World Library  
Flag as Inappropriate
Email this Article


Article Id: WHEBN0000062610
Reproduction Date:

Title: Polyploid  
Author: World Heritage Encyclopedia
Language: English
Subject: Watermelon, Somatic fusion, Ploidy, Parthenogenesis, Chromosome
Collection: Classical Genetics, Speciation
Publisher: World Heritage Encyclopedia


This image shows haploid (single), diploid (double), triploid (triple), and tetraploid (quadruple) sets of chromosomes. Triploid and tetraploid chromosomes are examples of polyploidy.

Polyploid bees and other Hymenoptera, for example, are monoploid.

Polyploidy refers to a numerical change in a whole set of chromosomes. Organisms in which a particular chromosome, or chromosome segment, is under- or overrepresented are said to be aneuploid (from the Greek words meaning "not", "good", and "fold"). Therefore the distinction between aneuploidy and polyploidy is that aneuploidy refers to a numerical change in part of the chromosome set, whereas polyploidy refers to a numerical change in the whole set of chromosomes.[2]

Polyploidy may occur due to abnormal cell division, either during mitosis, or commonly during metaphase I in meiosis.

Polyploidy occurs in some animals, such as goldfish,[3] salmon, and salamanders, but is especially common among ferns and flowering plants (see Hibiscus rosa-sinensis), including both wild and cultivated species. Wheat, for example, after millennia of hybridization and modification by humans, has strains that are diploid (two sets of chromosomes), tetraploid (four sets of chromosomes) with the common name of durum or macaroni wheat, and hexaploid (six sets of chromosomes) with the common name of bread wheat. Many agriculturally important plants of the genus Brassica are also tetraploids. Polyploidization is a mechanism of sympatric speciation because polyploids are usually unable to interbreed with their diploid ancestors.

Polyploidy can be induced in plants and cell cultures by some chemicals: the best known is colchicine, which can result in chromosome doubling, though its use may have other less obvious consequences as well. Oryzalin will also double the existing chromosome content.


  • Types 1
  • Animals 2
    • Humans 2.1
  • Plants 3
    • Crops 3.1
      • Examples 3.1.1
  • Fungi 4
  • Chromalveolata 5
  • Terminology 6
    • Autopolyploidy 6.1
    • Allopolyploidy 6.2
    • Paleopolyploidy 6.3
    • Karyotype 6.4
    • Paralogous 6.5
    • Homologous 6.6
    • Homoeologous 6.7
      • Example of homoeologous chromosomes 6.7.1
  • See also 7
  • References 8
  • Further reading 9
  • External links 10


Organ-specific patterns of endopolyploidy (from 2x to 64x) in the giant ant Dinoponera australis

Polyploid types are labeled according to the number of chromosome sets in the nucleus:


Examples in animals are more common in non-vertebrates[9] such as flatworms, leeches, and brine shrimp. Within vertebrates, examples of stable polyploidy include the salmonids and many cyprinids (i.e. carp).[10] Some fish have as many as 400 chromosomes.[10] Polyploidy also occurs commonly in amphibians; for example the biomedically-important Xenopus genus contains many different species with as many as 12 sets of chromosomes (dodecaploid).[11] Polyploid lizards are also quite common, but are sterile and must reproduce by parthenogenesis. Polyploid mole salamanders (mostly triploids) are all female and reproduce by kleptogenesis,[12] "stealing" spermatophores from diploid males of related species to trigger egg development but not incorporating the males' DNA into the offspring. While mammalian liver cells are polyploid, rare instances of polyploid mammals are known, but most often result in prenatal death.

An octodontid rodent of Argentina's harsh desert regions, known as the Plains Viscacha-Rat (Tympanoctomys barrerae) has been reported as an exception to this 'rule'.[13] However, careful analysis using chromosome paints shows that there are only two copies of each chromosome in T. barrerae, not the four expected if it were truly a tetraploid.[14] The rodent is not a rat, but kin to guinea pigs and chinchillas. Its "new" diploid [2n] number is 102 and so its cells are roughly twice normal size. Its closest living relation is Octomys mimax, the Andean Viscacha-Rat of the same family, whose 2n = 56. It was therefore surmised that an Octomys-like ancestor produced tetraploid (i.e., 2n = 4x = 112) offspring that were, by virtue of their doubled chromosomes, reproductively isolated from their parents.

