Abstract
Key message
Potatoes are highly heterozygous and the conventional breeding of superior germplasm is challenging, but use of a combination of MAS and EBVs can accelerate genetic gain.
Abstract
Cultivated potatoes are highly heterozygous due to their outbreeding nature, and suffer acute inbreeding depression. Modern potato cultivars also exhibit tetrasomic inheritance. Due to this genetic heterogeneity, the large number of target traits and the specific requirements of commercial cultivars, potato breeding is challenging. A conventional breeding strategy applies phenotypic recurrent selection over a number of generations, a process which can take over 10 years. Recently, major advances in genetics and molecular biology have provided breeders with molecular tools to accelerate gains for some traits. Marker-assisted selection (MAS) can be effectively used for the identification of major genes and quantitative trait loci that exhibit large effects. There are also a number of complex traits of interest, such as yield, that are influenced by a large number of genes of individual small effect where MAS will be difficult to deploy. Progeny testing and the use of pedigree in the analysis can provide effective identification of the superior genetic factors that underpin these complex traits. Recently, it has been shown that estimated breeding values (EBVs) can be developed for complex potato traits. Using a combination of MAS and EBVs for simple and complex traits can lead to a significant reduction in the length of the breeding cycle for the identification of superior germplasm.
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References
Andersen JR, Lübberstedt T (2003) Functional markers in plants. Trends Plant Sci 8:554–560
Andolfo G, Sanseverino W, Rombauts S, Van de Peer Y, Bradeen JM, Carputo D, Frusciante L, Ercolano MR (2013) Overview of tomato (Solanum lycopersicum) candidate pathogen recognition genes reveals important Solanum R locus dynamics. New Phytol 197:223–237
Anithakumari AM, Dolstra O, Vosman B, Visser RGF, van der Linden CG (2011) In vitro screening and QTL analysis for drought tolerance in diploid potato. Euphytica 181:357–369
Bakker E, Achenbach U, Bakker J, Vliet J, Peleman J, Segers B, Heijden S, Linde P, Graveland R, Hutten R, Eck H, Coppoolse E, Vossen E, Bakker J, Goverse A (2004) A high-resolution map of the H1 locus harbouring resistance to the potato cyst nematode Globodera rostochiensis. Theor Appl Genet 109:146–152
Bakker E, Borm T, Prins P, van der Vossen E, Uenk G, Arens M, de Boer J, van Eck H, Ml Muskens, Vossen J, van der Linden G, van Ham R, Klein-Lankhorst R, Visser R, Smant G, Bakker J, Goverse A (2011) A genome-wide genetic map of NB-LRR disease resistance loci in potato. Theor Appl Genet 123:493–508
Baldwin SJ, Dodds KG, Auvray B, Genet RA, Macknight RC, Jacobs JME (2011) Association mapping of cold-induced sweetening in potato using historical phenotypic data. Ann Appl Biol 158:248–256
Ballvora A, Hesselbach J, Niewöhner J, Leister D, Salamini F, Gebhardt C (1995) Marker enrichment and high-resolution map of the segment of potato chromosome VII harbouring the nematode resistance gene Gro1. Mol Gen Genet 249:82–90
Barone A (2004) Molecular marker-assisted selection for potato breeding. Am J Potato Res 81:111–117
Barone A, Ritter E, Schachtschabel U, Debener T, Salamini F, Gebhardt C (1990) Localization by restriction fragment length polymorphism mapping in potato of a major dominant gene conferring resistance to the potato cyst nematode Globodera rostochiensis. Mol Gen Genet 224:177–182
Barrell PJ, Meiyalaghan S, Jacobs JME, Conner AJ (2013) Applications of biotechnology and genomics in potato improvement. Plant Biotechnol J 11:907–920
Bendahmane A, Kanyuka K, Baulcombe D (1997) High-resolution genetical and physical mapping of the Rx gene for extreme resistance to potato virus X in tetraploid potato. Theor Appl Genet 95:153–162
