A cytological and molecular analysis of D-genome chromosome retention following F2–F6 generations of hexaploid×tetraploid wheat crosses

2018 ◽  
Vol 69 (2) ◽  
pp. 121 ◽  
Author(s):  
Sriram Padmanaban ◽  
Peng Zhang ◽  
Mark W. Sutherland ◽  
Noel L. Knight ◽  
Anke Martin
Keyword(s):  
Durum Wheat ◽  
Tetraploid Wheat ◽  
Triticum Aestivum L ◽  
Food Crops ◽  
Cytological Analysis ◽  
Genome Chromosome ◽  
D Genome ◽  
Ploidy Levels ◽  
F2 Generation ◽  
Global Food

Both hexaploid bread wheat (AABBDD) (Triticum aestivum L.) and tetraploid durum wheat (AABB) (T. turgidum spp. durum) are highly significant global food crops. Crossing these two wheats with different ploidy levels results in pentaploid (AABBD) F1 lines. This study investigated the differences in the retention of D chromosomes between different hexaploid × tetraploid crosses in subsequent generations by using molecular and cytological techniques. Significant differences (P < 0.05) were observed in the retention of D chromosomes in the F2 generation depending on the parents of the original cross. One of the crosses, 2WE25 × 950329, retained at least one copy of each D chromosome in 48% of its F2 lines. For this cross, the retention or elimination of D chromosomes was determined through several subsequent self-fertilised generations. Cytological analysis indicated that D chromosomes were still being eliminated at the F5 generation, suggesting that in some hexaploid × tetraploid crosses, D chromosomes are unstable for many generations. This study provides information on the variation in D chromosome retention in different hexaploid × tetraploid wheat crosses and suggests efficient strategies for utilising D genome retention or elimination to improve bread and durum wheat, respectively.

Aneuploid analyses of hybrid necrosis and hybrid chlorosis in tetraploid wheats using the D genome chromosome substitution lines of durum wheat

Genome ◽  
1992 ◽  
Vol 35 (4) ◽  
pp. 594-601 ◽  
Author(s):  
Koichiro Tsunewaki
Keyword(s):  
Durum Wheat ◽  
Tetraploid Wheat ◽  
Hybrid Necrosis ◽  
Chromosome Substitution ◽  
Substitution Lines ◽  
Genome Chromosome ◽  
D Genome ◽  
Chromosome Substitution Lines ◽  
Complementary Genes ◽  
Tetraploid Wheats

Chromosomal locations of the Ne1 gene, one of the two complementary genes for type 1 hybrid necrosis, and two complementary genes, Cs1 and Cs2, for type 2 hybrid chlorosis in tetraploid wheats were determined by aneuploid analyses employing the D genome chromosome substitution lines of 'Langdon' durum wheat. The Ne1 gene of 'Langdon' is located on chromosome 5B, whereas the Cs1 gene of Triticum dicoccum 'Hokudai' and the Cs2 gene of T. timopheevi are located on chromosomes 5A and 4G, respectively. Chromosomes 4B and 4G show almost complete functional compensation, though they rarely pair with each other, but chromosome 4D of T. aestivum 'Chinese Spring' has only half the ability of chromosome 4G in compensating for chromosome 4B on the fertilization ability of the male gamete. The results have demonstrated the usefulness of the D genome chromosome substitution lines of durum wheat for determining the chromosomes carrying major genes in tetraploid wheat. The results of these studies support the reallocation of chromosome 4A to the B genome.Key words: durum wheat, hybrid necrosis, hybrid chlorosis, aneuploid analyses, chromosome substitution lines.

