Alloplasmic wheat – Elymus ciliaris chromosome addition lines

Genome ◽  
1993 ◽  
Vol 36 (2) ◽  
pp. 327-333 ◽  
Author(s):  
Jiming Jiang ◽  
Peidu Chen ◽  
Bernd Friebe ◽  
W. John Raupp ◽  
Bikram S. Gill
Keyword(s):  
Fertility Restoration ◽  
Wheat Chromosome ◽  
Puccinia Recondita ◽  
Male Sterile ◽  
Chromosome Translocations ◽  
Chromosome Addition ◽  
Nucleolar Organizing Regions ◽  
Chromosome Addition Lines ◽  
The Relationship ◽  
Chromosome 3B

Alloplasmic euploid wheat with the cytoplasm of Elymus ciliaris (2n = 4x = 28, ScScYcYc) is male sterile and has reduced vigor. However, alloplasmic plants with E. ciliaris chromosomes 1Sc or 1Yc marked by gliadin genes Gli-Sc1 and Gli-Ycl, respectively, are vigorous and fertile. The Rf genes on 1Sc and 1Yc are named Rf-Sc1 and Rf-Yc1. Two chromosome translocations involving 1Yc were isolated. The first involved the short arm of 1Yc translocated to the short arm of wheat chromosome 3B. The second involved the short arm of 1Yc translocated to the short arm of a chromosome, designated L, of E. ciliaris. The second line also has another E. ciliaris chromosome designated A and lacks wheat chromosome 6A. This line is resistant to Puccinia recondita. The relationship between fertility restoration and nucleolar organizing regions is discussed. Key words : Triticum aestivum, Elymus ciliaris, chromosome addition, Rf genes, nucleolar organizing regions.

THE CYTOGENETIC STRUCTURE OF A 56-CHROMOSOME DERIVATIVE FROM A CROSS BETWEEN TRITICUM AESTIVUM AND AGROPYRON ELONGATUM (2n = 70)

1976 ◽  
Vol 18 (2) ◽  
pp. 271-279 ◽  
Author(s):  
Jan Dvořák
Keyword(s):  
Triticum Aestivum ◽  
Chromosome Pairing ◽  
Chinese Spring ◽  
Wheat Chromosome ◽  
Agropyron Elongatum ◽  
Synthetic Genome ◽  
Chromosome Associations ◽  
Chromosome Segments ◽  
The Relationship ◽  
Chromosome 3B

Chromosome pairing was studied in a number of hybrids involving a 56-chromosome wheat-Agropyron derivative, PW 327. PW 327 originated from the cross, Triticum aestivum cv. Chinese Spring (Chinese Spring × A. elongatum, 2n = 70). In hybrids between PW 327 and T. aestivum a number of multivalent chromosome associations were formed at metaphase I. These multivalents result from interchanges which occurred among wheat chromosomes 1A, 1D, 2A, 2D, 4D and 6D of PW 327. One chromosome of the Agropyron chromosome set of PW 327 occasionally pairs with wheat chromosome 3B. The rest of the Agropyron chromosomes present in PW 327 do not pair with the chromosomes of T. aestivum. It is proposed that the set of Agropyron chromosomes present in PW 327 is not an intact genome of decaploid A. elongatum but rather a modified synthetic genome combining chromosomes and/or chromosome segments from different genomes of the Agropyron parent. The incorporation of duplication-deletions into synthetic genomes of natural polyploids is discussed and it is shown that the set of Agropyron chromosomes which is present in PW 327 carries at least one such duplication-deletion. Pairing between chromosomes of diploid and decaploid A. elongatum was studied in a 56-chromosome hybrid from a cross between an amphiploid, T. aestivum × A. elongatum (2n = 14), and PW 327. It appeared that at least four chromosomes of these two Agropyrons occasionally paired with each other in this hybrid in which the diploidizing system of wheat was active. The relationship between chromosomes of diploid and decaploid A. elongatum is discussed.

Spontaneous somatic transfer of a segment from a wheat addition chromosome into the rye genome

Genome ◽  
1990 ◽  
Vol 33 (6) ◽  
pp. 794-797 ◽  
Author(s):  
G. Melz ◽  
V. Thiele
Keyword(s):  
Chromosome Pair ◽  
Wheat Chromosome ◽  
Centromeric Heterochromatin ◽  
Glutamate Oxaloacetate Transaminase ◽  
Specific Chromosome ◽  
Chromosome Addition ◽  
B Genome ◽  
Univalent Pair ◽  
Telomeric Heterochromatin ◽  
Chromosome 3B