Biryukova V, Zhuravlev A, Abrosimova S, Kostina L, Khromova L, Shmyglya I, Morozova N, Kirsanova S (2008) Use of molecular markers of potato golden nematode resistance genes H1 and GRO1. Russ Agric Sci 34:365–368
Bonierbale MW, Plaisted RL, Tanksley SD (1988) RFLP maps based on a common set of clones reveal modes of chromosomal evolution in potato and tomato. Genetics 120:1095–1103
Bradshaw J (2007a) The canon of potato science: four tetrasomic inheritance. Potato Res 50:219–222
Bradshaw JE (2007b) Potato-breeding strategy. In: Vreugdenhil D, Bradshaw J, Gebhardt C, Govers F, MacKerron DKL, Taylor MA, Ross HA (eds) Potato biology and biotechnology: advances and perspectives. Elsevier, Amsterdam, pp 157–177
Bradshaw JE, Mackay GR (1994) Breeding strategies for clonally propagated potatoes. In: Bradshaw JE, Mackay GR (eds) Potato Genetics. Cab International, Wallingford, pp 467–497
Bradshaw JE, Dale MFB, Mackay GR (2003) Use of mid-parent values and progeny tests to increase the efficiency of potato breeding for combined processing quality and disease and pest resistance. Theor Appl Genet 107:36–42
Bradshaw JE, Bryan GJ, Ramsay G (2006) Genetic resources (including wild and cultivated Solanum species) and progress in their utilisation in potato breeding. Potato Res 49:49–65
Bradshaw JE, Hackett CA, Pande B, Waugh R, Bryan GJ (2008) QTL mapping of yield, agronomic and quality traits in tetraploid potato (Solanum tuberosum subsp. tuberosum). Theor Appl Genet 116:193–211
Bradshaw JE, Dale MFB, Mackay GR (2009) Improving the yield, processing quality and disease and pest resistance of potatoes by genotypic recurrent selection. Euphytica 170:215–227
Brigneti G, Garcia-Mas J, Baulcombe DC (1997) Molecular mapping of the potato virus Y resistance gene Ry sto in potato. Theor Appl Genet 94:198–203
Brown CR (1993) Outcrossing rate in cultivated autotetraploid potato. Am Potato J 70:725–734
Celis-Gamboa C, Struik PC, Jacobsen E, Visser RGF (2003) Temporal dynamics of tuber formation and related processes in a crossing population of potato (Solanum tuberosum). Ann Appl Biol 143:175–186
Chen X, Salamini F, Gebhardt C (2001) A potato molecular-function map for carbohydrate metabolism and transport. Theor Appl Genet 102:284–295
Cockerham G (1970) Genetical studies on resistance to potato viruses X and Y. Heredity 25:309–348
Collard BC, Mackill DJ (2008) Marker-assisted selection: an approach for precision plant breeding in the twenty-first century. Philos Trans R Soc Lond B 363:557–572
Collard B, Jahufer M, Brouwer J, Pang E (2005) An introduction to markers, quantitative trait loci (QTL) mapping and marker-assisted selection for crop improvement: The basic concepts. Euphytica 142:169–196
Colton LM, Groza HI, Wielgus SM, Jiang J (2006) Marker-assisted selection for the broad-spectrum potato late blight resistance conferred by gene RB derived from a wild potato species. Crop Sci 46:589–594
Dale MFB, Mackay GR (1994) Inheritance of table and processing quality. In: Bradshaw JE, Mackay GR (eds) Potato Genetics. CAB International, Wallingford, UK, pp 285–315
Dalla Rizza M, Vilaró F, Torres D, Maeso D (2006) Detection of PVY extreme resistance genes in potato germplasm from the Uruguayan breeding program. Am J Potato Res 83:297–304
de Jong H (1981) Inheritance of russeting in cultivated diploid potatoes. Potato Res 24:309–313
De Jong WS, De Jong DM, Bodis M (2003) A fluorogenic 5’ nuclease (TaqMan) assay to assess dosage of a marker tightly linked to red skin color in autotetraploid potato. Theor Appl Genet 107:1384–1390
De Koeyer D, Douglass K, Murphy A, Whitney S, Nolan L, Song Y, de Jong W (2010) Application of high-resolution DNA melting for genotyping and variant scanning of diploid and autotetraploid potato. Mol Breed 25:67–90
