Transfer of a species cytoplasm specific (scs) gene from Triticum timopheevii to T. turgidum

Genome ◽  
1992 ◽  
Vol 35 (2) ◽  
pp. 238-243 ◽  
Author(s):  
S. S. Maan
Keyword(s):  
Common Wheat ◽  
Triticum Turgidum ◽  
Seed Viability ◽  
Male Parent ◽  
Alien Chromosome ◽  
Male Sterile ◽  
Male Sterile Plant ◽  
B Genome ◽  
Aegilops Longissima ◽  
Genome Donor

Initial attempts to substitute euploid nuclei of Triticum turgidum L. or T. aestivum L. into Aegilops longissima S. &L. cytoplasm failed because an alien chromosome remained fixed in the Triticum nucleus. The alien chromosome had gene(s) conditioning sporophytic sterility (also known as the gameticidal or Cuckoo effect). Subsequently, an exceptional 29-chromosome, male-sterile plant with spontaneously improved female fertility was used as a source of Ae. longissima cytoplasm, and a fully fertile alloplasmic common wheat 'Selkirk' line was developed. However, alloplasmic 'Selkirk' crossed with durum wheat as a recurrent male parent did not produce euploid plants. Instead, chromosome 1D or telocentric 1DL of 'Selkirk' was retained and male-sterile plants with 29 chromosomes were obtained. They set two seed types: a few that were plump and viable (PVi) and a large number that were shrivelled and inviable (SIv). The 1DL was deleted by crossing these plants to T. timopheevii, backcrossing the F1's to T. timopheevii, and repeatedly backcrossing the timopheevii-like plants to durum as the recurrent male parent. The resulting euploid durum plants with Ae. longissima cytoplasm were male sterile and set a 1:1 ratio of PVi and SIv seeds. Thus, a species cytoplasm specific (scs) gene of T. timopheevii was transferred to durum and caused male sterility and abortion of embryos lacking this gene. In conclusion, (i) the scs gene was expressed as a dominant sterility gene, restored seed viability, and partial compatibility between the durum nucleus and Ae. longissima cytoplasm and (ii) a scs gene on 1DL also caused dominant sterility in durum but not in alloplasmic common wheat. Hence, alien scs homoeoallele(s) conditioned sterility and seed abortion in alloplasmic durum but not in T. aestivum and T. timopheevii.Key words: interspecific nucleocytoplasmic genetics, sporophytically controlled sterility, B-genome donor, scs gene.

Cytological evidence bearing on the origin of the B genome in polyploid wheats

Genome ◽  
1988 ◽  
Vol 30 (1) ◽  
pp. 36-43 ◽  
Author(s):  
K. Kerby ◽  
J. Kuspira
Keyword(s):  
Dna Hybridization ◽  
Triticum Turgidum ◽  
Root Tip ◽  
Cytological Evidence ◽  
B Genome ◽  
Genome Donor ◽  
The One ◽  
Genome Donors ◽  
Tip Cells ◽  
Root Tip Cells

To help elucidate the origin of the B genome in polyploid wheats, karyotypes of Triticum turgidum, Triticum monoccum, and all six purported B genome donors were compared. The analysis utilized a common cytological procedure that employed the most advanced equipment for the measurement of chromosome lengths at metaphase in root tip cells. A comparison of the karyotypes of T. turgidum and T. monococcum permitted the identification of B genome chromosomes of T. turgidum. These consist of two SAT pairs, one ST pair, three SM pairs, and one M pair of homologues. Comparisons of the chromosomes of the B genome of T. turgidum with the karyotypes of the six putative B genome donors showed that only the karyotype of Aegilops searsii was similar to the one deduced for the donor of the B genome in T. turgidum, suggesting that Ae. searsii is, therefore, the most likely donor of the B genome to the polyploid wheats. Support for this conclusion has been derived from geographic, DNA-hybridization, karyotype, morphological, and protein data reported since 1977. Reasons why the B genome donor has not been unequivocally identified are discussed.Key words: phylogeny, karyotypes, Triticum turgidum, Triticum monococcum, B genome, B genome donors.

