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Thomas G. Ranney, Professor,
North Carolina State University
A paper from the Proceedings of the 11th Metropolitan Tree Improvement Alliance (METRIA) Conference held in Gresham, Oregon, August 23-24, 2000, and cosponsored by the Landscape Plant Development Center.
A polyploid is simply an organism that contains more than the usual two sets of chromosomes. For animals, this is a fairly rare occurrence (although a polyploid rat, the first polyploid mammal ever identified, was recently discovered in Argentina). In plants, however, this is much more common and has played an important role in plant evolution. The development of polyploids can also be a useful and valuable approach in plant improvement programs.
The term "ploidy" or "ploidy level" refers to the number of sets of chromosomes and is notated by an "x". An individual with two sets of chromosomes is referred to as a diploid (2x), three sets would be a triploid (3x), and so on with tetraploid (4x), pentaploid (5x), hexaploid (6x), etc. It is sometimes also important to identify if one is referring to the reduced number following meiosis as would be found in egg and sperm (denoted as "n") or in non-reduced tissue (denoted as "2n"). Thus, for example, a tetraploid birch tree would be represented as 2n=4x=56.
Polyploidy can naturally arise in a number of different ways. In some cases a somatic (non-reproductive) mutation can occur, due to a disruption in mitosis, resulting in chromosome doubling in a meristematic cell(s) that will subsequently produce a polyploid shoot. These mutations or sports are often evident on a tree by their enlarged "gigas" condition. Polyploids can also result from the union of unreduced gametes - eggs and sperm that have not undergone normal meiosis and still have a 2n constitution.
The origin of a polyploid can often determine if will be fertile and may further indicate how it can best be used in a plant improvement program. If a tetraploid arises from spontaneous doubling in a shoot or from the union of unreduced gametes from two closely related (e.g. same species) diploid individuals, it will have four similar (homologous) versions of each chromosome. Despite different origins, both of these polyploids behave similarly reproductively and are often referred to as autotetraploids (or polysomic tetraploids). Autopolyploids may or may not be fertile. In diploids, meiosis involves the pairing of homologous chromosomes, which eventually segregate to form two separate gametes, each with one set of chromosomes. Infertility can arises in autopolyploids due to the fact that there are more than two homologous chromosomes. The presence of multiple homologous chromosomes often results in spurious pairing between multiple chromosomes, unpaired chromosomes, and gametes with unbalanced chromosome numbers (anueploids).
Offspring that result from sexual reproduction from unreduced gametes of different species are referred to as allopolyploids (or sometimes amphidiploids or disomic polyploids). These plants also have four versions of each chromosome, but the two from one parent are sufficiently different (non-homologous) from the two from the other parent, that they generally don't pair during meiosis. Due to this composition, allopolyploids are typically fertile. During meiosis each chromosome can pair with its homologous partner, meiosis continues, resulting in fertile germ cells.
In contrast to the gradual evolutionary process whereby new species evolve from isolated populations, new species of plants can also arise abruptly. The most common mechanism for abrupt speciation is through the formation of natural polyploids. Once a tetraploid arises in a population, it can generally hybridize with other tetraploids. However, these tetraploids are reproductively isolated from their parental species. Tetraploids that cross with diploids of the parental species will result in triploids that are typically sterile. This phenomenon provides a "reproductive barrier" between the polyploids and the parental species - a driving force for speciation.
Various estimates suggest that as many as 30-70% of flowering plants are of polyploid origin (Grant, 1971; Goldblatt, 1980). For example, the plants in the rosaceous subfamily maloideae (Malus, Pyrus, Photinia, Chaenomeles, etc.) are believed to have originated from an ancient allopolyploids since they have n=17 base chromosomes whereas plants in other rosaceous subfamilies have n=8 or 9 (Rowley, 1993). In many genera, different species will have different ploidy levels (multiples of a base number) representing a series of polyploids. In the genus Dendranthema (Chrysanthemum), different species have chromosome numbers of 2n = 18, 36, 54, 72, 90, and 198 - all multiples of a base chromosome number of 9.
There are a number of factors that may provide polyploids with adaptive and evolutionary advantages. Perhaps most importantly, polyploids can be significantly more heterozygous than their diploid counterparts. Polyploids can have 4 different genes (alleles) present at any given locus (location on a chromosome). The degree of heterozygosity may be a key factor in the growth, performance, and adaptability of a polyploid. Allopolyploids can have a much greater degree of heterozygosity (dissimilar genes) which can contribute to heterosis or hybrid vigor. Furthermore, this heterozygosity is fixed (chromosomes that originated from a given species preferentially pair with similar homologous chromosomes during meiosis, ensuring that the genomes of both parental species will continue to be expressed). On the other hand, the addition of multiple copies of homozygous chromosomes (as would be the case with autopolyploids), does little to enhance genetic superiority and can actually reduce vigor and fertility by creating a more "inbred" situation.