De Koeyer D, Chen H, Gustafson V (2011) Molecular breeding for potato improvement. In: Bradeen J, Kole C (eds) Genetics, genomics and breeding of potato. Science Publishers, Enfield, New Hampshire, pp 41–67
D’Hoop BB, Paulo MJ, Mank RA, Van Eck HJ, Van Eeuwijk FA (2008) Association mapping of quality traits in potato (Solanum tuberosum L.). Euphytica 161:47–60
D’hoop B, Keizer PC, Paulo MJ, Visser RF, Eeuwijk F, Eck H (2014) Identification of agronomically important QTL in tetraploid potato cultivars using a marker–trait association analysis. Theor Appl Genet 127:731–748
Dong F, Song J, Naess SK, Helgeson JP, Gebhardt C, Jiang J (2000) Development and applications of a set of chromosome-specific cytogenetic DNA markers in potato. Theor Appl Genet 101:1001–1007
Donnelly DJ, Prasher SO, Patel RM (2007) Towards the development of salt-tolerant potato. In: Vreugdenhil D, Bradshaw J, Gebhardt C, Govers F, MacKerron DKL, Taylor M, Ross H (eds) Potato biology and biotechnology, advances and perspectives. Elsevier, Amsterdam, pp 415–437
Dreher K, Khairallah M, Ribaut J-M, Morris M (2003) Money matters (I): costs of field and laboratory procedures associated with conventional and marker-assisted maize breeding at CIMMYT. Mol Breed 11:221–234
Falconer DS, Mackay TFC (1996) Introduction to Quantitative Genetics, 4th edn. Pearson, Prentice Hall, Harlow, England
Felcher KJ, Coombs JJ, Massa AN, Hansey CN, Hamilton JP, Veilleux RE, Buell CR, Douches DS (2012) Integration of two diploid potato linkage maps with the potato genome sequence. PLoS ONE 7:e36347
Finkers-Tomczak A, Bakker E, de Boer J, van der Vossen E, Achenbach U, Golas T, Suryaningrat S, Smant G, Bakker J, Goverse A (2011) Comparative sequence analysis of the potato cyst nematode resistance locus H1 reveals a major lack of co-linearity between three haplotypes in potato (Solanum tuberosum ssp.). Theor Appl Genet 122:595–608
Flis B, Hennig J, Strzelczyk-Zyta D, Gebhardt C, Marczewski W (2005) The Ry-f sto gene from Solanum stoloniferum for extreme resistant to Potato virus Y maps to potato chromosome XII and is diagnosed by PCR marker GP122718 in PVY resistant potato cultivars. Mol Breed 15:95–101
Gebhardt C (2013) Bridging the gap between genome analysis and precision breeding in potato. Trends Genet 29:248–256
Gebhardt C, Valkonen JPT (2001) Organization of genes controlling disease resistance in the potato genome. Ann Rev Phytopathol 39:79–102
Gebhardt C, Ritter E, Debener T, Schachtschabel U, Walkemeier B, Uhrig H, Salamini F (1989) RFLP analysis and linkage mapping in Solanum tuberosum. Theor Appl Genet 78:65–75
Gebhardt C, Ritter E, Barone A, Debener T, Walkemeier B, Schachtschabel U, Kaufmann H, Thompson RD, Bonierbale MW, Ganal MW, Tanksley SD, Salamini F (1991) RFLP maps of potato and their alignment with the homoeologous tomato genome. Theor Appl Genet 83:49–57
Gebhardt C, Mugniery D, Ritter E, Salamini F, Bonnel E (1993) Identification of RFLP markers closely linked to the H1 gene conferring resistance to Globodera rostochiensis in potato. Theor Appl Genet 85:541–544
Gebhardt C, Ballvora A, Walkemeier B, Oberhagemann P, Schüler K (2004) Assessing genetic potential in germplasm collections of crop plants by marker-trait association: a case study for potatoes with quantitative variation of resistance to late blight and maturity type. Mol Breed 13:93–102
Gebhardt C, Lörz H, Wenzel G (2005) Potato genetics: Molecular maps and more. Molecular marker systems in plant breeding and crop improvement, Springer Berlin Heidelberg, pp 215–227
Gebhardt C, Bellin D, Henselewski H, Lehmann W, Schwarzfischer J, Valkonen J (2006) Marker-assisted combination of major genes for pathogen resistance in potato. Theor Appl Genet 112:1458–1464
Grube RC, Radwanski ER, Jahn M (2000) Comparative genetics of disease resistance within the solanaceae. Genetics 155:873–887
Hackett CA, Luo ZW (2003) TetraploidMap: construction of a linkage map in autotetraploid species. J Hered 94:358–359
