Gonzalo, M. J., Díaz, A., Dhillon, N. P. S., Reddy, U. K., Picó, B., & Monforte, A. J. (2019). Re-evaluation of the role of Indian germplasm as center of melon diversification based on genotyping-by-sequencing analysis. BMC Genomics, 20(1). doi:10.1186/s12864-019-5784-0
Telford, I. R. H., Schaefer, H., Greuter, W., & Renner, S. (2011). A new Australian species of Luffa (Cucurbitaceae) and typification of two Australian Cucumis names, all based on specimens collected by Ferdinand Mueller in 1856. PhytoKeys, 5(0), 21. doi:10.3897/phytokeys.5.1395
Filipowicz, N., Schaefer, H., & Renner, S. S. (2014). Revisiting <I>Luffa</I> (Cucurbitaceae) 25 Years After C. Heiser: Species Boundaries and Application of Names Tested with Plastid and Nuclear DNA Sequences. Systematic Botany, 39(1), 205-215. doi:10.1600/036364414x678215
[+]
Gonzalo, M. J., Díaz, A., Dhillon, N. P. S., Reddy, U. K., Picó, B., & Monforte, A. J. (2019). Re-evaluation of the role of Indian germplasm as center of melon diversification based on genotyping-by-sequencing analysis. BMC Genomics, 20(1). doi:10.1186/s12864-019-5784-0
Telford, I. R. H., Schaefer, H., Greuter, W., & Renner, S. (2011). A new Australian species of Luffa (Cucurbitaceae) and typification of two Australian Cucumis names, all based on specimens collected by Ferdinand Mueller in 1856. PhytoKeys, 5(0), 21. doi:10.3897/phytokeys.5.1395
Filipowicz, N., Schaefer, H., & Renner, S. S. (2014). Revisiting <I>Luffa</I> (Cucurbitaceae) 25 Years After C. Heiser: Species Boundaries and Application of Names Tested with Plastid and Nuclear DNA Sequences. Systematic Botany, 39(1), 205-215. doi:10.1600/036364414x678215
Kistler, L., Montenegro, A., Smith, B. D., Gifford, J. A., Green, R. E., Newsom, L. A., & Shapiro, B. (2014). Transoceanic drift and the domestication of African bottle gourds in the Americas. Proceedings of the National Academy of Sciences, 111(8), 2937-2941. doi:10.1073/pnas.1318678111
Sebastian, P., Schaefer, H., Telford, I. R. H., & Renner, S. S. (2010). Cucumber (Cucumis sativus) and melon (C. melo) have numerous wild relatives in Asia and Australia, and the sister species of melon is from Australia. Proceedings of the National Academy of Sciences, 107(32), 14269-14273. doi:10.1073/pnas.1005338107
Endl, J., Achigan-Dako, E. G., Pandey, A. K., Monforte, A. J., Pico, B., & Schaefer, H. (2018). Repeated domestication of melon (Cucumis melo
) in Africa and Asia and a new close relative from India. American Journal of Botany, 105(10), 1662-1671. doi:10.1002/ajb2.1172
Esteras, C., Formisano, G., Roig, C., Díaz, A., Blanca, J., Garcia-Mas, J., … Picó, B. (2013). SNP genotyping in melons: genetic variation, population structure, and linkage disequilibrium. Theoretical and Applied Genetics, 126(5), 1285-1303. doi:10.1007/s00122-013-2053-5
Zhao, G., Lian, Q., Zhang, Z., Fu, Q., He, Y., Ma, S., … Huang, S. (2019). A comprehensive genome variation map of melon identifies multiple domestication events and loci influencing agronomic traits. Nature Genetics, 51(11), 1607-1615. doi:10.1038/s41588-019-0522-8
Roy, A., Bal, S. S., Fergany, M., Kaur, S., Singh, H., Malik, A. A., … Dhillon, N. P. S. (2011). Wild melon diversity in India (Punjab State). Genetic Resources and Crop Evolution, 59(5), 755-767. doi:10.1007/s10722-011-9716-3
Díaz, A., Martín-Hernández, A. M., Dolcet-Sanjuan, R., Garcés-Claver, A., Álvarez, J. M., Garcia-Mas, J., … Monforte, A. J. (2017). Quantitative trait loci analysis of melon (Cucumis melo L.) domestication-related traits. Theoretical and Applied Genetics, 130(9), 1837-1856. doi:10.1007/s00122-017-2928-y
