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.
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.
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.