Molecular characterization and chromosome-specific TRAP-marker development for Langdon durum D-genome disomic substitution lines

Genome ◽  
2006 ◽  
Vol 49 (12) ◽  
pp. 1545-1554 ◽  
Author(s):  
J. Li ◽  
D.L. Klindworth ◽  
F. Shireen ◽  
X. Cai ◽  
J. Hu ◽  
...  
Keyword(s):  
Triticum Turgidum ◽  
Tetraploid Wheat ◽  
Substitution Lines ◽  
Genome Chromosome ◽  
D Genome ◽  
Single Chromosome ◽  
B Genome ◽  
The Individual ◽  
Trap Marker

The aneuploid stocks of durum wheat ( Triticum turgidum L. subsp. durum (Desf.) Husnot) and common wheat ( T. aestivum L.) have been developed mainly in ‘Langdon’ (LDN) and ‘Chinese Spring’ (CS) cultivars, respectively. The LDN-CS D-genome chromosome disomic substitution (LDN-DS) lines, where a pair of CS D-genome chromosomes substitute for a corresponding homoeologous A- or B-genome chromosome pair of LDN, have been widely used to determine the chromosomal locations of genes in tetraploid wheat. The LDN-DS lines were originally developed by crossing CS nulli-tetrasomics with LDN, followed by 6 backcrosses with LDN. They have subsequently been improved with 5 additional backcrosses with LDN. The objectives of this study were to characterize a set of the 14 most recent LDN-DS lines and to develop chromosome-specific markers, using the newly developed TRAP (target region amplification polymorphism)-marker technique. A total of 307 polymorphic DNA fragments were amplified from LDN and CS, and 302 of them were assigned to individual chromosomes. Most of the markers (95.5%) were present on a single chromosome as chromosome-specific markers, but 4.5% of the markers mapped to 2 or more chromosomes. The number of markers per chromosome varied, from a low of 10 (chromosomes 1A and 6D) to a high of 24 (chromosome 3A). There was an average of 16.6, 16.6, and 15.9 markers per chromosome assigned to the A-, B-, and D-genome chromosomes, respectively, suggesting that TRAP markers were detected at a nearly equal frequency on the 3 genomes. A comparison of the source of the expressed sequence tags (ESTs), used to derive the fixed primers, with the chromosomal location of markers revealed that 15.5% of the TRAP markers were located on the same chromosomes as the ESTs used to generate the fixed primers. A fixed primer designed from an EST mapped on a chromosome or a homoeologous group amplified at least 1 fragment specific to that chromosome or group, suggesting that the fixed primers might generate markers from target regions. TRAP-marker analysis verified the retention of at least 13 pairs of A- or B-genome chromosomes from LDN and 1 pair of D-genome chromosomes from CS in each of the LDN-DS lines. The chromosome-specific markers developed in this study provide an identity for each of the chromosomes, and they will facilitate molecular and genetic characterization of the individual chromosomes, including genetic mapping and gene identification.

INHERITANCE OF THE TYPE OF SOLID STEM IN GOLDEN BALL (TRITICUM DURUM): II. CYTOGENETICS OF THE RELATION BETWEEN SOLID STEM AND OTHER MORPHOLOGICAL CHARACTERS IN HEXAPLOID F5 LINES OF A HYBRID WITH RESCUE (T. AESTIVUM)

1959 ◽  
Vol 37 (6) ◽  
pp. 1207-1216 ◽  
Author(s):  
Ruby I. Larson
Keyword(s):  
Triticum Aestivum ◽  
Triticum Durum ◽  
Triticum Aestivum L ◽  
Morphological Characters ◽  
Genome Chromosome ◽  
D Genome ◽  
Stem Solidness ◽  
Pentaploid Hybrid ◽  
Golden Ball ◽  
Solid Stem

