Early seed development in hexaploid triticale

1973 ◽  
Vol 51 (12) ◽  
pp. 2291-2300 ◽  
Author(s):  
P. J. Kaltsikes

The development of the embryo, endosperm, and antipodals was studied in five hexaploid triticale lines. The egg cell was fertilized 10–15 h after pollination. The first division of the zygote occurred 15–20 h later. Ninety-six hours after pollination there was a twofold difference among the lines in the number of embryo cells, which ranged from 17 to 31. The polar nuclei were fertilized 4–5 h after pollination and the first division of the primary endosperm nucleus took place 2–3 h later. At 60 h the lines examined fell into two groups with respect to endosperm development: one group included 6A190 and 6A250, both raw amphiploids, which had 1032 and 486 endosperm nuclei, respectively; and another which included Rosner, Armadillo 458, and 6517, all products of artificial selection, with 209, 201, and 98 endosperm nuclei, respectively. The first five or six endosperm divisions were highly synchronized while later a gradient was established. Cellularization of endosperm was first observed 96 h after pollination. No appreciable amount of mitotic abnormalities was observed in the endosperm nuclei. In all lines examined endosperm nuclei were found with DNA amount exceeding 6C.The number of antipodals, some of which were highly endopolyploid (up to 256C), ranged from 10 to 30 within and among lines. Disintegration of the antipodals began about 3 days after pollination in 6A190, at 4 days in Rosner, and at 5 days in the other lines. The rate of endosperm development and especially the disintegration of the antipodal complement seemed to be positively related with the amount of seed shrivelling observed in the lines studied.

The rates of early seed development were compared in several species in the Triticeae which play a major role in human nutrition, and in several related genotypes whose reproductive development is of current interest to plant breeders. Embryo and endosperm development during the first five days after pollination was studied in plants of 22 genotypes grown at 20 °C with continuous light. Spikes were emasculated before anther dehiscence and then pollinated once full female receptivity was reached. The numbers of embryo and endosperm nuclei or cells in individual florets were ascertained by using large samples of fertilized florets fixed at various known times after pollination. The pattern of early seed development was essentially the same in wheat, rye, Triticale and barley, although some interspecific variation in the rate between genotypes was noted. Fertilization occurred in some florets of several genotypes studied within 40-60 min after pollination. Mitosis in the primary endosperm nucleus was completed about 6-7 h after pollination. During the next 24-48 h the number of endosperm nuclei increased geometrically, doubling about every 4-5 h. The endosperm was coenocytic at first but usually at about 72 h after pollination it became cellular. The rate of nuclear development in the endosperm declined on each successive day, the greatest fall occurring at the time of cell wall formation. Mitosis in the zygote occurred about 18-30 h after pollination which was later than mitosis in the primary endosperm nucleus. The cell cycle time in the embryo varied between species from about 12 to 18 h, and was similar to its duration in cells of other meristematic tissues in the same species. Cell cycle time in the embryo remained fairly constant during the first 5 days of seed development unlike the rate of nuclear development in the endosperm. Thus, at first the rate of embryo cell development was very slow compared with that of the endosperm nuclei, however, by the end of the fifth day the cell cycle time in the endosperm had increased to become equal to or longer than that of the cell cycle in embryo cells. The nature and possible cause (s) of rapid nuclear development in coenocytic endosperm is discussed. While embryo volume increased steadily over the period studied, the mean volume of embryo cells decreased about tenfold. This was because at first the rate of increase in embryo volume was lower than the rate of increase in embryo cell number. Eventually these two rates became similar and thereafter further development gave rise to embryo cells whose volume was constant and roughly equivalent to that of other meristematic cells in the same species. The rates of embryo and endosperm development were as a rule much faster in wheat species than in rye. By comparison, the rates in hexaploid Triticale genotypes were usually much slower than in wheat, and sometimes even slower than in rye. Results for wheat-rye chromosome addition lines, disomic for each rye chromosome, show that most rye chromosomes apparently had a pronounced effect on slowing both embryo and endosperm development. Indeed, rye chromosomes VI and V II apparently had an effect equal to that of the presence of a whole rye genome. Comparison of the maximum rates of endosperm development in diploid and related polyploid species shows that there was no effect of polyploidy during the first 48 h of the coenocytic phase of endosperm development. Concurrently, during development of the cellular embryo there was a clear effect of ploidy level, with a positive relation between ploidy level and developmental rate. These results are compared with the effects of polyploidy on the rate of development in other tissues in the same species. The rates of embryo and endosperm development in Hordeum vulgare were much faster than in diploid H. bulbosum . This result is discussed with reference to the mechanism of chromosome elimination from embryo and endosperm tissues of Fj-hybrids between these two species. The present results provide a detailed picture of the course of normal early seed development in a wide range of cereal genotypes which varied with respect to several characters known to affect rate of development in other tissues. They provide, therefore, a baseline for comparative studies which aim both to describe abnormal early seed development and to quantify its extent, in for instance Triticale withshrivelled grain. At the same time they provide some indication of the factors which apparently influence or control the rate and extent of early embryo and endosperm development in these important crop species.