Wheat chromosome 3B when added to the rye genome causes resistance to powdery mildew of rye (Erysiphe graminis DC. f.sp. secalis Marchal) as the result of the action of the gene Rpm1. Wheat chromosome 3B also carries the gene Got-B3 for glutamate oxaloacetate transaminase. In two independent, vegetatively reproduced additions of 3B to rye, the extra wheat chromosome appeared to have been lost spontaneously, but both genes were still present. The rye chromosome into which the genes had been transferred could not be identified. Chromosome 3R appeared to be morphologically unchanged, no telomeric heterochromatin normally present in any rye chromosome had disappeared, and no wheat B-genome centromeric heterochromatin was observed. At meiosis the chiasma frequency was reduced, resulting in the frequent formation of one univalent pair, and occasionally two univalent pairs. No specific chromosome pair was preferentially involved. The wheat genes could not be transferred to the progeny by selfing nor by reciprocal back-crossing, but gametes without these genes were functional. The plants were semisterile.Key words: wheat chromosome addition, rye, somatic translocation, univalents, mildew resistance.

The addition of Aegilops variabilis chromosomes to Triticum aestivum and their identification

1983 ◽  
Vol 25 (1) ◽  
pp. 76-84 ◽  
Author(s):  
D. C. Jewell ◽  
C. J. Driscoll
Keyword(s):  
Triticum Aestivum ◽  
Triticum Aestivum L ◽  
Addition Lines ◽  
Single Chromosome ◽  
Aegilops Umbellulata ◽  
Chromosome Addition ◽  
Aegilops Longissima ◽  
Chromosome Addition Lines ◽  
Aegilops Variabilis ◽  
The Relationship

Nine of the 14 possible single chromosome addition lines of the tetraploid species Aegilops variabilis Eig. (CuCuSvSv) to Triticum aestivum L. cv. Chinese Spring (AA BB DD) have been isolated and identified. The nine Aegilops variabilis addition lines were compared with the available addition lines of Aegilops umbellulata (CuCu) and Aegilops longissima (SvSv) to further elucidate the relationship between these two diploids and the tetraploid Aegilops variabilis. Differences were observed between the same chromosomes isolated from the diploid and the tetraploid and discussed. After taking into account banding pattern polymorphisms, Aegilops umbellulata was confirmed as the donor of the Cu genome, and evidence indicated that Aegilops longissima probably is the donor of the other genome (Sv) in the tetraploid Aegilops variabilis.

scholarly journals Production and Characterization of Maize Chromosome 9 Radiation Hybrids Derived From an Oat-Maize Addition Line

Genetics ◽  
2000 ◽  
Vol 156 (1) ◽  
pp. 327-339 ◽  
Author(s):  
O Riera-Lizarazu ◽  
M I Vales ◽  
E V Ananiev ◽  
H W Rines ◽  
R L Phillips
Keyword(s):  
Radiation Hybrid ◽  
Chromosome Region ◽  
Chromosome 9 ◽  
Addition Line ◽  
Addition Lines ◽  
Organization Studies ◽  
Maize Chromosome ◽  
Chromosome Addition ◽  
Radiation Hybrids ◽  
Chromosome Addition Lines

Abstract In maize (Zea mays L., 2n = 2x = 20), map-based cloning and genome organization studies are often complicated because of the complexity of the genome. Maize chromosome addition lines of hexaploid cultivated oat (Avena sativa L., 2n = 6x = 42), where maize chromosomes can be individually manipulated, represent unique materials for maize genome analysis. Maize chromosome addition lines are particularly suitable for the dissection of a single maize chromosome using radiation because cultivated oat is an allohexaploid in which multiple copies of the oat basic genome provide buffering to chromosomal aberrations and other mutations. Irradiation (gamma rays at 30, 40, and 50 krad) of a monosomic maize chromosome 9 addition line produced maize chromosome 9 radiation hybrids (M9RHs)—oat lines possessing different fragments of maize chromosome 9 including intergenomic translocations and modified maize addition chromosomes with internal and terminal deletions. M9RHs with 1 to 10 radiation-induced breaks per chromosome were identified. We estimated that a panel of 100 informative M9RHs (with an average of 3 breaks per chromosome) would allow mapping at the 0.5- to 1.0-Mb level of resolution. Because mapping with maize chromosome addition lines and radiation hybrid derivatives involves assays for the presence or absence of a given marker, monomorphic markers can be quickly and efficiently mapped to a chromosome region. Radiation hybrid derivatives also represent sources of region-specific DNA for cloning of genes or DNA markers.

scholarly journals A Duplicated Copy of the Meiotic Gene ZIP4 Preserves up to 50% Pollen Viability and Grain Number in Polyploid Wheat

Biology ◽  
2021 ◽  
Vol 10 (4) ◽  
pp. 290
Author(s):  
Abdul Kader Alabdullah ◽  
Graham Moore ◽  
Azahara C. Martín
Keyword(s):  
Pollen Viability ◽  
Pollen Grains ◽  
Wheat Chromosome ◽  
Grain Number ◽  
Meiotic Gene ◽  
Chromosome 5B ◽  
Mutant Pollen ◽  
Female Gametogenesis ◽  
Chromosome 3B

