Skip to main content

Advertisement

Springer Nature Link
Log in
Menu
Find a journal Publish with us Track your research
Search
Saved research
Cart
  1. Home
  2. Science China Life Sciences
  3. Article

Polyploid organisms

  • Review
  • Open access
  • Published: 15 June 2012
  • Volume 55, pages 301–311 (2012)
  • Cite this article

You have full access to this open access article

Download PDF
View saved research
Image Science China Life Sciences Aims and scope Submit manuscript
Polyploid organisms
Download PDF
  • Can Song1,
  • ShaoJun Liu1,
  • Jun Xiao1,
  • WeiGuo He1,
  • Yi Zhou1,
  • QinBo Qin1,
  • Chun Zhang1 &
  • …
  • Yun Liu1 
  • 10k Accesses

  • 113 Citations

  • 6 Altmetric

  • Explore all metrics

Abstract

Polyploids are organisms with three or more complete chromosome sets. Polyploidization is widespread in plants and animals, and is an important mechanism of speciation. Genome sequencing and related molecular systematics and bioinformatics studies on plants and animals in recent years support the view that species have been shaped by whole genome duplication during evolution. The stability of polyploids depends on rapid genome recombination and changes in gene expression after formation. The formation of polyploids and subsequent diploidization are important aspects in long-term evolution. Polyploids can be formed in various ways. Among them, hybrid organisms formed by distant hybridization could produce unreduced gametes and thus generate offspring with doubled chromosomes, which is a fast, efficient method of polyploidization. The formation of fertile polyploids not only promoted the interflow of genetic materials among species and enriched the species diversity, but also laid the foundation for polyploidy breeding. The study of polyploids has both important theoretical significance and valuable applications. The production and application of polyploidy breeding have brought remarkable economic and social benefits.

Article PDF

Download to read the full article text

Similar content being viewed by others

Image

Introduction to Polyploidy

Chapter © 2017
Image

Polyploidy: Evolution and Crop Improvement

Chapter © 2017
Image

Learning to tango with four (or more): the molecular basis of adaptation to polyploid meiosis

Article Open access 23 September 2022

Explore related subjects

Discover the latest articles, books and news in related subjects, suggested using machine learning.
  • Doubled Haploids
  • Genetic hybridization
  • Plant Hybridization
  • Polyploidy
  • Polyploidy in plants
  • Aneuploidy
  • Parthenogenesis and Genetic Diversity in Vertebrate Lineages

References

  1. Otto S P. The evolutionary consequences of polyploidy. Cell, 2007, 131: 452–462

    PubMed  CAS  Google Scholar 

  2. Ohno S. Evolution by Gene Duplication. New York: Springer-Verlag, 1970

    Google Scholar 

  3. Holland P W H, Garcia-Fernàndez J, Williams N A, et al. Gene duplications and the origins of vertebrate development. Development (Supplement), 1994, 125–133

  4. Meyer A, Van de Peer Y. From 2R to 3R: evidence for a fish-specific genome duplication (FSGD). Bioessays, 2005, 27: 937–945

    PubMed  CAS  Google Scholar 

  5. Dehal P, Boore J L. Two rounds of whole genome duplication in the ancestral vertebrate. PLoS Biol, 2005, 3: 1700–1708

    CAS  Google Scholar 

  6. Blomme T, Vandepoele K, De Bodt S, et al. The gain and loss of genes during 600 million years of vertebrate evolution. Genome Biol, 2006, 7: R43

    PubMed  PubMed Central  Google Scholar 

  7. Amores A, Force A, Yan Y L, et al. Zebrafish hox clusters and vertebrate genome evolution. Science, 1998, 282: 1711–1714

    PubMed  CAS  Google Scholar 

  8. Taylor J S, Van de Peer Y, Braasch I, et al. Comparative genomics provides evidence for an ancient genome duplication event in fish. Philos Trans R Soc, 2001a, 356: 1661–1679

