Rye C-banding patterns and meiotic stability of hexaploid triticale (× Triticosecale) selections differing in kernel shriveling

Genome ◽  
1990 ◽  
Vol 33 (5) ◽  
pp. 686-689 ◽  
Author(s):  
Charles M. Papa ◽  
R. Morris ◽  
J. W. Schmidt

Two winter hexaploid triticale populations derived from the same cross were selected on the basis of grain appearance and agronomic performance. The five lines from 84LT402 showed more kernel shriveling than the four lines from 84LT401. The derived lines were analyzed for aneuploid frequencies, rye chromosome banding patterns, and meiotic stability to detect associations with kernel development. The aneuploid frequencies were 16% in 84LT401 and 18% in 84LT402. C-banding showed that both selection groups had all the rye chromosomes except 2R. The two groups had similar telomeric patterns but differed in the long-arm interstitial patterns of 4R and 5R. Compared with lines from 84LT402, those from 84LT401 had significantly fewer univalents and rod bivalents, and more paired arms at metaphase I; fewer laggards and bridges at anaphase I; and a higher frequency of normal tetrads. There were no significant differences among lines within each group for any meiotic character. Since there were no differences within or between groups in telomeric banding patterns, the differences in kernel shriveling and meiotic stability might be due to genotypic factors and (or) differences in the interstitial patterns of 4R and 5R. By selecting plump grains, lines with improved kernel characteristics along with improved meiotic stability are obtainable.Key words: triticale, meiotic stability, C-banding, Secale cereale, heterochromatin.

1978 ◽  
Vol 20 (2) ◽  
pp. 199-204 ◽  
Author(s):  
J. P. Gustafson ◽  
K. D. Krolow

Three tetraploid triticales were analysed by C-banding techniques in order to establish their chromosome constitutions. All three tetraploid triticales contained seven rye chromosomes with the banding pattern of Secale cereale L. A mixture of A- and B-genome chromosomes from Triticum turgidum L. constituted the wheat genome present in the tetraploid triticales. Triticale Trc 4x3 contained 1A, 2B, 3A, 4A, 5B, 6A, and 7B. Triticale Trc 4x2 contained 1A, 2B, 3B, 4B, 5B, 6A, and 7B, while triticale Trc 4x5 contained 1A, 2B, 3B, 4A, 5A, 6A, and 7B. The reliability of the staining technique is subject to errors in identification, which are discussed.


Genome ◽  
1987 ◽  
Vol 29 (1) ◽  
pp. 58-62 ◽  
Author(s):  
Friedrich J. Zeller ◽  
Mari-Carmen Cermeño ◽  
Bernd Friebe

Seven telotrisomic lines (1RS, 1RL, 2RS, 2RL, 3RS acro, 5RS, and 6RS), two double monotelosomic, and two double ditelosomic lines of Secale cereale cv. Heines Hellkorn were analyzed by means of Giemsa C-banding techniques. In crosses with several wheat–rye chromosome addition lines, the telosomic chromosomes in double ditelosomic lines 1/23 and 3/23 were found to be homologous to chromosomes 1R and 2RL of cv. Imperial rye. The C-banding pattern observed for the telosomes in these lines was similar to that detected in the 1R and 2R telosomics of the corresponding telotrisomic lines. Key words: Secale cereale, telotrisomics, double ditelosomics, C-banding pattern.


Genome ◽  
1991 ◽  
Vol 34 (1) ◽  
pp. 109-120 ◽  
Author(s):  
J. H. de Jong ◽  
F. Havekes ◽  
A. Roca ◽  
T. Naranjo

Synapsis and chiasma formation were analyzed in a ditelo-substituted haploid of rye (Secale cereale), in which chromosome 1R was replaced by its telosomes. The study was made by comparing synaptonemal complex formation at early meiotic prophase I, chromosome associations at metaphase I, and recombinant chromosomes at anaphase I and prophase II. For the analysis of synaptonemal complexes, 41 nuclei at stages ranging from leptotene to early diplotene were selected. In the leptotene and early zygotene nuclei, numerous alignments of axial cores involving the same or different chromosomes were observed. Pairing initiation sites occurred at both interstitial and distal segments. Throughout zygotene the extent of pairing gradually increases, with values up to 84.8% at a stage that is morphologically comparable with late pachytene. Pairing-partner exchanges were frequently observed in zygotene nuclei, giving rise to multiple associations encompassing all or most of the chromosomes. In cells at metaphase I multivalents were very rare (2%), indicating elimination of most pairing-partner exchanges. In cells at metaphase I, anaphase I, and prophase II chromosome length, centromere position, and C-banding pattern enable the identification of the chromosomes 1RS, 1RL, 4R, 5R, and 6R, and the distinction of three metacentric chromosomes (RM1, RM2, and RM3). Metaphase I bonds were found to be nonrandomly distributed. Associations between the arms 4RL, 5RL, 6RL, and RM1L, all of them without telomeric C-bands, were more frequent than between the remaining arms. The bonds were mainly located at the distal parts of the chromosomes. The frequency of recombinant chromosomes at anaphase I or prophase II suggests that metaphase I bonds were true chiasmata.Key words: Secale cereale, haploid, synaptonemal complex, chiasmate bonds, C-banding.


Genome ◽  
1993 ◽  
Vol 36 (4) ◽  
pp. 641-651 ◽  
Author(s):  
Zhi-Wu Liu ◽  
Richard R.-C. Wang

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.


1971 ◽  
Vol 13 (3) ◽  
pp. 592-596 ◽  
Author(s):  
S. Shigenaga ◽  
E. N. Larter ◽  
R. C. McGinnis

Detailed karyotype analyses were conducted on root-tip cells of aneuploid plants of hexaploid triticale, cultivar 'Rosner.' Although complete meiotic stability in this cultivar has not as yet been achieved, it currently represents the standard for triticale improvement in Canada. Rosner characteristically exhibits an average of 0.8 univalents per cell at metaphase I and approximately 10% of its progeny are aneuploid. The results of the present study clearly indicated that both wheat and rye chromosomes of the triticale complement contribute to the aneuploid condition, not primarily those of rye as believed earlier.


1976 ◽  
Vol 18 (1) ◽  
pp. 85-91 ◽  
Author(s):  
T. J. Ennis

Chromosome replication has been analysed in four species of Chilocorus. In C. orbus Csy., C. tricyclus Smith, and C. hexacyclus Smith, centric regions of all chromosomes are last to replicate, preceded in order by heterochromatic arms and euchromatic arms. In C. stigma Say, very late replication of centric regions can be detected only in otherwise wholly euchromatic chromosomes (= monophasics); in chromosomes with one arm heterochromatic (= diphasics), these arms are last to replicate. Based on pachytene bivalent morphology and chromosome banding patterns, and supported by autoradiographic data, models are presented for the general organisation of Chilocorus chromosomes. All chromosomes in the first three species are subdivided into euchromatic arm, centric heterochromatin, and either a second euchromatic arm (monophasics) or a heterochromatic arm (diphasics). Chilocorus stigma diphasics apparently lack distinct centric organisation, and are therefore divided into euchromatic and heterochromatic arms only.


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