Centromere association is an unlikely mechanism by which the wheat Ph1 locus regulates metaphase I chromosome pairing between homoeologous chromosomes

Chromosoma ◽  
2000 ◽  
Vol 109 (6) ◽  
pp. 410-414 ◽  
Author(s):  
Jan Dvorak ◽  
Adam J. Lukaszewski
Genome ◽  
1988 ◽  
Vol 30 (5) ◽  
pp. 639-646 ◽  
Author(s):  
T. Naranjo ◽  
A. Roca ◽  
R. Giraldez ◽  
P. G. Goicoechea

Metaphase I pairing was studied in five ph1b mutant wheat × rye hybrids to verify the presence of translocations between homoeologous chromosomes in ph1b mutant wheat and to establish the pairing homoeology between wheat and rye chromosomes. Three 5B-deficient ABDR hybrids with standard chromosome structure were used as controls. Chromosomes 1R and 5R of rye and most wheat chromosomes, as well as their arms, were identified by means of C-banding. The presence of 5BS in ph1b hybrids raised the overall pairing level. The pattern of pairing between wheat chromosomes in ph1b hybrids, as in 5B-deficient hybrids, was characterized by the occurrence of preferential pairing between chromosomes of the A and D genomes in most homoeologous groups. The existence of a double translocation involving 4BL, 5AL, and 7BS in common wheat was confirmed. Deviation from the standard pairing pattern suggested the existence of a translocation involving 1BL and 1DL in one ph1b ABDR plant and another translocation involving 3AL and 3DL in three other ph1b hybrids. In ph1b hybrids, wheat – rye pairing was relatively frequent for 1RL, 5RL, and an arm of a metacentric rye chromosome, probably 2R, that is homoeologous to 2BL, and the homoeologous arms of 2A and 2D. The existence of a translocation involving 5RL and 4RL in rye was confirmed.Key words: homoeologous, homologous, 5B-deficient, translocations, C-banding.


Genetics ◽  
2003 ◽  
Vol 164 (2) ◽  
pp. 645-653 ◽  
Author(s):  
Eric Jenczewski ◽  
Frédérique Eber ◽  
Agnès Grimaud ◽  
Sylvie Huet ◽  
Marie Odile Lucas ◽  
...  

Abstract Precise control of chromosome pairing is vital for conferring meiotic, and hence reproductive, stability in sexually reproducing polyploids. Apart from the Ph1 locus of wheat that suppresses homeologous pairing, little is known about the activity of genes that contribute to the cytological diploidization of allopolyploids. In oilseed rape (Brassica napus) haploids, the amount of chromosome pairing at metaphase I (MI) of meiosis varies depending on the varieties the haploids originate from. In this study, we combined a segregation analysis with a maximum-likelihood approach to demonstrate that this variation is genetically based and controlled mainly by a gene with a major effect. A total of 244 haploids were produced from F1 hybrids between a high- and a low-pairing variety (at the haploid stage) and their meiotic behavior at MI was characterized. Likelihood-ratio statistics were used to demonstrate that the distribution of the number of univalents among these haploids was consistent with the segregation of a diallelic major gene, presumably in a background of polygenic variation. Our observations suggest that this gene, named PrBn, is different from Ph1 and could thus provide complementary information on the meiotic stabilization of chromosome pairing in allopolyploid species.


1970 ◽  
Vol 12 (4) ◽  
pp. 790-794 ◽  
Author(s):  
Chi-Chang Chen ◽  
Pryce B. Gibson

Both Trifolium repens (2n = 32) and T. nigrescens (2n = 16) formed bivalents during meiosis. However, their triploid hybrid showed an average of 4.27 trivalents per microsporocyte at metaphase I. The frequency of trivalents in the hybrid between T. nigrescens and autotetraploid T. occidentale (2n = 32) was 5.69. The data are interpreted to indicate: (1) a possible autotetraploid origin of T. repens; and (2) a close phylogenetic relationship among T. repens, T. nigrescens and T. occidentale.


1977 ◽  
Vol 19 (4) ◽  
pp. 651-656 ◽  
Author(s):  
J. M. Leggett

Chromosome pairing and the frequency of secondary associations in two aneupolyhaploid plants of A. sativa are described. There was little evidence of pairing between homoeologous chromosomes in either plant. The results are discussed in relation to the genetic control of bivalent pairing in A. sativa and the possible divergence between the constituent genomes.