Hackett CA, Milne I, Bradshaw JE, Luo Z (2007) TetraploidMap for Windows: Linkage map construction and QTL mapping in autotetraploid species. J Hered 98:727–729
Hackett CA, McLean K, Bryan GJ (2013) Linkage analysis and QTL mapping using SNP dosage data in a tetraploid potato mapping population. PLoS One 8:e63939
Hämäläinen JH, Watanabe KN, Valkonen JPT, Arihara A, Plaisted RL, Pehu E, Miller L, Slack SA (1997) Mapping and marker-assisted selection for a gene for extreme resistance to potato virus Y. Theor Appl Genet 94:192–197
Hämäläinen JH, Sorri VA, Watanabe KN, Gebhardt C, Valkonen JPT (1998) Molecular examination of a chromosome region that controls resistance to potato Y and A potyviruses in potato. Theor Appl Genet 96:1036–1043
Hamilton J, Hansey C, Whitty B, Stoffel K, Massa A, Van Deynze A, De Jong W, Douches D, Buell CR (2011) Single nucleotide polymorphism discovery in elite north american potato germplasm. BMC Genom 12:302
Hanneman REJ (1989) The potato germplasm resource. Am J Potato Res 66:655–667
Hawkes JG (1990) The potato; evolution, biodiversity and genetic resources. Belhaven Press, London
Hawkes JG (1994) Origins of cultivated potatoes and species relationships. In: Bradshaw JE, Mackay GR (eds) Potato Genetics. Cab International, Wallingford, pp 3–42
Hayes BJ, Cogan NOI, Pembleton LW, Goddard ME, Wang J, Spangenberg GC, Forster JW (2013) Prospects for genomic selection in forage plant species. Plant Breed 132:133–143
Heffner EL, Sorrells ME, Jannink J-L (2009) Genomic selection for crop improvement. Crop Sci 49:1–12
Heldák J, Bežo M, Štefúnová V, Galliková A (2007) Selection of DNA markers for detection of extreme resistance to potato virus Y in tetraploid potato (Solanum tuberosum L.) F1 progenies. Czech J Genet Plant Breed 43:125–134
Henderson CR (1984) Applications of Linear Models in Animal Breeding. University of Guelph, Guelph
Howard HW (1970) The Genetics of the Potato. Logos Press, London
Jacobs JME, Eck HJ, Horsman K, Arens PFP, Verkerk-Bakker B, Jacobsen E, Pereira A, Stiekema WJ (1996) Mapping of resistance to the potato cyst nematode Globodera rostochiensis from the wild potato species Solanum vernei. Mol Breed 2:51–60
Jacobs M, Vosman B, Vleeshouwers V, Visser R, Henken B, van den Berg R (2010) A novel approach to locate Phytophthora infestans resistance genes on the potato genetic map. Theor Appl Genet 120:785–796
Jannink J-L, Lorenz AJ, Iwata H (2010) Genomic selection in plant breeding: from theory to practice. Brief Funct Genomics 9:166–177
Jansky S (2009) Breeding, genetics and cultivar development. In: Singh J, Kaur L (eds) Advances in potato chemistry and technology. Academic Press, New York, pp 27–62
Jupe F, Pritchard L, Etherington G, MacKenzie K, Cock P, Wright F, Sharma SK, Bolser D, Bryan G, Jones J, Hein I (2012) Identification and localisation of the NB-LRR gene family within the potato genome. BMC Genom 13:75
Jupe F, Witek K, Verweij W, Śliwka J, Pritchard L, Etherington GJ, Maclean D, Cock PJ, Leggett RM, Bryan GJ, Cardle L, Hein I, Jones JDG (2013) Resistance gene enrichment sequencing (RenSeq) enables reannotation of the NB-LRR gene family from sequenced plant genomes and rapid mapping of resistance loci in segregating populations. Plant J 76:530–544
Kasai K, Morikawa Y, Sorri VA, Valkonen JP, Gebhardt C, Watanabe KN (2000) Development of SCAR markers to the PVY resistance gene Ry adg based on a common feature of plant disease resistance genes. Genome 43:1–8
Kawchuk L, Lynch D, Yada R, Bizimungu B, Lynn J (2008) Marker assisted selection of potato clones that process with light chip color. Am J Potato Res 85:227–231
Kearsey MJ, Pooni HS (1998) The genetical analysis of quantitative traits. Stanley Thornes Ltd, Cheltenham