Garcia-Mas, J., Monforte, A. J., & Ar�s, P. (2004). Phylogenetic relationships among Cucumis species based on the ribosomal internal transcribed spacer sequence and microsatellite markers. Plant Systematics and Evolution, 248(1-4). doi:10.1007/s00606-004-0170-y
Studer, A., Zhao, Q., Ross-Ibarra, J., & Doebley, J. (2011). Identification of a functional transposon insertion in the maize domestication gene tb1. Nature Genetics, 43(11), 1160-1163. doi:10.1038/ng.942
Li, C., Zhou, A., & Sang, T. (2006). Rice Domestication by Reducing Shattering. Science, 311(5769), 1936-1939. doi:10.1126/science.1123604
Frary, A., Nesbitt, T. C., Frary, A., Grandillo, S., Knaap, E. van der, Cong, B., … Tanksley, S. D. (2000). fw2.2
: A Quantitative Trait Locus Key to the Evolution of Tomato Fruit Size. Science, 289(5476), 85-88. doi:10.1126/science.289.5476.85
Sanseverino, W., Hénaff, E., Vives, C., Pinosio, S., Burgos-Paz, W., Morgante, M., … Casacuberta, J. M. (2015). Transposon Insertions, Structural Variations, and SNPs Contribute to the Evolution of the Melon Genome. Molecular Biology and Evolution, 32(10), 2760-2774. doi:10.1093/molbev/msv152
Elshire, R. J., Glaubitz, J. C., Sun, Q., Poland, J. A., Kawamoto, K., Buckler, E. S., & Mitchell, S. E. (2011). A Robust, Simple Genotyping-by-Sequencing (GBS) Approach for High Diversity Species. PLoS ONE, 6(5), e19379. doi:10.1371/journal.pone.0019379
Garcia-Mas, J., Benjak, A., Sanseverino, W., Bourgeois, M., Mir, G., Gonzalez, V. M., … Puigdomenech, P. (2012). The genome of melon (Cucumis melo L.). Proceedings of the National Academy of Sciences, 109(29), 11872-11877. doi:10.1073/pnas.1205415109
Brewer, M. T., Lang, L., Fujimura, K., Dujmovic, N., Gray, S., & van der Knaap, E. (2006). Development of a Controlled Vocabulary and Software Application to Analyze Fruit Shape Variation in Tomato and Other Plant Species. Plant Physiology, 141(1), 15-25. doi:10.1104/pp.106.077867
Lander, E. S., & Botstein, D. (1989). Mapping mendelian factors underlying quantitative traits using RFLP linkage maps. Genetics, 121(1), 185-199. doi:10.1093/genetics/121.1.185
KOSAMBI, D. D. (1943). THE ESTIMATION OF MAP DISTANCES FROM RECOMBINATION VALUES. Annals of Eugenics, 12(1), 172-175. doi:10.1111/j.1469-1809.1943.tb02321.x
Zeng, Z. B. (1994). Precision mapping of quantitative trait loci. Genetics, 136(4), 1457-1468. doi:10.1093/genetics/136.4.1457
Windows QTL Cartographer V2.5_011http://statgen.ncsu.edu/qtlcart/WQTLCart.htm
Argyris, J. M., Pujol, M., Martín-Hernández, A. M., & Garcia-Mas, J. (2015). Combined use of genetic and genomics resources to understand virus resistance and fruit quality traits in melon. Physiologia Plantarum, 155(1), 4-11. doi:10.1111/ppl.12323
Sun, S., Wang, X., Wang, K., & Cui, X. (2019). Dissection of complex traits of tomato in the post-genome era. Theoretical and Applied Genetics, 133(5), 1763-1776. doi:10.1007/s00122-019-03478-y
Fisher, R. A. (1919). XV.—The Correlation between Relatives on the Supposition of Mendelian Inheritance. Transactions of the Royal Society of Edinburgh, 52(2), 399-433. doi:10.1017/s0080456800012163
Causse, M., Chaïb, J., Lecomte, L., Buret, M., & Hospital, F. (2007). Both additivity and epistasis control the genetic variation for fruit quality traits in tomato. Theoretical and Applied Genetics, 115(3), 429-442. doi:10.1007/s00122-007-0578-1
Würschum, T., Maurer, H. P., Schulz, B., Möhring, J., & Reif, J. C. (2011). Genome-wide association mapping reveals epistasis and genetic interaction networks in sugar beet. Theoretical and Applied Genetics, 123(1), 109-118. doi:10.1007/s00122-011-1570-3