Genome ◽  
1993 ◽  
Vol 36 (6) ◽  
pp. 1032-1041 ◽  
Author(s):  
J. H. de Jong ◽  
A. M. A. Wolters ◽  
J. M. Kok ◽  
H. Verhaar ◽  
J. van Eden

Three somatic hybrids resulting from protoplast fusions of a diploid kanamycin-resistant line of tomato (Lycopersicon esculentum) and a dihaploid hygromycin-resistant transformant of a monohaploid potato (Solanum tuberosum) line were used for a cytogenetic study on chromosome pairing and meiotic recombination. Chromosome counts in root-tip meristem cells revealed two hypotetraploids with chromosome complements of 2n = 46 and one with 2n = 47. Electron microscope analyses of synaptonemal complex spreads of hypotonically burst protoplasts at mid prophase I showed abundant exchanges of pairing partners in multivalents involving as many as eight chromosomes. In the cells at late pachytene recombination nodules were found in multivalents on both sides of pairing partner exchanges, indicating recombination at both homologous and homoeologous sites. Light microscope observations of pollen mother cells at late diakinesis and metaphase I also revealed multivalents, though their occurrence in low frequencies betrays the reduction of multivalent number and complexity. Precocious separation of half bivalents at metaphase I and lagging of univalents at anaphase I were observed frequently. Bridges, which may result from an apparent inversion loop found in the synaptonemal complexes of a mid prophase I nucleus, were also quite common at anaphase I, though the expected accompanying fragments could be detected in only a few cells. Most striking were the high frequencies of first division restitution in preparations at metaphase II/anaphase II, giving rise to unreduced gametes. In spite of the expected high numbers of balanced haploid and diploid gametes, male fertility, as revealed by pollen staining, was found to be negligible.Key words: synaptonemal complex, recombination, chromosome pairing, somatic hybrid, Lycopersicon esculentum (+) Solanum tuberosum.


Genome ◽  
1990 ◽  
Vol 33 (4) ◽  
pp. 465-471 ◽  
Author(s):  
Hum M. Thomas ◽  
W. G. Morgan

The synaptonemal complexes in the diploid hybrid Lolium multiflorum × Festuca drymeja were examined by the surface spreading technique, and chromosome pairing at metaphase I was analysed. Synaptonemal complex analysis revealed "illegitimate" pairing, including multivalents and foldback pairing. At metaphase I, most chiasmata were between chromosomes of the same genome, and again multivalents were found. It was concluded that most synaptonemal complexes resulted in chiasma formation. The effects of the large differences in DNA values of the two species and the possible genotypic effect of F. drymeja on chromosome pairing are discussed.Key words: Lolium-Festuca, synaptonemal complexes, nonhomologous pairing, DNA values.


Genome ◽  
1993 ◽  
Vol 36 (1) ◽  
pp. 147-151 ◽  
Author(s):  
J. Torabinejad ◽  
R. J. Mueller

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.


1982 ◽  
Vol 24 (4) ◽  
pp. 397-408 ◽  
Author(s):  
U. Kushnir ◽  
G. M. Halloran

Two mutants, each promoting homoeologous chromosome pairing in hexaploid wheat (Triticum × aestivum L. emend gr. aestivum), in the cultivar Chinese Spring, ph1b at the Ph locus on chromosome 5BL and the other, ph2, on chromosome 3DS, were compared for their influence on chromosome pairing and fertility in pentaploid hybrids with Triticum turgidum L. emend var. dicoccoides (Korn. in litt. in Schweinf.). The mutants induced increased multivalent frequency over the normal pentaploid. Lower univalent frequencies in the ph2-pentaploid, compared with the normal pentaploid, indicated that D-genome chromosomes of the former were substantially involved in homoeologous pairing. Certain differences in other meiotic processes and fertility among the pentaploids may reflect differences in the activity of the pairing genes. There appeared to be a higher level of univalent elimination in pollen and egg cells in the ph2-, compared with the ph1b-pentaploid. Tetrad formation was close to normal in the ph2- pentaploid but exhibited high levels of abnormality (monads, dyads, triads and apolar tetrads) in the ph1b-pentaploid. Fertility levels in crosses of the pentaploids with hexaploid wheat, while low, were much lower for the ph1b-, compared with the ph2-pentaploid.


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