Polyploidy was induced in fish by Har Swarup (1956) using a cold-shock treatment of the eggs close to the time of fertilization, which produced triploid embryos that successfully matured.[15][16] Cold or heat shock has also been shown to result in unreduced amphibian gametes, though this occurs more commonly in eggs than in sperm.[17] John Gurdon (1958) transplanted intact nuclei from somatic cells to produce diploid eggs in the frog, Xenopus (an extension of the work of Briggs and King in 1952) that were able to develop to the tadpole stage.[18] The British Scientist, J. B. S. Haldane hailed the work for its potential medical applications and, in describing the results, became one of the first to use the word “clone” in reference to animals. Later work by Shinya Yamanaka showed how mature cells can be reprogrammed to become pluripotent, extending the possibilities to non-stem cells. Gurdon and Yamanaka were jointly awarded the Nobel Prize in 2012 for this work.[18]


True polyploidy rarely occurs in humans, although polyploid cells occur in highly differentiated tissue, such as liver parenchyma and heart muscle, and in bone marrow.[19] Aneuploidy is more common.

Polyploidy occurs in humans in the form of triploidy, with 69 chromosomes (sometimes called 69,XXX), and tetraploidy with 92 chromosomes (sometimes called 92,XXXX). Triploidy, usually due to polyspermy, occurs in about 2–3% of all human pregnancies and ~15% of miscarriages. The vast majority of triploid conceptions end as a miscarriage; those that do survive to term typically die shortly after birth. In some cases, survival past birth may extend longer if there is mixoploidy with both a diploid and a triploid cell population present.

Triploidy may be the result of either digyny (the extra haploid set is from the mother) or diandry (the extra haploid set is from the father). Diandry is mostly caused by reduplication of the paternal haploid set from a single sperm, but may also be the consequence of dispermic (two sperm) fertilization of the egg.[20] Digyny is most commonly caused by either failure of one meiotic division during oogenesis leading to a diploid oocyte or failure to extrude one polar body from the oocyte. Diandry appears to predominate among early miscarriages, while digyny predominates among triploidy that survives into the fetal period. However, among early miscarriages, digyny is also more common in those cases <8.5 weeks gestational age or those in which an embryo is present. There are also two distinct phenotypes in triploid placentas and fetuses that are dependent on the origin of the extra haploid set. In digyny, there is typically an asymmetric poorly grown fetus, with marked adrenal hypoplasia and a very small placenta. In diandry, a partial hydatidiform mole develops.[20] These parent-of-origin effects reflect the effects of genomic imprinting.

Complete tetraploidy is more rarely diagnosed than triploidy, but is observed in 1–2% of early miscarriages. However, some tetraploid cells are commonly found in chromosome analysis at prenatal diagnosis and these are generally considered 'harmless'. It is not clear whether these tetraploid cells simply tend to arise during in vitro cell culture or whether they are also present in placental cells in vivo. There are, at any rate, very few clinical reports of fetuses/infants diagnosed with tetraploidy mosaicism.

Mixoploidy is quite commonly observed in human preimplantation embryos and includes haploid/diploid as well as diploid/tetraploid mixed cell populations. It is unknown whether these embryos fail to implant and are therefore rarely detected in ongoing pregnancies or if there is simply a selective process favoring the diploid cells.


Speciation via polyploidy: A diploid cell undergoes failed meiosis, producing diploid gametes, which self-fertilize to produce a tetraploid zygote.

Polyploidy is pervasive in plants and some estimates suggest that 30–80% of living plant species are polyploid, and many lineages show evidence of ancient polyploidy (paleopolyploidy) in their genomes.[21][22][23] Huge explosions in angiosperm species diversity appear to have coincided with the timing of ancient genome duplications shared by many species.[24] It has been established that 15% of angiosperm and 31% of fern speciation events are accompanied by ploidy increase.[25]

Polyploid plants can arise spontaneously in nature by several mechanisms, including meiotic or mitotic failures, and fusion of unreduced (2n) gametes.[26] Both autopolyploids (e.g. potato [27]) and allopolyploids (e.g. canola, wheat, cotton) can be found among both wild and domesticated plant species.

Most polyploids display novel variation or morphologies relative to their parental species, that may contribute to the processes of speciation and eco-niche exploitation.[22][26] The mechanisms leading to novel variation in newly formed allopolyploids may include gene dosage effects (resulting from more numerous copies of genome content), the reunion of divergent gene regulatory hierarchies, chromosomal rearrangements, and epigenetic remodeling, all of which affect gene content and/or expression levels.[28][29][30][31] Many of these rapid changes may contribute to reproductive isolation and speciation. However seed generated from interploidy crosses, such as between polyploids and their parent species, usually suffer from aberrant endosperm development which impairs their viability,[32][33] thus contributing to polyploid speciation.

Lomatia tasmanica is an extremely rare Tasmanian shrub that is triploid and sterile; reproduction is entirely vegetative, with all plants having the same genetic constitution.

