Genetic control of meiotic chromosome pairing in polyploids in the genus Hordeum

1985 ◽  
Vol 27 (5) ◽  
pp. 515-530 ◽  
Author(s):  
P. K. Gupta ◽  
George Fedak
Keyword(s):  
Chromosome Pairing ◽  
Interspecific Hybrids ◽  
Meiotic Chromosome ◽  
Intergeneric Hybrid ◽  
Meiotic Pairing ◽  
Major Locus ◽  
In The Wild ◽  
Hordeum Species ◽  
Homoeologous Chromosomes ◽  
Existing Data

Existing data on meiosis in hexaploid and tetraploid species of Hordeum, their respective polyhaploids, and intergeneric – interspecific hybrids indicate that a meiotic pairing control system exists in this genus. The system is probably polygenic and it is therefore unlikely that a major locus such as Ph in Triticum controls chromosome pairing. It is more efficient in the tetraploids than hexaploids, permitting some intergenomic pairing in the latter. In the polyhaploids the pairing control is somewhat hemizygous ineffective. The pairing of homoeologous chromosomes in the wild polyploid Hordeum species is generally inhibited by H. vulgare and variably enhanced by genomes of Secale species.Key words: Hordeum, synapsis regulation, intergeneric hybrid, polyhaploids, hemizygous.

Genome constitution of the Australian hexaploid grass Elymus scabrus (Poaceae: Triticeae)

Genome ◽  
1993 ◽  
Vol 36 (1) ◽  
pp. 147-151 ◽  
Author(s):  
J. Torabinejad ◽  
R. J. Mueller
Keyword(s):  
Chromosome Pairing ◽  
Interspecific Hybrids ◽  
Intergeneric Hybrid ◽  
Meiotic Pairing ◽  
Genome Constitution ◽  
Psathyrostachys Juncea ◽  
Hybrid Plants ◽  
Thinopyrum Bessarabicum ◽  
Mother Cells ◽  
Metaphase I

Eight intergeneric hybrid plants were obtained between Elymus scabrus (2n = 6x = 42, SSYY??) and Australopyrum pectinatum ssp. retrofractum (2n = 2x = 14, WW). The hybrids were vegetatively vigorous but reproductively sterile. Examination of pollen mother cells at metaphase I revealed an average of 16.63 I, 5.29 II, 0.19 III, and 0.05 IV per cell for the eight hybrids. The average chiasma frequency of 6.77 per cell in the above hybrids strongly supports the presence of a W genome from A. pectinatum ssp. retrofractum in E. scabrus. Meiotic pairing data of some other interspecific hybrids suggest the existence of the SY genomes in E. scabrus. Therefore, the genome constitution of E. scabrus should be written as SSYYWW. Two other hybrid plants resulted from Elymus yezoensis (2n = 4x = 28, SSYY) crosses with A. pectinatum ssp. pectinatum (2n = 2x = 14, WW). Both were weak and sterile. An average of 0.45 bivalents per cell were observed at metaphase I. This clearly indicates a lack of pairing between W genome of Australopyrum and S or Y genomes of E. yezoensis. In addition, six hybrid plants of E. scabrus with Psathyrostachys juncea (2n = 2x = 14, NN) and one with Thinopyrum bessarabicum (2n = 2x = 14, JJ) were also obtained. The average bivalents per cell formed in both combinations were 2.84 and 0.70, respectively. The results of the latter two combinations showed that there is no N or J genome in E. scabrus.Key words: wide hybridization, chromosome pairing, genome analysis, Australopyrum, Elymus.

scholarly journals Wheat mutants permitting homoeologous meiotic chromosome pairing

1971 ◽  
Vol 18 (3) ◽  
pp. 311-328 ◽  
Author(s):  
A. M. Wall ◽  
Ralph Riley ◽  
Victor Chapman
Keyword(s):  
Triticum Aestivum ◽  
Chromosome Pairing ◽  
Secale Cereale ◽  
Meiotic Chromosome ◽  
Meiotic Pairing ◽  
Homoeologous Pairing ◽  
Homozygous Condition ◽  
Meiotic Chromosome Pairing ◽  
Homoeologous Chromosomes

SUMMARYPlants of Triticum aestivum (2n = 6x = 42) ditelocentric 5BL were treated with EMS in order to produce mutations in the 5B system by which meiotic pairing between homoeologous chromosomes is normally prevented. To check for the occurrence of mutation T. aestivum ditelo-5BL plants were pollinated with rye (Secale cereale 2n = 14) and meiosis was examined in the resulting hybrids.Wheat-rye hybrids were scored for the presence of mutants when the wheat parents were either the EMS-treated wheat plants, or their selfed derivatives, or their progenies obtained after pollination with untreated euploid individuals.Mutants were detected by each of these procedures and mutant gametes were produced by the treated ditelocentric plants with frequencies between 1·5 and 2·5%, but there were differences between the mutants in the extent to which homoeologous pairing occurred in the derived wheat-rye hybrids. The differences may have resulted from the occurrence of mutation at different loci or to different extents at the same locus.Two mutants, Mutant 10/13 and Mutant 61, were fixed in the homozygous condition. Mutant 10/13 was made homozygous both in the 5BL ditelocentric and in the euploid conditions but these genotypes regularly formed 21 bivalents at meiosis, and there was no indication of homoeologous pairing although the mutant 10/13 gave rise to homoeologous pairing in wheat-rye hybrids.

