Academic Journal
Optimum recombination rates for genetic gains in simulated recurrent selection in empirical maize populations.
| Title: | Optimum recombination rates for genetic gains in simulated recurrent selection in empirical maize populations. |
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| Authors: | Anilkumar C; Department of Agronomy and Plant Genetics, University of Minnesota, Saint Paul, Minnesota, USA.; Indian Council of Agricultural Research-Central Rice Research Institute, Cuttack, India., Bernardo R; Department of Agronomy and Plant Genetics, University of Minnesota, Saint Paul, Minnesota, USA. |
| Source: | The plant genome [Plant Genome] 2026 Jun; Vol. 19 (2), pp. e70229. |
| Publication Type: | Journal Article |
| Language: | English |
| Journal Info: | Publisher: Crop Science Society of America Country of Publication: United States NLM ID: 101273919 Publication Model: Print Cited Medium: Internet ISSN: 1940-3372 (Electronic) Linking ISSN: 19403372 NLM ISO Abbreviation: Plant Genome Subsets: MEDLINE |
| Imprint Name(s): | Original Publication: Madison, WI : Crop Science Society of America |
| MeSH Terms: | Zea mays*/genetics , Recombination, Genetic* , Selection, Genetic*, Haplotypes ; Polymorphism, Single Nucleotide ; Crossing Over, Genetic ; Phenotype ; Genetic Linkage |
| Abstract: | Meiotic recombination creates new allelic combinations, but it also disrupts favorable parental haplotypes. Our objective was to assess if optimum recombination rates exist in elite maize (Zea mays L.) populations undergoing simulated short-term and long-term recurrent selection. Genomewide marker effects were calculated for eight populations genotyped with 3072 single nucleotide polymorphism markers and phenotyped in up to 18 environments for yield, moisture, test weight, and plant and ear height. The recombination rate was altered by multiplying the sizes of linkage maps by 0.25-10. The regression of genetic gain on the number of crossovers was often curvilinear, and an optimum number of crossovers (CO (© 2026 The Author(s). The Plant Genome published by Wiley Periodicals LLC on behalf of Crop Science Society of America.) |
| References: | Allard, R. W. (1960). Principles of plant breeding. John Wiley & Sons, Inc. Battagin, M., Gorjanc, G., Faux, A.‐M., Johnston, S. E., & Hickey, J. M. (2016). Effect of manipulating recombination rates on response to selection in livestock breeding programs. Genetics Selection Evolution, 48, Article 44. https://doi.org/10.1186/s12711‐016‐0221‐1. Bauer, E., Falque, M., Walter, H., Bauland, C., Camisan, C., Campo, L., Meyer, N., Ranc, N., Rincent, R., Schipprack, W., Altmann, T., Flament, P., Melchinger, A. E., Menz, M., Moreno‐González, J., Ouzunova, M., Revilla, P., Charcosset, A., Martin, O. C., & Schön, C.‐C. (2013). Intraspecific variation of recombination rate in maize. Genome Biology, 14, Article R103. https://doi.org/10.1186/gb‐2013‐14‐9‐r103. Bernardo, R. (1991). Retrospective index weights used in multiple trait selection in a maize breeding program. Crop Science, 31, 1174–1179. https://doi.org/10.2135/cropsci1991.0011183X003100050020x. Bernardo, R. (2017). Prospective targeted recombination and genetic gains for quantitative traits in maize. The Plant Genome, 10, plantgenome2016.11.0118. https://doi.org/10.3835/plantgenome2016.11.0118. Bernardo, R. (2020). Breeding for quantitative traits in plants (3rd ed.). Stemma Press. Bernardo, R. (2025). Contribution of crossing over to genetic variance in maize and wheat populations. The Plant Genome, 18, e20552. https://doi.org/10.1002/tpg2.20552. Bernardo, R., Moreau, L., & Charcosset, A. (2006). Number and fitness of selected individuals in marker‐assisted and phenotypic recurrent selection. Crop Science, 46, 1972–1980. https://doi.org/10.2135/cropsci2006.01‐0057. Blary, A., & Jenczewski, E. (2019). Manipulation of crossover frequency and distribution for plant breeding. Theoretical and Applied Genetics, 132, 