Since all polyploids have a certain amount of genetic redundancy, extra copies of genes can mutate and diverge resulting in new traits without compromising essential functions. Polyploid populations often demonstrate extensive genomic rearrangement including the origin of novel regions of DNA (Arnold, 1997; Song et al., 1995). Ancient polyploids can eventually undergo such changes to the extent that they effectively become "diploidized" where single gene ratios are restored.
Polyploids also tend to be more self-fertile and apomictic (producing seeds with embryos derived directly from maternal tissue, not sexual hybridization). Since polyploids generally arise at a low frequency, greater self fertility and apomixis would help to compensate for their minority-disadvantage (Briggs and Walters, 1977) and would provide further benefits in areas where breeding systems are compromised in stressful environments. Furthermore, inbreeding is less deleterious for allopolyploids due to their extreme heterozygous nature.
One question that frequently arises is whether or not polyploids inherently have greater stress tolerance. For example, it has often been observed that disproportionate number of polyploids are found in cold, dry regions. Some argue that this is a spurious correlation (Sanford, 1983) or possibly the result of intermixing of species and formation of allopolyploids during glacial periods (Stebbins, 1984). However, polyploids may also have certain characteristics that do provide some adaptive benefits. Molecular studies have demonstrated that allopolyploids exhibit "enzyme multiplicity" (Soltis and Soltis, 1993). Since allopolyploids represent a fusion of two distinctly different genomes, these polyploids can potentially produce all of the enzymes produced by each parent as well as new hybrid enzymes. This enzyme multiplicity may provide polyploids with greater biochemical flexibility; possibly extending the range of environments in which the plant can grow (Roose and Gottlieb, 1976).
Considering the profound importance of polyploidy in plant evolution, it is understandable that there was considerable interest in developing induced polyploids when mitotic inhibitors were first discovered in the 1930s. However, despite the fact that polyploids have been developed for many major crops, these plants are almost always found to be inferior to their diploid progenitors. Somatic doubling does not introduce any new genetic material, but rather produces additional copies of existing chromosomes. This extra DNA must be replicated with each cell division. Enlarged cell size is often associated with polyploids which can result in anatomical imbalances. Other deleterious effects can include erratic bearing, brittle wood, and watery fruit (Sanford, 1983). High level polyploids (e.g. octaploids) can be stunted and malformed, possibly resulting from the extreme genetic redundancy and somatic instability that leads to chimeral tissue.
Despite the drawbacks of somatically induced polyploides, they may be valuable if they are in turn used in a breeding program to enhance the degree of heterozygosity and select for desirable traits. In most cases it appears that inducing autopolyploids will do little for plant improvement unless substantial heterozygosity can be incorporated (Sanford, 1983). Historically, work with polyploids has not progressed much beyond somatic doubling - resulting in considerable genetic redundancy. Based on our knowledge of natural systems and evolution, it appears that much greater advances can be made by working towards enhance heterozygosity, including the development of allopolyploids.
Polyploidy can result in a wide range of effects on plants, but the specific effects will vary dramatically based on the species in question, the degree of heterozygosity, the ploidy level, and the mechanisms that relate to gene silencing, gene interactions, gene dose effects, and regulation of specific traits and processes.
Overcoming barriers to hybridization. In some cases, desirable crosses are difficult to obtain due to differences in ploidy levels between prospective parents. Such interploid barriers typically arise due to endosperm imbalance. In species where there is an interploid block, seeds will only develop normally if there is a 2 maternal : 1 paternal ratio in the genomic makeup of the endosperm, which would be the normal case for two diploid parents. Seeds that don't meet this criterion, are often underdeveloped or abort. In some cases this ratio is not exact, but the greater the disparity, the lower the viability of the seeds (Sanford, 1983). In cases, where interploid blocks exist, barriers to hybridization may be overcome by manipulating the ploidy levels to match prior to hybridization.