Sáez, C., Esteras, C., Martínez, C., Ferriol, M., Dhillon, N. P. S., López, C., & Picó, B. (2017). Resistance to tomato leaf curl New Delhi virus in melon is controlled by a major QTL located in chromosome 11. Plant Cell Reports, 36(10), 1571-1584. doi:10.1007/s00299-017-2175-3
Díaz, A., Zarouri, B., Fergany, M., Eduardo, I., Álvarez, J. M., Picó, B., & Monforte, A. J. (2014). Mapping and Introgression of QTL Involved in Fruit Shape Transgressive Segregation into ‘Piel de Sapo’ Melon (Cucucumis melo L.). PLoS ONE, 9(8), e104188. doi:10.1371/journal.pone.0104188
Wallace, J. G., Larsson, S. J., & Buckler, E. S. (2013). Entering the second century of maize quantitative genetics. Heredity, 112(1), 30-38. doi:10.1038/hdy.2013.6
Stitzer, M. C., & Ross‐Ibarra, J. (2018). Maize domestication and gene interaction. New Phytologist, 220(2), 395-408. doi:10.1111/nph.15350
Studer, A. J., & Doebley, J. F. (2011). Do Large Effect QTL Fractionate? A Case Study at the Maize Domestication QTL teosinte branched1. Genetics, 188(3), 673-681. doi:10.1534/genetics.111.126508
Mu, Q., Huang, Z., Chakrabarti, M., Illa-Berenguer, E., Liu, X., Wang, Y., … van der Knaap, E. (2017). Fruit weight is controlled by Cell Size Regulator encoding a novel protein that is expressed in maturing tomato fruits. PLOS Genetics, 13(8), e1006930. doi:10.1371/journal.pgen.1006930
Czerednik, A., Busscher, M., Bielen, B. A. M., Wolters-Arts, M., de Maagd, R. A., & Angenent, G. C. (2012). Regulation of tomato fruit pericarp development by an interplay between CDKB and CDKA1 cell cycle genes. Journal of Experimental Botany, 63(7), 2605-2617. doi:10.1093/jxb/err451
Doebley, J., Stec, A., & Gustus, C. (1995). teosinte branched1 and the origin of maize: evidence for epistasis and the evolution of dominance. Genetics, 141(1), 333-346. doi:10.1093/genetics/141.1.333
Von Korff, M., Léon, J., & Pillen, K. (2010). Detection of epistatic interactions between exotic alleles introgressed from wild barley (H. vulgare ssp. spontaneum). Theoretical and Applied Genetics, 121(8), 1455-1464. doi:10.1007/s00122-010-1401-y
Azhaguvel, P., Vidya-Saraswathi, D., & Komatsuda, T. (2006). High-resolution linkage mapping for the non-brittle rachis locus btr1 in cultivated × wild barley (Hordeum vulgare). Plant Science, 170(6), 1087-1094. doi:10.1016/j.plantsci.2006.01.013
Sakuma, S., Salomon, B., & Komatsuda, T. (2011). The Domestication Syndrome Genes Responsible for the Major Changes in Plant Form in the Triticeae Crops. Plant and Cell Physiology, 52(5), 738-749. doi:10.1093/pcp/pcr025
Monforte, A. J., Friedman, E., Zamir, D., & Tanksley, S. D. (2001). Comparison of a set of allelic QTL-NILs for chromosome 4 of tomato: Deductions about natural variation and implications for germplasm utilization. Theoretical and Applied Genetics, 102(4), 572-590. doi:10.1007/s001220051684
Gur, A., & Zamir, D. (2004). Unused Natural Variation Can Lift Yield Barriers in Plant Breeding. PLoS Biology, 2(10), e245. doi:10.1371/journal.pbio.0020245
Kovach, M., & McCouch, S. (2008). Leveraging natural diversity: back through the bottleneck. Current Opinion in Plant Biology, 11(2), 193-200. doi:10.1016/j.pbi.2007.12.006
Doust, A. N., Lukens, L., Olsen, K. M., Mauro-Herrera, M., Meyer, A., & Rogers, K. (2014). Beyond the single gene: How epistasis and gene-by-environment effects influence crop domestication. Proceedings of the National Academy of Sciences, 111(17), 6178-6183. doi:10.1073/pnas.1308940110
[-]