    CAS  Google Scholar 

  9. Volff J N. Genome evolution and biodiversity in teleost fish. Heredity, 2005, 94: 280–294

    PubMed  CAS  Google Scholar 

  10. Soltis D E, Soltis P S, Tate J A. Advances in the study of polyploidy since plant speciation. New Phytol, 2003, 161: 173–191

    Google Scholar 

  11. Comai L. The advantages and disadvantages of being polyploid. Nat Rev Genet, 2005, 6: 836–845

    PubMed  CAS  Google Scholar 

  12. Kassahn K S, Dang V T, Wilkins S J, et al. Evolution of gene function and regulatory control after whole-genome duplication: comparative analyses in vertebrates. Genome Res, 2009, 19: 1404–1418

    PubMed  CAS  PubMed Central  Google Scholar 

  13. Soltis D E, Soltis P S. Molecular data and the dynamic nature of polyploidy. Crit Rev Plant Sci, 1993, 12: 243–273

    CAS  Google Scholar 

  14. Grant V. Plant Speciation, 2nd ed. New York: Columbia University Press, 1981

    Google Scholar 

  15. Ahuja M R, Neale D B. Evolution of genome size in conifers. Silvae Genet, 2005, 54: 126–137

    Google Scholar 

  16. Hair J B. The chromosomes of the Cupressaceae. I. Tetraclineae and Actinostrobeae (Callitroideae). New Zeal J Bot, 1968, 6: 277–284

    Google Scholar 

  17. Gates R R. The stature and chromosomes of Oenothera gigas De Vries. Arch F Zellforsch, 1909, 3: 525–552

    Google Scholar 

  18. Goldblatt P. Polyploidy in Angiosperms: Monocotyledons. In: Lewis W H, ed. Polyploidy: Biological Relevance. New York: Plenum Press, 1980. 219–239

    Google Scholar 

  19. Lewis W H. Polyploidy in Angiosperms: Dicotyledons. In: Lewis W H, ed. Polyploidy: Biological Relevance. New York: Plenum Press, 1980. 241–268

    Google Scholar 

  20. Masterson J. Stomatal size in fossil plants: evidence for polyploidy in majority of angiosperms. Science, 1994, 264: 421–423

    PubMed  CAS  Google Scholar 

  21. Bowers J E, Chapman B A, Rong J K, et al. Unravelling angiosperm genome evolution by phylogenetic analysis of chromosomal duplication events. Nature, 2003, 422: 433–438

    PubMed  CAS  Google Scholar 

  22. Soltis D E, Albert V A, Leebens-Mack J, et al. Polyploidy and angiosperm diversification. Am J Bot, 2009, 96: 336–348

    PubMed  Google Scholar 

  23. Veron A S, Kaufmann K, Bornberg-Bauer E. Evidence of interaction network evolution by whole-genome duplications: a case study in MADS-box proteins. Mol Biol Evol, 2007, 24: 670–678

    PubMed  CAS  Google Scholar 

  24. Albert V A, Soltis D E, Carlson J E, et al. Floral gene resources from basal angiosperms for comparative genomics research. BMC Plant Biol, 2005, 5: 5–16

    PubMed  PubMed Central  Google Scholar 

  25. Cui L, Wall P K, Leebens-Mack J, et al. Widespread genome duplications throughout the history of flowering plants. Genome Res, 2006, 16: 738–749

    PubMed  CAS  PubMed Central  Google Scholar 

  26. Zhang F W, Wang Y R. Progress of polyploidy breeding technology applied in medical plants scale (in Chinese). Guiding J TCM, 2006, 12: 83–85

    Google Scholar 

  27. Paterson A H, Bowers J, Burow M, et al. Comparative genomics of plant chromosomes. Plant Cell, 2000, 12: 1523–1539

    PubMed  CAS  PubMed Central  Google Scholar 

  28. Severin A J, Cannon S B, Graham M M, et al. Changes in twelve homoeologous genomic regions in soybean following three rounds of polyploidy. Plant Cell, 2011, 23: 3129–3136

    PubMed  CAS  PubMed Central  Google Scholar 

  29. Jaillon O, Aury J M, Noel B, et al. The grapevine genome sequence suggests ancestral hexaploidization in major angiosperm phyla. Nature, 2007, 449: 463–467

