CHROMOSOME PAIRING IN TWO INTERSPECIFIC HYBRIDS OF TRIFOLIUM

1970 ◽  
Vol 12 (4) ◽  
pp. 790-794 ◽  
Author(s):  
Chi-Chang Chen ◽  
Pryce B. Gibson
Keyword(s):  
Phylogenetic Relationship ◽  
Chromosome Pairing ◽  
Trifolium Repens ◽  
Interspecific Hybrids ◽  
Triploid Hybrid ◽  
Close Phylogenetic Relationship ◽  
Metaphase I

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.

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.

Interspecific hybrids between a transgenic rapeseed (Brassica napus) and related species: cytogenetical characterization and detection of the transgene

Genome ◽  
1993 ◽  
Vol 36 (6) ◽  
pp. 1099-1106 ◽  
Author(s):  
M. C. Kerlan ◽  
A. M. Chevre ◽  
F. Eber
Keyword(s):  
Chromosome Pairing ◽  
Related Species ◽  
Interspecific Hybrids ◽  
Plant Production ◽  
Triploid Hybrid ◽  
Bar Gene ◽  
Meiotic Behavior ◽  
Gene Dispersal ◽  
Gene Characterization ◽  
Transgenic Rapeseed

In interspecific hybrids produced between a transgenic rapeseed, an allotetraploid species, resistant to herbicide, phosphinotricin, and five diploid related species, the risk for gene introgression in weed genomes was explored through cytogenetic and bar gene characterizations. Among the 75 hybrids studied, most had the expected triploid structure, with the exception of B. napus – B. oleracea amphidiploid plants and one B. napus – S. arvensis amphidiploid plant. In triploid hybrid plants, the reciprocal hybrids did not exhibit any difference in their meiotic behavior. The comparison of the percentage of chromosome pairing in the hybrids with that of haploid rapeseed permit to conclude that allosyndesis between AC genomes and related species genomes took place. This possibility of recombination was confirmed by the presence of multivalent associations in all the interspecific hybrids. Nevertheless, in B. napus – B. adpressa hybrids a control of chromosome pairing seemed to exist. The possibility of amphidiploid plant production directly obtained in the F1 generation increased the risk of gene dispersal. The B. napus – B. oleracea amphidiploid plant presented a meiotic behavior more regular than that of the B. napus – S. arvensis amphidiploid plant. Concerning the herbicide bar gene characterization, the presence of the gene detected by DNA amplification was correlated with herbicide resistance, except for two plants. Different hypotheses were proposed to explain these results. A classification of the diploid species was established regarding their gene dispersal risk based on the rate of allosyndesis between chromosomes of AC genomes of rapeseed and the genomes of the related species.Key words: Brassicaceae, transgenic rapeseed, risk assessment, interspecific hybrids, chromosome pairing, bar gene characterization.

Chromosome pairing in triploid and tetraploid hybrids in Elytrigia (Triticeae; Poaceae)

1984 ◽  
Vol 26 (5) ◽  
pp. 519-522 ◽  
Author(s):  
Patrick E. McGuire
Keyword(s):  
Chromosome Pairing ◽  
Genome Analysis ◽  
Triploid Hybrid ◽  
Pollen Mother Cells ◽  
Tetraploid Hybrid ◽  
A Genome ◽  
Mother Cells ◽  
Metaphase I

Mean chromosome pairing of 5.14I + 1.28II (rod) + 3.86II (ring) + 1.47III + 0.11IV (open) + 0.11V was observed in pollen mother cells at metaphase I in the triploid hybrid Elytrigia scirpea (K. Presl) Holub, 2n = 4x = 28 × E. bessarabica (Savul. et Rayss) Dubrovik, 2n = 4x = 14. Mean chromosome pairing of 3.71I + 2.29II (rod) + 1.82II (ring) + 2.64III + 0.29IV (open) was observed in the triploid hybrid E. curvifolia (Lange) Holub, 2n = 4x = 28 × E. bessarabica. Mean chromosome pairing of 3.00I + 0.93II (rod) + 1.57II (ring) + 1.36III + 1.79IV (open) + 1.I4IV (closed) + 0.79V was observed in the tetraploid hybrid E. junceiformis Löve et Löve, 2n = 4x = 28 × E. curvifolia. The first hybrid provides the first evidence by genome analysis that E. bessarabica possesses a genome (designated Eb) which is closely related to the genomes of E. scirpea (ES and ESC) and hence to the E genome of E. elongata (Host) Nevski, 2n = 2x = 14. The second and third hybrids provide the first evidence that the two genomes of E. curvifolia (designated EC and ECU) are related to the Eb genome of E. bessarabica and thus to the E genome of E. elongata.Key words: Elytrigia, homoeology, Triticum, phylogeny, triploid, tetraploid.

