Incorporation of restoring gene of Aegilops umbellulata into wheat

Genome ◽  
1991 ◽  
Vol 34 (5) ◽  
pp. 727-732 ◽  
Author(s):  
Zheng-Qiang Ma ◽  
Yin-Hai Zhao ◽  
Da-Jun Liu

Six 'Chinese Spring' – Aegilops umbellulata Zhuk. addition lines (UAD, UBD, UCD, UDD, UED, and UFM) were assayed for their effects on the fertility of timopheevi cytoplasm male sterile lines (T-type). Chromosome 6U of disomic addition line UAD was found to be able to restore the fertility of T-type male sterility and 'Chinese Spring' was verified to lack restoring genes, indicating that 6U carries at least one fertility restoration gene. From about 200 plants with 42 somatic chromosomes derived from the progeny of crosses Qu Xian Early A × UAD and Sumai No. 3 A × UAD, eight self-fertile plants were selected. Their self-fertility in timopheevi cytoplasm implies that they carry the restoring gene(s) from 6U. Cytological analysis was conducted on the hybrid F1 of the selected fertile plants (040-5, 060-1, and 061-4) as female parents crossed with 'Chinese Spring'. The self-fertility segregation and the chromosome pairing of pollen mother cells of F1 fertile plants from 040-5, 060-1, and 061-4 × 'Chinese Spring' during meiosis suggested that they were heterozygous translocation lines with restoring gene(s) from 6U.Key words: Aegilops umbellulata Zhuk., restoring genes, alien gene transfer, timopheevi cytoplasmic male sterile fertility, Triticum aestivum L.

Genetics ◽  
1981 ◽  
Vol 97 (2) ◽  
pp. 391-414
Author(s):  
Jan Dvořák ◽  
Patrick E McGuire

ABSTRACT Wheat cultivar Chinese Spring (Triticum aestivum L. em. Thell.) was crossed with cultivars Hope, Cheyenne and Timstein. In all three hybrids, the frequencies of pollen mother cells (PMCs) with univalents at metaphase I (MI) were higher than those in the parental cultivars. No multivalents were observed in the hybrids, indicating that the cultivars do not differ by translocations. Thirty-one Chinese Spring telosomic lines were then crossed with substitution lines in which single chromosomes of the three cultivars were substituted for their Chinese Spring homologues. The telosomic lines were also crossed with Chinese Spring. Data were collected on the frequencies (% of PMCs) of pairing of the telesomes with their homologues at MI and the regularity of pairing of the remaining 20 pairs of Chinese Spring chromosomes in the monotelodisomics obtained from these crosses. The reduced MI pairing in the intercultivar hybrids was caused primarily by chromosome differentiation, rather than by specific genes. Because the differentiation involved a large part of the chromosome complement in each hybrid, it was concluded that it could not be caused by structural changes such as inversions or translocations. In each case, the differentiation appeared to be unevenly distributed among the three wheat genomes. It is proposed that the same kind of differentiation, although of greater magnitude, differentiates homoeologous chromosomes and is responsible, together with structural differentiation, for poor chromosome pairing in interspecific hybrids.


2008 ◽  
Vol 59 (3) ◽  
pp. 206 ◽  
Author(s):  
A. C. Martín ◽  
S. G. Atienza ◽  
M. C. Ramírez ◽  
F. Barro ◽  
A. Martín

We report a new cytoplasmic male sterility (CMS) source in bread wheat (Triticum aestivum L.) designated as msH1. CMS has been identified during the process of obtaining alloplasmic bread wheat in different Hordeum chilense Roem. Schultz. cytoplasms. It was observed that when using the H. chilense H1 accession, the corresponding alloplasmic line was male sterile. This alloplasmic wheat is stable under different environmental conditions and it does not exhibit developmental or floral abnormalities, showing only slightly reduced height and some delay in heading. On examining microsporogenesis in the alloplasmic line, it was found that different stages of meiosis were completed normally, but abnormal development occurred at the uninucleate-pollen stage at the first mitosis, resulting in failure of anther exertion and pollen abortion. Fertility restoration of the CMS phenotype caused by the H. chilense cytoplasm was associated with the addition of chromosome 6HchS from H. chilense accession H1. Thus, some fertility restoration genes appear to be located in this chromosome arm. Considering the features displayed by the msH1 system, we consider that it has a great potential for the development of viable technology for hybrid wheat production.