There are few naturally occurring polyploid conifers. One example is the Coast Redwood Sequoia sempervirens, which is a hexaploid (6x) with 66 chromosomes (2n = 6x = 66), although the origin is unclear.[34]

Aquatic plants, especially the Monocotyledons, include a large number of polyploids.[35]


The induction of polyploidy is a common technique to overcome the sterility of a hybrid species during plant breeding. For example, Triticale is the hybrid of wheat (Triticum turgidum) and rye (Secale cereale). It combines sought-after characteristics of the parents, but the initial hybrids are sterile. After polyploidization, the hybrid becomes fertile and can thus be further propagated to become triticale.

In some situations, polyploid crops are preferred because they are sterile. For example, many seedless fruit varieties are seedless as a result of polyploidy. Such crops are propagated using asexual techniques, such as grafting.

Polyploidy in crop plants is most commonly induced by treating seeds with the chemical colchicine.


Some crops are found in a variety of ploidies: tulips and lilies are commonly found as both diploid and triploid; daylilies (Hemerocallis cultivars) are available as either diploid or tetraploid; apples and kinnows can be diploid, triploid, or tetraploid.


Schematic phylogeny of the fungi. Red circles indicate polyploidy, blue squares indicate hybridization. From Albertin and Marullo, 2012[38]

Besides plants and animals, the evolutionary history of various fungal species is dotted by past and recent whole-genome duplication events (see Albertin and Marullo 2012[38] for review). Several examples of polyploids are known:

In addition, polyploidy is frequently associated with hybridization and reticulate evolution that appear to be highly prevalent in several fungal taxa. Indeed, homoploid speciation (i.e., hybrid speciation without a change in chromosome number) has been evidenced for some fungal species (e.g., the basidiomycota Microbotryum violaceum [46]).

Schematic phylogeny of the Chromalveolata. Red circles indicate polyploidy, blue squares indicate hybridization. From Albertin and Marullo, 2012[38]

As for plants and animals, fungal hybrids and polyploids display structural and functional modifications compared to their progenitors and diploid counterparts. In particular, the structural and functional outcomes of polyploid Saccharomyces genomes strikingly reflect the evolutionary fate of plant polyploid ones. Large chromosomal rearrangements[47] leading to chimeric chromosomes[48] have been described, as well as more punctual genetic modifications such as gene loss.[49] The homoealleles of the allotetraploid yeast S. pastorianus show unequal contribution to the transcriptome.[50] Phenotypic diversification is also observed following polyploidization and/or hybridization in fungi,[51] producing the fuel for natural selection and subsequent adaptation and speciation.


Other eukaryotic taxa have experienced one or more polyploidization events during their evolutionary history (see Albertin and Marullo, 2012[38] for review). The oomycetes, which are non-true fungi members, contain several examples of paleopolyploid and polyploid species, such as within the Phytophthora genus.[52] Some species of brown algae (Fucales, Laminariales [53] and diatoms [54]) contain apparent polyploid genomes. In the Alveolata group, the remarkable species Paramecium tetraurelia underwent three successive rounds of whole-genome duplication [55] and established itself as a major model for paleopolyploid studies.



Autopolyploids are polyploids with multiple chromosome sets derived from a single species. Autopolyploids can arise from a spontaneous, naturally occurring genome doubling, like the potato.[27] Others might form following fusion of 2n gametes (unreduced gametes). Bananas and apples can be found as autotriploids. Autopolyploid plants typically display polysomic inheritance, and therefore have low fertility, but may be propagated clonally.


Allopolyploids are polyploids with chromosomes derived from different species. Precisely it is the result of multiplying the chromosome number in an F1 hybrid. Triticale is an example of an allopolyploid, having six chromosome sets, allohexaploid, four from wheat (Triticum turgidum) and two from rye (Secale cereale). Amphidiploids are a type of allopolyploids (they are tetraploid, containing the diploid chromosome sets of both parents[56]). Some of the best examples of allopolyploids come from the Brassicas, and the Triangle of U describes the relationships between the three common diploid Brassicas (B. oleracea, B. rapa, and B. nigra) and three allotetraploids (B. napus, B. juncea, and B. carinata) derived from hybridization among the diploids.


This phylogenetic tree shows the relationship between the best-documented instances of paleopolyploidy in eukaryotes.

Ancient genome duplications probably occurred in the evolutionary history of all life. Duplication events that occurred long ago in the history of various evolutionary lineages can be difficult to detect because of subsequent diploidization (such that a polyploid starts to behave cytogenetically as a diploid over time) as mutations and gene translations gradually make one copy of each chromosome unlike the other copy. Over time, it is also common for duplicated copies of genes to accumulate mutations and become inactive pseudogenes.[57]

In many cases, these events can be inferred only through comparing sequenced genomes. Examples of unexpected but recently confirmed ancient genome duplications include baker's yeast (Saccharomyces cerevisiae), mustard weed/thale cress (Arabidopsis thaliana), rice (Oryza sativa), and an early evolutionary ancestor of the vertebrates (which includes the human lineage) and another near the origin of the teleost fishes. Angiosperms (flowering plants) have paleopolyploidy in their ancestry. All eukaryotes probably have experienced a polyploidy event at some point in their evolutionary history.


