Interaction between wheat chromosomes and rye telomeric heterochromatin on meiotic pairing of chromosome pair 1R of rye in wheat-rye derivatives

Chromosoma ◽  
1980 ◽  
Vol 81 (2) ◽  
pp. 249-261 ◽  
Author(s):  
T. Naranjo ◽  
J. R. Lacadena
Genetics ◽  
1983 ◽  
Vol 104 (4) ◽  
pp. 677-684
Author(s):  
J L Santos ◽  
J Orellana ◽  
R Giraldez

ABSTRACT Meiotic pairing preferences between identical and homologous but not identical chromosomes were analyzed in spontaneous tetraploid/diploid chimeras of three male grasshoppers (Eyprepocnemis plorans) whose chromosome pair 11 were heterozygous for C-banding pattern and in four induced tetraploid/diploid chimaeral rye plants (Secale cereale) heterozygous for telomeric heterochromatin C-bands in chromosomes 1R and 2R. In the grasshoppers, a preference for identical over homologous pairing was observed, whereas in rye both a preference for homologous rather than identical pairing and random pairing between the four chromosomes of the set was found. From the results in rye, it can be deduced that pairing preferences do not depend exclusively on the similarities between chromosomes involved. It is suggested that genotypic or cryptic structural differences between the homologous chromosomes of each pair analyzed might be responsible for the pairing preferences found. This hypothesis can also explain the results obtained in grasshoppers, although the possibility of premeiotic association cannot be excluded in this material.


1986 ◽  
Vol 28 (3) ◽  
pp. 420-425 ◽  
Author(s):  
P. K. Gupta ◽  
George Fedak

Intergeneric hybrids were obtained between Hordeum parodii Covas s.1. (6x) and three cultivars of triticale (×Triticosecale) at frequencies of 0.47 to 1.21% of pollinated florets. The triticale cultivars varied in their chromosome constitutions of the rye genome as well as the telomeric heterochromatin content of some of the rye chromosomes. The average chiasmata frequency per cell varied from 0.58 to 13.14 in different hybrid combinations. The differences in the chiasmata frequencies in the different hybrid combinations were attributed to a meiotic pairing control mechanism in H. parodii whose function was affected primarily by the rye chromosome constitutions of the triticale cultivars and to a lesser extent by the heterochromatin content of the rye chromosomes.Key words: hybrids (intergeneric), Hordeum, meiotic pairing control, chiasma.


Genome ◽  
1990 ◽  
Vol 33 (6) ◽  
pp. 794-797 ◽  
Author(s):  
G. Melz ◽  
V. Thiele

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.


Genome ◽  
1987 ◽  
Vol 29 (4) ◽  
pp. 554-561 ◽  
Author(s):  
Adam J. Lukaszewski ◽  
Barbara Apolinarska ◽  
J. Perry Gustafson ◽  
K.-D. Krolow

Among 38 lines of tetraploid triticale analyzed at meiosis, the number of paired arms per rye chromosome ranged from 1.14 to 1.76 and from 1.46 to 1.96 per wheat chromosome. The frequency of cells without univalents ranged from 22 to 90%. Pairing frequencies within rye and wheat genomes were correlated in all groups of lines. Lines without wheat chromosome 3B showed reduced pairing in both genomes, while lines with an additional pair of 5R chromosomes substituted for group-5 wheat chromosomes showed improved pairing of the rye genome but not of the wheat genome. In the rye genome, the chromosome arms that carry major blocks of telomeric heterochromatin paired with an average of 25.1% lower frequency than the arms without the telomeric heterochromatin, the difference being attributed to the difference in arm length and not to the presence of heterochromatic blocks. In the wheat genome, chromosome arms IBS, 5AS, and 5BS and chromosomes 4A and 7B paired with significantly lower frequency than the remaining arms of wheat chromosomes. Average aneuploid frequency in a sample of 1383 plants was 4.55%, with the mean value of 5.77% in lines with 14 wheat and 14 rye chromosomes, and 2.01% in lines with an extra pair of 5R chromosomes. The results indicate that while the meiotic pairing is poorer and aneuploid frequency is higher than previously believed, tetraploid triticales are nevertheless chromosomally much more stable than hexaploid or octoploid triticales. Key words: C-banding, heterochromatin, paired arms, chromosome substitution.