575–592. https://doi.org/10.1007/s00122‐018‐3240‐1. Bogdanove, A. J., & Voytas, D. F. (2011). TAL effectors: Customizable proteins for DNA targeting. Science, 333(6051), 1843–1846. https://doi.org/10.1126/science.1204094. Crismani, W., & Mercier, R. (2012). What limits meiotic crossovers? Cell Cycle, 11, 3527–3528. https://doi.org/10.4161/cc.21963. Dudley, J. W. (1993). Molecular markers in plant improvement: Manipulation of genes affecting quantitative traits. Crop Science, 33, 660–668. https://doi.org/10.2135/cropsci1993.0011183X003300040003x. Dudley, J. W., Dijkhuizen, A., Paul, C., Coates, S. T., & Rocheford, T. R. (2004). Effects of random mating on marker–QTL associations in the cross of the Illinois high protein × Illinois low protein maize strains. Crop Science, 44, 1419–1428. https://doi.org/10.2135/cropsci2004.1419. Epstein, R., Sajai, N., Zelkowski, M., Zhou, A., Robbins, K. R., & Pawlowski, W. P. (2023). Exploring impact of recombination landscapes on breeding outcomes. Proceedings of the National Academy of Sciences of the USA, 120, e2205785119. https://doi.org/10.1073/pnas.2205785119. Gaynor, R. C., Gorjanc, G., & Hickey, J. M. (2021). AlphaSimR: An R package for breeding program simulations. G3 Genes|Genomes|Genetics, 11, jkaa017. https://doi.org/10.1093/g3journal/jkaa017. Gonen, S., Battagin, M., Johnston, S. E., Gorjanc, G., & Hickey, J. M. (2017). The potential of shifting recombination hotspots to increase genetic gain in livestock breeding. Genetics Selection Evolution, 49, Article 55. https://doi.org/10.1186/s12711‐017‐0330‐5. Jannink, J. L. (2010). Dynamics of long‐term genomic selection. Genetics Selection Evolution, 42, Article 35. https://doi.org/10.1186/1297‐9686‐42‐35. King, K., Ferela, A., Vyn, T. J., Trifunovic, S., Eudy, D., Hurburgh, C., Lamkey, K. R., & Archontoulis, S. V. (2024). Genetic gains in short‐season corn hybrids: Grain yield, yield components, and grain quality traits. Crop Science, 64, 710–725. https://doi.org/10.1002/csc2.21199. Krchov, L.‐M., Gordillo, G. A., & Bernardo, R. (2015). Multienvironment validation of the effectiveness of phenotypic and genomewide selection within biparental maize populations. Crop Science, 55, 1068–1075. https://doi.org/10.2135/cropsci2014.09.0608. Meng, L., Li, H., Zhang, L., & Wang, J. (2015). QTL IciMapping: Integrated software for genetic linkage map construction and quantitative trait locus mapping in biparental populations. The Crop Journal, 3, 269–283. https://doi.org/10.1016/j.cj.2015.01.001. Mercier, R., Mézard, C., Jenczewski, E., Macaisne, N., & Grelon, M. (2015). The molecular biology of meiosis in plants. Annual Review of Plant Biology, 66, 297–327. https://doi.org/10.1146/annurev‐arplant‐050213‐035923. Mieulet, D., Aubert, G., Bres, C., Klein, A., Droc, G., Vieille, E., Rond‐Coissieux, C., Sanchez, M., Dalmais, M., Mauxion, J. P., Rothan, C., Guiderdoni, E., & Mercier, R. (2018). Unleashing meiotic crossovers in crops. Nature Plants, 4, 1010–1016. https://doi.org/10.1038/s41477‐018‐0311‐x. Moyers, B. T., Morrell, P. L., & McKay, J. K. (2018). Genetic costs of domestication and improvement. Journal of Heredity, 109, 103–116. https://doi.org/10.1093/jhered/esx069. Parée, T., Noble, L., Ferreira Gonçalves, J., & Teotónio, H. (2024). rec‐1 loss of function increases recombination in the central gene clusters at the expense of autosomal pairing centers. Genetics, 226, iyad205. Presting, G. G. (2018). Centromeric retrotransposons and centromere function. Current Opinion in Genetics & Development, 49, 79–84. https://doi.org/10.1016/j.gde.2018.03.004. Rey, M.