A karyotype is the characteristic chromosome complement of a eukaryote species.[58][59] The preparation and study of karyotypes is part of cytology and, more specifically, cytogenetics.

Although the replication and transcription of DNA is highly standardized in eukaryotes, the same cannot be said for their karotypes, which are highly variable between species in chromosome number and in detailed organization despite being constructed out of the same macromolecules. In some cases, there is even significant variation within species. This variation provides the basis for a range of studies in what might be called evolutionary cytology.


The term is used to describe the relationship between duplicated genes or portions of chromosomes that derived from a common ancestral DNA. Paralogous segments of DNA may arise spontaneously by errors during DNA replication, copy and paste transposons, or whole genome duplications.


The term is used to describe the relationship of similar chromosomes that pair at mitosis and meiosis. In a diploid, one homolog is derived from the male parent (sperm) and one is derived from the female parent (egg). During meiosis and gametogenesis, homologous chromosomes pair and exchange genetic material by recombination, leading to the production of sperm or eggs with chromosome haplotypes containing novel genetic variation.


The term homoeologous, also spelled homeologous, is used to describe the relationship of similar chromosomes or parts of chromosomes brought together following inter-species hybridization and allopolyploidization, and whose relationship was completely homologous in an ancestral species. In allopolyploids, the homologous chromosomes within each parental sub-genome should pair faithfully during meiosis, leading to disomic inheritance; however in some allopolyploids, the homoeologous chromosomes of the parental genomes may be nearly as similar to one another as the homologous chromosomes, leading to tetrasomic inheritance (four chromosomes pairing at meiosis), intergenomic recombination, and reduced fertility.

Example of homoeologous chromosomes

Durum wheat is the result of the inter-species hybridization of two diploid grass species Triticum urartu and Aegilops speltoides. Both diploid ancestors had two sets of 7 chromosomes, which were similar in terms of size and genes contained on them. Durum wheat contains two sets of chromosomes derived from Triticum urartu and two sets of chromosomes derived from Aegilops speltoides. Each chromosome pair derived from the Triticum urartu parent is homoeologous to the opposite chromosome pair derived from the Aegilops speltoides parent, though each chromosome pair unto itself is homologous.

