Meiotic pairing in new hybrids of Hordeum procerum (6x) with H. parodii (6x) and Elymus virginicus (4x)

1986 ◽  
Vol 28 (3) ◽  
pp. 416-419 ◽  
Author(s):  
P. K. Gupta ◽  
George Fedak

Hybrids of Hordeum procerum were readily produced with H. parodii (7.9%) and Elymus virginicus (14.3%). The average meiotic pairing per cell in the interspecific hybrid between H. procerum and H. parodii was 14.56 I + 12.19 II + 1.04 III, which indicated that the species have two genomes in common. In the hybrid between H. procerum and E. virginicus the average metaphase I configuration was 20.35 I + 6.86 II + 0.31 III indicating one common genome. Keywords: interspecific, intergeneric hybrids, chromosome pairing, Hordeum, Elymus.

Genome ◽  
1991 ◽  
Vol 34 (6) ◽  
pp. 860-867 ◽  
Author(s):  
Kevin B. Jensen ◽  
Richard R.-C. Wang

Two accessions of Elymus caucasicus (Koch) Tzvelev and three accessions of Elymus longearistatus (Boiss.) Tzvelev were studied to determine the meiotic behavior and chromosome pairing in the two taxa, their interspecific hybrid, and their hybrids with various "analyzer" parents. Interspecific and intergeneric hybrids of the target taxa were obtained with the following analyzer species: Pseudoroegneria spicata (Pursh) A. Löve (2n = 14, SS), Pseudoroegneria libanotica (Hackel) D. R. Dewey (2n = 14, SS), Hordeum violaceum Boiss. &Hohenacker (2n = 14, HH) (= Critesion violaceum (Boiss. &Hohenacker) A. Löve), Elymus lanceolatus (Scribn. &Smith) Gould (2n = 28, SSHH), Elymus abolinii (Drob.) Tzvelev (2n = 28, SSYY), Elymus pendulinus (Nevski) Tzvelev (2n = 28, SSYY), Elymus fedtschenkoi Tzvelev (2n = 28, SSYY), Elymus panormitanus (Parl.) Tzvelev (2n = 28, SSYY), and Elymus drobovii (Nevski) Tzvelev (2n = 42, SSHHYY). Cytological analysis of their F1 hybrids showed that E. caucasicus and E. longearistatus were allotetraploids comprising the same basic genomes. Chromosome pairing in the E. caucasicus × P. libanotica hybrid demonstrated that the target taxa contained the S genome, based on 6.1 bivalents per cell. The lack of chromosome pairing, less than one bivalent per cell, in the E. longearistatus × H. violaceum hybrid showed that the H genome was absent. Increased pairing in the tetraploid and pentaploid hybrids when the Y genome was introduced indicated that the second genome in the two taxa was a segmental homolog of the Y genome. The S and Y genomes in E. caucasicus and E. longearistatus have diverged from each other and from those in many of the eastern and central Asian SY tetraploids.Key words: genome, meiosis, chromosome pairing, morphology, hybrid, Triticeae.


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.


Genome ◽  
1992 ◽  
Vol 35 (6) ◽  
pp. 951-956 ◽  
Author(s):  
Richard R.-C. Wang

Amphiploids of the hybrid Thinopyrum elongatum (Host) D.R. Dewey (2n = 2x = 14; JeJe) × Pseudoroegneria spicata (Pursh) A. Löve (2n = 2x = 14; SS) were obtained by the colchicine treatment of regenerants from inflorescence culture. Meiotic pairings in the JJSS amphiploids averaged 2.90 I + 4.44 rod II + 7.50 ring II + 0.14 III + 0.20 IV at metaphase I but had 13.38 ring II + 0.30 IV at diakinesis. This amphidiploid was crossed with that of T. bessarabicum (Savul. &Rayss) A. Löve (2n = 2x = 14; JbJb) × T. elongatum and the latter was also crossed with T. scirpeum (K. Presl) D.R. Dewey (2n = 4x = 28; JeJeJeJe) to obtain JbJeJeS and JeJeJeJb hybrids, respectively. The former hybrid had a metaphase I pairing pattern of 7.82 I + 4.33 rod II + 2.76 ring II + 1.51 III + 0.35 IV. The latter hybrid had 3.04 I + 4.05 rod II + 4.31 ring II + 1.26 III + 1.08 IV. These meiotic pairing data are in agreement with the genomic relationships based on the diploid hybrids involving these genomes. Fertility of the hybrid between T. scirpeum and the amphiploid of T. bessarabicum × T. elongatum suggested that their genomes were similar and balanced and that gene flow could occur between the JJ diploids and the JJJJ tetraploid.Key words: hybrid, amphidiploid, genome, isozyme, chromosome pairing, Triticeae, Thinopyrum.


Genome ◽  
1992 ◽  
Vol 35 (1) ◽  
pp. 98-102 ◽  
Author(s):  
Qin Chen ◽  
Joseph Jahier ◽  
Yvonne Cauderon

Triticum aestivum cv. Chinese Spring (2n = 6x = 42, ABD genomes) was crossed with diploid Inner Mongolian Agropyron Gaertn. species A. cristatum and A. mongolicum and reciprocal hybrids between them (2n = 2x = 14, P genome, with or without B chromosomes). Intergeneric hybrids with 2n = 27, 28, 32, and 33 chromosomes were produced by the aid of embryo rescue. The extra chromosomes in two hybrids were assumed to be B chromosomes transmitted by the male Agropyron parent. Average meiotic pairing in the euploid hybrid with 28 chromosomes was 14.38 univalents + 4.92 bivalents + 1.26 trivalents. This level of pairing higher than expected was likely due to homeologous associations between wheat chromosomes. This data indicates that the P genome of diploid as well as tetraploid Agropyron originating from Inner Mongolia possess a genetic system interfering with 5B homoeologous restricting system of wheat.Key words: intergeneric hybrids, Triticum aestivum, diploid Agropyron species, chromosome pairing.


