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

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.

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.


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.


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.


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