1985 ◽  
Vol 27 (2) ◽  
pp. 134-142 ◽  
Author(s):  
J. P. Gustafson ◽  
A. J. Lukaszewski

The early embryo and endosperm development patterns of five annual taxa and three perennial taxa of the genus Secale were analyzed. The results showed that there was considerable variation in the speed of early embryo and endosperm development within the genus Secale, and that the developmental patterns of the annual and perennial taxa overlapped. Comparisons indicated that DNA content per se did not have any influence on the speed of early embryo development or aberrant endosperm nucleus production in either the annual or perennial taxa. However, comparisons between the percent telomeric heterochromatin and the number of embryo cells produced showed a significant positive correlation in the annual taxa, and a nonsignificant correlation in the perennial taxa. There was a positive correlation between the number of aberrant endosperm nuclei and percent telomeric heterochromatin in the annual taxa, while the perennial taxa showed a nonsignificant but negative correlation. The results suggest that percent telomeric heterochromatin has a different effect on early seed development in the annual taxa than in the perennial taxa.Key words: Secale, heterochromatin, DNA content, embryo cell cycle.


1988 ◽  
Vol 8 (10) ◽  
pp. 4322-4327
Author(s):  
M A Harrington ◽  
F Gonzales ◽  
P A Jones

Three developmentally determined myogenic cell lines derived from C3H 10T1/2 C18 (10T1/2) mouse embryo cells treated with 5-azacytidine were compared with the parental 10T1/2 line for their susceptibility to oncogenic transformation by 3-methylcholanthrene or the activated human c-Ha-ras oncogene. Neither the 10T1/2 cells nor the myogenic derivatives grew in soft agar or formed tumors in nude mice. In contrast to 10T1/2 cells, the three myogenic derivatives were not susceptible to transformation by 3-methylcholanthrene, so that cellular determination altered the response of 10T1/2 cells to chemical carcinogen. On the other hand, all cell types were transformed to a tumorigenic phenotype following transfection with the activated c-Ha-ras gene. The transfected myogenic cells expressed both the c-Ha-ras gene and the muscle determination gene MyoD1. In contrast to other reports, the presence of as many as six copies of the c-Ha-ras gene per genome did not prevent the formation of striated muscle cells which expressed immunologically detectable muscle-specific myosin. The expression of the c-Ha-ras gene does not therefore necessarily preclude the expression of the determination gene for myogenesis or prevent end-stage myogenic differentiation.


2009 ◽  
Vol 56 (1) ◽  
pp. 33-41 ◽  
Author(s):  
Hideki Takanashi ◽  
Takayuki Ohnishi ◽  
Mirai Mogi ◽  
Takashi Okamoto ◽  
Shin-ichi Arimura ◽  
...  

1983 ◽  
Vol 25 (3) ◽  
pp. 278-282
Author(s):  
Julian B. Thomas ◽  
P. J. Kaltsikes ◽  
S. Shigenaga

Chromosome 1B in 'Rosner' and chromosome 6B in line 125 both reduced the frequency with which chromosomes were paired at first meiotic metaphase of hexaploid triticale. On the other hand, chromosome 6B in 'Rosner' and chromosomes 1B and 6B in line 110 had no such effect. The 1B pairing suppressor in 'Rosner' was located on the short arm of the chromosome (1Bs). Between 10 and 30 °C, pairing frequency was quite stable in 'Rosner' triticale in comparison with common wheat, although the level was consistently lower in the triticale. Some reduction of pairing frequency was noted at 10 °C in 'Rosner'. This effect of low temperature did not interact with 1B dosage to cause a disproportionate decrease in pairing frequency when plants with high 1B dosage were grown at 10 °C.