See also


  1. ^ Parmacek, Michael S.; Epstein, Jonathan A. (2009). "Cardiomyocyte Renewal". New England Journal of Medicine 361 (1): 86–8.  
  2. ^ Griffiths, Anthony J. F. (1999). An Introduction to genetic analysis. San Francisco: W.H. Freeman.  
  3. ^ Ohno, Susumu; Muramoto, Junichi; Christian, Lawrence; Atkin, Niels B. (1967). "Diploid-tetraploid relationship among old-world members of the fish family Cyprinidae". Chromosoma 23 (1): 1–9.  
  4. ^ Bertolani R (2001). "Evolution of the reproductive mechanisms in Tardigrades: a review". Zoologischer Anzeiger 240 (3–4): 247–252.  
  5. ^ Stouder, Deanna J.; Bisson, Peter A.; Naiman, Robert J. (1997). Pacific Salmon and Their Ecosystems: Status and Future Options. Springer. pp. 30–1.  
  6. ^ Adams, Keith L; Wendel, Jonathan F (2005). "Polyploidy and genome evolution in plants". Current Opinion in Plant Biology 8 (2): 135–41.  
  7. ^ a b Crowhurst, Ross N.; Whittaker, D.; Gardner, R. C. "The genetic origin of kiwifruit". 
  8. ^ Ainouche, M. L.; Fortune, P. M.; Salmon, A.; Parisod, C.; Grandbastien, M.-A.; Fukunaga, K.; Ricou, M.; Misset, M.-T. (2008). "Hybridization, polyploidy and invasion: Lessons from Spartina (Poaceae)". Biological Invasions 11 (5): 1159–73.  
  9. ^ Otto, Sarah P; Whitton, Jeannette (2000). "Polyploidincidence Andevolution". Annual Review of Genetics 34: 401–437.  
  10. ^ a b Leggatt, Rosalind A.; Iwama, George K. (2003). "Occurrence of polyploidy in the fishes". Reviews in Fish Biology and Fisheries 13 (3): 237–46.  
  11. ^ Cannatella, David C.; De Sa, Rafael O. (1993). "Xenopus laevis as a Model Organism". Society of Systematic Biologists 42 (4): 476–507.  
  12. ^ Bonen, L.; Bi, James P.; Fu, Ke; Noble, Jinzong; Niedzwiecki, Daniel W.A.; Niedzwiecki, John (2007). "Unisexual salamanders (genus Ambystoma) present a new reproductive mode for eukaryotes". Genome 50 (2): 119–36.  
  13. ^ Gallardo, M.H.; González, C.A.; Cebrián, I. (2006). "Molecular cytogenetics and allotetraploidy in the red vizcacha rat, Tympanoctomys barrerae (Rodentia, Octodontidae)". Genomics 88 (2): 214–21.  
  14. ^ Svartman, Marta; Stone, Gary; Stanyon, Roscoe (2005). "Molecular cytogenetics discards polyploidy in mammals". Genomics 85 (4): 425–30.  
  15. ^ Swarup, H. (1956). "Production of Heteroploidy in the Three-Spined Stickleback, Gasterosteus aculeatus (L.)". Nature 178 (4542): 1124.  
  16. ^ Swarup, H. (1959). "Production of triploidy ingasterosteus aculeatus (L)". Journal of Genetics 56 (2): 129.  
  17. ^ Mable, B.K.; Alexandrou, M. A.; Taylor, M. I. (2011). "Genome duplication in amphibians and fish: an extended synthesis". Journal of Zoology 284: 151–182.  
  18. ^ a b "Nobel Prize in Physiology or Medicine 2012 Awarded for Discovery That Mature Cells Can Be Reprogrammed to Become Pluripotent". ScienceDaily. 8 Oct 2012. 
  19. ^ Winkelmann, M; Pfitzer, P; Schneider, W (1987). "Significance of polyploidy in megakaryocytes and other cells in health and tumor disease". Klinische Wochenschrift 65 (23): 1115–31.  
  20. ^ a b Baker, Phil; Monga, Ash; Baker, Philip (2006). Gynaecology by ten teachers. London: Arnold.  
  21. ^ Meyers, Lauren Ancel; Levin, Donald A. (2006). "On the Abundance of Polyploids in Flowering Plants". Evolution 60 (6): 1198–206.  
  22. ^ a b Rieseberg, L. H.; Willis, J. H. (2007). "Plant Speciation". Science 317 (5840): 910–4.  
  23. ^ Otto, Sarah P. (2007). "The Evolutionary Consequences of Polyploidy". Cell 131 (3): 452–62.  
  24. ^ Debodt, S; Maere, S; Vandepeer, Y (2005). "Genome duplication and the origin of angiosperms". Trends in Ecology & Evolution 20 (11): 591–7.  
  25. ^ Wood, T. E.; Takebayashi, N.; Barker, M. S.; Mayrose, I.; Greenspoon, P. B.; Rieseberg, L. H. (2009). "The frequency of polyploid speciation in vascular plants". Proceedings of the National Academy of Sciences 106 (33): 13875–9.  
  26. ^ a b Comai, Luca (2005). "The advantages and disadvantages of being polyploid". Nature Reviews Genetics 6 (11): 836–46.  
