Tetrasomic inheritance and chromosome pairing behaviour in the naturally occurring autotetraploid Heuchera grossulariifolia (Saxifragaceae)

Genome ◽  
1989 ◽  
Vol 32 (4) ◽  
pp. 655-659 ◽  
Author(s):  
Paul G. Wolf ◽  
Pamela S. Soltis ◽  
Douglas E. Soltis
Keyword(s):  
Chromosome Pairing ◽  
Meiotic Chromosome ◽  
Low Frequency ◽  
Small Chromosome ◽  
Tetrasomic Inheritance ◽  
Naturally Occurring ◽  
Chromatid Segregation ◽  
Marker Loci ◽  
Allozyme Loci ◽  
Pairing Behaviour

Inheritance patterns at four allozyme loci and chromosome pairing behaviour at diakinesis were examined in the naturally occurring autotetraploid Heuchera grossulariifolia. Segregation patterns for Tpi, Pgi, Pgm-2, and Lap deviated significantly from all possible disomic models. All patterns were consistent with tetrasomic inheritance of these marker loci. No chromatid segregation was detected electrophoretically. Meiotic chromosome configurations at diakinesis in 45 cells were compared with a previously published model to test for autopolyploid-like chromosome pairing. Using the observed chiasma frequencies, the frequency of quadrivalents was consistent with the expectations for an autotetraploid. We suggest that the low frequency of quadrivalents at diakinesis in Heuchera grossulariifolia is due to small chromosome size, which results in a low chiasma frequency.Key words: autopolyploidy, tetrasomic inheritance, chromosome pairing, isozyme genetics, Heuchera.

THE SIGNIFICANCE OF MEIOTIC CHROMOSOME PAIRING IN TETRAPLOID (2n = 28) BROMUS PUMPELLIANUS SCRIBN. SSP. DICKSONII

1972 ◽  
Vol 14 (4) ◽  
pp. 763-771 ◽  
Author(s):  
K. C. Armstrong
Keyword(s):  
Chromosome Pairing ◽  
High Frequency ◽  
Chiasma Frequency ◽  
Karyotype Analysis ◽  
Meiotic Chromosome ◽  
Low Frequency ◽  
Meiotic Chromosome Pairing ◽  
Ring Bivalents ◽  
Bivalent Formation

Bivalent formation was predominant at meiosis in B. pumpellianus ssp. dicksonii. The average in 15 plants ranged from 11.38 to 13.77 bivalents per cell. The high chiasma frequency (23.41-26.74) was a reflection of the high frequency of ring bivalents (9.48-12.42). A low frequency of quadrivalents occurred (0.06-1.22). A karyotype of this species was presented from both a highly contracted and moderately contracted cell and the differences between these two were noted. Four satellites were found, two large and two minute. There were 3-5 submedian and 5-7 median chromosomes depending on the cell studied. In addition two subterminal chromosomes were present. The meiotic and karyotype analysis suggest a deviation from an autotetraploid behaviour, but the presence of quadrivalents and similarities between pairs in the karyotype suggested closely related genomes. Alternatively it was considered that the quadrivalents could be due to translocation heterozygotes. The implications of these results were discussed in relation to the reported meiotic events in the octoploids, B. inermis and B. pumpellianus.

scholarly journals Meiotic chromosome pairing in triploid and tetraploid Saccharomyces cerevisiae.

Genetics ◽  
1995 ◽  
Vol 139 (4) ◽  
pp. 1511-1520 ◽  
Author(s):  
J Loidl
Keyword(s):  
Saccharomyces Cerevisiae ◽  
Complex Formation ◽  
Chromosome Segregation ◽  
Chromosome Pairing ◽  
Meiotic Chromosome ◽  
Low Frequency ◽  
Spore Viability ◽  
Homologous Chromosomes ◽  
Meiotic Chromosome Pairing ◽  
Synaptonemal Complex Formation