The scs and Vi genes correct a syndrome of cytoplasmic effects in alloplasmic durum wheat

Genome ◽  
1992 ◽  
Vol 35 (5) ◽  
pp. 780-787 ◽  
Author(s):  
S. S. Maan
Keyword(s):  
Durum Wheat ◽  
Triticum Turgidum ◽  
Seed Viability ◽  
Male Sterile ◽  
Selfed Progeny ◽  
Alloplasmic Lines ◽  
Preferential Transmission ◽  
Cytoplasmic Effects ◽  
True Breeding ◽  
Aegilops Squarrosa

The nucleus of Triticum turgidum L. var. durum is incompatible with cytoplasms of Aegilops squarrosa L., Ae. cylindrica Host, Ae. uniaristata Vis., and Ae. longissima S. &M. However, durum lines with these cytoplasms were obtained by adding a telosome from Ae. uniaristata (un telosome) or a 1DL telosome from T. aestivum L. 'Selkirk'. The Ae. squarrosa and Ae. cylindrica 29-chromosome plants with 1DL telosome were partially fertile. While Ae. uniaristata or Ae. longissima 29-chromosome plants with 1DL or un telosome were male sterile. The four alloplasmic lines set a few plump and a large number of shrivelled seed from crosses with euploid durum. Only plump seed germinated and produced 29-chromosome plants in successive backcrosses. The telosomes must have a species cytoplasm specific (scs) gene(s) that improved nucleocytoplasmic (NCC) and embryo–endosperm compatibility (EEC), but scs was not transferred to a durum chromosome because telosomes remained meiotically unpaired in 29-chromosome plants. However, a scs gene with similar effects was transferred from T. timopheevii Zhuk. to Ae. longissima euploid durum. The resulting plants were male sterile and set a 1:1 ratio of plump and shrivelled seed. This paper reports that a vitality gene (Vi) restored NCC, EEC, seed viability, fertility, and vigor to Ae. longissima euploid F1's with scs from T. timopheevii. F1 progeny had a 1:1 ratio of fertile plants of normal vigor and low vigor plants (LVP). Thus, Vi had xenia effect, improved EEC, and corrected a syndrome of cytoplasmic effects in 50% of the F1's where Vi was epistatic or dominant to scs. The F2 and sucessive selfed progeny segregated for LVP but true breeding fertile plants were not obtained. Either scs and Vi were alleles, heterosexual gametes with scs and Vi were incompatible, scs had preferential transmission through the heterosexual gametophytes, or Vi was inactivated or remained unexpressed. Thus, scs and Vi had an unorthodox manner of inheritance and expression.Key words: Triticum, dfs, xenia effect, zygotic sterility, embryo–endosperm compatibility.

EVIDENCE FOR AEGILOPS SHARONENSIS EIG AS THE DONOR OF THE B GENOME OF WHEAT

Genetics ◽  
1981 ◽  
Vol 99 (3-4) ◽  
pp. 495-512
Author(s):  
U Kushnir ◽  
G M Halloran
Keyword(s):  
Triticum Turgidum ◽  
Tetraploid Wheat ◽  
Grain Morphology ◽  
B Genome ◽  
Aegilops Sharonensis ◽  
Genome Donor ◽  
Low Levels ◽  
High Level ◽  
Karyotype Morphology ◽  
Donor Species

ABSTRACT A number of lines of evidence are advanced for the candidacy of Aegilops sharonensisEig as the donor of the B genome of wheat. The cytoplasm of Ae. shuronensis iscompatible with tetraploid wheat Triticum turgidum dicoccoides,as evidenced bythe high level of chromosome pairing and fertility of the amphiploid Ae. sharonensisx T. turgidum dicoccoides. Ae. sharonensischromosomes exhibit high levels of pairing with those of the B genome of wheat in hybrids with Ph-deficient hexaploid wheat and low levels of homoeologous pairing with T. monocmcumchromosomes.——The amphidiploid between Ae. sharonensisand T. monococcumis very similar to T. turgidum dicoccoidesin spike, spikelet and grain morphology. The karyotype of Ae. sharonensisresembles more closely that of extrapolated Bgenome karyotypes of wheat than do the karyotypes of other proposed B-genome donor species of Aegilops. Because of distinctiveness in cytological aftinity and karyotype morphology between Ae. sharonensisand Ae. longissima,a separate genome symbol Sshis proposed for the former species.

