Frigessi, A., Edvardsen, H., Kristensen, V. N., & Wojnowski, L. (2007) · Genetic Epidemiology · doi:10.1002/gepi.20273 · Cited by 10
Structural Genomics: Correlation Blocks, Population Structure, and Genome Architecture
Hu, X., Yeh, F. C., & Wang, Z. (2011) · Current Genomics · doi:10.2174/138920211794520141 · Cited by 10
Genomic features of meiotic crossovers in diploid potato
Jiang, X., Li, D., Du, H., Wang, P., Guo, L., Zhu, G., & Zhang, C. (2023) · Horticulture Research · doi:10.1093/hr/uhad079 · Cited by 9
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Metadata
- Authors
- Coop, G., & Przeworski, M.
- Affiliations
- University of Chicago (US)
- Corresponding author
- Przeworski, Molly
- Venue
- Nature Reviews Genetics
- Published
- 2006-12-05
- Volume
- 8
- Issue
- 1
- Pages
- 23-34
- ISSN
- 1471-0056 (ISSN-L)
- 1471-0064
- OpenAlex
- W2085231911
- Cited by
- 344
- References
- 143
- Citations by year
- 2026: 5 · 2025: 15 · 2024: 12 · 2023: 12 · 2022: 18 · 2021: 53 · 2020: 10 · 2019: 14 · 2018: 13 · 2017: 25 · 2016: 15 · 2015: 17 · 2014: 12 · 2013: 14 · 2012: 12
- FWCI
- 1.35
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Reviews Genetics (publishedVersion)
- PubMed (publishedVersion)
- Funders
- University of Chicago
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Chromosomal and Genetic Variations
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Keywords
- meiotic recombination, recombination rate variation, mammalian meiosis, recombination hotspots, recombination rate evolution, comparative genomics, human genetics
- MeSH terms
- Animals, Crossing Over, Genetic, Biological Evolution, Female, Humans, Male, Mammals, Meiosis, Models, Genetic, Recombination, Genetic, Selection, Genetic, Sex Characteristics, Species Specificity, Linkage Disequilibrium, Genome, Human
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