Genome ◽  
1990 ◽  
Vol 33 (1) ◽  
pp. 9-12 ◽  
Author(s):  
J. P. Gustafson ◽  
K. Ross

The expression of aluminum tolerance from rye (Secale cereale L.) when present in a wheat (Triticum aestivum L. em. Thell.) background has been observed to be much lower than that in rye itself. By crossing each of the ditelocentric lines of 'Chinese Spring' wheat with a tolerant rye, the effects of the presence or absence of each arm of wheat on the expression of rye aluminum tolerance could be established. Of 42 wheat chromosome arms, 18 affected the expression of rye aluminum tolerance. Tolerance was increased over that observed in the euploid wheat–rye hybrid when arms 4AL, 5AL, 6AL, 7BS, 7BL, and 3DS were absent. Tolerance was reduced when arms 2AL, 5AS, 6BS, 1DS, 1DL, 2DL, 4DL, 5DS, 5DL, 6DL, 7DS, and 7DL were absent. Thus, the control of aluminum tolerance expression from rye in a wheat background was evidently under the influence of genes located on a number of wheat chromosome arms, with a few arms tending to enhance expression and many others tending to reduce it. In fact, 5AS of 'Chinese Spring' enhances expression, while 5AL suppresses it. The D genome of bread wheat appears to have the most pronounced effect on the expression of rye aluminum tolerance.Key words: rye, activator genes, suppressor genes, alien manipulation.


1972 ◽  
Vol 14 (2) ◽  
pp. 335-340 ◽  
Author(s):  
L. R. Joppa ◽  
F. H. McNeal

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.


Genome ◽  
1990 ◽  
Vol 33 (1) ◽  
pp. 16-22 ◽  
Author(s):  
Kay L. D. Morris ◽  
W. John Raupp ◽  
Bikram S. Gill

A combination of cytological and biochemical methods were used to isolate and identify six Triticum aestivum 'Chinese Spring' – Elymus trachycaulus (= Agropyron trachycaulum, 2n = 28, genomes StStHtHt) Ht genome disomic and ditelosomic chromosome addition lines. Protein and morphological markers indicated that Elymus chromosomes 1Ht, 1Htp, 5Ht, 6Ht, 7Ht, and 7Htp have been added to the wheat genome. Two alloplasmic addition lines, 1Ht and 1Htp, were determined to have favorable nucleocytoplasmic interactions by the presence of vegetative vigor and fertility restoration. The gene(s) for vigor and fertility restoration were located on the short arm of 1Ht. The Elymus chromosomes of each line were found to affect plant morphology and fertility, with the exception of disomic addition 6Ht, which appeared similar to 'Chinese Spring'. Phenotypic differences between each line may be attributed to the expression of genes from specific Elymus chromosomes, the cumulative dosage of homoeoalleles, or nucleocytoplasmic interactions. These morphological traits, in combination with biochemical markers, provide evidence of the gene synteny relationships between the Elymus and Triticum species. Knowledge of the homoeologous relationships among wheat and Elymus chromosomes may be useful for the eventual transfer of disease-resistance genes from Elymus to wheat.Key words: Elymus, wheat, addition line, polyploidy.