  27. ^ a b Xu, Xun; Xu, Shengkai; Pan, Shifeng; Cheng, Bo; Zhang, Desheng; Mu, Peixiang; Ni, Gengyun; Zhang, Shuang; Yang, Ruiqiang; Li, Jun; Wang, Gisella; Orjeda, Frank; Guzman, Michael; Torres, Roberto; Lozano, Olga; Ponce, Diana; Martinez, Germán; De La Cruz, S. K.; Chakrabarti, Virupaksh U.; Patil, Konstantin G.; Skryabin, Boris B.; Kuznetsov, Nikolai V.; Ravin, Tatjana V.; Kolganova, Alexey V.; Beletsky, Andrei V.; Mardanov, Alex; Di Genova, Daniel M.; Bolser, David M. A.; Martin, Guangcun; Li, Yu (2011). "Genome sequence and analysis of the tuber crop potato". Nature 475 (7355): 189–95.  
  28. ^ Osborn, Thomas C.; Pires, J.; Birchler, James A.; Auger, Donald L.; Chen, Z.; Lee, Hyeon-Se; Comai, Luca; Madlung, Andreas; Doerge, R.W.; Colot, Vincent; Martienssen, Robert A. (2003). "Understanding mechanisms of novel gene expression in polyploids". Trends in Genetics 19 (3): 141–7.  
  29. ^ Chen, Z. Jeffrey; Ni, Zhongfu (2006). "Mechanisms of genomic rearrangements and gene expression changes in plant polyploids". BioEssays 28 (3): 240–52.  
  30. ^ Chen, Z. Jeffrey (2007). "Genetic and Epigenetic Mechanisms for Gene Expression and Phenotypic Variation in Plant Polyploids". Annual Review of Plant Biology 58: 377–406.  
  31. ^ Albertin, W.; Balliau, T; Brabant, P; Chèvre, AM; Eber, F; Malosse, C; Thiellement, H (2006). "Numerous and Rapid Nonstochastic Modifications of Gene Products in Newly Synthesized Brassica napus Allotetraploids". Genetics 173 (2): 1101–13.  
  32. ^ Pennington, PD; Costa, LM; Gutierrez-Marcos, JF; Greenland, AJ; Dickinson, HG (Apr 2008). "When genomes collide: aberrant seed development following maize interploidy crosses.". Annals of botany 101 (6): 833–43.  
  33. ^ von Wangenheim, Karl-Hartmut; Peterson, Hans-Peter. "Aberrant endosperm development in interploidy crosses reveals a timer of differentiation". Developmental Biology 270 (2): 277–289.  
  34. ^ Ahuja MR, Neale DB (2002). "Origins of Polyploidy in Coast Redwood (Sequoia sempervirens (D. DON) ENDL.) and Relationship of Coast Redwood to other Genera of Taxodiaceae". Silvae Genetica 51: 2–3. 
  35. ^ Les, D.H.; Philbrick, C.T. (1993). "Studies of hybridization and chromosome number variation in aquatic angiosperms: Evolutionary implications". Aquatic Botany 44 (2–3): 181.  
  36. ^ Seedless Fruits Make Others Needless
  37. ^ Emshwiller, E. (2006). "Origins of polyploid crops: The example of the octaploid tuber crop Oxalis tuberosa". In M.A. Zeder; D. Decker-Walters; E. Emshwiller; D. Bradley; B.D. Smith. Documenting domestication: new genetic and archaeological paradigms. Berkeley, USA: University of California Press. pp. 153–168. 
  38. ^ a b c d Albertin, W.; Marullo, P. (2012). "Polyploidy in fungi: Evolution after whole-genome duplication".  
  39. ^ Emerson, Ralph; Wilson, Charles M. (1954). "Interspecific Hybrids and the Cytogenetics and Cytotaxonomy of Euallomyces". Mycologia 46 (4): 393–434.  
  40. ^ Albertin, W.; Marullo, P.; Aigle, M.; Bourgais, A.; Bely, M.; Dillmann, C.; De Vienne, D.; Sicard, D. (2009). "Evidence for autotetraploidy associated with reproductive isolation inSaccharomyces cerevisiae: Towards a new domesticated species". Journal of Evolutionary Biology 22 (11): 2157–70.  
  41. ^ Lu, Benjamin C. (1964). "Polyploidy in the Basidiomycete Cyathus stercoreus". American Journal of Botany 51 (3): 343–7.  
  42. ^ Libkind, D.; Hittinger, C. T.; Valerio, E.; Goncalves, C.; Dover, J.; Johnston, M.; Goncalves, P.; Sampaio, J. P. (2011). "Microbe domestication and the identification of the wild genetic stock of lager-brewing yeast". Proceedings of the National Academy of Sciences 108 (35): 14539–44.  
  43. ^