Although most flowering plants are polyploid, little is known of how the meiotic process evolves after polyploidisation to stabilise and preserve fertility. On wheat polyploidisation, the major meiotic gene ZIP4 on chromosome 3B duplicated onto 5B and diverged (TaZIP4-B2). TaZIP4-B2 was recently shown to promote homologous pairing, synapsis and crossover, and suppress homoeologous crossover. We therefore suspected that these meiotic stabilising effects could be important for preserving wheat fertility. A CRISPR Tazip4-B2 mutant was exploited to assess the contribution of the 5B duplicated ZIP4 copy in maintaining pollen viability and grain setting. Analysis demonstrated abnormalities in 56% of meiocytes in the Tazip4-B2 mutant, with micronuclei in 50% of tetrads, reduced size in 48% of pollen grains and a near 50% reduction in grain number. Further studies showed that most of the reduced grain number occurred when Tazip4-B2 mutant plants were pollinated with the less viable Tazip4-B2 mutant pollen rather than with wild type pollen, suggesting that the stabilising effect of TaZIP4-B2 on meiosis has a greater consequence in subsequent male, rather than female gametogenesis. These studies reveal the extraordinary value of the wheat chromosome 5B TaZIP4-B2 duplication to agriculture and human nutrition. Future studies should further investigate the role of TaZIP4-B2 on female fertility and assess whether different TaZIP4-B2 alleles exhibit variable effects on meiotic stabilisation and/or resistance to temperature change.

scholarly journals Mutator-Induced Mutations of the rf1 Nuclear Fertility Restorer of T-Cytoplasm Maize Alter the Accumulation of T-urfl3 Mitochondrial Transcripts

Genetics ◽  
1996 ◽  
Vol 143 (3) ◽  
pp. 1383-1394
Author(s):  
Roger P Wise ◽  
Carren L Dill ◽  
Patrick S Schnable
Keyword(s):  
Pollen Fertility ◽  
Fertility Restoration ◽  
Mitochondrial Rna ◽  
Induced Mutations ◽  
Male Sterile ◽  
Fertility Restorer ◽  
Restorer Genes ◽  
Mitochondrial Transcripts ◽  
Ecori Restriction ◽  
Fertility Restorer Genes

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.

scholarly journals Cosegregation of Single Genes Associated with Fertility Restoration and Transcript Processing of Sorghum Mitochondrial orf107 and urf209

Genetics ◽  
1998 ◽  
Vol 150 (1) ◽  
pp. 383-391 ◽  
Author(s):  
Hoang V Tang ◽  
Ruying Chang ◽  
Daryl R Pring
Keyword(s):  
Fertility Restoration ◽  
Mitochondrial Gene ◽  
Pollen Viability ◽  
Single Gene ◽  
Dominant Gene ◽  
Nuclear Gene ◽  
Male Sterile ◽  
Reading Frame ◽  
Transcript Processing ◽  
Backcross Populations

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.

scholarly journals The Dynamics of Gynodioecy in Plantago lanceolatu L. II. Mode of Action and Frequencies of Restorer Alleles

Genetics ◽  
1997 ◽  
Vol 147 (3) ◽  
pp. 1317-1328
Author(s):  
Anita A de Haan ◽  
Hans P Koelewijn ◽  
Maria P J Hundscheid ◽  
Jos M M Van Damme
Keyword(s):  
Cytoplasmic Male Sterility ◽  
Male Sterility ◽  
Allele Frequency ◽  
Mode Of Action ◽  
Male Fertility ◽  
Fertility Restoration ◽  
Plantago Lanceolata ◽  
Allele Frequencies ◽  
Male Sterile ◽  
Male Fertility Restoration

Male fertility in Plantago lanceolata is controlled by the interaction of cytoplasmic and nuclear genes. Different cytoplasmic male sterility (CMS) types can be either male sterile or hermaphrodite, depending on the presence of nuclear restorer alleles. In three CMS types of P. lanceolata (CMSI, CMSIIa, and CMSIIb) the number of loci involved in male fertility restoration was determined. In each CMS type, male fertility was restored by multiple genes with either dominant or recessive action and capable either of restoring male fertility independently or in interaction with each other (epistasis). Restorer allele frequencies for CMSI, CMSIIa and CMSIIb were determined by crossing hermaphrodites with “standard” male steriles. Segregation of male steriles vs. non-male steriles was used to estimate overall restorer allele frequency. The frequency of restorer alleles was different for the CMS types: restorer alleles for CMSI were less frequent than for CMSIIa and CMSIIb. On the basis of the frequencies of male steriles and the CMS types an “expected” restorer allele frequency could be calculated. The correlation between estimated and expected restorer allele frequency was significant.

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