‐D., Martín, A. C., Smedley, M., Hayta, S., Harwood, W., Shaw, P., & Moore, G. (2018). Magnesium increases homoeologous crossover frequency during meiosis in ZIP4 (Ph1 gene) mutant wheat‐wild relative hybrids. Frontiers in Plant Science, 9, 509. https://doi.org/10.3389/fpls.2018.00509. Sadhu, M. J., Bloom, J. S., Day, L., & Kruglyak, L. (2016). CRISPR‐directed mitotic recombination enables genetic mapping without crosses. Science, 352, 1113–1116. https://doi.org/10.1126/science.aaf5124. Sarno, R., Vicq, Y., Uematsu, N., Luka, M., Lapierre, C., Carroll, D., Bastianelli, G., Serero, A., & Nicolas, A. (2017). Programming sites of meiotic crossovers using Spo11 fusion proteins. Nucleic Acids Research, 45, e164. https://doi.org/10.1093/nar/gkx739. Serra, H., Lambing, C., Griffin, C. H., Topp, S. D., Nageswaran, D. C., Underwood, C. J., Ziolkowski, P. A., Séguéla‐Arnaud, M., Fernandes, J. B., Mercier, R., & Henderson, I. R. (2018). Massive crossover elevation via combination of HEI10 and recq4a recq4b during Arabidopsis meiosis. Proceedings of the National Academy of Sciences of the USA, 115, 2437–2442. https://doi.org/10.1073/pnas.1713071115. Stapley, J., Feulner, P. G. D., Johnston, S. E., Santure, A. W., & Smadja, C. M. (2017). Variation in recombination frequency and distribution across eukaryotes: Patterns and processes. Philosophical Transactions of the Royal Society B: Biological Sciences, 372, 20160455. https://doi.org/10.1098/rstb.2016.0455. Stevison, L. S., Sefick, S., Rushton, C., & Graze, R. M. (2017). Recombination rate plasticity: Revealing mechanisms by design. Philosophical Transactions of the Royal Society B: Biological Sciences, 372(1736), 20160459. https://doi.org/10.1098/rstb.2016.0459. Taagen, E., Jordan, K., Akhunov, E., Sorrells, M. E., & Jannink, J.‐L. (2022). If it ain't broke, don't fix it: Evaluating the effect of increased recombination on response to selection for wheat breeding. G3 Genes|Genomes|Genetics, 12, jkac291. https://doi.org/10.1093/g3journal/jkac291. Tourrette, E., Bernardo, R., Falque, M., & Martin, O. C. (2019). Assessing by modeling the consequences of increased recombination in recurrent selection of Oryza sativa and Brassica rapa. G3 Genes|Genomes|Genetics, 9, 4169–4181. https://doi.org/10.1534/g3.119.400545. Underwood, C. J., Choi, K., Lambing, C., Zhao, X., Serra, H., Borges, F., Simorowski, J., Ernst, E., Jacob, Y., Henderson, I. R., & Martienssen, R. A. (2018). Epigenetic activation of meiotic recombination near Arabidopsis thaliana centromeres via loss of H3K9me2 and non‐CG DNA methylation. Genome Research, 28, 519–531. https://doi.org/10.1101/gr.227116.117. Wang, S., Zickler, D., Kleckner, N., & Zhang, L. (2015). Meiotic crossover patterns: Obligatory crossover, interference and homeostasis in a single process. Cell Cycle, 14, 305–314. https://doi.org/10.4161/15384101.2014.991185. Weir, B. S., Cockerham, C. C., & Reynolds, J. (1980). The effects of linkage and linkage disequilibrium on the covariances of noninbred relatives. Heredity, 45, 351–359. https://doi.org/10.1038/hdy.1980.77. Yao, Y., & Kovalchuk, I. (2011). Abiotic stress leads to somatic and heritable changes in homologous recombination frequency, point mutation frequency and microsatellite stability in Arabidopsis plants. Mutation Research, 707, 61–66. https://doi.org/10.1016/j.mrfmmm.2010.12.013. |
| Contributed Indexing: | Local Abstract: [plain-language-summary] Genes for characters are present on chromosome pairs. During meiotic cell division, crossing over can exchange segments between these chromosomes, creating new gene combinations in offspring. We aimed to see if there is an ideal number of crossovers that maximize offspring performance. Using data from eight commercial‐grade maize populations and five traits, we simulated longer chromosomes to allow more crossovers. Our findings showed that increasing crossovers up to an optimal level maximized progeny performance. However, too many crossovers can break apart useful combinations of genes already present in the parents. |
| Entry Date(s): | Date Created: 20260328 Date Completed: 20260714 Latest Revision: 20260714 |
| Update Code: | 20260714 |
| PubMed Central ID: | PMC13032164 |
| DOI: | 10.1002/tpg2.70229 |
| PMID: | 41902534 |
| Database: | MEDLINE |
| ISSN: | 1940-3372 |
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| DOI: | 10.1002/tpg2.70229 |