Cytogenetic analysis of selected F5 lines of the pentaploid hybrid, Rescue (Triticum aestivum L. emend. Thell.) × Golden Ball (T. durum Desf.) showed that chromosome XVI is the member of the D genome of Rescue that prevents transfer of the more solid top culm internode of Golden Ball to hexaploid segregates. It also produces a lax spike. Chromosome XX, which is the D-genome chromosome mainly responsible for the hollowness of hollow-stemmed hexaploids, probably has little effect in Rescue. Long awns were associated with low chromosome number but not with stem solidness or dense spike; therefore, the chromosome that suppresses awn development is probably not XVI.Three 42-chromosome segregates from the cross were more solid in the top internode than Rescue, presumably because of segregation of genes in the A and B genomes. It is unlikely, however, that a fully hexaploid segregate with a top internode as solid as that of Golden Ball can be selected from this hybrid.

scholarly journals The Use of Pentaploid Crosses for the Introgression of Amblyopyrum muticum and D-Genome Chromosome Segments Into Durum Wheat

2019 ◽  
Vol 10 ◽  
Author(s):  
Manel Othmeni ◽  
Surbhi Grewal ◽  
Stella Hubbart-Edwards ◽  
Caiyun Yang ◽  
Duncan Scholefield ◽  
...  
Keyword(s):  
Durum Wheat ◽  
Genome Chromosome ◽  
D Genome ◽  
Chromosome Segments

COLD HARDINESS IN HEXAPLOID TRITICALE

1985 ◽  
Vol 65 (3) ◽  
pp. 487-490 ◽  
Author(s):  
A. E. LIMIN ◽  
J. DVORAK ◽  
D. B. FOWLER
Keyword(s):  
Cold Hardiness ◽  
Tetraploid Wheat ◽  
Triticum Aestivum L ◽  
Hexaploid Triticale ◽  
D Genome ◽  
Potential Source ◽  
Secale Cereale L ◽  
Cold Hardy ◽  
Triticosecale Wittmack ◽  
X Triticosecale Wittmack

The excellent cold hardiness of rye (Secale cereale L.) makes it a potential source of genetic variability for the improvement of this character in related species. However, when rye is combined with common wheat (Triticum aestivum L.) to produce octaploid triticale (X Triticosecale Wittmack, ABDR genomes), the superior rye cold hardiness is not expressed. To determine if the D genome of hexaploid wheat might be responsible for this lack of expression, hexaploid triticales (ABR genomes) were produced and evaluated for cold hardiness. All hexaploid triticales had cold hardiness levels similar to their tetraploid wheat parents. Small gains in cold hardiness of less than 2 °C were found when very non-hardy wheats were used as parents. This similarity in expression of cold hardiness in both octaploid and hexaploid triticales indicates that the D genome of wheat is not solely, if at all, responsible for the suppression of rye cold hardiness genes. There appears to be either a suppressor(s) of the rye cold hardiness genes on the AB genomes of wheat, or the expression of diploid rye genes is reduced to a uniform level by polyploidy in triticale. The suppression, or lack of expression, of rye cold hardiness genes in a wheat background make it imperative that cold-hardy wheats be selected as parents for the production of hardy triticales.Key words: Triticale, Secale, winter wheat, cold hardiness, gene expression

TRANSFER OF CORNERSTONE MALE-STERILITY MUTANT TO TETRAPLOID WHEAT AND HEXAPLOID AND OCTOPLOID TRITICALES

1981 ◽  
Vol 23 (3) ◽  
pp. 493-496 ◽  
Author(s):  
M. A. Hossain ◽  
C. J. Driscoll
Keyword(s):  
Triticum Aestivum ◽  
Male Sterility ◽  
Secale Cereale ◽  
Tetraploid Wheat ◽  
Colchicine Treatment ◽  
Triticum Aestivum L ◽  
Male Sterile ◽  
Ploidy Levels ◽  
Secale Cereale L ◽  
Γ Ray

A γ-ray induced male-sterility mutant on chromosome 4A of Triticum aestivum L. (Cornerstone mutant ms1c) was transferred to T. durum Desf. by backcrossing. Selfed heterozygotes of T. durum produced fewer male-sterile plants than those of T. aestivum. Male-sterile plants of T. durum and T. aestivum were crossed with diploid rye (Secale cereale L.) and fertile hexaploid and octoploid triticales were obtained following colchicine treatment of the F1's. Thus, rye is able to restore fertility at both of these ploidy levels.

