Production and cytogenetics of Triticum turgidum L. hybrids with some perennial Triticeae.

A. Cortés, V. Rosas, and A. Mujeeb-Kazi.

Several new, intergeneric hybrids in the Triticeae were produced and cytogenetically described during the last decade. Intergeneric crossability barriers have been circumvented more recently, leading to novel success in achieving extremely divergent cross combinations. So far, our major emphasis is bread wheat, and although this genetic base continues to be exploited, a shift was made to address the biotic/abiotic stress constraints of durum wheats (T. turgidum, 2n = 4x = 28, AABB). Some stress constraints in durum wheats are associated with resistance to Fusarium graminearum, and Helminthosporium sativum and tolerance to salinity. Several other stresses can be added to these. We attempted to combine durum wheats with perennial Triticeae species recognized for their diversified stress tolerances and document here several of these F1 hybrids with their meiotic and mitotic data. Advanced derivatives from these hybrids are anticipated to serve the needs in durum wheats for resistances to biotic/abiotic stresses as these relate to resistance/tolerance for H. sativum, F. graminearum, barley yellow dwarf virus, salinity, and drought, with quality standing as a common base across all objectives.

Two of the 13 F1 hybrid combinations reported in Table 9, i.e., Ps. juncea and Th. elongatum, initially were targeted by advancing them for stress-objective outputs.

Meiotic analyses demonstrate that complexities exist for durum wheat-alien chromosome recombinations at the F1 stage; hence, special manipulation strategies appear essential. The genomic diversity of the F1 combinations (Table 9) is seen as an important prerequisite for achieving stable outputs through gene pyramiding.

Table 9. Cytological details of some Triticum turgidum/perennial Triticeae species hybrids.

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Mean meiotic chromosome association

Somatic I II II III Xta

Hybrid combination count (Rings) (Rods) /cell

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4x*/Th. junceum 2n=5x=35 19.9 1.0 5.53 0.67 8.87

4x/Th. junceiforme 2n=4x=28 21.2 3.40 3.40

4x/Th. acutum 2n=5x=35 23.2 0.5 4.95 0.30 6.55

4x/Th. intermedium 2n=5x=35 29.2 2.90 2.90

4x/Th. pulcherrimum 2n=5x=35 21.3 0.3 6.40 0.1 7.20

4x/Th. trichophorum 2n=5x=35 28.6 0.1 3.00 0.05 3.30

4x/Th. varnense 2n=5x=35 27.4 0.3 2.50 3.10

4x/Th. scirpeum 2n=4x=28 16.3 1.4 4.33 0.07 7.27

4x/Th. scythicum 2n=4x=28 22.6 0.3 2.40 3.00

4x/Et. pungens 2n=5x=35 29.5 2.60 0.10 2.80

4x/Ps. juncea 2n=4x=28 20.3 0.29 3.36 0.14 4.36

4x/Th elongatum 2n=3x=21 20.4 0.28 0.02 0.60

E. fibrosum/4x 2n=4x=28 27.6 0.20 0.20

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* 4x = T. turgidum cultivar (2n = 4x = 28, AABB)

Characterization of an elite set of new synthetic hexaploid wheats (2n = 6x = 42, AABBDD).
n

J. Sanchez, R. Delgado, V. Rosas, S. Cano, and A. Mujeeb-Kazi.

Triticum aestivum L. (2n = 6x = 42, AABBDD) improvement has been accomplished predominantly through conventional plant breeding methodologies, and this approach will continue to be the predominant procedure in the future. Novel approaches that complement plant breeding have emerged and are attracting research interest. The practical gains of alien genetic variability would be separated into short and longterm time frames. The shortterm benefits have a high potential with fewer constraints. For this to materialize, interspecific hybridization is a priority, with emphasis assigned to T. tauschii (Coss.) Schmal. (Ae. squarrosa auct. non L., 2n = 2x = 14, DD), because of its genetic proximity to the D genome of wheat. Triticum tauschii is attributed with a wide range of resistances/ tolerances to biotic/abiotic stresses. One mechanism, of a few that exist for exploiting T. tauschii variation, involves bridge crosses where `T. turgidum L./T. tauschii' hybrids (2n = 3x = 21, ABD) lead to the generation of synthetic hexaploids (2n = 6x = 42, AABBDD) upon colchicine treatment or by spontaneous induction.

We have emphasized indiscriminate hybridization of different T. turgidum cultivars with several T. tauschii accessions ultimately accompanied by screening the resulting synthetic hexaploids for characterization and reactions to some biotic/abiotic stresses.

From the 570 synthetic hexaploid wheats, an elite set of 95 SH wheats based upon growth habit under two locations in Mexico was prepared; seed was increased and transferred to our germplasm bank for global distribution. Several stress descriptors are being established to facilitate utilization of SH wheats in crop improvement.

