Chromosome C-banding of Zea mays and its closest relatives

1983 ◽  
Vol 25 (3) ◽  
pp. 203-209 ◽  
Author(s):  
Ineke Mastenbroek ◽  
J. M. J. de. Wet

An established C-banding technique was modified to consistently yield complete sets of distinct, sharply banded chromosomes in Zea. It was used to demonstrate similarities and differences among heterochromatin patterns of different Zea taxa. The C-banding patterns showed a general agreement with heterochromatic knob positions known from pachytene studies. Two groups of banding patterns could be distinguished. Those taxa with bands that were almost exclusively terminally positioned included Z. mays ssp. parviglumis var. huehuetenangensis, Z. diploperennis, Z. perennis, and Z. luxurians. In the last mentioned, previously unknown heterochromatic regions were found. Both terminal and subterminal band positions were found in Z. mays, Z. mays ssp. mexicana, and Z. mays ssp. parviglumis var. parviglumis. On the basis of these results, and those of other workers, the taxonomic treatments of Z. mays ssp. parviglumis var. huehuetenangensis, and of Z. diploperennis and its autotetraploid derivative Z. perennis are questioned.

1984 ◽  
Vol 71 (1) ◽  
pp. 111-120
Author(s):  
I. Schubert ◽  
R. Rieger ◽  
P. Dobel

Similarities and differences become evident from comparisons of centromeric and non-centromeric banding patterns in plant and animal chromosomes. Similar to C and G-banding in animals (at least most of the reptiles, birds and mammals), centromeric and nucleolus-organizing region bands as well as interstitially and/or terminally located non-centromeric bands may occur in plants, depending on the kind and strength of pretreatment procedures. The last group of bands may sometimes be subdivided into broad regularly occurring ‘marker’ bands and thinner bands of more variable appearance. Non-centromeric bands in plants often correspond to blocks of constitutive heterochromatin that are rich in simple sequence DNA and sometimes show polymorphism; they thus resemble C-bands. However, most of these bands contain late-replicating DNA. Also they are sometimes rich A X T base-pairs, closely adjacent to each other and positionally identical to Feulgen+ and Q+ bands, thus being comparable to mammalian G-bands. Although banding that is reverse to the non-centromeric bands after Giemsa staining is still uncertain in plants, reverse banding patterns can be obtained with Feulgen or with pairs of A X T versus G X C-specific fluorochromes. It is therefore concluded that not all of the plant Giemsa banding patterns correspond to C-banding of mammalian chromosomes. Before the degree of homology between different Giemsa banding patterns in plants and G and/or C-bands in mammals is finally elucidated, the use of the neutral term ‘Giemsa band’, specified by position (e.g. centromeric, proximal, interstitial, terminal), is suggested to avoid confusion.


1984 ◽  
Vol 26 (6) ◽  
pp. 669-678 ◽  
Author(s):  
T. Ryu Endo ◽  
Bikram S. Gill

The acetocarmine–Giemsa C-banding technique was used to study heterochromatin distribution in somatic chromosomes of diploid Elymus junceus (= Psathyrostachys juncea) (2n = 14) (genome designation Ju = N) and nine diploid Agropyron species (2n = 14): A. cristatum (C = P), A. imbricatum (C = P), A. elongatum (= Elytrigia elongata = Thinopyrum elongatum) (E = J), A. junceum (= E. bessarabicum = T. bessarabicum) (J = E), A. spicatum (= Pseudoroegneria spicata) (S), A. libanoticum (= P. libanotica) (S), A. ferganense (S), A. stipifolium (= P. stipifolia) (S), and A. velutinum (V). With the exception of A. elongatum and A. velutinum, which were self-fertile, all species were cross-pollinating and self-sterile. The cross-pollinating species showed large terminal C-bands and a high level of C-band polymorphism. Agropyron elongatum, moderately self-fertile, showed small terminal and interstitial bands and a minimal C-band polymorphism. Agropyron velutinum, fully self-fertile, almost totally lacked C-bands. The Ju, C, E, and J genomes appeared to be distinctive and the equivalence of the E and J genomes was not supported from their C-banding patterns. Four species sharing the S genome, A. spicatum, A. libanoticum, A. ferganense, and A. stipifolium had C-band patterns similar to one another, although C-bands were less prominent in A. stipifolium than others.Key words: C-banding, karyotype, wheatgrass, cytology.


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.


