Progress in Polyhaploid Production Techniques of Hexaploid Wheat through Wide Crosses

(Triticum aestivum L.) through wide crosses were evaluated in terms of pollen sources, 2,4-D application, embryo rescue and chromosome retention. Pollen sources included Hordeum bulbosum L., Zea mays L., Pennisetum glaucum (L.) R. Br., Sorghum bicolor (L.) Moench, and Tripsacum dactyloides (L.) L. Maize-mediated polyhaploid production was more stable than the other methods because of a lesser genotypic influence on embryo formation. Application of 2,4-D onto wheat after pollination was critical to promote seed setting and embryo formation in all cross combinations. Embryo rescue was necessary at an appropriate embryo developmental stage to obtain plant regeneration. Paternal chromosomes were eliminated by the stage of active growth of the polyhaploid seedlings. Polyhaploid production frequencies ranged between 10 and 20% of pollinated wheat florets, suggesting germ plasm genotypic effects

Cytological, Phenological and Molecular Characterization of B (S)-Genome Synthetic Hexaploids (2n = 6x = 42; AABBSS)

The B(S) genome diploids (2n = 2x = 14) are a unique reservoir of genetic diversity that can provide wheat breeders a rich source of allelic variation for stress traits that limit productivity. Restricted in practical use essentially due to their complex chromosomal behavior, these diploids have been in limited practical usage. The classic utilization example has been the suppression activity of the Ph locus and role in alien genetic transfer aspects that has been a standard in cytogenetic manipulation studies. For applied efforts focusing on Aegilops speltoides researchers in CIMMYT initiated an ambitious program to make AABBBB(SS) synthetics and made progress by generating over 50 such synthetics. Of these 20 were available for this study in which phenology and powdery mildew screening were evaluated. Four of these 20 synthetics appeared to be useful sources for further exploitation in breeding. These were entries 6, 9, 10 and 11 suited for exploitation in pre-breeding, with positive phenological characters particularly high thousand-kernel weight and are cytologically near euploid at 2n = 6x = 42. The subtle hyper (43) and hypoploid number would not negate their applied use potential. Preference however goes to genotypes 9 and 11

Molecular analysis of genetic diversity in elite II synthetic hexaploid wheat screened against Barley yellow dwarf virus

The presence of sufficient genetic diversity in the germplam is an important prerequisite for the improve-ment and efficient use of available material. Traditionally, the data on agronomic, morphological and physiological plants traits are used to estimate the genetic diversity. But now molecular markers are available for authenticated and reliable studies for genetic diversity. The present study was conducted to assess the genetic diversity of Elite-II synthetic hexaploid (SH) wheat by genome DNA fingerprinting as revealed by random amplified polymorphic DNA (RAPD) analysis. Ten decamer RAPD primers (OPG-1, OPG-2, OPG-3, OPG-4, OPG-5, OPA-3, OPA-4, OPA-5, OPA-8, and OPA-15) were used to evaluate the diversity profile of the selected SH entries. Primers OPG-2 andOPA-4 gave the highly polymorphic results. The pair wise similarity values shows that genotypes 1, 20 and 30 have most closest relationship with highest similarity values i.e., 100% while genotypes 9and 13 show dictinct relationship with minimum similarity value that is, 54%. Therefore, the allelic variation of the SH resistance germplasm is a potent means to enrich and improve bread wheat cultivars where BYDV is a production threat and these can be used in future wheat breeding programme

Resistance to Wheat streak mosaic virus identified in synthetic wheat lines

Citation: Shoup Rupp, J. L., Simon, Z. G., Gillett-Walker, B., & Fellers, J. P. (2014). Resistance to Wheat streak mosaic virus identified in synthetic wheat lines. Retrieved from http://krex.ksu.eduWheat streak mosaic virus (WSMV) is an important pathogen in wheat that causes significant yield losses each year. WSMV is typically controlled using cultural practices such as the removal of volunteer wheat. Genetic resistance is limited. Until recently, no varieties have been available with major resistance genes to WSMV. Two resistance genes have been derived from Thinopyrum intermedium through chromosome engineering, while a third gene was transferred from bread wheat through classical breeding. New sources of resistance are needed and synthetic wheat lines provide a means of accessing genetic variability in wheat progenitors. A collection of wheat synthetic lines was screened for WSMV resistance. Four lines, 07-SYN-27, -106, -164, and -383 had significant levels of resistance. Resistance was effective at 18 °C and virus accumulation was similar to the resistant control, WGGRC50 containing Wsm1. At 25 °C, resistance was no longer effective and virus accumulation was similar to the susceptible control, Tomahawk

Wheat-barley hybridization – the last forty years

Abstract Several useful alien gene transfers have been reported from related species into wheat (Triticum aestivum), but very few publications have dealt with the development of wheat/barley (Hordeum vulgare) introgression lines. An overview is given here of wheat 9 barley hybridization over the last forty years, including the development of wheat 9 barley hybrids, and of addition and translocation lines with various barley cultivars. A short summary is also given of the wheat 9 barley hybrids produced with other Hordeum species. The meiotic pairing behaviour of wheat 9 barley hybrids is presented, with special regard to the detection of wheat– barley homoeologous pairing using the molecular cytogenetic technique GISH. The effect of in vitro multiplication on the genome composition of intergeneric hybrids is discussed, and the production and characterization of the latest wheat/barley translocation lines are presented. An overview of the agronomical traits (b-glucan content, earliness, salt tolerance, sprouting resistance, etc.) of the newly developed introgression lines is given. The exploitation and possible use of wheat/barley introgression lines for the most up-to-date molecular genetic studies (transcriptome analysis, sequencing of flow-sorted chromosomes) are also discussed