Control of Meiotic Chromosome Pairing by the Chromosomes of Homoeologous Group 5 of Triticum aestivum

Nature ◽  
1966 ◽  
Vol 212 (5069) ◽  
pp. 1475-1477 ◽  
Author(s):  
RALPH RILEY ◽  
VICTOR CHAPMAN ◽  
R. M. YOUNG ◽  
ANGELA M. BELFIELD
Keyword(s):  
Triticum Aestivum ◽  
Chromosome Pairing ◽  
Meiotic Chromosome ◽  
Homoeologous Group ◽  
Meiotic Chromosome Pairing ◽  
Group 5

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.

Induced Mutation Affecting the Control of Meiotic Chromosome Pairing in Triticum aestivum

Nature ◽  
1966 ◽  
Vol 211 (5047) ◽  
pp. 368-369 ◽  
Author(s):  
RALPH RILEY ◽  
VICTOR CHAPMAN ◽  
ANGELA M. BELFIELD
Keyword(s):  
Triticum Aestivum ◽  
Chromosome Pairing ◽  
Meiotic Chromosome ◽  
Induced Mutation ◽  
Meiotic Chromosome Pairing

scholarly journals Aneuhaploids in bread wheat

1976 ◽  
Vol 28 (1) ◽  
pp. 37-45 ◽  
Author(s):  
T. E. Miller ◽  
Victor Chapman
Keyword(s):  
Triticum Aestivum ◽  
Genetic Control ◽  
Bread Wheat ◽  
Chromosome Pairing ◽  
Chinese Spring ◽  
Meiotic Chromosome ◽  
Hordeum Bulbosum ◽  
Meiotic Abnormalities ◽  
Meiotic Chromosome Pairing

SUMMARYEuploid and aneuploid plants of Triticum aestivum, variety Chinese Spring were pollinated with, pollen of Hordeum bulbosum. Euhaploids and aneuhaploids of Chinese Spring were obtained from the crosses. Meiotic chromosome pairing was analysed in 25 different aneuhaploids and the results were compared with those obtained from euhaploids. The evidence provided by the meiotic studies was used to identify chromosomes whose activities affected the genetic control of chromosome pairing.Meiosis was abnormal in a 23-chromosome aneuhaploid and in the 22-chromosome sectors of a chimaeral plant. Both plants were thought to have resulted from the incomplete elimination of the genome of H. bulbosum from hybrid embryos. It is suggested that the meiotic abnormalities in the two aneuhaploids were caused by the residual barley chromosomes.

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.

Construction of comparative genetic maps of two 4Bs.4Bl-5Rl translocations in bread wheat (Triticum aestivum L.)

Genome ◽  
2006 ◽  
Vol 49 (7) ◽  
pp. 729-734 ◽  
Author(s):  
R C Leach ◽  
I S Dundas ◽  
A Houben
Keyword(s):  
Triticum Aestivum ◽  
Bread Wheat ◽  
Rflp Analysis ◽  
Triticum Aestivum L ◽  
Genetic Maps ◽  
Homoeologous Group ◽  
Group 4 ◽  
Translocation Breakpoints ◽  
Group 5 ◽  
Wheat Lines

The physical length of the rye segment of a 4BS.4BL–5RL translocation derived from the Cornell Wheat Selection 82a1-2-4-7 in a Triticum aestivum 'Chinese Spring' background was measured using genomic in situ hybridization (GISH) and found to be 16% of the long arm. The size of this translocation was similar to previously published GISH measurements of another 4BS.4BL–5RL translocation in a Triticum aestivum 'Viking' wheat background. Molecular maps of both 4BS.4BL–5RL translocations for 2 different wheat backgrounds were developed using RFLP analysis. The locations of the translocation breakpoints of the 2 4BS.4BL–5RL translocations were similar even though they arose in different populations. This suggests a unique property of the region at or near the translocation breakpoint that could be associated with their similarity and spontaneous formation. These segments of rye chromosome 5 also contain a gene for copper efficiency that improves the wheat's ability to cope with low-copper soils. Genetic markers in these maps can also be used to screen for copper efficiency in bread wheat lines derived from the Cornell Wheat Selection 82a1 2-4-7.Key words: Triticum aestivum, wheat–rye translocation, homoeologous group 4, homoeologous group 5, GISH, comparative map, copper efficiency, hairy peduncle.

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