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.

Genome constitutions of Thinopyrum curvifolium, T. scirpeum, T. distichum, and T. junceum (Triticeae: Gramineae)

Genome ◽  
1993 ◽  
Vol 36 (4) ◽  
pp. 641-651 ◽  
Author(s):  
Zhi-Wu Liu ◽  
Richard R.-C. Wang
Keyword(s):  
Chromosome Pairing ◽  
Banding Pattern ◽  
Triploid Hybrid ◽  
Target Species ◽  
Banding Patterns ◽  
C Banding ◽  
Geographical Separation ◽  
Basic Genome ◽  
Karyotype Analyses ◽  
Metaphase I

The objective of this study is to elucidate genome constitutions of Thinopyrum curvifolium (Lange) D.R. Dewey, T. scirpeum (K. Presl) D.R. Dewey, T. distichum (Thunb.) A. Löve, and T. junceum (L.) A. Löve. Hybrids of T. sartorii (Boiss. &Heidr.) A. Löve with T. scirpeum and T. junceum, as well as the hybrid between T. curvifolium and Pseudoroegneria geniculata ssp. scythica (Nevski) A. Löve, were made and chromosome pairing at metaphase I was studied. The karyotype analyses of mitotic cells stained by aceto-orcein were conducted for both hybrids and the four target species. The Giemsa C-banding following acetocarmine staining was carried out for the above species and the triploid hybrid T. curvifolium × T. bessarabicum (Savul &Rayss) A. Löve. Meiotic data indicate that all target species have two sets of the basic genome J, but they behave like true allopolyploids because of bivalentization. Karyotypes of T. curvifolium and its triploid hybrid with T. bessarabicum indicate that T. curvifolium contains two different versions of the Jb genome, designated as Jb3 and Jb4, rather than two Je genomes as previously believed. Thinopyrum scirpeum and T. elongatum (4x) have similar karyotypes. Both are segmental allotetraploids carrying two forms of the Je genome. Their genome formulae are Je2 Je3 and Je1 Je3, respectively. Thinopyrum distichum has a karyotype similar to T. junceiforme, which has the Jb2 Je2 genome formula. However, the two species differ in C-banding patterns, reflecting their geographical separation. Thinopyrum junceum is a hexaploid with two pairs of Jb2 genomes and one pair of the Je2 genome, and it has a C-banding pattern similar to that of T. junceiforme, which has one pair each of the Jb2 and Je2 genomes.Key words: genome, meiosis, karyotype, C-banding, Triticeae, Thinopyrum.

Chromosome pairing in the allotetraploid Aegilops biuncialis and a triploid intergeneric hybrid

Genome ◽  
1996 ◽  
Vol 39 (4) ◽  
pp. 664-670 ◽  
Author(s):  
N. Cuñado ◽  
S. Callejas ◽  
M. J. García ◽  
J. L Santos ◽  
A. Fernández
Keyword(s):  
Synaptonemal Complex ◽  
Chromosome Pairing ◽  
Complex Analysis ◽  
Intergeneric Hybrid ◽  
Chiasma Formation ◽  
Triploid Hybrid ◽  
Homologous Chromosomes ◽  
Prophase I ◽  
Surface Spread ◽  
Metaphase I

Chromosome pairing behaviour of the natural allotetraploid Aegilops biuncialis (genome UUMM) and a triploid hybrid Ae. biuncialis × Secale cereale (genome UMR) was analyzed by electron microscopy in surface-spread prophase I nuclei. Synaptonemal-complex analysis at zygotene and pachytene revealed that synapsis in the allotetraploid was mostly between homologous chromosomes, although a few quadrivalents were also formed. Only homologous bivalents were observed at metaphase I. In contrast, homoeologous and heterologous chromosome associations were common at prophase I and metaphase I of the triploid hybrid. It is concluded that the mechanism controlling bivalent formation in Ae. biuncialis acts mainly at zygotene by restricting pairing to homologous chromosomes, but also acts at pachytene by preventing chiasma formation in the homoeologous associations. In the hybrid the mechanism fails at both stages. Key words : Aegilops biuncialis, allotetraploid, intergeneric hybrid, pairing control, synaptonemal complex.