Developing sterile cultivars. The introduction and movement of invasive species can be a significant threat to certain ecosystems. Development of sterile forms of important nursery crops is an ideal approach for addressing this problem. In doing so, plants can be grown and used for landscaping while virtually eliminating any possibility that these plants could sexually reproduce and become invasive. There are a number of methods available for developing sterile plants. However, one of the most rapid and cost effective approaches for inducing sterility in a plant is by creating polyploids. In most cases these plants function normally with the exception of reproduction, specifically meiosis. In some cases doubling the chromosomes of an individual plant (autotetrapoid) will result in sterility due to multiple homologous chromosomes and complications during meiosis (as discussed previously). Despite these complications, autotetraploids of some species can produce fertile seeds. In this case, tetraploids can then be hybridized with diploids to create sterile triploids. Triploids have an additional reproductive barrier in that the 3 sets of chromosomes cannot be divided evenly during meiosis yielding unequal segregation of the chromosomes (aneuploids). Even in the very unusual case when a triploid plant can produce a seed (apples are an example), it happens infrequently, and seedlings rarely survive.
Development of triploids of some species can be complicated due to the presence of an interploid block that prevents the normal development of a triploid embryo. However, embryo culture is an additional technique that can be employed to overcoming this problem and produce sterile triploid plants.
An alternative approach for creating triploid plants is regeneration of plants from endosperm found in seeds. Although the embryo in most angiosperm seeds is diploid, the adjoining endosperm (nutritive tissue) originates from the fusion of three haploid nuclei (one from the male gametophyte and two from the female) resulting in triploid tissue. This tissue can be excised from developing seeds and cultured in vitro (tissue culture) to eventually give rise to a regenerated embryos and plantlets. This approach has been successful for a range of plants including citrus, kiwifruit, loquat, passionflower, acacia, rice, and pawpaw.
Restoring fertility in wide hybrids. It is not unusual for hybrids between distant taxa (different species or genera) to be sterile. This generally occurs due to failure of the chromosomes to pair correctly during meiosis. By doubling the chromosomes of a wide hybrid, one essentially creates an allopolyploid and thereby restores fertility (as described above).
Enhancing pest resistance and stress tolerance. There are a number of strategies for inducing polyploids as a means of enhancing pest resistance. Increasing the chromosome number and related gene dose can sometimes enhance the expression and concentration of certain secondary metabolites and defense chemicals. For example, autotetraploid ryegrass had better disease resistance and more structural carbohydrates than diploid counterparts (van Bogaert, 1975). However, this is not always the case and little is generally known about the relationship between gene dose, gene silencing, and expression of secondary metabolites. A more promising approach would be to create allopolyploids between plants with diverse endogenous defense chemicals. A unique and valuable characteristic of allopolyploids, is that the secondary metabolites from the parental species are typically additive. That is to say that allopolyploids often produce all the enzymes and metabolites (including defense chemicals) of both parents, effectively combining the pest resistant characteristics of each, and potentially contributing to a much broader, more horizontal form of pest resistance. A similar approach may have utility for enhancing tolerance to certain environmental stresses.
Enlargement and enhanced vigor. Although enlarged cell size found in some polyploids can have undesirable effects, it can sometimes also be beneficial. In some plants, polyploidy results in significant enlargement. Fruit from tetraploid apples can be twice as large as diploid fruit, though they tend to be watery and misshapen. For apples, triploids have proven to be a happy medium that combines larger fruit while retaining good quality and are often grown for commercial production. This type of enlargement can be particularly desirable for ornamental flowers. Flower petals can also be thicker and flowers can be longer lasting in polyploid plants (Kehr, 1996).
In the late 1930s it was discovered by that colchicine inhibits the formation of spindle fibers and effectively arrests mitosis at the anaphase stage. At this point, the chromosmes have multiplied but cell division has not yet taken place resulting in polyploid cells. In later years, a number of other mitotic inhibitors, including oryzalin, trifluralin, amiprophos-methyl, and N2O gas have been identified and used as doubling agents (Bouvier et al., 1994; van Tuyl et al., 1992; Taylor et al., 1976).
Methods for applying these agents varies. One of the easiest and most effective methods is to work with a large number of seedlings with small, actively growing meristems. Seedlings can be soaked or the apical meristems can be submerged or sprayed with different concentrations, durations, or frequencies of a given doubling agent.
Shoots on older plants can be treated, but it is often less successful. Treatment of smaller axillary or sub-axillary meristems is sometimes more effective. Chemical solutions can be applied to buds using cotton, agar, or lanolin or by dipping branch tips into a solution for a few hours or days. Surfactants, wetting agents, and other carriers (dimethyl sulfoxide) are sometimes used to enhance efficacy.