Kloosterman B, Abelenda JA, Gomez MdMC, Oortwijn M, de Boer JM, Kowitwanich K, Horvath BM, van Eck HJ, Smaczniak C, Prat S, Visser RGF, Bachem CWB (2013) Naturally occurring allele diversity allows potato cultivation in northern latitudes. Nature 495:246–250
Kuchel H, Ye G, Fox R, Jefferies S (2005) Genetic and economic analysis of a targeted marker-assisted wheat breeding strategy. Mol Breed 16:67–78
Leister D, Ballvora A, Salamini F, Gebhardt C (1996) A PCR-based approach for isolating pathogen resistance genes from potato with potential for wide application in plants. Nat Genet 14:421–429
Li X-Q, De Jong H, De Jong DM, De Jong WS (2005) Inheritance and genetic mapping of tuber eye depth in cultivated diploid potatoes. Theor Appl Genet 110:1068–1073
Li L, Paulo M-J, Strahwald J, Lübeck J, Hofferbert H-R, Tacke E, Junghans H, Wunder J, Draffehn A, van Eeuwijk F, Gebhardt C (2008a) Natural DNA variation at candidate loci is associated with potato chip color, tuber starch content, yield and starch yield. Theor Appl Genet 116:1167–1181
Li XQ, Griffiths R, De Koeyer D, Rothwell C, Gustafson V, Regan S, Flinn B (2008b) Functional genomic resources for potato. Can J Plant Sci 88:573–581
Luo ZW, Zhang RM, Kearsey MJ (2004) Theoretical basis for genetic linkage analysis in autotetraploid species. Proc Natl Acad Sci USA 101:7040–7045
Luo ZW, Zhang Z, Leach L, Zhang RM, Bradshaw JE, Kearsey MJ (2006) Constructing genetic linkage maps under a tetrasomic model. Genetics 172:2635–2645
Marczewski W, Flis B, Syller J, Schäfer-Pregl R, Gebhardt C (2001) A major quantitative trait locus for resistance to Potato leafroll virus is located in a resistance hotspot on potato chromosome XI and is tightly linked to N-gene-like markers. Mol Plant-Microbe Interact 14:1420–1425
Marczewski W, Hennig J, Gebhardt C (2002) The Potato virus S resistance gene Ns maps to potato chromosome VIII. Theor Appl Genet 105:564–567
Marczewski W, Flis B, Syller J, Strzelczyk-Zyta D, Hennig J, Gebhardt C (2004) Two allelic or tightly linked genetic factors at the PLRV.4 locus on potato chromosome XI control resistance to potato leafroll virus accumulation. Theor Appl Genet 109:1604–1609
Marczewski W, Strzelczyk-Żyta D, Hennig J, Witek K, Gebhardt C (2006) Potato chromosomes IX and XI carry genes for resistance to potato virus M. Theor Appl Genet 112:1232–1238
Maris B (1986) The effect of seed tuber weight on characters in the first and the second clonal generation of potato populations. Euphytica 35:465–482
Maris B (1988) Correlations within and between characters between and within generations as a measure for the early generation selection in potato breeding. Euphytica 37:205–224
Meuwissen THE, Hayes BJ, Goddard ME (2001) Prediction of total genetic value using genome-wide dense marker maps. Genetics 157:1819–1829
Milbourne D, Meyer RC, Collins AJ, Ramsay LD, Gebhardt C, Waugh R (1998) Isolation, characterisation and mapping of simple sequence repeat loci in potato. Mol Gen Genet 259:233–245
Milbourne D, Bradshaw JE, Hackett CA (2008) Molecular mapping and breeding in polyploid crop plants. In: Kole C, Abbott AG (eds) Principles and practices of plant genomics. Science Publishers, Enfield, pp 355–394
Moloney C, Griffin D, Jones P, Bryan G, McLean K, Bradshaw J, Milbourne D (2010) Development of diagnostic markers for use in breeding potatoes resistant to Globodera pallida pathotype Pa2/3 using germplasm derived from Solanum tuberosum ssp. andigena CPC 2802. Theor Appl Genet 120:679–689
Moose SP, Mumm RH (2008) Molecular plant breeding as the foundation for 21st century crop improvement. Plant Physiol 147:969–977
Morris M, Dreher K, Ribaut J-M, Khairallah M (2003) Money matters (II): costs of maize inbred line conversion schemes at CIMMYT using conventional and marker-assisted selection. Mol Breed 11:235–247
Naess SK, Bradeen JM, Wielgus SM, Haberlach GT, McGrath JM, Helgeson JP (2000) Resistance to late blight in Solanum bulbocastanum is mapped to chromosome 8. Theor Appl Genet 101:697–704