Biochemical data bearing on the relationship between the genome of Triticum urartu and the A and B genomes of the polyploid wheats

Genome ◽  
1988 ◽  
Vol 30 (4) ◽  
pp. 576-581 ◽  
Author(s):  
K. Kerby ◽  
J. Kuspira ◽  
B. L. Jones
Keyword(s):  
Amino Acid ◽  
Triticum Turgidum ◽  
Amino Acid Sequences ◽  
Triticum Monococcum ◽  
Triticum Urartu ◽  
B Genome ◽  
Genome Donor ◽  
A Genome ◽  
The Relationship ◽  
Donor Species

To determine whether the Triticum urartu genome is more closely related to the A or B genome of the polyploid wheats, the amino acid sequence of its purothionin was compared to the amino acid sequences of the purothionins in Triticum monococcum, Triticum turgidum, and Triticum aestivum. The residue sequence of the purothionin from T. urartu differs by five and six amino acid substitutions respectively from the α1 and α2 forms coded for by genes in the B and D genomes, and is identical to the β form specified by a gene in the A genome. Therefore, the T. urartu purothionin is either coded by a gene in the A genome or a chromosome set highly homologous to it. The results demonstrate that at least a portion of the T. urartu and T. monococcum genomes is homologous and probably identical. A variety of other studies have also shown that T. urartu is very closely related to T. monococcum and, in all likelihood, also possesses the A genome. Therefore, it could be argued that either T. urartu and T. monococcum are the same species or that T. urartu rather than T. monococcum is the source of the A genome in T. turgidum and T. aestivum. Except for Johnson's results, our data and that of others suggest a revised origin of polyploid wheats. Specifically, the list of six putative B genome donor species is reduced to five, all members of the Sitopsis section of the genus Aegilops.Key words: Triticum monococcum, Triticum urartu, polyploid wheats, genomes A and B, purothionins.

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.

Natural or induced nucleocytoplasmic heterogeneity in Triticum longissimum

Genome ◽  
1996 ◽  
Vol 39 (1) ◽  
pp. 71-76 ◽  
Author(s):  
S. S. Maan
Keyword(s):  
Durum Wheat ◽  
Common Wheat ◽  
Meiotic Chromosome ◽  
Nuclear Gene ◽  
Meiotic Pairing ◽  
Alien Chromosome ◽  
Male Sterile ◽  
Substitution Lines ◽  
Selfish Gene ◽  
Group 4

Alien cytoplasms produce a variety of phenotypes in durum wheat (Triticum turgidum) and common wheat (Triticum aestivum) cultivars, which indicate the prevalence of cytoplasmic variability in the subtribe Triticinae. Intraspecific cytoplasmic differences have been demonstrated between the subspecies of Triticum speltoides, Triticum dichasians, and Triticum comosum. In this study, durum wheat lines with cytoplasm from two accessions, B and C, of Triticum longissimum were compared, and meiotic chromosome pairing between the group 4 homoeologues from the same two accessions was examined in common wheat. First, monosomic addition or monosomic substitution lines of common wheat with cytoplasm and one chromosome (designated B) from accession B were crossed with those having cytoplasm and a chromosome designated C-1 or C-2 from accession C. In each substitution line, an alien chromosome substituted for a group 4 homoeologue. Each alien chromosome had a "selfish" (Sf) gene, which remained fixed in the wheat nucleus. The F1s had greatly reduced meiotic pairing between chromosomes B and C-1 and B and C-2, which indicated greatly reduced homology between the group 4 homoeologues from the two accessions. Second, by using Triticum timopheevii as a bridging species, chromosome B in a common wheat line was eliminated and an euploid durum line with cytoplasm from accession B was obtained. This line was fertile. In contrast, a similarly produced durum line with cytoplasm from accession C was male sterile and retained a species cytoplasm specific (scs) nuclear gene from T. timopheevii. In conclusion, nuclear and cytoplasmic heterogeneity pre-existed between accessions B and C and they represent varieties or incipient subspecies in T. longissimum. Alternatively, the Sf genes produced chromosomal heterogeneity and mutated cytoplasmic genes from one or both accessions. Key words : meiotic drive, selfish gene (Sf), gametocidal gene (Gc), Triticum, Aegilops.

