Cytological and molecular characterization of a Triticum aestivum × Lophopyrum ponticum backcross derivative resistant to barley yellow dwarf

Genome ◽  
1994 ◽  
Vol 37 (5) ◽  
pp. 876-881 ◽  
Author(s):  
Gan-Yuan Zhong ◽  
Patrick E. Mcguire ◽  
Calvin O. Qualset ◽  
Jan Dvořák

Barley yellow dwarf is the most damaging virus-caused disease in bread wheat (Triticum aestivum L.). A resistant line, SW335.1.2-13-11-1-5 (2n = 47), derived from a cross of T. aestivum × Lophopyrum ponticum was characterized by meiotic chromosome pairing, by in situ DNA hybridization and by expression of molecular markers to determine its chromosome constitution. All progeny of this line had three pairs of L. ponticum chromosomes from homoeologous chromosome groups 3, 5, and 6 and the 2n = 47 progeny had an additional L. ponticum monosome. The pairs from groups 3 and 6 were in the added state, while the group 5 pair was substituted for wheat chromosome 5D. Several wheat–wheat translocations with respect to the parental wheat genotype occurred in this line, presumably owing to the promotion of homoeologous chromosome pairing by L. ponticum chromosomes. It was hypothesized that homoeologous recombination results in homoeologous duplication–deletions in wheat chromosomes. An aberrant 3:1 disjunction creates the potential at each meiosis for replacement of these wheat chromosomes by homoeologous L. ponticum chromosomes. Wheat chromosomes 3A and 6A appeared to be in intermediate stages of this substitution process.Key words: wheat, wheatgrass, Lophopyrum, barley yellow dwarf virus, disease resistance, homoeologous chromosome recombination, homoeologous pairing, alien chromosome substitution.

Genome ◽  
1987 ◽  
Vol 29 (2) ◽  
pp. 221-224
Author(s):  
G. Ganeva ◽  
B. Bochev

The effect of nullisomy for D-genome chromosomes and chromosome 5B on the meiotic behaviour of pollen mother cell chromosomes of pentaploid F1 hybrids of Triticum aestivum (cv. Bezostaya 1) × T. dicoccoides (Körn) was studied. The functional ability of female gametes with diverse chromosome constitution and the frequency of their inheritance in BC1 was assessed. Absence of individual T. aestivum D-genome chromosomes had a specific effect on meiotic chromosome pairing. The genetic systems involving chromosome 5B of the two species did not have the same effect on homologous and homoeologous chromosome pairing. Chromosome 5B of T. dicoccoides reduced bivalent pairing and increased multivalent associations. In BC1 the frequency of female gametes with n = 16–18 chromosomes was highest. Key words: nullisomy, chromosome pairing, Triticum, pentaploid hybrids.


1992 ◽  
Vol 109 (2) ◽  
pp. 123-129 ◽  
Author(s):  
K. K. Nkongolo ◽  
K. C. Armstrong ◽  
A. Comeau ◽  
C. A. St. Pierre

1977 ◽  
Vol 19 (3) ◽  
pp. 549-556 ◽  
Author(s):  
J. Dvořák

The number of chiasmata per cell at metaphase I was scored in eight haploid plants of Triticum aestivum L. emend. Thell. cv. 'Chinese Spring' and 100 hybrid plants of Chinese Spring × Secale cereale L. Mean chiasma frequency per cell ranged from 0.00 to 3.59 in the hybrids and from 0.17 to 0.35 in the haploids. Since the same wheat genotype was present in both the haploids and hybrids, it is concluded that some of the rye genotypes promoted homoeologous chromosome pairing. The absence of distinct segregation classes among the hybrids suggests that these genes constitute a polygenic system.