scholarly journals A locus for sodium exclusion (Nax1), a trait for salt tolerance, mapped in durum wheat

2004 ◽  
Vol 31 (11) ◽  
pp. 1105 ◽  
Author(s):  
Megan P. Lindsay ◽  
Evans S. Lagudah ◽  
Ray A. Hare ◽  
Rana Munns
Keyword(s):  
Salt Tolerance ◽  
Durum Wheat ◽  
Triticum Turgidum ◽  
Tetraploid Wheat ◽  
Triticum Aestivum L ◽  
Wheat Breeding ◽  
Lower Yield ◽  
Diverse Backgrounds ◽  
Salt Affected Soils ◽  
Sodium Exclusion

Salinity affects durum wheat [Triticum turgidum L. ssp. durum (Desf.)] more than it affects bread wheat (Triticum aestivum L.), and results in lower yield for durum wheat cultivars grown on salt-affected soils. A novel source of salt tolerance in the form of a sodium exclusion trait, identified previously in a screen of tetraploid wheat germplasm, was mapped using a QTL approach. The trait, measured as low Na+ concentration in the leaf blade, was mapped on a population derived from a cross between the low Na+ landrace and the cultivar Tamaroi. The use of AFLP, RFLP and microsatellite markers identified a locus, named Nax1 (Na exclusion), on chromosome 2AL, which accounted for approximately 38% of the phenotypic variation in the mapping population. Markers linked to the Nax1 locus also associated closely with low Na+ progeny in a genetically unrelated population. A microsatellite marker closely linked to the Nax1 locus was validated in genetically diverse backgrounds, and proven to be useful for marker-assisted selection in a durum wheat breeding program.

scholarly journals Screening of Diverse Ethiopian Durum Wheat Accessions for Aluminum Tolerance

Agronomy ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 440
Author(s):  
Edossa Fikiru Wayima ◽  
Ayalew Ligaba-Osena ◽  
Kifle Dagne ◽  
Kassahun Tesfaye ◽  
Eunice Magoma Machuka ◽  
...  
Keyword(s):  
Durum Wheat ◽  
Bread Wheat ◽  
Rapid Method ◽  
Triticum Turgidum ◽  
Aluminum Tolerance ◽  
Acid Soils ◽  
Triticum Aestivum L ◽  
D Genome ◽  
Potential Source ◽  
Seminal Roots

Acid soils and associated Al3+ toxicity are prevalent in Ethiopia where normally Al3+-sensitive durum wheat (Triticum turgidum ssp durum Desf.) is an important crop. To identify a source of Al3+ tolerance, we screened diverse Ethiopian durum germplasm. As a center of diversity for durum wheat coupled with the strong selection pressure imposed by extensive acid soils, it was conceivable that Al3+ tolerance had evolved in Ethiopian germplasm. We used a rapid method on seedlings to rate Al3+ tolerance according to the length of seminal roots. From 595 accessions screened using the rapid method, we identified 21 tolerant, 180 intermediate, and 394 sensitive accessions. When assessed in the field the accessions had tolerance rankings consistent with the rapid screen. However, a molecular marker specific for the D-genome showed that all accessions rated as Al3+-tolerant or of intermediate tolerance were hexaploid wheat (Triticum aestivum L.) that had contaminated the durum grain stocks. The absence of Al3+ tolerance in durum has implications for how Al3+ tolerance evolved in bread wheat. There remains a need for a source of Al3+-tolerance genes for durum wheat and previous work that introgressed genes from bread wheat into durum wheat is discussed as a potential source for enhancing the Al3+ tolerance of durum germplasm.

