FUSION OF CHROMOCENTERS IN PREMEIOTIC INTERPHASE OF SECALE CEREALE AND ITS POSSIBLE RELATIONSHIP TO CHROMOSOME PAIRING

1977 ◽  
Vol 19 (2) ◽  
pp. 313-321 ◽  
Author(s):  
J. G. Bowman ◽  
Tibor Rajhathy
Keyword(s):  
Chromosome Pairing ◽  
Secale Cereale ◽  
Disruptive Effect ◽  
Immature Inflorescence ◽  
Multivalent Formation ◽  
Relationship Of ◽  
The Relationship ◽  
Metaphase I

The premeiotic interphase of rye has been found to exhibit a synchronized fusion of chromocenters. This results in a solid knot of heterochromatin localized to one side of the nucleus. Colchicine injected into the immature inflorescence of diploid rye has been found to induce univalent and multivalent formation at metaphase I. The early premeiotic interphase was the phase of development most sensitive to colchicine. Colchicine was also found to have a similar disruptive effect on fusion of chromocenters in the premeiotic interphase. The relationship of these observations to chromosome pairing is discussed.

Dilemma of genome relationship in the diploid species Thinopyrum bessarabicum and Thinopyrum elongatum (Triticeae: Poaceae)

Genome ◽  
1990 ◽  
Vol 33 (6) ◽  
pp. 944-946 ◽  
Author(s):  
Prem P. Jauhar
Keyword(s):  
Chromosome Pairing ◽  
Constitutive Heterochromatin ◽  
Diploid Species ◽  
Total Content ◽  
Ploidy Levels ◽  
5S Dna ◽  
Thinopyrum Bessarabicum ◽  
Thinopyrum Elongatum ◽  
Relationship Of ◽  
The Relationship

Evidence on the relationship of the J genome of diploid Thinopyrum bessarabicum and the E genome of diploid Thinopyrum elongatum (= Lophopyrum elongatum) is discussed. Low chromosome pairing between J and E at different ploidy levels, suppression of J–E pairing by the Ph1 pairing regulator that inhibits homoeologous pairing, complete sterility of the diploid hybrids (JE), karyotypic differentiation of the two genomes and differences in their biochemical organization as reflected in total content and distribution of constitutive heterochromatin, and marked differences in isozymes, 5S DNA, and rDNA indicate that J and E are distinct genomes. These genomes are homoeologous and not homologous. There is no justification for the merger of J and E genomes.Key words: chromosome pairing, Ph1 pairing regulator, C-banding, isozymes, 5S DNA, rDNA.

Homology of chromosomes of the X genomes in common and Uruguayan dallisgrass, Paspalum dilatatum

Genome ◽  
1991 ◽  
Vol 34 (6) ◽  
pp. 950-953 ◽  
Author(s):  
Byron L. Burson
Keyword(s):  
Chromosome Pairing ◽  
Chromosome Numbers ◽  
The Other ◽  
Paspalum Dilatatum ◽  
Intraspecific Hybridization ◽  
The Common ◽  
Complete Sets ◽  
The Relationship ◽  
Metaphase I

Two biotypes of dallisgrass, Paspalum dilatatum Poir., designated common and Uruguayan, have chromosome numbers and genome formulas of 2n = 5x = 50 (IIJJX) and 2n = 6x = 60 (IIJJXX), respectively. The relationship between the X genomes in these two biotypes is unknown, and each was arbitrarily assigned the letter X to designate an unknown genome. This study was undertaken to determine the relationship between the X genomes in these two biotypes. Because both biotypes are apomicts and cannot be crossed, a sexual intraspecific F1 hybrid (2n = 45) between sexual yellow-anthered (2n = 4x = 40; IIJJ) and common dallisgrass biotypes was crossed with Uruguayan dallisgrass. This F1 hybrid has complete sets of the I and J genomes but only 5 of the 10 chromosomes of the X genome from common dallisgrass. Two hybrids were recovered. One had 52 and the other had 53 chromosomes, which associated at metaphase I as 22 bivalents + 8 univalents and 23 bivalents + 7 univalents, respectively. Twenty bivalents represent pairing of members of the I and J genomes, and those in excess of 20 represent pairing between members of the two X genomes. The remaining members of the X genome from the Uruguayan biotype were present as univalents at metaphase I. This demonstrates that those chromosomes of the X genome from the common biotype that were present are homologous to members of the X genome of the Uruguayan biotype. Both hybrids are aposporous facultative apomicts with some sterility.Key words: meiosis, intraspecific hybridization, chromosome pairing, genome relations, apomixis.