1984 ◽  
Vol 26 (1) ◽  
pp. 46-49 ◽  
Author(s):  
J. E. Dillé ◽  
J. P. Gustafson ◽  
M. D. Bennett

The relationship between the frequency of aneuploids and blocks of telomeric heterochromatin on rye (Secale cereale L.) chromosomes in a triticale (× Triticosecale Wittmack) background was investigated. Lines with or without blocks of telomeric heterochromatin were examined to determine the percentage of aneuploid progeny. The results showed that the amount of telomeric heterochromatin present on rye chromosomes 4R and 6R had little effect (2%) on lowering the proportion of aneuploids. When rye chromosome pair 2R was replaced by wheat chromosome 2D in the presence of chromosomes 4R and 6R lacking heterochromatin, the percentage of aneuploids increased slightly (2.7%) over that found in the control population.


1982 ◽  
Vol 24 (1) ◽  
pp. 93-100 ◽  
Author(s):  
M. D. Bennett ◽  
J. P. Gustafson

The influence of telomeric heterochromatin blocks on early embryo and endosperm development, and on various agronomic parameters seen at maturity, was investigated using triticales (× Triticosecale Wittmack) isogenic for the presence or absence of the heterochromatin blocks on rye (Secale cereale L.) chromosomes 6R and 7R/4R. Absence of the telomeric heterochromatin blocks from the long arm of rye chromosome pair 7R/4R in DRIRA, and from the short arm of rye chromosome pair 6R in Rosner was significantly related with a lower production of aberrant endosperm nuclei and an increased kernel weight. The loss of the heterochromatin block on rye chromosome pair 7R/4R in DRIRA resulted in a significant yield increase, while there was no increase in yield when the heterochromatin block was missing from rye chromosome pair 6R in Rosner. The lack of yield increase in Rosner was apparently due to a significant decrease in fertility when the heterochromatin block on 6R was lost. The loss of the heterochromatin block on the short arm of rye chromosome 6R appears to have the same effect on aberrant endosperm nuclei production and kernel weight in two different genetic backgrounds. The rate of embryo and endosperm development showed a small but significant increase when the heterochromatin blocks were lost from both 6R and 7R/4R.


Genetics ◽  
1998 ◽  
Vol 149 (1) ◽  
pp. 143-155 ◽  
Author(s):  
Bruce D McKee ◽  
Kathy Wilhelm ◽  
Cynthia Merrill ◽  
Xiao-jia Ren

Abstract In Drosophila melanogaster, deletions of the pericentromeric X heterochromatin cause X-Y nondisjunction, reduced male fertility and distorted sperm recovery ratios (meiotic drive) in combination with a normal Y chromosome and interact with Y-autosome translocations (T(Y;A)) to cause complete male sterility. The pericentromeric heterochromatin has been shown to contain the male-specific X-Y meiotic pairing sites, which consist mostly of a 240-bp repeated sequence in the intergenic spacers (IGS) of the rDNA repeats. The experiments in this paper address the relationship between X-Y pairing failure and the meiotic drive and sterility effects of Xh deletions. X-linked insertions either of complete rDNA repeats or of rDNA fragments that contain the IGS were found to suppress X-Y nondisjunction and meiotic drive in Xh−/Y males, and to restore fertility to Xh−/T(Y;A) males for eight of nine tested Y-autosome translocations. rDNA fragments devoid of IGS repeats proved incapable of suppressing either meiotic drive or chromosomal sterility. These results indicate that the various spermatogenic disruptions associated with X heterochromatic deletions are all consequences of X-Y pairing failure. We interpret these findings in terms of a novel model in which misalignment of chromosomes triggers a checkpoint that acts by disabling the spermatids that derive from affected spermatocytes.


1984 ◽  
Vol 26 (5) ◽  
pp. 564-568 ◽  
Author(s):  
Orlando Moreira-Filho ◽  
Luiz Antonio Carlos Bertollo ◽  
Pedro Manoel Galetti Jr.

Nucleolar organizer regions (NORs) were studied in mitotic chromosomes of four species of fish of family Parodontidae: Parodon tortuosus, Apareiodon affinis, Apareiodon ibitiensis, and Apareiodon piracicabae. All four species exhibited only a single nucleolar chromosome pair in their karyotypes. Intraspecific differences were observed in the size of these chromosomes; however, these were not very clear for A. affinis and A. piracicabae, Apareiodon piracicabae exhibited two clearly visible NORs in each of the nucleolar chromosomes, which was the only configuration practically found in this species. This trait therefore predominates in a homozygous condition in the population investigated. Regions of constitutive heterochromatin adjacent to the two NORs were detected. Possible mechanisms that may have originated the two NORs are discussed.Key words: nucleolar organizing regions, fish.


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