Cytological identification of telotrisomic and double ditelosomic lines in Secale cereale cv. Heines Hellkorn by means of Giemsa C-banding patterns and crosses with wheat–rye addition lines

Genome ◽  
1987 ◽  
Vol 29 (1) ◽  
pp. 58-62 ◽  
Author(s):  
Friedrich J. Zeller ◽  
Mari-Carmen Cermeño ◽  
Bernd Friebe
Keyword(s):  
Key Words ◽  
Secale Cereale ◽  
Banding Pattern ◽  
Addition Lines ◽  
Banding Patterns ◽  
Chromosome Addition ◽  
C Banding ◽  
Chromosome Addition Lines

Seven telotrisomic lines (1RS, 1RL, 2RS, 2RL, 3RS acro, 5RS, and 6RS), two double monotelosomic, and two double ditelosomic lines of Secale cereale cv. Heines Hellkorn were analyzed by means of Giemsa C-banding techniques. In crosses with several wheat–rye chromosome addition lines, the telosomic chromosomes in double ditelosomic lines 1/23 and 3/23 were found to be homologous to chromosomes 1R and 2RL of cv. Imperial rye. The C-banding pattern observed for the telosomes in these lines was similar to that detected in the 1R and 2R telosomics of the corresponding telotrisomic lines. Key words: Secale cereale, telotrisomics, double ditelosomics, C-banding pattern.

Cytogenetic identification of Triticum peregrinum chromosomes added to common wheat

Genome ◽  
1996 ◽  
Vol 39 (2) ◽  
pp. 272-276 ◽  
Author(s):  
B. Friebe ◽  
E. D. Badaeva ◽  
B. S. Gill ◽  
N. A. Tuleen
Keyword(s):  
Triticum Aestivum ◽  
Key Words ◽  
Common Wheat ◽  
Addition Lines ◽  
Karyotypic Analysis ◽  
Chromosome Addition ◽  
C Banding ◽  
Chromosome Addition Lines ◽  
Complete Set ◽  
Donor Species

C-banded karyotypes of a complete set of 14 Triticum peregrinum whole chromosome addition lines and 25 telosomic addition lines are reported. The added T. peregrinum chromosomes were not structurally rearranged compared with the corresponding chromosomes of the donor accession. Comprehensive karyotypic analysis confirmed Triticum umbellulatum as the donor species of the Uv genome and identified Triticum longissimum as the donor species of the Sv genome of T. peregrinum. Neither the Uv nor Sv genome chromosomes of the T. peregrinum accession showed large modifications when compared with the ancestral U and S1 genomes. Key words : Triticum aestivum, Triticum peregrinum, Triticum umbellulatum, Triticum longissimum, chromosome addition lines, C-banding.

A TENTATIVE IDENTIFICATION OF CHROMOSOMES PRESENT IN TETRAPLOID TRITICALE BASED ON HETEROCHROMATIC BANDING PATTERNS

1978 ◽  
Vol 20 (2) ◽  
pp. 199-204 ◽  
Author(s):  
J. P. Gustafson ◽  
K. D. Krolow
Keyword(s):  
Secale Cereale ◽  
Banding Pattern ◽  
Triticum Turgidum ◽  
Staining Technique ◽  
Wheat Genome ◽  
Banding Patterns ◽  
Tentative Identification ◽  
C Banding ◽  
B Genome ◽  
Secale Cereale L

Three tetraploid triticales were analysed by C-banding techniques in order to establish their chromosome constitutions. All three tetraploid triticales contained seven rye chromosomes with the banding pattern of Secale cereale L. A mixture of A- and B-genome chromosomes from Triticum turgidum L. constituted the wheat genome present in the tetraploid triticales. Triticale Trc 4x3 contained 1A, 2B, 3A, 4A, 5B, 6A, and 7B. Triticale Trc 4x2 contained 1A, 2B, 3B, 4B, 5B, 6A, and 7B, while triticale Trc 4x5 contained 1A, 2B, 3B, 4A, 5A, 6A, and 7B. The reliability of the staining technique is subject to errors in identification, which are discussed.

Standard karyotype of Triticum longissimum and its cytogenetic relationship with T. aestivum

Genome ◽  
1993 ◽  
Vol 36 (4) ◽  
pp. 731-742 ◽  
Author(s):  
Bernd Friebe ◽  
Neal Tuleen ◽  
Jiming Jiang ◽  
Bikram S. Gill
Keyword(s):  
In Situ Hybridization ◽  
Addition Line ◽  
Addition Lines ◽  
Substitution Lines ◽  
Chromosome Addition ◽  
C Banding ◽  
Chromosome Addition Lines ◽  
Standard Karyotype ◽  
Fertility Genes