Abstract Meiotic chromosome pairing in isogenic triploid and tetraploid strains of yeast and the consequences of polyploidy on meiotic chromosome segregation are studied. Synaptonemal complex formation at pachytene was found to be different in the triploid and in the tetraploid. In the triploid, triple-synapsis, that is, the connection of three homologues at a given site, is common. It can even extend all the way along the chromosomes. In the tetraploid, homologous chromosomes mostly come in pairs of synapsed bivalents. Multiple synapsis, that is, synapsis of more than two homologues in one and the same region, was virtually absent in the tetraploid. About five quadrivalents per cell occurred due to the switching of pairing partners. From the frequency of pairing partner switches it can be deduced that in most chromosomes synapsis is initiated primarily at one end, occasionally at both ends and rarely at an additional intercalary position. In contrast to a considerably reduced spore viability (approximately 40%) in the triploid, spore viability is only mildly affected in the tetraploid. The good spore viability is presumably due to the low frequency of quadrivalents and to the highly regular 2:2 segregation of the few quadrivalents that do occur. Occasionally, however, quadrivalents appear to be subject to 3:1 nondisjunction that leads to spore death in the second generation.

Meiotic duration in wheat genotypes with or without homoeologous meiotic chromosome pairing

1974 ◽  
Vol 187 (1087) ◽  
pp. 191-207 ◽  
Keyword(s):  
Chromosome Pairing ◽  
Chinese Spring ◽  
Meiotic Chromosome ◽  
Meiotic Pairing ◽  
Homoeologous Pairing ◽  
Meiotic Chromosome Pairing ◽  
Chromosome 5B ◽  
Homoeologous Chromosome Pairing ◽  
The Cross ◽  
Pairing Behaviour

In order to investigate the possible relation between meiotic time and meiotic chromosome pairing behaviour, meiosis was timed in various forms of wheat and wheat hybrids. First, meiosis was timed in ten Triticum aestivum (var. Chinese Spring) genotypes with different chromosome constitutions which differed widely in the meiotic pairing behaviour. Secondly, in order to escape from the disadvantage of aneuploid material, meiosis was also timed in plants which differed in the extent of homoeologous pairing because of the activities of different alleles at one or two loci. For this experiment use was made of F 1 -hybrids from the cross T. aestivum x Aegilops mutica which, although they all have 28 chromosomes, differ widely in the amount of homoeologous pairing. Thirdly, meiosis was also timed in 28-chromosome and 29-chromosome plants derived from the cross between rye (Secale cereale) x 43-chromosome T. aestivum containing a single Ae. mutica addition chromosome known to carry genes which greatly affect the level of homoeologous pairing in wheat. Although the 28-chromosome plants display very little pairing (chiasma frequency per cell (c. f.) = 0.5) while 29-chromosome plants display a much higher amount of pairing (c. f. = 7.8) no difference in meiotic time was detected between them. Similarly, the duration of meiosis was not significantly different between the three types of F 1 -hybrids between T. aestivum x Ae. mutica which had chiasma frequencies of 14.3, 7.4 and 0.9. Thus, these results agree in showing that there was no correlation between the duration of meiosis and the amount of homoeologous chromosome pairing. The results obtained for genotypes of Chinese Spring also provided no evidence to support the notion that there is a relation between the level of chromosome pairing and the duration of the pairing process. Consequently some doubt must be cast upon the idea that the time available for pairing is limiting to the pairing process. It was shown that individual wheat chromosomes in Chinese Spring differed in their effects on meiotic duration. For instance, the absence of chromosome 7B has no detectable effect on meiotic duration. The absence of chromosome 5B in two genotypes resulted in an increase in meiotic time from that found in euploid plants (24 h) to that found in tetraploid wheat species (about 30 h). By using plants ditelosomic for chromosome 5B L it was shown that most, if not all, of the genetic effects of chromosome 5B on meiotic time are determined by the short arm.

Inferences from genetical evidence on the course of meiotic chromosome pairing in plants

1977 ◽  
Vol 277 (955) ◽  
pp. 313-326 ◽  
Keyword(s):  
Chromosome Pairing ◽  
Developmental Stages ◽  
Meiotic Chromosome ◽  
Critical Assessment ◽  
Gene Control ◽  
Meiotic Pairing ◽  
Homologous Chromosomes ◽  
Meiotic Chromosome Pairing ◽  
Combined Use ◽  
Or Gene

Meiotic chromosome pairing is a process that is amenable to genetic and experimental analysis. The combined use of these two approaches allows for the process to be dissected into several finite periods of time in which the developmental stages of pairing can be precisely located. Evidence is now available, in particular in plants, that shows that the pairing of homologous chromosomes, as observed at metaphase I, is affected by events occurring as early as the last premeiotic mitosis; and that the maintenance of this early determined state is subsequently maintained by constituents (presumably proteins) that are sensitive to either colchicine, temperature or gene control. A critical assessment of this evidence in wheat and a comparison of the process of pairing in wheat with the course of meiotic pairing in other plants and animals is presented.

