Variation in induction of homoeologous chromosome pairing in 6x Aegilops crassa by genomes of six different species of Secale

1985 ◽  
Vol 27 (5) ◽  
pp. 531-537 ◽  
Author(s):  
P. K. Gupta ◽  
George Fedak

Meiosis was studied in hybrids between Aegilops crassa (Boiss.) Hitch and Hensl. (2n = 6x = 42) having the genomes DD2MCr and six species of Secale. The chiasmata frequency per cell ranged from 6.86 in hybrids with S. cereale to 9.93 in hybrids with S. montanum ssp. dalmaticum. These results provide further evidence that a meiotic pairing control system is operating in Ae. crassa. The Secale genotypes suppress the function of this system in a manner which was inversely related to their heterochromatin content and total DNA content.Key words: Secale, Aegilops, chiasmata, meiotic pairing control, hybrids.

Genome ◽  
1991 ◽  
Vol 34 (2) ◽  
pp. 228-235 ◽  
Author(s):  
A. E. Dollin ◽  
J. D. Murray ◽  
C. B. Gillies

The mechanisms of homoeologous chromosome pairing were studied in synaptonemal complex (SC) spreads of F1 Brahman (Bos indicus) × Hereford (Bos taurus) cattle. The most common SC abnormalities were bivalents with partial pairing failure and interlocks. While C-band polymorphisms could underlie most of the SC abnormalities observed in the full-blood cattle, other causes seem also to be contributing in the hybrids. The pattern of the abnormalities indicates that genie differences between the species were probably involved. Pachytene substaging data suggest that in some spreads, early pachytene bivalents with partial pairing failure may achieve complete synapsis or may be converted to interlocks by late pachytene.Key words: synaptonemal complex, hybrid cattle, interlocks.


Genome ◽  
1988 ◽  
Vol 30 (2) ◽  
pp. 204-210 ◽  
Author(s):  
R. von Bothmer ◽  
N. C. Subrahmanyam

Meiotic pairing was studied in the following species and their haploid derivatives: Hordeum cordobense 2x, H. marinum 2x and 4x, H. secalinum 4x, H. capense 4x, H. jubatum 4x, H. brachyantherum 4x and 6x, H. lechleri 6x, and H. procerum 6x. The study revealed (i) homologous pairing in diploid species and very little nonhomologous associations in their mono-haploids; (ii) the alloploid nature of the polyploid taxa; (iii) a certain degree of homoeologous pairing in polyhaploids despite the diploid-like meiotic behaviour of the polyploids; (iv) genetic variation in the suppression of homoeologous chromosome pairing in different Hordeum species.Key words: Hordeum, meiotic pairing, haploids.


1982 ◽  
Vol 24 (6) ◽  
pp. 715-719 ◽  
Author(s):  
E. R. Sears

An X-ray-induced mutation in common wheat (Triticum aestivum L.), designated ph2, conditions an intermediate level of homoeologous chromosome pairing in hybrids with Triticum kotschyi var. variabilis. The number of chromosomes paired averaged 9.2 per sporocyte, compared with 2.0 in the control and 27.9 in the same hybrid involving ph1b, an apparent deficiency for Ph1 obtained in the same mutation experiment. The ph2 mutation is located on chromosome 3D and is believed to be a deficiency for a terminal segment of the short arm that includes the locus of Ph2, a minor suppressor of homoeologous pairing. Although no pairing of the ph2-carrying chromosome with telosome 3DS was observed, the mutation is clearly not a deficiency for the entire arm. It has little effect on pairing in wheat itself. Male transmission of the mutation is approximately normal, and fertility, while reduced, is sufficient for easy maintenance of the homozygous line.


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.


1983 ◽  
Vol 61 (6) ◽  
pp. 1809-1814 ◽  
Author(s):  
Kathryn Carvey Crist ◽  
Donald R. Farrar

Solitary plants of Asplenium platyneuron occur disjunctively on recently produced coal spoils in southern Iowa. They are assumed to have been produced by self-fertilization of isolated gametophytes and therefore highly homozygous. Cultures of isolated and paired gametophytes originating from these solitary sporophytes produced second-generation sporophytes with 89 and 93% success, respectively, indicating a low genetic load as expected. The failure of gametophytes from coal-spoil plants to produce sporophytes with even greater success may result from homoeologous chromosome pairing and recombination at meiosis which allows production of variable spores and expression of genetic load from plants produced by self-fertilization of single gametophytes. Cultures of isolated and paired gametophytes originating from sporophytes in populations central to the species' range produced second-generation sporophytes with 83 and 90% success, respectively, indicating a significantly greater genetic load in populations but still a relatively low genetic load for the species. Through low genetic load, regularity of sporophyte production from isolated gametophytes, and ability of such plants to release variability through homoeologous chromosome pairing, Asplenium platyneuron is remarkably adapted for, and successful in, colonizing distant habitats through long-range spore dispersal.


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.


1979 ◽  
Vol 21 (1) ◽  
pp. 65-71 ◽  
Author(s):  
K. C. Armstrong

Homoeology between the A and B genomes of allotetraploid (2n = 4x = 28) AiAiBiBi and autoallooctoploid (2n = 8x = 56) AIAIAIAIBIBIBIBI cytotypes of B. inermis Leyss. was studied in a tetraploid F1 hybrid (AeAeAiBi) from 4x B. erectus × 4x B. inermis and in a haplo-triploid (AIeAIeBI) which occurred spontaneously in the F2 from open-pollination among plants of the hexaploid F1 hybrid (AeAeAIAIBIBI) from 4x B. erectus × 8x B. inermis. Chromosome pairing at metaphase I in both the tetraploid (AeAeAiBi) and haplo-triploid (AIeAIeBI) indicated that for each A genome chromosome there was a corresponding B genome homoeologue. There was no convincing evidence of gross structural differences between the two homoeologous genomes. The frequency of trivalent formation in the haplo-triploid was approximately one-half that found in two pentaploids (2n = 5x = 35) AIeAIeAIBIBI. This indicates that the pairing affinity between the A and B genomes is one-half that between homologues as expressed by trivalent formation in triploids of the type AAB and AAA. Homoeologous chromosome pairing (A with B) may be controlled by a gene which is hemizygous ineffective.


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