    PubMed  CAS  Google Scholar 

  30. Ming R, Hou S, Feng Y, et al. The draft genome of the transgenic tropical fruit tree papaya (Carica papaya Linnaeus). Nature, 2008, 452: 991–996

    PubMed  CAS  PubMed Central  Google Scholar 

  31. Otto S P, Whitton J. Polyploid incidence and evolution. Annu Rev Genet, 2000, 34: 401–437

    PubMed  CAS  Google Scholar 

  32. Liu Z D. Yichuanxue (in Chinese). Beijing: Higher Education Press, 1991

    Google Scholar 

  33. Yang Y G, Zhuang Y, Chen L Z, et al. Vegetable polyploid and polyploidy breeding (in Chinese). Acta Agricult Univ Jiangxi, 2006, 28: 534–538

    Google Scholar 

  34. Hilu K W. Polyploidy and the evolution of domesticated plants. Am J Bot, 1993, 80: 1494–1499

    Google Scholar 

  35. Fedorov A. Chromosome Numbers of Flowering Plants. Leningrad: Acad Sci USSR Komarov Botanical Institute, 1969

    Google Scholar 

  36. Dai S L, Wang W K, Huang J P. Advances of researches on phylogeny of Dendranthema and origin of chrysanthemum (in Chinese). J Beijing Forest Univ, 2002, 24: 230–234

    Google Scholar 

  37. Jin X X, Zhang Q X. Advances in the studies of breeding Primula (in Chinese). Chin Bull Bot, 2005, 22: 738–745

    Google Scholar 

  38. Gregory T R, Mable B K. Polyploidy in Animals. In: Gregory T R, ed. The Evolution of the Genome. San Diego: Elsevier, 2005. 427–517

    Google Scholar 

  39. Wu M. Genetics and evolution of animal polyploid (in Chinese). Chin J Zool, 1988, 23: 48–51

    Google Scholar 

  40. Chen D W, Daoye M Y. Chromosomes and systematic classification of molluscs. Chin J Zool, 1988, 23: 48–51

    Google Scholar 

  41. Ye M W. The polyploidy phenomenon and formation in animals and plants (in Chinese). Bull Biol, 1998, 33: 21–23

    Google Scholar 

  42. Li S W. Polyploid insects (in Chinese). Entomol Knowledge, 2002, 39: 147–151

    CAS  Google Scholar 

  43. Naruse K, Tanaka M, Mita K, et al. A medaka gene map: the trace of ancestral vertebrate proto-chromosomes revealed by comparative gene mapping. Genome Res, 2004, 14: 820–828

    PubMed  CAS  PubMed Central  Google Scholar 

  44. Woods I G, Wilson C, Friedlander B, et al. The zebrafish gene map defines ancestral vertebrate chromosomes. Genome Res, 2005, 15: 1307–1314

    PubMed  CAS  PubMed Central  Google Scholar 

  45. Gui J F, Zhou L. Genetic basis and breeding application of clonal diversity and dual reproduction modes in polyploid Carassius auratus gibelio. Sci China Life Sci, 2010, 53: 409–415

    PubMed  Google Scholar 

  46. Zhou L, Gui J F. Karyotypic diversity in polyploid gibel carp, Carassius auratus gibelio bloch. Genetica, 2002, 115: 223–232

    PubMed  CAS  Google Scholar 

  47. Xiao J, Zou T M, Chen Y B, et al. Coexistence of diploid, triploid and tetraploid crucian carp (Carassius auratus) in natural waters. BMC Genet, 2011, 12: 20

    PubMed  CAS  PubMed Central  Google Scholar 

  48. Luo J R. Polyploid fishes and fish polyploidy breeding (in Chinese). Pearl River Fisheries, 1991, 17: 69–74

    Google Scholar 

  49. Lampert K P, Schartl M. The origin and evolution of a unisexual hybrid: Poecilia formosa. Philos Trans R Soc Lond B Biol Sci, 2008, 363: 2901–2909