Genome ◽  
1988 ◽  
Vol 30 (3) ◽  
pp. 438-442 ◽  
Author(s):  
William Tai ◽  
Peter B. E. McVetty

Crosses were made between Brassica napus (2n = 38) with the 'Polima' cytoplasmic male sterile system and variety 'Zem' of B. juncea. Fertility was partially restored in backcross progeny with an extra chromosome (2n = 39) that was believed to be a member of the B genome of B. juncea. Among more than 40 self-pollinated offspring plants studied, fertility restoration was transmitted only through those plants with two extra chromosomes (2n = 40). Anthers of these plants were either full or shriveled with small swollen protrusions. Full and round pollen grains were found in full anthers and in the swollen portion of shriveled anthers. These pollen grains were stained darkly with I2-KI solution and full seed set was obtained from bagged flowers. Meiotic studies in plants with 2n = 40 showed 18 bivalents + 1 quadrivalent at diakinesis in most of the pollen mother cells analyzed. The chromosomes segregated equally at anaphase I and behaved normally at other meiotic stages. The presence of a single quadrivalent in the backcross progeny was highly consistent and occurred in very high frequencies. It is believed that the extra chromosomes belong to the B genome of B. juncea and take part in the quadrivalent formation.Key words: Brassica napus, cytoplasmic male sterility, aneuploidy, Polima, Brassica juncea, rapeseed cytogenetics.


Author(s):  
Fahimeh Shahinnia ◽  
Manuel Geyer ◽  
Annette Block ◽  
Volker Mohler ◽  
Lorenz Hartl

AbstractWheat (Triticum aestivum L.) is a self-pollinating crop whose hybrids offer the potential to provide a major boost in yield. Male sterility induced by the cytoplasm of Triticum timopheevii is a powerful method for hybrid seed production. Hybrids produced by this method are often partially sterile and full fertility restoration is crucial for wheat production using hybrid cultivars. To identify genetic loci controlling fertility restoration in wheat, we produced two CMS-based backcross (BC1) mapping populations. The restorer lines Gerek 79 and 71R1203 were used to pollinate the male-sterile winter wheat line CMS-Sperber. Seed set and numbers of sterile spikelets per spike were evaluated in 340 and 206 individuals of the populations derived from Gerek 79 and 71R1203, respectively. Genetic maps were constructed using 930 and 994 SNPs, spanning 2,160 and 2,328 cM over 21 linkage groups in the two populations, respectively. Twelve quantitative trait loci (QTL) controlled fertility restoration in both BC1 populations, including a novel restorer-of-fertility (Rf) locus flanked by the single nucleotide polymorphism (SNP) markers IWB72413 and IWB1550 on chromosome 6AS. The locus was mapped as a qualitative trait in the BC1 Gerek 79 population and was designated Rf9. Ninety-three putative candidate genes were predicted for the QTL region on chromosome 6AS. Among them were genes encoding tetratricopeptide and pentatricopeptide repeat-containing proteins in rice known to be associated with fertility restoration. This finding is a promising step to better understand the functions of genes for improving hybrid wheat.


Author(s):  
Hao Fu ◽  
N. P. Goncharov

Aim. To present the wheat endemics of China as source material for breeding and historical heritage. Results and Discussion. Wheat in China is the second most widely distributed cereal crop after rice. It is cultivated in China from the extreme northern border to the southern one, at altitudes from 154 m below sea level to 4450 m above sea level. The Chinian wheat is originated from South-West and West Asia and has a history of more than 2.8 thousand years. Since ancient times, the wheat species have been grown in China: bread (Triticum aestivum L.), compactum (T. compactum Host), polonicum (T. polonicum L.), turgidum (T. turgidum L.), durum (T. durum Desf.), turanian (T. turanicum Jakubz.). The Chinese ancient bread wheats are of interest for breeders because presence among them of early ripening, multi-flowering with the grain number in a spikelet up to 7-8 and in the ear up to 90-100, drought and winter hardy, resistant to powdery mildew and leaf rust; forms with good crossability with rye and Aegilops species. Among the endemic Chinese wheat, an important place belongs to the Chinese Spring variety which played an outstanding role in wheat genetics; super dwarfs Tom Pouce and Tibetan Dwarf; three-grain wheat, in which 3 grains are formed in one flower; Charklyk ancient wheat – a boneless form of polonicum wheat; dwarf blue wheat turgidum – with a strong waxy coating; Taigu-Male-Sterile Wheat – with gene male sterility; a wheats having species and subspecies status: wheat of Petropavlovskyi – Triticum petropavlovskyi Udacz. et Migusch.; Tibetan wheat – T. spelta L. ssp. tibetanum (Shao) N.P. Gontsch comb. nov .; Yunnan wheat – T. spelta L. ssp. yunnanse (King ex S.L. Chen) N.P. Gontsch comb. nov. The origin and genetic characteristics of China's endemic wheats are discussed. Conclusions. China's wheat endemics need careful study and conservation as a reserve of valuable genes and their complexes for breeding, and as an embodiment of the history, culture, talent and work of the people who created them, and an integral part of human cultural heritage.