scholarly journals CYTOGENETICS OF CHROMOSOME PAIRING IN WHEAT

Genetics ◽  
1974 ◽  
Vol 78 (1) ◽  
pp. 193-203
Author(s):  
Ralph Riley
Keyword(s):  
Chromosome Pairing ◽  
Meiotic Chromosome ◽  
Meiotic Pairing ◽  
Homoeologous Pairing ◽  
Aegilops Species ◽  
Temperature Dependent ◽  
Supernumerary Chromosomes ◽  
Chromosome 5B ◽  
Two Stages ◽  
Homoeologous Chromosomes

ABSTRACT Meiotic chromosome pairing in Triticum aestivum is controlled by genetic systems promoting and reducing pairing. The pairing of homoeologous chromosomes is prevented principally by the activity of a single locus (Ph) distally located on the long arm of chromosome 5B. In certain hybrids, supernumerary chromosomes (B chromosomes) from Aegilops species can compensate for the absence of chromosome 5B preventing or reducing homoeologous pairing. Temperature-dependent variants and colchicine sensitivity have been used to show that there are at least two stages in the G1 of meiosis at which the occurrence of meiotic pairing is determined. Wheat may differ from lily in the detailed organization of meiosis.

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.

scholarly journals Meiotic Chromosome Pairing in Interspecific Hybrids ofNicotiana

1975 ◽  
Vol 13 (4) ◽  
pp. 601-609 ◽  
Author(s):  
Elizabeth Williams
Keyword(s):  
Chromosome Pairing ◽  
Interspecific Hybrids ◽  
Meiotic Chromosome ◽  
Meiotic Chromosome Pairing

The Effect of Spindle Inhibitors Applied before Meiosis on Meiotic Chromosome Pairing

1973 ◽  
Vol 12 (1) ◽  
pp. 143-161 ◽  
Author(s):  
G. A. DOVER ◽  
R. RILEY
Keyword(s):  
Chromosome Pairing ◽  
Chloral Hydrate ◽  
Control Mechanism ◽  
Meiotic Chromosome ◽  
Chiasma Formation ◽  
Meiotic Pairing ◽  
Mitotic Spindles ◽  
Pollen Mother Cells ◽  
Meiotic Chromosome Pairing ◽  
Mother Cells

Injection of 0.5% colchicine into immature tillers of genotypes of Triticum aestivum, T. aestivum x Aegilops mutica and T. aestivum x Secale cereale hybrids induces asynapsis at first meiotic metaphase irrespective of the homologous or homoeologous nature of the potential pairing chromosomes. The induction of asynapsis occurs at a time during and immediately following the last premeiotic mitosis of pollen mother cells. No disruption of synapsis and chiasma formation occurs in anthers having pollen mother cells originally at leptotene or immediately prior to leptotene when cultured in White's medium plus colchicine. Tetraploid and octaploid pollen mother cells resulting from the disruption of premeiotic spindles by colchicine show pairing of chromosomes only in bivalents, in genotypes normally having a degree of multivalent pairing configurations. The induction of multipolar mitotic spindles with 0.01% colchicine results in the development of pollen mother cell mosaics with different numbers of chromosomes. Such cells show high levels of chromosome pairing, including multivalents, in some genotypes that normally have very little chromosome pairing. The injection of 0.5% chloral hydrate during the last premeiotic mitosis of the archesporium causes no disturbances of meiotic pairing. The results are discussed with reference to the hypothesis that the control mechanism of meiotic chromosome pairing involves centromeric microtubules of the spindle (not affected by chloral hydrate) that are responsible for the positional adjustment, during the last mitotic anaphase, of potential pairing partners.

scholarly journals The position of a locus on chromosome 5B of Triticum aestivum affecting homoeologous meiotic pairing

1971 ◽  
Vol 18 (3) ◽  
pp. 329-339 ◽  
Author(s):  
A. M. Wall ◽  
Ralph Riley ◽  
M. D. Gale
Keyword(s):  
Triticum Aestivum ◽  
Chromosome Pairing ◽  
Single Locus ◽  
Meiotic Pairing ◽  
Homoeologous Pairing ◽  
Chromosome 5B ◽  
Homoeologous Chromosome Pairing ◽  
Mutant Locus ◽  
Homoeologous Chromosomes ◽  
Pairing Behaviour