    PubMed  CAS  PubMed Central  Google Scholar 

  50. Zan R G. The polyploids in fish and their roles in fish evolution (in Chinese). J Yunnan Univ, 1985, 7: 235–243

    Google Scholar 

  51. Abbas K, Li M Y, Wang W M, et al. First record of the natural occurrence of hexaploids loach Misgurnus anguillicaudatus in Hubei Province, China. J Fish Biol, 2009, 75: 435–441

    PubMed  CAS  Google Scholar 

  52. Ráb P, Rábová M, Bohlen J, et al. Genetic differentiation of the two hybrid diploid-polyploid complexes of loaches, genus Cobitis (Cobitidae) involving C. taenia, C. elongatoides and C. spp. in the Czech Republic: karyotypes and cytogenetic diversity. Folia Zool, 2000, 49: S55–S66

    Google Scholar 

  53. Boroň A, Kotusz J. The preliminary data on diploid-polyploid complexes of the genus Cobitis in the Odra River basin, Poland (Pisces, Cobitidae). Folia Zool, 2000, 49: S79–S84

    Google Scholar 

  54. Li S S. Amphibians’s chromosomes and their evolution (in Chinese). Chin J Zool, 1991, 26: 47–52

    CAS  Google Scholar 

  55. Li S S. Parthenogenesis in reptiles (in Chinese). Chin J Zool, 1992, 27: 41–44

    Google Scholar 

  56. Li S S. Vertebrate’s polyploid (in Chinese). Chin J Zool, 1980, 2: 52–54

    Google Scholar 

  57. Ramsey J, Schemske D W. Pathways, mechanisms, and rates of polyploid formation in flowering plants. Annu Rev Ecol Syst, 1998, 29: 467–501

    Google Scholar 

  58. Newton W C F, Pellew C. Primula kewensis and its derivatives. J Genet, 1929, 20: 405–467

    Google Scholar 

  59. Liu S J, Qin Q B, Xiao J, et al. The formation of the polyploid hybrids from different subfamily fish crossing and its evolutionary significance. Genetics, 2007, 176: 1023–1034

    PubMed  CAS  PubMed Central  Google Scholar 

  60. Liu S J. Distant hybridization leads to different ploidy fishes. Sci China Life Sci, 2010, 53: 416–425

    PubMed  Google Scholar 

  61. Karpechenko G D. The production of polyploid gametes in hybrids. Hereditas, 1927, 9: 349–368

    Google Scholar 

  62. Liu S J, Liu Y, Zhou G J, et al. The formation of tetraploid stocks of red crucian carp × common carp hybrids as an effect of interspecific hybridization. Aquaculture, 2001, 192: 171–186

    Google Scholar 

  63. Zhang C, Sun Y D, Liu S J, et al. Evidence of the unreduced diploid eggs generated from the diploid gynogenetic progeny of allotetraploid hybrids (in Chinese). Acta Genet Sin, 2005, 32: 136–144

    PubMed  Google Scholar 

  64. Ullah Z, Lee C Y, DePamphilis M L. Cip/Kip cyclin-dependent protein kinase inhibitors and the road to polyploidy. Cell Div, 2009, 4: 10

    PubMed  PubMed Central  Google Scholar 

  65. Bretagnolle F, Thompson J D. Gametes with the somatic chromosome number: mechanisms of their formation and role in the evolution of autopolyploid plants. New phytol, 1995, 129: 1–22

    Google Scholar 

  66. Werner J E, Peloquin S J. Occurrence and mechanisms of 2n egg formation in 2x potato. Genome, 1991, 34: 975–982

    Google Scholar 

  67. Seehausen O. Hybridization and adaptive radiation. Trends Ecol Evol, 2004, 19: 198–207

    PubMed  Google Scholar 

  68. Mallet J. Hybridization as an invasion of the genome. Trends Ecol Evol, 2005, 20: 229–237

    PubMed  Google Scholar 

  69. Mallet J. Hybrid speciation. Nature, 2007, 446: 279–283

    PubMed  CAS  Google Scholar 

  70. Yu X J, Zhou T, Li Y C. Chromosomes of Chinese Fresh-water Fishes (in Chinese). Beijing: Science Press, 1989

    Google Scholar 

  71. Meyer A, Salzburger W, Schartl M. Hybrid origin of a swordtail species (Teleostei: Xiphophorus clemenciae) driven by sexual selection. Mol Ecol, 2006, 15: 721–730