C-banding polymorphism was analyzed in 17 accessions of Triticum longissimum from Israel and Jordan, and a generalized idiogram of this species was established. C-banding analysis was further used to identify two sets of disomic T. aestivum – T. longissimum chromosome addition lines and 13 ditelosomic addition lines and one monotelosomic (6S1L) addition line. C-banding was also used to identify T. aestivum – T. longissimum chromosome substitution and translocation lines. Two major nucleolus organizing regions (NORs) on 5S1 and 6S1 and one minor NOR on 1S1 were detected by in situ hybridization using a 18S–26S rDNA probe. Sporophytic and gametophytic compensation tests were used to determine the homoeologous relationships of T. longissimum chromosomes. The T. longissimum chromosomes compensate rather well and fertility was restored even in substitution lines involving wheat chromosomes 2A, 4B, and 6B that contain major fertility genes. Except for the deleterious gametocidal genes, T. longissimum can be considered as a suitable donor of useful genes for wheat improvement.Key words: Triticum aestivum, Triticum longissimum, homoeology, C-banding, in situ hybridization.

Development and identification of a complete set of Triticum aestivum - Aegilops geniculata chromosome addition lines

Genome ◽  
1999 ◽  
Vol 42 (3) ◽  
pp. 374-380 ◽  
Author(s):  
Bernd R Friebe ◽  
Neal A Tuleen ◽  
Bikram S Gill
Keyword(s):  
Triticum Aestivum ◽  
Chromosome Breakage ◽  
Meiotic Pairing ◽  
Addition Lines ◽  
Aegilops Geniculata ◽  
Chromosome Addition ◽  
C Banding ◽  
Chromosome Addition Lines ◽  
Complete Set ◽  
Gametocidal Gene

The production and identification of a complete set of intact Aegilops geniculata chromosome and telosome additions to common wheat is described. All Ug and Mg genome chromosomes were tentatively assigned to their homoeologous groups based on C-banding, meiotic metaphase I pairing analyses and plant morphologies. Thirteen disomic and one monosomic wheat-Ae. geniculata chromosome additions were identified. Furthermore, two monotelosomic (MtA7UgL, MtA7MgL) and nine ditelosomic (DtA1UgS, DtA1UgL, DtA2UgS, DtA1MgL, DtA2MgL, DtA3MgS, DtA5MgS, DtA6MgL, DtA7MgS) wheat-Ae. geniculata additions were recovered. C-banding and meiotic pairing analyses revealed that all added Ug and Mg genome chromosomes are structurally unaltered compared to the Ae. geniculata parent accession. Chromosome 4Mg has a strong gametocidal gene that, when transferred to wheat, causes extensive chromosome breakage mainly in gametes lacking it. The relationships of Ae. geniculata chromosomes with those of the diploid progenitor species and derived polyploids is discussed.Key words: Triticum aestivum, Aegilops geniculata, chromosome addition lines, C-banding, genome evolution.

scholarly journals The genetic control of triosephosphate isomerase of hexaploid wheat and other Triticeae species

1985 ◽  
Vol 45 (2) ◽  
pp. 127-142 ◽  
Author(s):  
Michael E. Pietro ◽  
Gary E. Hart
Keyword(s):  
Triticum Aestivum ◽  
Hordeum Vulgare ◽  
Secale Cereale ◽  
Hexaploid Wheat ◽  
Chinese Spring ◽  
Triosephosphate Isomerase ◽  
Addition Lines ◽  
Chromosome Addition ◽  
Chromosome Addition Lines ◽  
Derivatives Of

SummaryThe zymogram phenotypes of triosephosphate isomerase (TPI) were determined for a large number of aneuploid derivatives of Triticum aestivum cv. ‘Chinese Spring’ and for six wheat-alien species chromosome addition series. Examination of the available compensating nullisomic-tetrasomic and homoeologous groups 3 and 5 ditelosomic lines of Chinese Spring disclosed that T. aestivum possesses two systems of dimeric TPI isozymes, designated TPI-1 and TPI-2. The genes TPI-A1, TPI-B1 and TPI-D1 were located in Chinese Spring chromosome arms 3Ap, 3Bp and 3Dp, respectively and the genes TPI-A2, TPI-B2 and TPI-D2 in chromosome arms 5Aq, 5Bq and 5Dq, respectively. TPI-1 genes were also located in Hordeum vulgare cv. Betzes chromosome 3H, T. longissimum chromosome G, Elytrigia elongata chromosome 3E, and Secale cereale cvs. Imperial and Dakold chromosome 3R. TPI-2 genes were found in Betzes chromosome 5H, T. umbellulatum chromosome 5U, T. longissimum chromosome F, and Imperial and Dakold chromosome 5R. These gene locations provide evidence of homoeology between the alien chromosomes in which the genes are located and the chromosomes of homoeologous groups 3 and 5 of Chinese Spring, respectively. Evidence was obtained for the presence of a TPI-R2 gene in each of the T. aestivum cv. Kharkov -S. cereale cv. Dakold chromosome addition lines studied suggesting that this gene is present in the wheat genome in each member of this addition series.

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.

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