Ortega F, Lopez-Vizcon C (2012) Application of molecular marker-assisted selection (MAS) for disease resistance in a practical potato breeding programme. Potato Res 55:1–13
Ortiz R, Huaman Z (1994) Inheritance of morphological and tuber characteristics. In: Bradshaw JE, Mackay GR (eds) Potato Genetics. CAB International, Wallingford, UK, pp 263–283
Ottoman R, Hane D, Brown C, Yilma S, James S, Mosley A, Crosslin J, Vales M (2009) Validation and implementation of marker-assisted selection (MAS) for PVY resistance (Ry adg gene) in a tetraploid potato breeding program. Am J Potato Res 86:304–314
Oud JSN, Schneiders H, Kool AJ, van Grinsven MQJM (1995) Breeding of transgenic orange Petunia hybrida varieties. Euphytica 84:175–181
Ovchinnikova A, Krylova E, Gavrilenko T, Smekalova T, Zhuk M, Knapp S, Spooner DM (2011) Taxonomy of cultivated potatoes (Solanum section Petota: Solanaceae). Bot J Linn Soc 165:107–155
Paal J, Henselewski H, Muth J, Meksem K, Menéndez CM, Salamini F, Ballvora A, Gebhardt C (2004) Molecular cloning of the potato Gro1-4 gene conferring resistance to pathotype Ro1 of the root cyst nematode Globodera rostochiensis, based on a candidate gene approach. Plant J 38:285–297
Pavek JJ, Corsini DL (1994) Inheritance of resistance to warm-growing-season fungal diseases. In: Bradshaw JE, Mackay GR (eds) Potato Genetics. CAB International, Wallingford, pp 403–409
Peters SA, Bargsten JW, Szinay D, van de Belt J, Visser RGF, Bai Y, de Jong H (2012) Structural homology in the Solanaceae: analysis of genomic regions in support of synteny studies in tomato, potato and pepper. Plant J 71:602–614
Phillips MS (1994) Inheritance of resistance to nematodes. In: Bradshaw JE, Mackay GR (eds) Potato Genetics. CAB International, Wallingford, pp 319–337
Pineda O, Bonierbale MW, Plaisted RL, Brodie BB, Tanksley SD (1993) Identification of RFLP markers linked to the H1 gene conferring resistance to the potato cyst nematode Globodera rostochiensis. Genome 36:152–156
Plaisted R, Hoopes R (1989) The past record and future prospects for the use of exotic potato germplasm. Am J Potato Res 66:603–627
Potato Genome Sequencing Consortium (2011) Genome sequence and analysis of the tuber crop potato. Nature 475:189–195
Quirin EA, Mann H, Meyer RS, Traini A, Chiusano ML, Litt A, Bradeen JM (2012) Evolutionary meta-analysis of solanaceous resistance gene and Solanum resistance gene analog sequences and a practical framework for cross-species comparisons. Mol Plant-Microbe Interact 25:603–612
Ribaut J-M, Hoisington D (1998) Marker-assisted selection: new tools and strategies. Trends Plant Sci 3:236–239
Ross H (1986) Potato breeding—problems and perspectives. In: Parey P (ed) Advances in Plant Breeding, Verlag Berlin
Sattarzadeh A, Achenbach U, Lübeck J, Strahwald J, Tacke E, Hofferbert H-R, Rothsteyn T, Gebhardt C (2006) Single nucleotide polymorphism (SNP) genotyping as basis for developing a PCR-based marker highly diagnostic for potato varieties with high resistance to Globodera pallida pathotype Pa2/3. Mol Breed 18:301–312
Schmidt MA, Martin GS, Artelt BJ, Parrott WA (2004) Increased transgene expression by breeding and selection in white clover. Crop Sci 44:963–967
Schultz L, Cogan NOI, Forster JW, Slater AT (2010) Evaluation and optimisation of the TG689 marker linked to PCN resistance. Potato Res 53:247–248
Schultz L, Cogan NOI, McLean K, Dale MFB, Bryan GJ, Forster JW, Slater AT (2012) Evaluation and implementation of a potential diagnostic molecular marker for H1-conferred potato cyst nematode resistance in potato (Solanum tuberosum L.). Plant Breed 131:315–321
Simko I, Costanzo S, Haynes KG, Christ BJ, Jones RW (2004) Linkage disequilibrium mapping of a Verticillium dahliae resistance quantitative trait locus in tetraploid potato (Solanum tuberosum) through a candidate gene approach. Theor Appl Genet 108:217–224