    PubMed  CAS  Google Scholar 

  72. Saitoh K, Chen W J, Mayden R L. Extensive hybridization and tetrapolyploidy in spined loach fish. Mol Phylogenet Evol, 2010, 56: 1001–1010

    PubMed  CAS  Google Scholar 

  73. Harlan J R, deWet J M J. On Ö. Winge and a prayer: the origins of polyploidy. Bot Rev, 1975, 41: 361–390

    Google Scholar 

  74. Belling J. The origin of chromosomal mutations in Uvularia. J Genet, 1925, 15: 245–266

    Google Scholar 

  75. McHale N A. Environmental induction of high frequency 2n pollen formation in diploid Solanum. Can J Genet Cytol, 1983, 25: 609–615

    Google Scholar 

  76. Mable B K. ’Why polyploidy is rarer in animals than in plants’: myths and mechanisms. Biol J Linn Soc, 2004, 82: 453–466

    Google Scholar 

  77. Comai L. Genetic and epigenetic interactions in allopolyploid plants. Plant Mol Biol, 2000, 43: 387–399

    PubMed  CAS  Google Scholar 

  78. Chen Z J, Ni Z F. Mechanisms of genomic rearrangements and gene expression changes in plant polyploids. Bioessays, 2006, 28: 240–252

    PubMed  Google Scholar 

  79. Song K, Lu P, Tang K, et al. Rapid genome change in synthetic polyploids of Brassica and its implications for polyploid evolution. Proc Natl Acad Sci USA, 1995, 92: 7719–7723

    PubMed  CAS  PubMed Central  Google Scholar 

  80. Kenton A, Parokonny A S, Gleba Y Y, et al. Characterization of the Nicotiana tabacum L. Genome by molecular cytogenetics. Mol Gen Genet, 1993, 240: 159–169

    PubMed  CAS  Google Scholar 

  81. Jellen E N, Gill B S, Cox T S. Genomic in situ hybridization differentiates between A/D-and C-genome chromatin and detects intergenomic translocations in polyploid oat species (genus Avena). Genome, 1994, 37: 613–618

    PubMed  CAS  Google Scholar 

  82. Kellogg E A. What happens to genes in duplicated genomes. Proc Natl Acad Sci USA, 2003, 100: 4369–4371

    PubMed  CAS  PubMed Central  Google Scholar 

  83. Se’mon M, Wolfe K H. Preferential subfunctionalization of slow-evolving genes after allopolyploidization in Xenopus laevis. Proc Natl Acad Sci USA, 2008, 105: 8333–8338

    Google Scholar 

  84. Lee H S, Chen Z J. Protein-coding genes are epigenetically regulated in Arabidopsis polyploids. Proc Natl Acad Sci USA, 2001, 98: 6753–6758

    PubMed  CAS  PubMed Central  Google Scholar 

  85. Chen Z J. Genetic and epigenetic mechanisms for gene expression and phenotypic variation in plant polyploids. Annu Rev Plant Biol, 2007, 58: 377–406

    PubMed  CAS  PubMed Central  Google Scholar 

  86. Liu B, Wendel J F. Epigenetic phenomena and the evolution of plant allopolyploids. Mol Phylogenet Evol, 2003, 29: 365–379

    PubMed  CAS  Google Scholar 

  87. Madlung A, Masuelli R W, Watson B, et al. Remodeling of DNA methylation and phenotypic and transcriptional changes in synthetic Arabidopsis allotetraploids. Plant Physiol, 2002, 129: 733–746