Genome analysis of Elymus alatavicus and E. batalinii (Poaceae: Triticeae)

1986 ◽  
Vol 28 (5) ◽  
pp. 770-776 ◽  
Author(s):  
Kevin B. Jensen ◽  
Douglas R. Dewey ◽  
Kay H. Asay
Keyword(s):  
Chromosome Pairing ◽  
Genome Analysis ◽  
Taxonomic Classification ◽  
Meiotic Behaviour ◽  
Pseudoroegneria Spicata ◽  
Mode Of Reproduction ◽  
The Relationship ◽  
Partial Fertility ◽  
Metaphase I

Elymus alatavicus (Drob.) A. Love and E. batalinii (Krasn.) A. Love were studied to determine (i) meiotic behaviour, (ii) the mode of reproduction, (iii) the relationship between the two species, (iv) genomic constitutions, and (v) the most logical taxonomic classification of both species. A series of F1 hybrids between E. alatavicus, E. batalinii, and six "analyzer" species were developed. Chromosome pairing was studied at metaphase I to identify genomic similarities or differences. The results showed that E. alatavicus and E. batalinii are caespitose, self-fertile allohexaploids (2n = 42) with the same genomic formula SSYYXX. The F1 hybrids between E. alatavicus and E. batalinii had complete pairing (21 bivalents) at metaphase I in 7% of the cells and almost complete pairing in the remaining cells. High chromosome pairing and partial fertility (4 seeds/plant) in the F1 hybrids shows that the two species are closely related. Hybrids were obtained between E. alatavicus or E. batalinii and the following "analyzer" species with known genomic formulas: Pseudoroegneria spicata (Pursh) A. Love, 2n = 14, SS; P. cognata (Hack.) A. Love, 2n = 14, SS; E. lanceolatus (Scribn. &Smith) Gould, 2n = 28, SSHH; E. trachycaulus1 (Link) Gould ex Shinners, 2n = 28, SSHH; E. mutabilis (Drob.) Tzvelev, 2n = 28, SSHH; and E. drobovii (Nevski) Tzvelev, 2n = 42, SSHHYY. Chromosome pairing in this series of hybrids demonstrated that E. alatavicus and E. batalinii contain an S and probably a Y genome plus an unknown genome, X, that may have been derived from Psathryostachys huashanica Keng or from Agropyron. Elymus alatavicus and E. batalinii are correctly classified in the genus Elymus.Key words: cytotaxonomy, Agropyron, meiosis, chromosome.

Relationship between pachytene synapsis, metaphase I associations, and transmission of 2B and 4B chromosomes in rye

Genome ◽  
2000 ◽  
Vol 43 (2) ◽  
pp. 232-239 ◽  
Author(s):  
Guillermo Jiménez ◽  
Silvia Manzanero ◽  
María J Puertas
Keyword(s):  
Secale Cereale ◽  
Maternal Effect ◽  
Chiasma Frequency ◽  
Transmission Rate ◽  
Chiasma Formation ◽  
B Chromosomes ◽  
Bivalent Formation ◽  
The Relationship ◽  
Variable Efficiency ◽  
Metaphase I

2B rye plants selected for high (H) or low (L) B transmission rate were studied at pachytene and metaphase I of meiosis to determine the relationship between synapsis, bivalents at metaphase I, and B transmission rate. The results show that the 2 B chromosomes (Bs) form bivalents at pachytene in both the H and L lines, whereas the frequency of bivalents at metaphase I is much higher in the H than in the L line. This demonstrates that B transmission is mainly related to the proper association of Bs at metaphase I, as well as that synapsis of the 2 Bs in the L line is normal, but the bivalent is not consolidated by a chiasma in most cases. Crosses were made between 2B plants of the H and L lines in all combinations (H × H, H × L, L × H, and L × L) to obtain 4B plants. Similarly, bivalent formation at pachytene and metaphase I was studied. The results show that 4B plants of the H × H and L × L classes differ significantly at pachytene and metaphase I since the former forms more bivalents. The heterozygous 4 Bs of the H × L and L × H classes show intermediate values. The relation H × H > H × L > L × H > L × L was consistently found for the variables transmission rate, bivalents at pachytene, bivalents at metaphase I, and B mean chiasma frequency. A maternal effect was also found. Our data suggest that there are two separate mechanisms acting upon synapsis and chiasma formation in H and L B chromosomes: (i) there is variable efficiency of the control of synapsis at early stages of meiosis; and (ii) there is variable efficiency of the control of the number of chiasmata. Key words: B chromosomes, synaptonemal complex, Secale cereale.