Pairing affinities of the B- and G-genome chromosomes of polyploid wheats with those of Aegilops speltoides

Genome ◽  
2000 ◽  
Vol 43 (5) ◽  
pp. 814-819 ◽  
Author(s):  
S Rodríguez ◽  
B Maestra ◽  
E Perera ◽  
M Díez ◽  
T Naranjo
Keyword(s):  
Chromosome Pairing ◽  
Interspecific Hybrids ◽  
Triticum Turgidum ◽  
Aegilops Speltoides ◽  
Meiotic Pairing ◽  
Triticum Timopheevii ◽  
C Banding ◽  
Tetraploid Wheats ◽  
B Genome ◽  
Metaphase I

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.

Three new species of Sectonema Thorne, 1930 (Dorylaimida: Aporcelaimidae) from Vietnam

Nematology ◽  
2016 ◽  
Vol 18 (5) ◽  
pp. 517-536 ◽  
Author(s):  
Sergio Álvarez-Ortega ◽  
Thi Anh Duong Nguyen ◽  
Joaquín Abolafia ◽  
Thi Thanh Tam Vu ◽  
Michael Bonkowski ◽  
...  
Keyword(s):  
New Species ◽  
Phylogenetic Relationship ◽  
Ventral Side ◽  
Molecular Data ◽  
Evolutionary Tree ◽  
Neck Length ◽  
Natural Habitats ◽  
Line Drawings ◽  
Close Phylogenetic Relationship ◽  
Three New Species

Three new species of the genus Sectonema collected from natural habitats in Vietnam are studied, described and illustrated, including line drawings, LM and/or SEM pictures. Sectonema birrucephalum sp. n. is characterised by its 2.73-4.35 mm long body, lip region 18-20 μm broad and offset by deep constriction, odontostyle 10.0-11.5 μm long on its ventral side, 659-989 μm long neck, pharyngeal expansion occupying 63-68% of total neck length, uterus a simple tube, 221-277 μm long, pars refringens vaginae present, V = 54-56, tail short (31-43 μm, c = 85-111, c′ = 0.6-0.8) and rounded, spicules 72-75 μm long, and four or five irregularly spaced ventromedian supplements beyond the range of the spicules. Sectonema buccociliatum sp. n. is distinguished by its 2.00-2.46 mm long body, lip region offset by constriction, 19-20 μm broad and bearing perioral cilia-like structures, odontostyle 13-14 μm long at its ventral side, 530-625 μm long neck, pharyngeal expansion occupying 62-69% of total neck length, uterus a simple tube, 116-152 μm long, pars refringens vaginae present, V = 56-62, tail short (23-31 μm, c = 72-104, c′ = 0.6-0.8) and rounded, spicules 56-68 μm long, and 3-5 spaced and weakly developed ventromedian supplements beyond the range of the spicules. Sectonema ciliatum sp. n. is characterised by its 2.79-3.13 mm long body, lip region offset by constriction, 21-22 μm broad and bearing perioral cilia-like structures, odontostyle 14-15 μm long at its ventral side, 699-722 μm long neck, pharyngeal expansion occupying 60% of total neck length, uterus a simple tube, 201-244 μm long, pars refringens vaginae present, V = 52-53, tail short (33-35 μm, c = 82-92, c′ = 0.6-0.7) and rounded, spicules 70-72 μm long, and three or four spaced and weakly developed ventromedian supplements beyond the range of the spicules. Molecular data obtained for S. ciliatum sp. n. and the derived evolutionary tree show a close phylogenetic relationship with other species of the genus.

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