Genome ◽  
1995 ◽  
Vol 38 (6) ◽  
pp. 1271-1278 ◽  
Author(s):  
Jun-Zhi Wei ◽  
W. F. Campbell ◽  
G. J. Scoles ◽  
A. E. Slinkard ◽  
R. Ruey-Chyi Wang

Russian wildrye, Psathyrostachys juncea (Fisch.) Nevski (2n = 2x = 14; NsNs), is an important forage grass and a potential source of germplasm for cereal crop improvement. Because of genetic heterogeneity as a result of its self-incompatibility, it is difficult to identify trisomics of this diploid species based on morphological characters alone. Putative trisomies (2n = 2x + 1 = 15), derived from open pollination of a triploid plant by pollen grains of diploid plants, were characterized by Giemsa C-banding. Based on both karyotypic criteria and C-banding patterns, four of the seven possible primary trisomics, a double-deletion trisomic, and two tertiary trisomics were identified.Key words: Russian wildrye, Psathyrostachys juncea, trisomic, C-banding, karyotype.


Genome ◽  
1989 ◽  
Vol 32 (4) ◽  
pp. 629-639 ◽  
Author(s):  
Ib Linde-Laursen ◽  
Roland von Bothmer ◽  
Niels Jacobsen

Giemsa C-banding patterns of the predominantly self-pollinating, annual species Hordeum marinum (2x, 4x) and H. murinum (2x, 4x, 6x) showed mostly very small to small bands at centromeric and telomeric positions, at one or both sides of the nucleolar constrictions, and at intercalary positions with no preferential disposition. A similar distribution of bands has been observed in other Hordeum species, suggesting that the pattern is the basic one in the genus Hordeum. Hordeum murinum, especially the hexaploid cytotype, was distinguished from H. marinum by having more numerous and more conspicuous bands, resulting in a significantly higher percentage of constitutive heterochromatin (9–17 vs. 4–8%). The differences in C-banding patterns supported by differences in chromosome morphology confirm that H. marinum and H. murinum are not closely related. Banding-pattern polymorphism was prevalent among populations but unobserved within populations. In spite of this polymorphism, banding patterns in combination with chromosome morphology identified homologous chromosomes of different populations of a taxon and indicated that the chromosome complements of the polyploids of both species comprised the genome of the related diploid as well as one or two "unidentified" genomes. This agrees with an alloploid origin of polyploids. The C-banding patterns of H. marinum ssp. marinum and H. marinum ssp. gussoneanum (2x) showed some divergence in spite of the close relationship. The C-banded karyotypes of H. murinum ssp. murinum and H. murinum ssp. leporinum (4x) were very similar, supporting conspecificity. Chromosome lengths and longest/shortest chromosome ratios were fairly similar to those previously published, supporting the conclusion that linear relationships of chromosomes are normally stable within genomes. The taxonomy of the two species is discussed.Key words: C-banding, karyotypes, Hordeum.


Author(s):  
E. K. Gubar ◽  
V. A. Kunakh
Keyword(s):  
Zea Mays ◽  

1982 ◽  
Vol 24 (6) ◽  
pp. 667-673 ◽  
Author(s):  
T. A. Bongso ◽  
M. Hilmi

The chromosomes of the Murrah (River), Swamp (Malaysian kerbau), F1 hybrid (Murrah × Swamp) and first generation backcross (F1 hybrid female × Murrah male) buffaloes (Bubalus bubalis L.) were studied using Giemsa (G) and centromeric (C) banding techniques. The diploid chromosome number for the Murrah was 2n = 50, Swamp 2n = 48, F1 hybrid 2n = 49 and two backcross animals had 2n = 49 and 2n = 50, respectively. The largest two metacentric chromosomes of the Swamp resulted from a tandem fusion between the two chromosomes 4p and 9, respectively, of the Murrah karyotype. The F1 hybrid (2n = 49) and one of the backcrosses (2n = 49) had karyotypes intermediate to the Murrah and Swamp parents. The C banding patterns were useful in identifying the X and Y chromosomes of the buffalo and demonstrated that a major portion of the centromere region of chromosome 9 was not incorporated into chromosome 4 during the tandem fusion.


Caryologia ◽  
2014 ◽  
Vol 67 (4) ◽  
pp. 314-320
Author(s):  
Diego Mattos Penedo ◽  
Jorge Luís Azevedo de Armada ◽  
José Francisco Santos da Silva ◽  
Daniel Marchesi Neves ◽  
Alcides Pissinatti ◽  
...  

Genetica ◽  
1983 ◽  
Vol 61 (1) ◽  
pp. 65-74 ◽  
Author(s):  
J. L. Santos ◽  
P. Arana ◽  
R. Gir�ldez
Keyword(s):  

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