Simko I, Jansky S, Stephenson S, Spooner DM (2007) Genetics of resistance to pests and diseases. In: Vreugdenhil D, Bradshaw J, Gebhardt C, Govers F, MacKerron DKL, Taylor MA, Ross HA (eds) Potato biology and biotechnology: advances and perspectives. Elsevier, Amsterdam, pp 117–155
Simmonds NW (1964) The genetics of seed and tuber dormancy in the cultivated potatoes. Heredity 19:489–504
Slater AT, Cogan NOI, Forster JW (2013) Cost analysis of the application of marker-assisted selection in potato breeding. Mol Breed 32:299–310
Slater AT, Wilson GM, Cogan NOI, Forster JW, Hayes BJ (2014) Improving the analysis of low heritability complex traits for enhanced genetic gain in potato. Theor Appl Genet 127:809–820
Song YS, Schwarzfischer A (2008) Development of STS markers for selection of extreme resistance (Ry sto ) to PVY and maternal pedigree analysis of extremely resistant cultivars. Am J Potato Res 85:159–170
Song YS, Hepting L, Schweizer G, Hartl L, Wenzel G, Schwarzfischer A (2005) Mapping of extreme resistance to PVY (Ry sto ) on chromosome XII using anther-culture-derived primary dihaploid potato lines. Theor Appl Genet 111:879–887
Sorri VA, Watanabe KN, Valkonen JPT (1999) Predicted kinase-3a motif of a resistance gene analogue as a unique marker for virus resistance. Theor Appl Genet 99:164–170
Spooner DM, Bamberg JB (1994) Potato genetic resources: Sources of resistance and systematics. Am Potato J 71:325–337
Spooner DM, Hijmans RJ (2001) Potato systematics and germplasm collecting, 1989–2000. Am J Potato Res 78:237–268
Spooner DM, Nunez J, Trujillo G, del Rosario HM, Guzman F, Ghislain M (2007) Extensive simple sequence repeat genotyping of potato landraces supports a major reevaluation of their gene pool structure and classification. Proc Natl Acad Sci USA 104:19398–19403
Spooner DM, Ames M, Fajardo D, Rodriguez F (2009) Species boundaries and interrelationships of Solanum sect. Petota (wild and cultivated potatoes) are drastically altered as a result of PBI-funded research. Botany & Mycology 2009 Annual Meeting
Stein J, Quarin CL, Martinez EJ, Pessino SC, Ortiz JPA (2004) Tetraploid races of Paspalum notatum show polysomic inheritance and preferential chromosome pairing around the apospory-controlling locus. Theor Appl Genet 109:186–191
Swaminathan MS, Howard HW (1953) The cytology and genetics of the potato (Solanum tuberosum) and related species. Bibliogr Genet 16:1–192
Swiezynski KM (1994) Inheritance of resistance to viruses. In: Bradshaw JE, Mackay GR (eds) Potato Genetics. CAB International, Wallingford, pp 339–363
Tameling W, Takken F (2008) Resistance proteins: scouts of the plant innate immune system. Eur J Plant Pathol 121:243–255
Tanksley SD, Ganal MW, Prince JP, de Vicente MC, Bonierbale MW, Broun P, Fulton TM, Giovannoni JJ, Grandillo S, Martin GB et al (1992) High density molecular linkage maps of the tomato and potato genomes. Genetics 132:1141–1160
Tomato Genome Consortium (2012) The tomato genome sequence provides insights into fleshy fruit evolution. Nature 485:635–641
Toxopeus HJ, Huijsman CA (1953) Breeding for resistance to potato root eelworm. Euphytica 2:180–186
Uitdewilligen JGAML, Wolters A-MA, D’hoop BB, Borm TJA, Visser RGF, van Eck HJ (2013) A next-generation sequencing method for genotyping-by-sequencing of highly heterozygous autotetraploid potato. PLoS One 8:e62355
Umaerus V, Umaerus M (1994) Inheritance of resistance to late blight. In: Bradshaw JE, Mackay GR (eds) Potato Genetics. CAB International, Wallingford, UK, pp 365–401
Valkonen JPT, Wiegmann K, Hämäläinen JH, Marczewski W, Watanabe KN (2008) Evidence for utility of the same PCR-based markers for selection of extreme resistance to Potato virus Y controlled by Ry sto of Solanum stoloniferum derived from different sources. Ann Appl Biol 152:121–130