GENOME RELATIONS BETWEEN PASPALUM CONSPERSUM AND TWO DIPLOID PASPALUM SPECIES

1978 ◽  
Vol 20 (3) ◽  
pp. 365-372 ◽  
Author(s):  
Byron L. Burson
Keyword(s):  
Chromosome Number ◽  
Chromosome Pairing ◽  
Mean Frequency ◽  
Hybrid Plants ◽  
The Mean ◽  
The Cross ◽  
Relationship Of ◽  
The Relationship

Paspalum conspersum Schrad. ex Schult., 2n = 4x = 40, was crossed with P. intermedium Munro ex Morong, 2n = 2x = 20, and P. jurgensii Hackel, 2n = 2x = 20, and the hybrids were studied cytologically to determine the relationship between these species. Thirteen P. intermedium × P. conspersum hybrid plants were produced; however, only eight survived. They had a chromosome number of 2n = 3x = 30. Meiosis was irregular with a chromosome pairing relationship of 19.87 univalents, 5.03 bivalents, and 0.03 trivalents per cell. These findings suggested that the two species have a partially homologous genome. The two hybrids obtained from the cross between P. jurgensii and P. conspersum had a chromosome number of 2n = 3x = 30. The mean chromosome pairing in these hybrids was 10.12 univalents. 9.86 bivalents, 0.08 trivalents, and 0.004 quadrivalents. The close bivalent pairing and a mean frequency of 9.86 bivalents suggested that the P. jurgensii genome was homologous to one genome of P. conspersum. Limited autosyndetic pairing of the P. conspersum chromosomes was also detected in both groups of hybrids. A standardization of genome formulas for the genus was proposed in which P. intermedium, P. jurgensii, and P. conspersum were represented by genome formulas of II, JJ, and I2I2 JJ, respectively. The genome relationships and formulas were discussed for other related Paspalum species.

The relationship of the scleractinian corals to the rugose corals

Paleobiology ◽  
1980 ◽  
Vol 6 (02) ◽  
pp. 146-160 ◽  
Author(s):  
William A. Oliver
Keyword(s):  
Critical Points ◽  
Scleractinian Corals ◽  
Convincing Evidence ◽  
Early Triassic ◽  
Rugose Corals ◽  
History Of ◽  
The Subject ◽  
Relationship Of ◽  
The Relationship ◽  
Biologic Factors

The Mesozoic-Cenozoic coral Order Scleractinia has been suggested to have originated or evolved (1) by direct descent from the Paleozoic Order Rugosa or (2) by the development of a skeleton in members of one of the anemone groups that probably have existed throughout Phanerozoic time. In spite of much work on the subject, advocates of the direct descent hypothesis have failed to find convincing evidence of this relationship. Critical points are:(1) Rugosan septal insertion is serial; Scleractinian insertion is cyclic; no intermediate stages have been demonstrated. Apparent intermediates are Scleractinia having bilateral cyclic insertion or teratological Rugosa.(2) There is convincing evidence that the skeletons of many Rugosa were calcitic and none are known to be or to have been aragonitic. In contrast, the skeletons of all living Scleractinia are aragonitic and there is evidence that fossil Scleractinia were aragonitic also. The mineralogic difference is almost certainly due to intrinsic biologic factors.(3) No early Triassic corals of either group are known. This fact is not compelling (by itself) but is important in connection with points 1 and 2, because, given direct descent, both changes took place during this only stage in the history of the two groups in which there are no known corals.