Interactions between the scs and Vi genes in alloplasmic durum wheat

Genome ◽  
1994 ◽  
Vol 37 (2) ◽  
pp. 210-216 ◽  
Author(s):  
S. S. Maan
Keyword(s):  
Male Sterility ◽  
Chromosomal Location ◽  
Triticum Turgidum ◽  
Meiotic Chromosome ◽  
Seed Viability ◽  
Triticum Aestivum L ◽  
Male Sterile ◽  
Genome Chromosome ◽  
D Genome ◽  
Alien Cytoplasm

Two nuclear genes, vitality (Vi) on an A- or B-genome chromosome and species cytoplasm specific (scs) on a 1DL telosome from Triticum aestivum L. or a telosome from Aegilops uniaristata Vis. (un telosome), improved compatibility between the nucleus of Triticum turgidum L. var. durum and the cytoplasm of Ae. longissima S. &M. or Ae. uniaristata. To study interactions between Vi and scs and to determine the chromosomal location of Vi, 29-chromosome fertile plants were crossed with 13 D-genome disomic-substitution (d-sub) lines [except 5D(5A)] of 'Langdon' durum. F1 and backcross progenies were examined for meiotic chromosome number and pairing, fertility, and plant vigor. In 11 crosses, Vi restored seed viability but produced double-monosomics (d-monos) with greatly reduced growth and vigor. In contrast, crosses involving 1D(1A) and 1D(1B) d-sub lines produced d-monos with normal vigor and anthesis but nonfunctional pollen. A backcross of 1D + 1A d-mono F1 and 1D(1A) d-sub lines produced 11 male steriles; 3 had 13 II + 1 II 1D + 1 I 1A, 2 had 13 II + 2 I, 1 had 13 II + 1 II 1D(1A), and 5 were not examined. Crosses of 1D + 1A d-mono F1 with control durum, lo durum (with 1DL), and un durum (with un telosome) lines produced 16 male-sterile d-monos and 14 fertiles with 14 II + 1 I 1D, showing that 15-chromosome female gametes transmitted monosomes 1A and 1D. However, BC2F1's from 1D + 1B d-mono × fertile line with un telosome included 20 male-sterile d-monos, 6 fertile triple monosomics (13 II + 1 I 1D + 1 I 1B + t I un telosome), and 1 fertile plant with a 1B/1D translocation. Unlike d-mono 1A + 1D, d-mono 1B + 1D did not transmit 15-chromosome female gametes with monosomes 1D and 1B. Additional backcrosses also indicated that homozygous scs caused male sterility in 1D(1A) and 1D(1B) d-subs and that the procedure used was not suitable for the chromosomal location of Vi.Key words: alien cytoplasm, nucleocytoplasmic interactions, 1B/1D translocation, aneuploidy, cytoplasmic male sterility.

DEVELOPMENT OF D-GENOME DISOMIC ADDITION LINES OF DURUM WHEAT

1972 ◽  
Vol 14 (2) ◽  
pp. 335-340 ◽  
Author(s):  
L. R. Joppa ◽  
F. H. McNeal
Keyword(s):  
Triticum Aestivum ◽  
Durum Wheat ◽  
Chromosome Numbers ◽  
Chinese Spring ◽  
Triticum Aestivum L ◽  
Addition Lines ◽  
Male Sterile ◽  
D Genome ◽  
Disomic Addition Lines

Seven lines of 'Chinese Spring' (Triticum aestivum L. em Thell.), each tetrasomic for one of the D-genome chromosomes, were crossed to 'Wells' and to 'Lakota' durum (T. durum Desf.). Nearly all F1 plants had 15 pairs plus six univalents, as expected.The D-genome disomic addition lines 1D, 3D, 4D, 5D and 6D were obtained in the F3. The 1D, 3D and 6D disomic addition lines proved to be male-sterile. The 4D and 5D disomic addition lines had stable chromosome numbers, were partially male-fertile and could be maintained by selfing. The 2D and 7D disomic addition lines were not obtained.

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