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Modern Concepts & Developments in Agronomy

Registered Crop Cultivars Composed of Multiple Biotypes: What About “DUS” rules?

E Metakovsky1, VA Melnik2, L Pascual1, and CW Wrigley3*

1Unit of Genetics, Department of Biotechnology-Plant Biology, Universidad Politecnica de Madrid, Madrid 28040, Spain

2Vavilov Institute of General Genetics Academy of Sciences RAN, Moscow 119991, Russia

3QAAFI, University of Queensland, Brisbane, QLD 4072, Australia

*Corresponding author: CW Wrigley, QAAFI, University of Queensland, Brisbane, QLD 4072, Australia

Submission: August 18, 2020Published: September 01, 2020

DOI: 10.31031/MCDA.2020.07.000658

ISSN 2637-7659
Volume7 Issue 2

Background

To be officially registered and therefore to acquire the right to be called “a cultivar”, any newly bred common wheat genotype must pass a series of tests to confirm that it fits three requirements (called “DUS”-it must be genetically Distinct, Uniform and Stable). One of the more important of these requirements is that the candidate cultivar should be composed of genotypically identical homozygous individuals (seeds, plants). Thus, SW genotypic uniformity is one of the more important definitions of the officially registered cultivar [1]. The DUS procedure provides a basis for protecting the intellectual property of the breeder for a given cultivar [1-3].

History and Advances

Once any new wheat genotype has passed the tests of DUS, and is called "a registered cultivar", it will be always treated as being composed of genotypically identical homozygous individuals and its uniformity will be accepted as a self-evident truth. However, there is a multitude of previous ("aged") data certifying the intra-varietal non-uniformity of registered wheat cultivars, based on studies of polymorphic storage proteins of wheat grain [4-11] and of grain enzymes [12,13].

The non-uniformity of a cultivar (the concept is internally contradictory) may occur in two broad categories, authentic biotypes (genuine progeny from the original parental lines) and "foreign" seeds (originating from out-crossing or from mechanical admixture with foreign genotypes). The way to distinguish authentic biotypes from foreign seeds is the comparison of sets of alleles present in a non-uniform cultivar and in its parental cultivars. To do that, high-resolution genetic markers are needed.

In common wheat (Triticum aestivum), that requirement can be provided using the enormous polymorphism of the seed storage proteins, which provide multiple allelism at several gliadin-encoding (Gli) loci (from 16 to 44 alleles at each of the six major Gli loci are known). Thus, it is possible (theoretically) to distinguish more than a billion homozygous genotypes [14]. Using alleles at the Gli loci as genetic markers, it is possible to prove that any non-uniformity of registered cultivars is due to the presence of authentic biotypes (genotypes that originated from the initial cross, namely sister lines), but not to any type of admixture or error [15].

As a result of analyzing the gliadin genotypes of 8-10 individual seeds in each of 450 registered cultivars from 12 countries, an unexpected finding is now emerging that many (from 16% to 70% of registered varieties per country) of these cultivars are composed of multiple but authentic biotypes [16]. Equivalent findings have emerged from parallel studies involving microsatellite markers; for example, 74% of Bulgarian cultivars were non-uniform at least at one of 19 markers used, although the origin of this non-uniformity (authentic biotypes or foreign seeds) was not analyzed [17].

Outlook

The current Plant Breeders’ Rights rules have the strict demand for each cultivar to be genotypically uniform. Nevertheless, many registered cultivars have been found to be composed of multiple biotypes (although in many cases authenticity may have been demonstrated with respect to origins from the original cross). The presence of hidden (morphologically identical) biotypes, even as sister lines, may provide agronomic advantages for a cultivar, for example, improving its adaptability to the agro-ecological conditions of growth. Therefore, the demand of being “Uniform” may impose an unintended penalty on breeders, requiring yet a further hurdle in the processes of selection and registration of novel genotypes. There may thus be a need to re-evaluate relevant rules of cultivar registration for crop species in general.

References

  1. Сooke RJ, Wrigley CW (2004) In: Encyclopedia of grain science. Elsevier Ltd, Oxford, UK, 3: 314-321.
  2. Cooke RJ (1995) In: Identification of food-grain varieties. Wrigley CW (Ed.), AACC, St Paul, Minnesota, USA, pp.1-17.
  3. Law JR, Donini P, Koebner RMD, Reeves JC, Cooke RJ (1998) DNA profiling and plant variety registration. III: The statistical assessment of distinctness in wheat using amplified fragment length polymorphisms. Euphytica 102: 335-342.
  4. Appleyard DB, McCausland J, Wrigley CW (1979) Checking the identity and origin of off-types in the propagation of pedigreed wheat seed. Seed Sci Technol 7: 459-466.
  5. Wrigley CW, Autran JC, Bushuk W (1982) Identification of cereal varieties by gel electrophoresis of the grain proteins. Adv Cereal Sci Thecnol 5: 211-259.
  6. Lawrence GJ (1986) The high-molecular-weight glutenin subunit composition of Australian wheat cultivars. Austr J Agric Res 37(2): 125-133.
  7. Pogna NE, Mellini F, Baretta A, Peruffo ADB (1989) J Genet Breed 43: 17-24.
  8. Gupta RB, Shepherd KW (1990) Two-step one-dimensional SDS-PAGE analysis of LMW subunits of glutelin. Theor Appl Genet 80: 65-74.
  9. Morgunov AI, Rogers WJ, Sayers EJ, Metakovsky E (1990) The high-molecular-weight glutenin subunits composition of Soviet wheat varieties. Euphitica 51: 41-52.
  10. Graybosch RA (1992) High molecular weight glutenin subunit composition of cultivars, germplasm and parents of U. S. red winter wheat. Crop Sci 32(5): 1151-1155.
  11. Sobko TA, Sozinov AA (1999) Analysis of genotypic structure of common wheat cultivars licensed for growing in Ukraine using genetic markers. Tsitol Genet (Kiev) 33(5): 30-41.
  12. Chojecki AJS, Gale MD, Holt LM, Payne PI (1983) The intrachromosomal mapping of a glucose phosphate isomerase structural gene, using allelic variation among stocks of Chinese Spring wheat. Genet Res 41(3): 221-226.
  13. Illichevsky NN, Upelniek VP, Metakovsky E (1992) Genetika (Rus) 28: 97-110.
  14. Metakovsky E, Melnik VA, Rodriguez Quijano M, Upelniek VP, Carrillo JM (2018) A catalog of gliadin alleles: Polymorphism of 20th-century common wheat germplasm. The Crop J 6(6): 629-641.
  15. Metakovsky E, Melnik VA, Pascual L, Romanov G.A, Wrigley CW (2019) Types, frequencies and value of intra-varietal genotypic non-uniformity in common wheat cultivars: authentic biotypes and foreign seeds. J Cereal Sci 89: 102813.
  16. Metakovsky E, Melnik VA, Pascual L, Wrigley CW (2020) Over 40% of 450 registered wheat cultivars (Triticum aestivum) worldwide are composed of multiple biotypes. J Cereal Sci (in press).
  17. Landjeva S, Korzun V, Ganeva G (2006) Evaluation of genetic diversity among Bulgarian winter wheat (Triticum aestivum) varieties during the period 1925-2003 using microsatellites. Genet Res Crop Evol 53: 1605-1614.

© 2020 CW Wrigley. This is an open access article distributed under the terms of the Creative Commons Attribution License , which permits unrestricted use, distribution, and build upon your work non-commercially.