Crossing susceptible bread wheats with H. sativum-resistant SH wheats enabled selection of advanced derivatives with resistance and desirable breadmaking quality variation and is the most advanced output of our wide crosses breeding.

Synthetic wheats immune to Karnal bunt were registered in Crop Science in 1996. These germplasms are listed in Table 10. Seed is available for distribution. Requests may be made to A.M. Kazi or B. Skovmand at the CIMMYT germplasm bank.

Table 10. Pedigrees of four Karnal bunt-resistant, synthetic hexaploid wheat (Triticum turgidum/Triticum tauschii) registered germplasm1.

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Germplasm Pedigree Cross2

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WX-SYN.B-92-52 Altar84/T. tauschii (Acc.198) CIGM87.2768-1B-0Y-0M-0Y(SH12)

WX-SYN.B-92-81 Duergand/T. tauschii (Acc.221) CIGM86.953-1B-0Y-0M-0Y(SH46)

WX-SYN.B-92-87 Altar84/T. tauschii (Acc.223) CIGM87.2762-1B-0Y-0M-0Y(SH10)

WX-SYN.B-92-91 Chen `S'/T. tauschii (Acc.224) CIGM86.949-1B-0Y-0M-0Y(SH31)

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1Crop Sci 1996, 36:218.

2Locations in Mexico where selections were made: B = El Batan, M = Toluca, and Y = CAEVY, Obregon, Sonora,

Insert Table 11 here. Page 145-Table 11.

Cytogenetics of some amphiploids involving Triticum turgidum and T. aestivum cultivars with alien Triticeae species.

V. Rosas, R. Delgado, A. Cortés, and A. Mujeeb-Kazi.

Production of intergeneric hybrids is the initial step in exploiting alien genetic variability for crop improvement. The self-sterile F1 hybrids can be advanced to yield BC1 derivatives by pollinating the F1 plants with the same wheat parent or by using a different wheat cultivar. Additional crosses lead to advanced backcross generations, allowing for the production of alien chromosome addition lines, substitution lines, and wheat/alien chromosomal translocations, which through genetic manipulation procedures have the potential of yielding subtle, alien genetic exchanges. Amphiploids derived from F1 intergeneric hybrids significantly ease germplasm distribution and facilitate the systematic development of cytogenetic stocks. Here we report new amphiploids involving T. aestivum and T. turgidum cultivars with some perennial Triticeae and provide cytological/fertility data generated during their maintenance (Table 11). Amphiploid maintenance involves somatic/meiotic cytology, and those that are normal with a high seed set are advanced further in order to obtain larger seed samples for use, distribution, and storage.

Triticum aestivum x perennial Triticeae BC1 self-fertile derivatives with complete and partial synthetic genomes.

R. Delgado, A. Cortés, V. Rosas, and A. Mujeeb-Kazi.

Several intergeneric hybrids were produced and maintained in our program by annual clonal propagation. These hybrids are sources of producing BC1 derivatives by either pollinating the F1 plants with T. aestivum or, if possible, first producing amphiploids and then crossing these to give BC1 progeny. Selfing the BC1 derivatives yields seed set that is indicative of fertility that has a range associated with seed quantity and presumably is influenced by the cytogenetic status of the respective progenies. Such BC1 fertile derivatives form a unique germplasm base with the potential of screening for biotic/abiotic stresses. The alien species involved were Th. intermedium, Th. distichum, Th. elongatum, and Th. scirpeum. Backcrossing F1 hybrids with 2n = 6x = 42 chromosomes or 2n = 5x = 35 chromosomes results in BC1 progeny with 2n = 9x = 63 or 2n = 8x = 56 chromosomes. Selfing of the 63-chromosome derivatives yields 63, or near 63, and 56 chromosome derivatives that we categorize as BC1 fertiles with `complete' genomes (2n = 9x = 63) or with `partial' genomes (2n = 8x = 56), where a genome presumably has been eliminated. Complete genomes generally are maintained after selfing the 56 chromosome BC1 derivatives.

Sixteen BC1 self-fertile intergeneric derivatives are reported (Table 12) of which 15 were produced in our program and one produced elsewhere are maintained. The BC1 derivatives are an alternate germplasm source other than amphiploids for stress screening. The autosyndetic rearrangements during selfed advance of the BC1 plants through `n' generations has the potential to promote genomic modification. Multiple alien disomics that frequently result from selfing lend themselves to genetic manipulation of complex traits.

Selection of selfed derivatives with high seed fertility is a source for the building-up of seed reserves for use in biotic/abiotic stress screening, distribution, and germplasm storage, an area in which work is underway.

Insert Table 12 here. Page 147-Table 12.

Insert Table 13 here. Page 148-Table 13.