1970 ◽  
Vol 12 (2) ◽  
pp. 278-282 ◽  
Author(s):  
C. J. Driscoll ◽  
C. J. Quinn

Genetic differences which affect the extent of homoeologous chromosome pairing in intergeneric hybrids have been demonstrated between varieties of Triticum aestivum. Each of seven varieties of Triticum was crossed with the same strain of Aegilops variabilis. Significant differences in chiasma frequencies between varieties were found. Varieties Eureka, Gamut and Chinese Spring constitute one group with a relatively low chiasma frequency and varieties A. R. Falcon, Federation and Poso constitute a distinct second group with a relatively high chiasma frequency. The variety Bearded Yalta is intermediate to the two groups. Thus, this genetic variation appears to be common among varieties of Triticum. Presumably this variation does not become subject to natural selection as long as chromosome pairing in the parental varieties remains strictly homologous.


Plant Disease ◽  
2009 ◽  
Vol 93 (9) ◽  
pp. 964-964 ◽  
Author(s):  
J. K. Kundu

Barley yellow dwarf disease, a ubiquitous virus disease of cereal crops worldwide, is caused by a group of related, single-stranded RNA viruses assigned to Luteovirus (Barley yellow dwarf virus [BYDV] spp. PAV, PAS, MAV, and GAV) or Polerovirus (Cereal yellow dwarf virus-RPV) genera or unassigned to a genera (BYDV-SGV, BYDV-RMV, and BYDV-GPV) in the family Luteoviridae (1). Incidence of BYDV in cereal crops (e.g., barley, wheat, and oats) was high, and in recent years, reached epidemic levels in many regions of the Czech Republic. BYDV-PAV and BYDV-PAS have been identified in Czech cereal crops (2,4). Surveys of the incidence of BYDV were carried out using ELISA (SEDIAG SAS, Longvic, France) and one-step reverse transcription (RT)-PCR (Qiagen, Hilden, Germany) (2) during 2007 and 2008. Samples (125) were collected from different fields around the Czech Republic and 96 were BYDV positive. Three of the field isolates, CZ-6815, CZ-1561, and CZ-10844, from oat (Avena sativa; cv. Auron), winter wheat (Triticum aestivum; cv. Apache), and winter barley (Hordeum vulgare; cv. Merlot), respectively, were identified as BYDV-MAV by sequencing of the RT-PCR product (641-bp fragment) used to identify BYDV, which spanned 2839–3479 of the BYDV genome (GenBank Accession Nos. EF043235 and NC_002160) (2). The partial coat protein gene sequence of 483 nt was compared with the available sequences of 12 BYDV-PAV isolates (PAV-JP, PAV-NY, PAV-ILL, PAV-AUS, PAV-WG2, PAV-whG4y3, PAV-on21-4, Tahoe1, CA-PAV, HB3, FH3, and MA9501); nine BYDV-PAS isolates (PAS-129, PAS-64, WS6603, WG13, PAS-Tcb4-1, PASwaw5-9, FL2, PAS-Vd29, and PAS-MA9516); and six BYDV-MAV isolates (MAV-CA, MAV-PS1X1, MAV-Alameds268, LMB2a, SI-o4, and MAV-CN) by MEGA4 (3). Nucleotide and amino acid sequence identities for the three isolates ranged from 92.9 to 99.4% and 88.0 to 95.8%, respectively, for available BYDV-MAV isolates; 76.8 to 78.2% and 62.7 to 67.6%, respectively, for available BYDV-PAS isolates; and 77.6 to 79.3% and 65.5 to 70.4%, respectively, for available PAV isolates. The sequence data indicates that these isolates (CZ-6815, CZ-1561, and CZ10844; GenBank Accession Nos. FJ645747, FJ645758, and FJ645746, respectively) are BYDV-MAV. To my knowledge, this is the first record of BYDV-MAV in the Czech Republic. References: (1) C. J. D'Arcy and L. L. Domier. Page 891 in: Virus Taxonomy-8th Report of the ICTV. C. M. Fauquet et al., eds. Springer-Verlag, NY, 2005. (2) J. K. Kundu. Plant Dis. 92:1587, 2008. (3) K. Tamura et al. Mol. Biol. Evol. 24:1596, 2007. (4) J. Vacke. Page 100 in: Sbornik Referatu z Odborneho Seminare, Aktualni Problemy Ochrany Polnich Plodin, Praha, 1991.


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