SUMMARYAn investigation was made of the chromosomal position of the mutant locus, in Mutant 10/13 of Triticum aestivum (2n = 6x = 42), affecting homoeologous chromosome pairing at meiosis. In hybrids between Mutant 10/13 and rye (Secale cereale 2n = 14), homoeologous chromosomes frequently pair at meiosis although normally, in wheat-rye hybrids, this happens infrequently.The association of the mutant condition with chromosome 5B was determined by (i) the absence of segregation in hybrids obtained when Mutant 10/13 monosomic 5B was pollinated by rye; (ii) the occurrence of trisomie segregation for pairing behaviour in 28-chromosome wheat-rye hybrids, obtained from SB trisomie wheat parents with two 5B chromosome from a non-mutant and one from a mutant parent; (iii) the absence of segregation for pairing behaviour in the 29-chromosome wheat-rye hybrids obtained from the same trisomie wheat parents.The alternative pairing behaviours segregated independently of the centromere when wheat plants that were simultaneously heteromorphic, 5BL telocentric/5B complete, and heterozygous for the Mutant 10/13 state, were pollinated by rye. The alternative chromosome-pairing patterns segregated to give a ratio not different from 1:1, so that the association of homoeologous pairing with Mutant 10/13 probably derived from the occurrence of mutation at a single locus on 5BL. In the disomic heteromorphic state, 5BL was 91 map units in length.Trisomie wheats with two complete 5B chromosomes and one 5BL telocentric, that were also heterozygous for the Mutant 10/13 condition, were pollinated by rye. Among the resulting 28-chromosome hybrids there was a 2:1 segregation of hybrids with low pairing: high (homoeologous) pairing and also of hybrids with complete 5B: telocentric 5BL. However, there was no evidence of linkage in this trisomie segregation. All the 29-chromosome hybrids from this cross had low pairing and it could be concluded that the single mutant allele, in Mutant 10/13, was recessive. In the trisomie condition, relative to a simplex situation, 5BL was 33·05 map units in length.The critical locus on 5BL was designated Pairing homoeologous. The normal dominant allele was symbolized Ph and the recessive allele, in Mutant 10/13, ph.The prevention of homoeologous pairing by the activity of a single locus makes the evolution of the regular meiotic behaviour of T. aestivum more readily comprehensible.

CHROMOSOME PAIRING IN HEXAPLOID HYBRIDS FROM BROMUS ERECTUS (2n = 28) × B. INERMIS (2n = 56)

1973 ◽  
Vol 15 (3) ◽  
pp. 427-436 ◽  
Author(s):  
K. C. Armstrong
Keyword(s):  
Chromosome Pairing ◽  
Interspecific Hybrids ◽  
Meiotic Chromosome ◽  
The Other ◽  
Meiotic Chromosome Pairing ◽  
Hybrid Plants ◽  
Quadrivalent Frequency ◽  
Bromus Erectus ◽  
Metaphase I

Meiotic chromosome pairing was studied at metaphase I of B. erectus (2n = 28), B. inermis (2n = 56) and interspecific hybrids from B. erectus × B. inermis (2n = 42). The B. erectus material averaged 2.08 IV + 0.11 III + 9.51 II + 0.35 I and B. inermis 0.05 VIII + 0.06 VI + 0.02 V + 2.25 IV + 0.11 III + 22.95 II + 0.25 I. The hybrid plants (2n = 42) averaged 0.18 VI + 1.90 IV + 0.19 III + 16.10 II + 0.39 I and one hybrid with 2n = 41 averaged 0.08 VI + 0.02 V + 0.95 IV + 0.50 III + 17.42 II + 0.72 I. Karyotype evidence supported the conclusion that B. erectus was an autotetraploid. The karyotype contains four large satellites and four subterminal chromosomes but the other four groups of four are median, with one group possibly a submedian. Since chromosome pairing in the hybrids was complete and the quadrivalent frequency in the parents and hybrids was similar, it was concluded that the genomic formula of B. erectus, B. inermis, and the hybrid was AAAA, AAAABBBB, and AAAABB, respectively.

Meiosis in interspecific Hordeum hybrids. I. Diploid combinations

1986 ◽  
Vol 28 (4) ◽  
pp. 525-535 ◽  
Author(s):  
Roland Von Bothmer ◽  
Jan Flink ◽  
Thomas Landström
Keyword(s):  
Interspecific Hybrids ◽  
Genomic Structure ◽  
Genetic Regulation ◽  
The Other ◽  
South American ◽  
Meiotic Pairing ◽  
Hordeum Bulbosum ◽  
High Affinity ◽  
Hordeum Species ◽  
Pairing Behaviour

The meiotic pairing behaviour of 39 new interspecific combinations between diploid Hordeum species are reported. On the basis of this data, four "basic genomes" are probably present in the genus. Hordeum bulbosum and H. vulgare have the same genome (I); H. marinum ("X") and H. murinum ("Y") each have one distinct genome. All other diploid taxa have either the same or a somewhat modified form of genome H. In this latter group of diploids, the South American taxa together with H. pusillum and H. intercedens in North America constitue a homogeneous group with respect to genomic structure, which differs somewhat from that found in the other Asiatic and North American species. Hordeum roshevitzii from Central Asia is unique, showing high affinity to both the Asiatic and to the American taxa. Evidence suggesting genetic regulation of chromosome pairing (both pairing promoting and pairing reducing) was obtained from a number of the diploid hybrids.Key words: Hordeum, interspecific hybrids, meiosis, diploids.

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