Genetics ◽  
1996 ◽  
Vol 143 (3) ◽  
pp. 1383-1394
Author(s):  
Roger P Wise ◽  
Carren L Dill ◽  
Patrick S Schnable

Abstract Dominant alleles of the rf1 and rf2 nuclear-encoded fertility restorer genes are necessary for restoration of pollen fertility in T-cytoplasm maize. To further characterize fertility restoration mediated by the Rf1 allele, 123,500 gametes derived from plants carrying the Mutator transposable element family were screened for rf1-mutant alleles (rf1-m) Four heritable rf1-m alleles were recovered from these populations. Three rf1-m alleles were derived from the progenitor allele Rf1-IAl53 and one was derived from Rf1-Ky21. Cosegregation analysis revealed 5.5- and 2.4kb Mu1-hybridizing EcoRI restriction fragments in all of the male-sterile and none of the male-fertile plants in families segregating for rf1-m3207 and rf1-m3310, respectively. Mitochondrial RNA gel blot analyses indicated that all four rf1-m alleles in male-sterile plants cosegregated with the altered steady-state accumulation of 1.6 and O.6-kb T-urf13 transcripts, demonstrating that these transcripts are Rf1 dependent. Plants carrying a leaky mutant, rf1-m7323, revealed variable levels of Rf1-associated, T-urf13 transcripts and the degree of pollen fertility. The ability to obtain rf1-m derivatives from Rf1 indicates that Rf1 alleles produce a functional gene product necessary for the accumulation of specific T-urf13 transcripts in T-cytoplasm maize.


Genetics ◽  
1998 ◽  
Vol 150 (1) ◽  
pp. 383-391 ◽  
Author(s):  
Hoang V Tang ◽  
Ruying Chang ◽  
Daryl R Pring

Abstract Defective nuclear-cytoplasmic interactions leading to aberrant microgametogenesis in sorghum carrying the IS1112C male-sterile cytoplasm occur very late in pollen maturation. Amelioration of this condition, the restoration of pollen viability, involves a novel two-gene gametophytic system, wherein genes designated Rf3 and Rf4 are required for viability of individual gametes. Rf3 is tightly linked to, or represents, a single gene that regulates a transcript processing activity that cleaves transcriptsof orf107, a chimeric mitochondrial open reading frame specific to IS1112C. The mitochondrial gene urf 209 is also subject to nucleus-specific enhanced transcript processing, 5′ to the gene, conferred by a single dominant gene designated Mmt1. Examinations of transcript patterns in F2 and two backcross populations indicated cosegregation of the augmented orf107 and urf209 processing activities in IS1112C. Several sorghum lines that do not restore fertility or confer orf107 transcript processing do exhibit urf209 transcript processing, indicating that the activities are distinguishable. We conclude that the nuclear gene(s) conferring enhanced orf107 and urf209 processing activities are tightly linked in IS1112C. Alternatively, the similarity in apparent regulatory action of the genes may indicate allelic differences wherein the IS1112C Rf3 allele may differ from alleles of maintainer lines by the capability to regulate both orf107 and urf209 processing activities.


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