Van Eck HJ (2007) Genetics of morphological and tuber traits. In: Vreugdenhil D, Bradshaw J, Gebhardt C, Govers F, MacKerron DKL, Taylor MA, Ross HA (eds) Potato biology and biotechnology: advances and perspectives. Elsevier, Amsterdam, pp 91–115
Van Os H, Andrzejewski S, Bakker E, Barrena I, Bryan GJ, Caromel B, Ghareeb B, Isidore E, De Jong W, Van Koert P, Lefebvre V, Milbourne D, Ritter E, Rouppe Van Der Voort JNAM, Rousselle-Bourgeois F, Van Vliet J, Waugh R, Visser RGF, Bakker J, Van Eck HJ (2006) Construction of a 10,000-marker ultradense genetic recombination map of potato: Providing a framework for accelerated gene isolation and a genomewide physical map. Genetics 173:1075–1087
Van Sanford D, Anderson J, Campbell K, Costa J, Cregan P, Griffey C, Hayes P, Ward R (2001) Discovery and deployment of molecular markers linked to fusarium head blight resistance: An integrated system for wheat and barley. Crop Sci 41:638–644
Van Vleck LD, Westell RA, Schneider JC (1986) Genetic change in milk yield estimated from simultaneous genetic evaluation of bulls and cows. J Dairy Sci 69:2963–2965
Varshney RK, Graner A, Sorrells ME (2005) Genomics-assisted breeding for crop improvement. Trends Plant Sci 10:621–630
Vos J, Haverkort AJ (2007) Water availability and potato crop performance. In: Vreugdenhil D, Bradshaw J, Gebhardt C, Govers F, MacKerron DKL, Taylor M, Ross H (eds) Potato biology and biotechnology, advances and perspectives. Elsevier, Amsterdam, pp 333–351
Wallace AJ, Callow RS (1995) Meiotic variation in an intergenomic autopolyploid series. II. Pairing behaviour. Genome 38:133–139
Wastie RL (1991) Resistance to powdery scab of seedling progenies of Solanum tuberosum. Potato Res 34:249–252
Wastie RL (1994) Inheritance of fungal diseases of tubers. In: Bradshaw JE, Mackay GR (eds) Potato Genetics. CAB International, Wallingford, pp 411–427
Wastie RL, Caligari PDS, Stewart HE, Mackay GR (1988) Assessing the resistance to gangrene of progenies of potato (Solanum tuberosum L.) from parents differing in susceptibility. Potato Res 31:355–365
Whitworth J, Novy R, Hall D, Crosslin J, Brown C (2009) Characterization of broad spectrum potato virus Y resistance in a Solanum tuberosum ssp. andigena-derived population and select breeding clones using molecular markers, grafting, and field inoculations. Am J Potato Res 86:286–296
Witek K, Strzelczyk-Żyta D, Hennig J, Marczewski W (2006) A multiplex PCR approach to simultaneously genotype potato towards the resistance alleles Ry-f sto and Ns. Mol Breed 18:273–275
Xu Y, Lu Y, Xie C, Gao S, Wan J, Prasanna B (2012) Whole-genome strategies for marker-assisted plant breeding. Mol Breed 29:833–854
Yu K, Park SJ, Poysa V (2000) Marker-assisted selection of common beans for resistance to common bacterial blight: efficacy and economics. Plant Breed 119:411–415
Zhang L-H, Mojtahedi H, Kuang H, Baker B, Brown CR (2007) Marker-assisted selection of columbia root-knot nematode resistance introgressed from Solanum bulbocastanum. Crop Sci 47:2021–2026
Zhang Y, Jung C, De Jong W (2009) Genetic analysis of pigmented tuber flesh in potato. Theor Appl Genet 119:143–150
Acknowledgments
This work was supported by funding from Horticulture Australia Limited and the Victorian Department of Environment and Primary Industries.
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The authors declare that they have no conflict of interest.
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All experiments comply with the current laws of Australia and Scotland.
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Communicated by Rajeev K. Varshney.
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Slater, A.T., Cogan, N.O.I., Hayes, B.J. et al. Improving breeding efficiency in potato using molecular and quantitative genetics. Theor Appl Genet 127, 2279–2292 (2014). https://doi.org/10.1007/s00122-014-2386-8
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DOI: https://doi.org/10.1007/s00122-014-2386-8