In traditional agricultural systems, wheat populations consist of
landraces, informal and often diverse farmer-maintained populations. Landraces of wheat continue to be important outside America and Europe.
Formal wheat breeding began in the nineteenth century, when single line varieties were created by selecting seed from a plant with desired properties. Modern wheat breeding developed early in the twentieth century, linked to the development of
Mendelian genetics. The standard method of breeding inbred wheat cultivars is by crossing two lines using hand emasculation, then selfing or inbreeding the progeny. Selections are identified genetically ten or more generations before release as a cultivar. Wheat has been the subject of
mutation breeding, with the use of
gamma-,
x-rays,
ultraviolet light, and harsh chemicals. Since 1960, hundreds of varieties have been created through these methods, mostly in populous countries such as China. Bread wheat with high grain iron and zinc content has been developed through gamma radiation breeding, and through conventional selection breeding. International wheat breeding is led by the International Maize and Wheat Improvement Center in Mexico.
ICARDA is another major public sector international wheat breeder, but it was forced to relocate from Syria to Lebanon in the
Syrian Civil War.
For higher yields The presence of certain versions of wheat genes has been important for crop yields. Genes for the 'dwarfing' trait, first used by Japanese wheat breeders to produce
Norin 10 short-stalked wheat, have had a huge effect on wheat yields worldwide, and were major factors in the success of the
Green Revolution in Mexico and Asia, an initiative led by
Norman Borlaug. Dwarfing genes enable the carbon that is fixed in the plant during photosynthesis to be diverted towards seed production, and reduce lodging, when a tall ear stalk falls over in the wind. By 1997, 81% of the developing world's wheat area was planted to semi-dwarf wheats, giving both increased yields and better response to nitrogenous fertilizer.
T. turgidum subsp. polonicum, known for its longer
glumes and grains, has been bred into main wheat lines for its grain size effect, and likely has contributed these traits to
T. petropavlovskyi and the Portuguese
landrace group
Arrancada. As with many plants,
MADS-box influences flower development, and more specifically, as with other agricultural Poaceae, influences yield. Despite that importance, little research has been done into MADS-box and other such spikelet and flower genetics in wheat specifically. A project in the UK, led by
Rothamsted Research has aimed to raise wheat yields in the country to by 2020, but in 2018 the UK record stood at , and the average yield was just .
For disease resistance . The strains bred to be resistant have their leaves unaffected or relatively unaffected by the fungus. Wild grasses in the genus
Triticum and related genera, and grasses such as
rye have been a source of many disease-resistance traits for cultivated wheat
breeding since the 1930s. Some
resistance genes have been identified against
Pyrenophora tritici-repentis, especially races 1 and 5, those most problematic in Kazakhstan.
Wild relative,
Aegilops tauschii is the source of several genes effective against
TTKSK/Ug99 -
Sr33,
Sr45,
Sr46, and
SrTA1662. • ''
is an R gene, a dominant negative for partial adult resistance discovered and molecularly characterized by Moore et al.
, 2015. Lr67
is effective against all races of leaf, stripe, and stem rusts, and powdery mildew (Blumeria graminis''). This is produced by a
mutation of two
amino acids in what is
predicted to be a
hexose transporter. The result is to reduce
glucose uptake. • '''' is widely deployed in cultivars as it confers resistance against
leaf- and
stripe-rusts, and
powdery mildew. It is used intensively in wheat cultivation worldwide. It is an
ABC transporter, producing a 'slow rusting'/
adult resistance phenotype. (FHB, Fusarium ear blight) is an important breeding target.
Marker-assisted breeding panels involving
kompetitive allele specific PCR can be used. A KASP
genetic marker for a
pore-forming toxin-like gene provides FHB resistance. In 2003 the first resistance genes against fungal diseases in wheat were isolated. In 2021, novel resistance genes were identified in wheat against
powdery mildew and
wheat leaf rust. Modified resistance genes have been tested in transgenic wheat and barley plants.
To create hybrid vigour Because wheat self-pollinates, creating
hybrid seed to provide
heterosis, hybrid vigour (as in F1 hybrids of maize), is extremely labour-intensive; the high cost of hybrid wheat seed has kept farmers from adopting them widely despite nearly 90 years of effort. Commercial hybrid wheat seed has been produced using chemical hybridizing agents,
plant growth regulators that interfere with pollen development, or naturally occurring
cytoplasmic male sterility systems. Hybrid wheat has been a limited commercial success in France, the United States and South Africa. Synthetic hexaploids made by crossing the wild goatgrass wheat ancestor
Aegilops tauschii, and other
Aegilops, with durum wheats are being deployed, increasing the genetic diversity of cultivated wheats.
For gluten content Modern bread wheat varieties have been
cross-bred to contain greater amounts of gluten. However, a 2020 study found no changes in albumin/globulin and gluten content between 1891 and 2010.
For water efficiency Stomata (or leaf pores) are involved in both uptake of carbon dioxide gas from the atmosphere and water vapor losses from the leaf due to water
transpiration. Basic physiological investigation of these gas exchange processes has yielded carbon
isotope based method used for breeding wheat varieties with improved water-use efficiency. These varieties can improve crop productivity in rain-fed dry-land wheat farms.
For insect resistance The complex genome of wheat has made its improvement difficult. Comparison of hexaploid wheat genomes using a range of chromosome pseudomolecule and molecular scaffold assemblies in 2020 has enabled the resistance potential of its genes to be assessed. Findings include the identification of "a detailed multi-genome-derived nucleotide-binding leucine-rich repeat protein repertoire" which contributes to disease resistance, while the gene
Sm1 provides a degree of insect resistance, for instance against the
orange wheat blossom midge. == Genomics ==