The phylogeny of the polyploid wheats Triticum aestivum (bread wheat) and Triticum turgidum (macaroni wheat)

Genome ◽  
1987 ◽  
Vol 29 (5) ◽  
pp. 722-737 ◽  
Author(s):  
K. Kerby ◽  
J. Kuspira
Keyword(s):  
Triticum Aestivum ◽  
Triticum Turgidum ◽  
Diploid Species ◽  
Triticum Monococcum ◽  
Aegilops Speltoides ◽  
Triticum Urartu ◽  
B Genome ◽  
Aegilops Longissima ◽  
A Genome ◽  
Genome Donors

The phylogeny of the polyploid wheats has been the subject of intense research and speculation during the past 70 years. Various experimental approaches have been employed to ascertain the diploid progenitors of these wheats. The species having donated the D genome to Triticum aestivum has been unequivocally identified as Aegilops squarrosa. On the basis of evidence from many studies, Triticum monococcum has been implicated as the source of the A genome in both Triticum turgidum and Triticum aestivum. However, numerous studies since 1968 have shown that Triticum urartu is very closely related to Triticum monococcum and that it also carries the A genome. These studies have prompted the speculation that Triticum urartu may be the donor of this chromosome set to the polyploid wheats. The donor of the B genome to Triticum turgidum and Triticum aestivum remains equivocal and controversial. Six different diploid species have been implicated as putative B genome donors: Aegilops bicornis, Aegilops longissima, Aegilops searsii, Aegilops sharonensis, Aegilops speltoides, and Triticum urartu. Until recently, evidence presented by different researchers had not permitted an unequivocal identification of the progenitor of the B genome in polyploid wheats. Recent studies, involving all diploid and polyploid wheats and putative B genome donors, lead to the conclusion that Aegilops speltoides and Triticum urartu can be excluded as B genome donors and that Aegilops searsii is the most likely source of this chromosome set. The possibility of the B genome having arisen from an AAAA autotetraploid or having a polyphyletic origin is discussed. Key words: phylogeny; Triticum aestivum; Triticum turgidum; A, B, and D genomes.

scholarly journals Heteroalleles in Common Wheat: Multiple Differences between Allelic Variants of the Gli-B1 Locus

2021 ◽  
Vol 22 (4) ◽  
pp. 1832
Author(s):  
Eugene Metakovsky ◽  
Laura Pascual ◽  
Patrizia Vaccino ◽  
Viktor Melnik ◽  
Marta Rodriguez-Quijano ◽  
...  
Keyword(s):  
Common Wheat ◽  
Dna Sequences ◽  
Fragment Length Polymorphism ◽  
Snp Markers ◽  
Group Iv ◽  
Nucleotide Polymorphisms ◽  
High Genetic Diversity ◽  
Single Nucleotide ◽  
Allelic Variants ◽  
B Genome

The Gli-B1-encoded γ-gliadins and non-coding γ-gliadin DNA sequences for 15 different alleles of common wheat have been compared using seven tests: electrophoretic mobility (EM) and molecular weight (MW) of the encoded major γ-gliadin, restriction fragment length polymorphism patterns (RFLPs) (three different markers), Gli-B1-γ-gliadin-pseudogene known SNP markers (Single nucleotide polymorphisms) and sequencing the pseudogene GAG56B. It was discovered that encoded γ-gliadins, with contrasting EM, had similar MWs. However, seven allelic variants (designated from I to VII) differed among them in the other six tests: I (alleles Gli-B1i, k, m, o), II (Gli-B1n, q, s), III (Gli-B1b), IV (Gli-B1e, f, g), V (Gli-B1h), VI (Gli-B1d) and VII (Gli-B1a). Allele Gli-B1c (variant VIII) was identical to the alleles from group IV in four of the tests. Some tests might show a fine difference between alleles belonging to the same variant. Our results attest in favor of the independent origin of at least seven variants at the Gli-B1 locus that might originate from deeply diverged genotypes of the donor(s) of the B genome in hexaploid wheat and therefore might be called “heteroallelic”. The donor’s particularities at the Gli-B1 locus might be conserved since that time and decisively contribute to the current high genetic diversity of common wheat.

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.

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