Genome ◽  
1992 ◽  
Vol 35 (4) ◽  
pp. 676-680 ◽  
Author(s):  
Kevin B. Jensen ◽  
Ira W. Bickford

This paper describes the cytogenetics and fertility of intergeneric hybrids of Psathyrostachys stoloniformis × Agropyron cristatum and two Elymus species, E. dentatus ssp. ugamicus and E. grandiglumis × A. cristatum. Bivalent frequencies of metaphase I cells in the F1 hybrid P. stoloniformis (NN) × Agropyron cristatum (PP) ranged from 0 to 4 per cell, with an average of 0.87 bivalent per cell and a c value of 0.07. The hybrid E. dentatus ssp. ugamicus (SSYY) × A. cristatum (PP) averaged 3.07 bivalents per cell and ranged from 0 to 7 with a c-value of 0.27. Bivalents were predominantly end to end associations. Meiotic analysis in E. grandiglumis (SSYYPP) × A. cristatum (PP) revealed an average of 6.84 bivalents per metaphase I cell with a c value of 0.73. This hybrid had a chromosome number of 2n = 30 rather than the expected 2n = 28. All hybrids had less than 1% stainable pollen and set no seed under open-pollination.Key words: chromosome pairing, meiosis.


2015 ◽  
Vol 147 (4) ◽  
pp. 268-273 ◽  
Author(s):  
Yarui Su ◽  
Dale Zhang ◽  
Yuge Li ◽  
Suoping Li

Intergeneric hybrids and amphidiploid hybrids from crosses of Aegilopstauschii and Secale cereale were produced using young embryo rescue. The hybrids showed complete sets of both parental chromosomes. The dihaploid plants showed an average meiotic pairing configuration of 10.84 I + 1.57 II + 0.01 III. Genomic in situ staining revealed 3 types of bivalent associations, i.e. D-D, R-R and D-R at frequencies of 8.6, 8.2 and 83.3%, respectively. Trivalents consisted of D-R-D or R-D-R associations. These results suggested that both intra- and intergenomic chromosome homology were contributed to chromosome pairing. Derived amphidiploids with 2n = 28 paired at metaphase I of meiosis as 4.51 I + 11.70 II + 0.03 III. Chromosome pairing of amphidiploids appeared more or less regular, i.e. bivalent-like with some trivalent configurations.


Genome ◽  
2000 ◽  
Vol 43 (5) ◽  
pp. 814-819 ◽  
Author(s):  
S Rodríguez ◽  
B Maestra ◽  
E Perera ◽  
M Díez ◽  
T Naranjo

Chromosome pairing at metaphase I was studied in different interspecific hybrids involving Aegilops speltoides (SS) and polyploid wheats Triticum timopheevii (AtAtGG), T. turgidum (AABB), and T. aestivum (AABBDD) to study the relationships between the S, G, and B genomes. Individual chromosomes and their arms were identified by means of C-banding. Pairing between chromosomes of the G and S genomes in T. timopheevii × Ae. speltoides (AtGS) hybrids reached a frequency much higher than pairing between chromosomes of the B and S genomes in T. turgidum × Ae. speltoides (ABS) hybrids and T. aestivum × Ae. speltoides (ABDS) hybrids, and pairing between B- and G-genome chromosomes in T. turgidum × T. timopheevii (AAtBG) hybrids or T. aestivum × T. timopheevii (AAtBGD) hybrids. These results support a higher degree of closeness of the G and S genomes to each other than to the B genome. Such relationships are consistent with independent origins of tetraploid wheats T. turgidum and T. timopheevii and with a more recent formation of the timopheevi lineage.Key words: Triticum turgidum, Triticum timopheevii, Aegilops speltoides, meiotic pairing, evolution, C-banding.


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.


Genome ◽  
1990 ◽  
Vol 33 (6) ◽  
pp. 845-849 ◽  
Author(s):  
Richard R.-C. Wang

Intergeneric hybrids were synthesized for the first time from the diploid crosses Thinopyrum elongatum (JeJe) × Psathyrostachys juncea (NjNj), T. elongatum × P. fragilis (NfNf), T. bessarabicum (JbJb) × P. huashanica (NhNh), and T. bessarabicum × P. juncea, as well as from a cross between the amphidiploid of T. bessarabicum × T. elongatum (JbJbJeJe) and P. juncea. Spikes of these hybrids are morphologically intermediate between those of the parental species. Double spikelets occurred occasionally at central nodes of the spikes. Glaucous blue leaves appeared in the F1 only in the cross T. bessarabicum × P. huashanica, suggesting that the gene(s) for glaucous blue leaves in T. bessarabicum is (are) recessive to a gene(s) for green leaves in P. juncea but is (are) dominant to that for yellowish green leaves in P. huashanica. Meiotic pairing at metaphase I in these diploid (JN) and triploid (JJN) hybrids revealed a very low level of homology between the basic J and N genome. Therefore, the J and N genomes are nonhomologous and justifiably represented by different genome symbols. The triploid hybrids exhibited a pattern of chromosome associations that substantiated the earlier conclusion that the genomes in T. bessarabicum and T. elongatum are two versions of a basic genome (J). These hybrids will be useful in genome analysis, forming new Leymus species with the J and N genomes and broadening the diversity in the genus Pascopyrum with the SHJN genomes.Key words: hybrid, Thinopyrum, Psathyrostachys, genome.


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