    PubMed  CAS  PubMed Central  Google Scholar 

  88. Fedoroff N. Transposons and genome evolution in plants. Proc Natl Acad Sci USA, 2000, 97: 7002–7007

    PubMed  CAS  PubMed Central  Google Scholar 

  89. Doyle J J, Flagel L E, Paterson A H, et al. Evolutionary genetics of genome merger and doubling in plants. Annu Rev Genet, 2008, 42: 443–461

    PubMed  CAS  Google Scholar 

  90. Liu B, Wendel J F. Non-mendelian phenomena in allopolyploid genome evolution. Curr Genomics, 2002, 3: 489–506

    CAS  Google Scholar 

  91. Ma X F, Gustafson J P. Genome evolution of allopolyploids: a process of cytological and genetic diploidization. Cytogenet Genome Res, 2005, 109: 236–249

    PubMed  CAS  Google Scholar 

  92. De Bodt S, Maere S, Van de Peer Y. Genome duplication and the origin of angiosperms. Trends Ecol Evol, 2005, 20: 591–597

    PubMed  Google Scholar 

  93. Ma H Y, Zhang J F, Li Z D. Research advances on plant polyploidy breeding techniques (in Chinese). Protect Forest Sci Technol, 2008, 1: 43–46

    Google Scholar 

  94. Wang T K, Zhang J Z, Qi Y S, et al. Advances on polyploid breeding of fruit crops in China (in Chinese). J Fruit Sci, 2004, 21: 592–597

    Google Scholar 

  95. Shun M H, Zhang S N. The application of polyploidy breeding in horticultural crops (in Chinese). Jiangsu Agricult Sci, 2004, 1: 68–72

    Google Scholar 

  96. Zhang X Y, Liu J F, Wang L P. Polyploidy breeding and its application research progress of medicinal plants (in Chinese). J Jilin Normal Univ (Nat Sci Ed), 2009, 4: 128–131

    Google Scholar 

  97. Yuan J M, Dang X M, Zhan Y F. Advances on polyploid breeding in watermelon (in Chinese). Chin J Tropical Agricult, 2009, 29: 65–70

    Google Scholar 

  98. Shen A L, Yao W Z. The proceeding on triploid breeding of aquatic animals (in Chinese). Reserv Fish, 2004, 24: 1–3

    CAS  Google Scholar 

  99. Liu Y, Liu S J, Sun Y D, et al. Polyploid hybrids of crucian carp× common carp (in Chinese). Rev China Agricult Sci Technol, 2003, 5: 3–6

    Google Scholar 

  100. Wu P. Research progress of fish polyploid breeding in China (in Chinese). J Shanghai Fish Univ, 2005, 14: 72–78

    Google Scholar 

  101. Hu L L, Li J E. The review of fish polyploid breeding research(in Chinese). Fish Sci Technol, 2009, 7–10

  102. Yuan B J, Jiang N C, Lu J P, et al. A review of decapod crustacean multiploid breeding (in Chinese). Donghai Marine Sci, 1998, 16: 64–68

    Google Scholar 

  103. Wang Z P, Li K J, Yu R H, et al. Progress of tetraploid breeding in mollusks (in Chinese). J Ocean Univ China, 2004, 34: 195–200

    Google Scholar 

  104. Song L M, Yang Y, Wang W M, et al. Induction of triploidy in yellow catfish Pelteobagrus fulvidraco by heat shock (in Chinese). Fish Sci, 2010, 29: 352–355

    Google Scholar 

  105. Gui J F, Liang S C, Sun J M, et al. Studies on genome manipulation in fish I. Induction of triploid transparent colored crucian carp (Carassius auratus transparent colored variety) by hydrostatic pressure (in Chinese). Acta Hydrobiol Sin, 1990, 14: 336–344

    Google Scholar 

  106. Wu W X, Li C W, Liu G A, et al. Studies on tetraploid hybrid between red common carp (Cyprinus carpio) and grass carp (Ctenopharyngodon idellus) and its backcross triploid (in Chinese). Acta Hydrobiol Sin, 1988, 12: 355–363

    Google Scholar 

  107. Gui J F, Liang S C, Zhu L F, et al. Discovery and breeding potential of compound tetraploid allogynogenetic silver crucian carp in artificial population (in Chinese). Chin Sci Bull, 1992, 37: 646–648