Skeletal elements of crinoid echinoderms: High-resolution structural and microanalytical results

1983 ◽  
Vol 41 ◽  
pp. 194-195
Author(s):  
D. F. Blake ◽  
L. F. Allard ◽  
D. R. Peacor
Keyword(s):  
High Resolution ◽  
Marine Invertebrates ◽  
Sea Urchins ◽  
Structural Features ◽  
Sea Stars ◽  
High Resolution Tem ◽  
Relationship Of ◽  
The Relationship ◽  
Insight Into

Echinodermata is a phylum of marine invertebrates which has been extant since Cambrian time (c.a. 500 m.y. before the present). Modern examples of echinoderms include sea urchins, sea stars, and sea lilies (crinoids). The endoskeletons of echinoderms are composed of plates or ossicles (Fig. 1) which are with few exceptions, porous, single crystals of high-magnesian calcite. Despite their single crystal nature, fracture surfaces do not exhibit the near-perfect {10.4} cleavage characteristic of inorganic calcite. This paradoxical mix of biogenic and inorganic features has prompted much recent work on echinoderm skeletal crystallography. Furthermore, fossil echinoderm hard parts comprise a volumetrically significant portion of some marine limestones sequences. The ultrastructural and microchemical characterization of modern skeletal material should lend insight into: 1). The nature of the biogenic processes involved, for example, the relationship of Mg heterogeneity to morphological and structural features in modern echinoderm material, and 2). The nature of the diagenetic changes undergone by their ancient, fossilized counterparts. In this study, high resolution TEM (HRTEM), high voltage TEM (HVTEM), and STEM microanalysis are used to characterize tha ultrastructural and microchemical composition of skeletal elements of the modern crinoid Neocrinus blakei.

Studies on Leukemogenic and Sarcomagenic Viruses

1970 ◽  
Vol 28 ◽  
pp. 156-157
Author(s):  
Leon Dmochowski
Keyword(s):  
Electron Microscopy ◽  
Electron Microscope ◽  
Morphological Properties ◽  
Mode Of Development ◽  
Relationship Of ◽  
The Relationship

Electron microscopy has proved to be an invaluable discipline in studies on the relationship of viruses to the origin of leukemia, sarcoma, and other types of tumors in animals and man. The successful cell-free transmission of leukemia and sarcoma in mice, rats, hamsters, and cats, interpreted as due to a virus or viruses, was proved to be due to a virus on the basis of electron microscope studies. These studies demonstrated that all the types of neoplasia in animals of the species examined are produced by a virus of certain characteristic morphological properties similar, if not identical, in the mode of development in all types of neoplasia in animals, as shown in Fig. 1.

The relationship of IGE receptor topography to signaling activity in RBL-2H3 mast cells

1991 ◽  
Vol 49 ◽  
pp. 236-237
Author(s):  
J.R. Pfeiffer ◽  
J.C. Seagrave ◽  
C. Wofsy ◽  
J.M. Oliver
Keyword(s):  
Mast Cells ◽  
Protein A ◽  
Scattered Electron ◽  
Ige Receptor ◽  
Receptor Complexes ◽  
Ige Binding ◽  
Electron Imaging ◽  
Small Clusters ◽  
Relationship Of ◽  
The Relationship

In RBL-2H3 rat leukemic mast cells, crosslinking IgE-receptor complexes with anti-IgE antibody leads to degranulation. Receptor crosslinking also stimulates the redistribution of receptors on the cell surface, a process that can be observed by labeling the anti-IgE with 15 nm protein A-gold particles as described in Stump et al. (1989), followed by back-scattered electron imaging (BEI) in the scanning electron microscope. We report that anti-IgE binding stimulates the redistribution of IgE-receptor complexes at 37“C from a dispersed topography (singlets and doublets; S/D) to distributions dominated sequentially by short chains, small clusters and large aggregates of crosslinked receptors. These patterns can be observed (Figure 1), quantified (Figure 2) and analyzed statistically. Cells incubated with 1 μg/ml anti-IgE, a concentration that stimulates maximum net secretion, redistribute receptors as far as chains and small clusters during a 15 min incubation period. At 3 and 10 μg/ml anti-IgE, net secretion is reduced and the majority of receptors redistribute rapidly into clusters and large aggregates.

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