  44. ^ Ma, Li-Jun; Ibrahim, Ashraf S.; Skory, Christopher; Grabherr, Manfred G.; Burger, Gertraud; Butler, Margi; Elias, Marek; Idnurm, Alexander; Lang, B. Franz; Sone, Teruo; Abe, Ayumi; Calvo, Sarah E.; Corrochano, Luis M.; Engels, Reinhard; Fu, Jianmin; Hansberg, Wilhelm; Kim, Jung-Mi; Kodira, Chinnappa D.; Koehrsen, Michael J.; Liu, Bo; Miranda-Saavedra, Diego; O'Leary, Sinead; Ortiz-Castellanos, Lucila; Poulter, Russell; Rodriguez-Romero, Julio; Ruiz-Herrera, José; Shen, Yao-Qing; Zeng, Qiandong; Galagan, James; Birren, Bruce W. (2009). Madhani, Hiten D, ed. "Genomic Analysis of the Basal Lineage Fungus Rhizopus oryzae Reveals a Whole-Genome Duplication". PLoS Genetics 5 (7): e1000549.  
  45. ^ Wong, S.; Butler, G.; Wolfe, K. H. (2002). "Gene order evolution and paleopolyploidy in hemiascomycete yeasts". Proceedings of the National Academy of Sciences 99 (14): 9272–7.  
  46. ^ Devier, B.; Aguileta, G.; Hood, M. E.; Giraud, T. (2009). "Using phylogenies of pheromone receptor genes in the Microbotryum violaceum species complex to investigate possible speciation by hybridization". Mycologia 102 (3): 689–96.  
  47. ^ Dunn, B.; Sherlock, G. (2008). "Reconstruction of the genome origins and evolution of the hybrid lager yeast Saccharomyces pastorianus". Genome Research 18 (10): 1610–23.  
  48. ^ Nakao, Y.; Kanamori, T.; Itoh, T.; Kodama, Y.; Rainieri, S.; Nakamura, N.; Shimonaga, T.; Hattori, M.; Ashikari, T. (2009). "Genome Sequence of the Lager Brewing Yeast, an Interspecies Hybrid". DNA Research 16 (2): 115–29.  
  49. ^ Scannell, Devin R.; Byrne, Kevin P.; Gordon, Jonathan L.; Wong, Simon; Wolfe, Kenneth H. (2006). "Multiple rounds of speciation associated with reciprocal gene loss in polyploid yeasts". Nature 440 (7082): 341–5.  
  50. ^ Minato, Toshiko; Yoshida, Satoshi; Ishiguro, Tatsuji; Shimada, Emiko; Mizutani, Satoru; Kobayashi, Osamu; Yoshimoto, Hiroyuki (2009). "Expression profiling of the bottom fermenting yeastSaccharomyces pastorianusorthologous genes using oligonucleotide microarrays". Yeast 26 (3): 147–65.  
  51. ^ Lidzbarsky, Gabriel A.; Shkolnik, Tamar; Nevo, Eviatar (2009). Idnurm, Alexander, ed. "Adaptive Response to DNA-Damaging Agents in Natural Saccharomyces cerevisiae Populations from "Evolution Canyon", Mt. Carmel, Israel". PLoS ONE 4 (6): e5914.  
  52. ^ Ioos, Renaud; Andrieux, Axelle; Marçais, Benoît; Frey, Pascal (2006). "Genetic characterization of the natural hybrid species Phytophthora alni as inferred from nuclear and mitochondrial DNA analyses". Fungal Genetics and Biology 43 (7): 511–29.  
  53. ^ Phillips, N.; Kapraun, D. F.; Gómez Garreta, A.; Ribera Siguan, M. A.; Rull, J. L.; Salvador Soler, N.; Lewis, R.; Kawai, H. (2011). "Estimates of nuclear DNA content in 98 species of brown algae (Phaeophyta)". AoB Plants 2011: plr001.  
  54. ^ Chepurnov, Victor A.; Mann, David G.; Vyverman, Wim; Sabbe, Koen; Danielidis, Daniel B. (2002). "Sexual Reproduction, Mating System, and Protoplast Dynamics of Seminavis (Bacillariophyceae)". Journal of Phycology 38 (5): 1004–19.  
  55. ^ Aury, Jean-Marc; Jaillon, Olivier; Duret, Laurent; Noel, Benjamin; Jubin, Claire; Porcel, Betina M.; Ségurens, Béatrice; Daubin, Vincent; Anthouard, Véronique; Aiach, Nathalie; Arnaiz, Olivier; Billaut, Alain; Beisson, Janine; Blanc, Isabelle; Bouhouche, Khaled; Câmara, Francisco; Duharcourt, Sandra; Guigo, Roderic; Gogendeau, Delphine; Katinka, Michael; Keller, Anne-Marie; Kissmehl, Roland; Klotz, Catherine; Koll, France; Le Mouël, Anne; Lepère, Gersende; Malinsky, Sophie; Nowacki, Mariusz; Nowak, Jacek K.; Plattner, Helmut (2006). "Global trends of whole-genome duplications revealed by the ciliate Paramecium tetraurelia". Nature 444 (7116): 171–8.  
  56. ^ Rieger, R.; Michaelis, A.; Green, M.M. (1968). A glossary of genetics and cytogenetics: Classical and molecular. 
  57. ^ Edger, Patrick P.; Pires, Chris J. (2009). "Gene and genome duplications: the impact of dosage-sensitivity on the fate of nuclear genes". Chromosome Research 17 (5): 699–717.  
  58. ^ White M.J.D. 1973. The chromosomes. 6th ed, Chapman & Hall, London. p28
  59. ^ Stebbins G.L. 1950. Variation and evolution in plants. Chapter XII: The Karyotype. Columbia University Press N.Y.