    Google Scholar 

  108. Wu C, Ye Y, Chen R, et al. An artificial multiple triploid carp and its biological characteristics. Aquaculture, 1993, 111: 255–262

    Google Scholar 

  109. Luo K K, Xiao J, Liu S J, et al. Massive production of all-female diploids and triploids in the crucian carp. Int J Biol Sci, 2011, 7: 487–495

    PubMed  PubMed Central  Google Scholar 

  110. Hu W, Zhu Z Y. Integration mechanisms of transgenes and population fitness of GH transgenic fish. Sci China Life Sci, 2010, 53: 401–408

    PubMed  CAS  Google Scholar 

  111. Hu W, Wang Y P, Zhu Z Y. Progress in the evaluation of transgenic fish for possible ecological risk and its containment strategies. Sci China Life Sci, 2007, 50: 573–579

    CAS  Google Scholar 

  112. Yu F, Xiao J, Liang X Y, et al. Rapid growth and sterility of growth hormone gene transgenic triploid carp. Chin Sci Bull, 2011, 56: 1679–1684

    Google Scholar 

  113. Qin Q B, He W G, Liu S J, et al. Analysis of 5S rDNA organization and variation in polyploid hybrids from crosses of different fish subfamilies. J Exp Zool (Mol Dev Evol), 2010, 314: 403–411

    Google Scholar 

Download references

Author information

Authors and Affiliations

  1. Key Laboratory of Protein Chemistry and Fish Developmental Biology of Ministry of Education of China, College of Life Sciences, Hunan Normal University, Changsha, 410081, China

    Can Song, ShaoJun Liu, Jun Xiao, WeiGuo He, Yi Zhou, QinBo Qin, Chun Zhang & Yun Liu

Authors
  1. Can Song
    View author publications

    Search author on:PubMed Google Scholar

  2. ShaoJun Liu
    View author publications

    Search author on:PubMed Google Scholar

  3. Jun Xiao
    View author publications

    Search author on:PubMed Google Scholar

  4. WeiGuo He
    View author publications

    Search author on:PubMed Google Scholar

  5. Yi Zhou
    View author publications

    Search author on:PubMed Google Scholar

  6. QinBo Qin
    View author publications

    Search author on:PubMed Google Scholar

  7. Chun Zhang
    View author publications

    Search author on:PubMed Google Scholar

  8. Yun Liu
    View author publications

    Search author on:PubMed Google Scholar

Corresponding author

Correspondence to ShaoJun Liu.

Additional information

This article is published with open access at Springerlink.com

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 2.0 International License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and permissions

About this article

Cite this article

Song, C., Liu, S., Xiao, J. et al. Polyploid organisms. Sci. China Life Sci. 55, 301–311 (2012). https://doi.org/10.1007/s11427-012-4310-2

Download citation

  • Received: 09 January 2012

  • Accepted: 29 February 2012

  • Published: 15 June 2012

  • Issue date: April 2012

  • DOI: https://doi.org/10.1007/s11427-012-4310-2

Share this article

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

Keywords

  • polyploid
  • whole genome duplication
  • diploidization
  • distant hybridization
  • polyploidy breeding

Advertisement

Search

Navigation

  • Find a journal
  • Publish with us
  • Track your research

Footer Navigation

Discover content

  • Journals A-Z
  • Books A-Z
  • Subjects A-Z

Publish with us

  • Journal finder
  • Publish your research
  • Language editing
  • Open access publishing

Products and services

  • Our products
  • Librarians
  • Societies
  • Partners and advertisers

Our brands

  • Springer
  • Nature Portfolio
  • BMC
  • Palgrave Macmillan
  • Apress
  • Discover

Corporate Navigation

  • Your US state privacy rights
  • Accessibility statement
  • Terms and conditions
  • Privacy policy
  • Help and support
  • Legal notice
  • Cancel contracts here

104.23.243.228

Not affiliated

Springer Nature

© 2026 Springer Nature