Plants with increased ploidy levels are often apparent by their distinct morphology. Increasing ploidy often results in increased cell size that in turn results in thicker, broader leaves and larger flowers and fruit. Shoots are often thicker and can have shortened internodes and wider crotch angles. Plants with high ploidy levels (e.g. octaploids) can have distorted growth and reduced growth rates. When screening large numbers of plants, these visual characteristics are often helpful for identifying putative polyploids. Other effective, but more time consuming, measures that indicate polyploidy include larger pollen size, greater number of chloroplasts per guard cell (Solov'eva, 1990), and larger guard cells and stomates. Flow cytometry has also been used as a method for measuring DNA content which can be correlated with ploidy level for a given crop (Sharma and Sharma, 1999).
Ultimately, however, it is necessary to count the chromosomes to definitively document the ploidy level. Techniques include measurements on young leaves, root tips and anthers (Ruzin, 1999). When doing so, it should be recognized that induced polyploids can sometimes be cytochimeras where the ploidy level varies in different types of tissue. Meristems are typically divided into three histogenic layers L-1, L-2, and L-3. Mutations and doubling agents may result in increased ploidy levels in one, two, or all three layers. For information on reproductive behavior, it is important to measure the ploidy level of L-2, or cortical layer, which is reflected in pollen size and chromosome counts from reproductive tissue (e.g. anthers). Root tips would reflect the L-3 layer while the guard cells would reflect the L-1 layer.
In the vast majority of cases, induction of autopolyploids will not, in of itself, result in substantially improved landscape plants. However, with knowledge of the origins of, variations in, and characteristics of different types of polyploids, there are many opportunities for developing and utilizing polyploids in plant improvement programs. Significant opportunities include developing sterile cultivars, overcoming barriers to hybridization, restoring fertility in wide hybrids, enhancing flower size, increasing heterosis and vigor, and improving pest resistance and tolerance to environmental stresses.
Arnold, M.L. Natural hybridization and evolution. 1997. Oxford Univ. Press. New York.
Bouvier, L., F.R. Fillon and Y. Lespinasse. 1994. Oryzalin as an efficient agent for chromosome doubling of haploid apple shoots in vitro. Plant Breeding. 113:343-346.
Briggs, D. and S.M. Walters. 1997. Plant variation and evolution, 3rd. ed. Cambridge Univ. Press, Cambridge.
Goldblatt, P. 1980. Polyploidy in angiosperms: monocotyledons, p. 219-239. In: W.H. Lewis (ed.). Polyploidy. Plenum Press, New York.
Rowley, G.D. 1993. Rosaceae: The rose family, p. 141-144. In: V.H. Heywood (ed.). Flowering plants of the world. Batsford Pub., London.
Grant, B. 1971. Plant speciation. Columbia University Press, New York.
Kehr, A.E. 1996. Woody plant polyploidy. Am. Nurseryman 183(3):38-47.
Roose, M.L. and L.D. Gottlieb. 1976. Genetic and biochemical consequences of polyploidy in Tragopogon. Evolution 30:818-830.
Ruzin, S.E. Plant microtechnique and microscopy. Oxford University Press, New York.
Sanford, J.C. 1983. Ploidy manipulations, p. 100-123. In: J.N. Moore and J. Janick (eds.). Methods in fruit breeding. Purdue Unv. Press, West Lafayette, Ind.
Sharma, A.K. and A. Sharma. 1999. Plant chromosomes: Analysis, manipulation and engineering. Harwood Academic Pub., Amsterdam.
Solov'eva, L.V. 1990. Number of chloroplasts in guard cells of stomata as an indicator of the ploidy level of apple seedlings. Cytol. Genet. 24:1-4.
Song, K., P. Lu, K. Tank, and T.C. Osborn. 1995. Rapid genome change in synthetic polyploids of Brassica and its implications for polyploid evolution. Proceedings of the National Acad. of Sci., USA. 92: 7719-7723.
Soltis, D.E. and P.S. Soltis. 1993. Molecular data and the dynamic nature of polyploidy. Critical Rev.Plant Sci. 12:243-273.
Stebbins, G.L. 1984. Polyploidy and the distribution of the arctic-alpine flora: new evidence and a new approach. Botanica Helvetica. 94:1-13.
Taylor, N.L., M.K. Anderson, K.H. Wuesenberry, and L. Watson. 1976. Doubling the chromosome number of Trifolium species using nitrous oxide. Crop Sci. 16:516-518.
van Bogaert, G. 1975. A comparison between colchicine induced tetraploid and diploid cultivars of Lolium species. In Ploidy in Fodder Crops, Neusch, B. (ed.), Eucarpia Report, Zurich.
van Tuyl, J.M., B. Meijer, and M.P. van Diën. 1992. The use of oryzalin as an alternative for colchicine in in-vitro chromosome doubling of Lilium and Nerine. Acta Hort. 325:625-629.
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