Further reading

  • Snustad, D. Peter et al. (2006). Principles of Genetics (4th ed.). Hoboken, NJ: John Wiley & Sons.  
  • The Arabidopsis Genome Initiative (2000). "Analysis of the genome sequence of the flowering plant Arabidopsis thaliana".  
  • Eakin, Guy S.; Behringer, Richard R. (2003). "Tetraploid development in the mouse". Developmental Dynamics 228 (4): 751–66.  
  • Gaeta, R. T.; Pires, J. C.; Iniguez-Luy, F.; Leon, E.; Osborn, T. C. (2007). "Genomic Changes in Resynthesized Brassica napus and Their Effect on Gene Expression and Phenotype". The Plant Cell Online 19 (11): 3403.  
  • Gregory, T.R.; Mable, B.K. (2005). "Polyploidy in animals". In Gregory, T.R. The Evolution of the Genome. San Diego: Elsevier. pp. 427–517. 
  • Jaillon, Olivier; Aury, Jean-Marc; Brunet, Frédéric; Petit, Jean-Louis et al. (2004). "Genome duplication in the teleost fish Tetraodon nigroviridis reveals the early vertebrate proto-karyotype".  
  • Paterson, Andrew H.; Bowers, John E.; Van De Peer, Yves; Vandepoele, Klaas (2005). "Ancient duplication of cereal genomes".  
  • Raes, Jeroen; Vandepoele, Klaas; Simillion, Cedric; Saeys, Yvan; Van De Peer, Yves (2003). "Investigating ancient duplication events in the Arabidopsis genome". Journal of Structural and Functional Genomics 3 (1–4): 117–29.  
  • Simillion, C.; Vandepoele, K; Van Montagu, MC; Zabeau, M; Van De Peer, Y (2002). "Arabidopsis thaliana"The hidden duplication past of . Proceedings of the National Academy of Sciences 99 (21): 13627–32.  
  • Soltis, Douglas E.; Soltis, Pamela S.; Schemske, Douglas W.; Hancock, James F.; Thompson, John N.; Husband, Brian C.; Judd, Walter S. (2007). "Autopolyploidy in Angiosperms: Have We Grossly Underestimated the Number of Species?". Taxon 56 (1): 13–30.  
  • Soltis DE, Buggs RJA, Doyle JJ, Soltis PS (2010). "What we still don't know about polyploidy". Taxon 59: 1387–403. 
  • Taylor, J. S.; Braasch, I; Frickey, T; Meyer, A; Van De Peer, Y (2003). "Genome Duplication, a Trait Shared by 22,000 Species of Ray-Finned Fish". Genome Research 13 (3): 382–90.  
  • Tate, J.A.; Soltis, D.E.; Soltis, P.S. (2005). "Polyploidy in plants". In Gregory, T.R. The Evolution of the Genome. San Diego: Elsevier. pp. 371–426. 
  • Van De Peer, Yves; Taylor, John S.; Meyer, Axel (2003). "Are all fishes ancient polyploids?". Journal of Structural and Functional Genomics 3 (1–4): 65–73.  
  • Van De Peer, Yves (2004). "Tetraodon genome confirms Takifugu findings: Most fish are ancient polyploids". Genome Biology 5 (12): 250.  
  • Van de Peer, Y.; Meyer, A. (2005). "Large-scale gene and ancient genome duplications". In Gregory, T.R. The Evolution of the Genome. San Diego: Elsevier. pp. 329–68. 
  • Wolfe, Kenneth H.; Shields, Denis C. (1997). "Molecular evidence for an ancient duplication of the entire yeast genome". Nature 387 (6634): 708–13.  
  • Wolfe, Kenneth H. (2001). "Yesterday's polyploids and the mystery of diploidization". Nature Reviews Genetics 2 (5): 333–41.  

External links

  • Polyploidy on Kimball's Biology Pages
  • The polyploidy portal a community-editable project with information, research, education, and a bibliography about polyploidy.
This article was sourced from Creative Commons Attribution-ShareAlike License; additional terms may apply. World Heritage Encyclopedia content is assembled from numerous content providers, Open Access Publishing, and in compliance with The Fair Access to Science and Technology Research Act (FASTR), Wikimedia Foundation, Inc., Public Library of Science, The Encyclopedia of Life, Open Book Publishers (OBP), PubMed, U.S. National Library of Medicine, National Center for Biotechnology Information, U.S. National Library of Medicine, National Institutes of Health (NIH), U.S. Department of Health & Human Services, and, which sources content from all federal, state, local, tribal, and territorial government publication portals (.gov, .mil, .edu). Funding for and content contributors is made possible from the U.S. Congress, E-Government Act of 2002.
Crowd sourced content that is contributed to World Heritage Encyclopedia is peer reviewed and edited by our editorial staff to ensure quality scholarly research articles.
By using this site, you agree to the Terms of Use and Privacy Policy. World Heritage Encyclopedia™ is a registered trademark of the World Public Library Association, a non-profit organization.

Copyright © World Library Foundation. All rights reserved. eBooks from Project Gutenberg are sponsored by the World Library Foundation,
a 501c(4) Member's Support Non-Profit Organization, and is NOT affiliated with any governmental agency or department.