Intergeneric hybrids of Hordeum vulgare with Agropyron caninum and A. dasystachyum

1985 ◽  
Vol 27 (4) ◽  
pp. 387-392 ◽  
Author(s):  
George Fedak
Keyword(s):  
Hordeum Vulgare ◽  
Chromosome Pairing ◽  
Meiotic Chromosome ◽  
Intergeneric Hybrids ◽  
Spindle Fibre ◽  
Chromosome Behavior ◽  
Paternal Parent ◽  
Agropyron Caninum

Hybrids were obtained by pollinating Hordeum vulgare cv. Betzes with Agropyron caninum (4x) and A. dasystachyum (4x) at frequencies of 1.4 and 6.1% of pollinated florets, respectively. The hybrids were sterile and phenotypically resembled the paternal parent, except for floret structure which was intermediate between the parental types. Chromosome pairing at meiosis was very low and thus provided no indication of homoeology between parental genomes. Abnormal meiotic chromosome behavior in meiocytes that occurred in sectors on the 'Betzes' × A. dasystachyum hybrid was attributed to abnormal spindle fibre function.Key words: intergeneric hybrids, Hordeum vulgare, Agropyron caninum, Agropyron dasystachyum.

Estimating meiotic chromosome pairing and recombination parameters in telocentric trisomics

Genome ◽  
2007 ◽  
Vol 50 (11) ◽  
pp. 1014-1028 ◽  
Author(s):  
J. Sybenga ◽  
H. Verhaar ◽  
D.G.A. Botje
Keyword(s):  
Gene Transfer ◽  
Chromosome Pairing ◽  
Genome Analysis ◽  
Meiotic Chromosome ◽  
Chiasma Formation ◽  
Chromosome Morphology ◽  
Test Material ◽  
Gene Localization ◽  
Maximum Information ◽  
Chromosome 1R

Telocentric trisomics (telotrisomics; one arm of a metacentric chromosome present in addition to two complete genomes) are used in theoretical studies of pairing affinities and chiasma formation in competitive situations and applied in genome analysis, gene localization, gene transfer, and breakage of close linkages. These applications require knowledge of the recombination characteristics of telotrisomics. Appropriate cytological and molecular markers and favorable chromosome morphology are not always available or applicable for quantitative analyses. We developed new mathematical models for extracting the maximum information from simple metaphase I observations. Two types of telotrisomics of the short arm of chromosome 1R of rye ( Secale cereale ), including several genotypes, were used as test material. In simple telotrisomics, pairing between morphologically identical complete chromosomes was more frequent than pairing between the telocentric and either of the normal chromosomes. In the telocentric substitution, morphologically identical telocentrics paired less frequently with each other than either one with the normal chromosome. Pairing partner switch was significant. Interaction between the two arms was variable. Variation within plants was considerable. Telotrisomics without markers are suitable for analyzing pairing preferences, for gene localization and gene transfer, and for breaking tight linkages, but less so for genome analysis.

ANTIBODY RESPONSES OF YOUNG INFANTS TO NATURALLY OCCURRING VIRAL INFECTIONS

PEDIATRICS ◽  
1966 ◽  
Vol 38 (4) ◽  
pp. 564-570
Author(s):  
Hugh L. Moffet ◽  
Henry G. Cramblett
Keyword(s):  
Neutralizing Antibodies ◽  
Virus Isolation ◽  
Viral Infections ◽  
Low Frequency ◽  
Severity Of Illness ◽  
Antibody Responses ◽  
Older Children ◽  
Young Infants ◽  
Naturally Occurring ◽  
Significant Difference

A fourfold rise in neutralizing antibodies was demonstrated for 45% of infants 1 through 6 months of age compared to 63% of older children or adults from whom an adenovirus or an enterovirus was recovered. This difference appeared to be related to severity of illness rather than to age, as there was no significant difference between young infants and older patients when only clinically severe illnesses were analyzed. The isolation of virus from more than one specimen increased the probability of a significant response in either age group. Infants with minor symptoms had a low frequency of significant fourfold antibody responses after virus isolation, but this was not significantly different from older children with minor symptoms. Failure to develop an increase in antibody titer could not be related to the presence of maternal antibodies.

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