1973 ◽  
Vol 51 (5) ◽  
pp. 879-890 ◽  
Author(s):  
William Newcomb

The degeneration of one synergid denotes the initiation of embryo and endosperm development in the embryo sac of sunflower Helianthus annuus L. The other synergid, the persistent synergid, is present until the late globular stage of embryogenesis. The primary endosperm nucleus divides before the zygote nucleus forming a coenocytic nuclear endosperm. When about eight endosperm nuclei are present during the early globular stage of embryogenesis, endosperm wall formation starts at the micropylar end of the embryo sac. The walls continue to grow toward the chalazal end of the embryo sac apparently as a result of the activity of Golgi located at the tips of the growing walls. Most endosperm wall formation is not associated with a mitotic spindle apparatus in sunflower. The suspensor of the embryo consists of a large basal cell during the proembryo stages, a single row of cells during the early globular stages, and at the late globular stage a double tier of cells near the radicle end of the embryo and a single row at the micropylar end of the embryo sac. Occasionally embryo development occurs in the absence of endosperm when only single fertilization has taken place. The development and nutritional implications of post-fertilization events in the sunflower embryo sac are discussed.


2004 ◽  
Vol 52 (1) ◽  
pp. 81 ◽  
Author(s):  
Guohua Ma ◽  
Xuelin Huang ◽  
Nanxian Zhao ◽  
Qiusheng Xu

The cytology, development of aposporous embryo sac, pro-embryo and pseudogamy in Paspalum thunbergii Kunth ex Steud. was studied. P. thunbergii was found to be a tetraploid cytotype, with a chromosome number of 40. Meiosis of the pollen mother cells was irregular, pollen viability was low and multiporate pollens were often observed. Megasporogenesis began normally; however, the megaspore deteriorated at the developmental stage of tetrad, while one to five specific nucellar cells became active and began enlarging, and then developed into aposporous embryo sacs. The mature aposporous sacs usually had three nuclei characterised by one egg cell and two polar nuclei. The egg cell developed spontaneously to form pro-embryos prior to anthesis. When several aposporous sacs occurred in the same ovule, usually one sac near the micropyle was involved in pseudogamy, while the other sacs were not involved. Low frequency of twin-embryo seedlings was observed after seeds matured. Examination of three successive generations by paraffin-section and clearing methods revealed that no sexual sac was present. Therefore, the species P. thunbergii is considered to be an obligate apomict that reproduces by apospory.


Botany ◽  
2011 ◽  
Vol 89 (4) ◽  
pp. 263-273 ◽  
Author(s):  
Edward C. Yeung ◽  
Steve Bowra

Coriander ( Coriandrum sativum L.) seeds are rich in lipids and are potentially important sources of oils for industrial use. The objective of this study was to determine the details of embryo and endosperm development and the sites of storage reserves using microscopy and histochemistry. In coriander, the zygote divides unequally, giving rise to a large basal cell and a smaller terminal cell. Subsequent divisions in the basal cell result in the formation of a suspensor, and divisions in the terminal cell give rise to cells of the embryo proper. A defined cell lineage is absent in the formation of the proembryo. Contrary to other flowering plants, the suspensor persists as the embryo matures and storage products are present within the cytoplasm of the suspensor cells. After fertilization, the primary endosperm nucleus divides rapidly, resulting in a large syncytium of nuclei and cytoplasm. The rapid nuclear divisions occur prior to the first division of the zygote. Cellularization of the endosperm occurs soon after. Within the developing seed, the endosperm can be separated into two main regions, i.e., the “embryo surround region” (ESR) of endosperm and the persistent endosperm. The endosperm cells in these two regions have different cell fates and storage products. In the ESR, the endosperm cells undergo distinct structural changes and are destined to degenerate. These endosperm cells produce a significant amount of polysaccharides and these materials appear to aid in cell separation prior to cell degeneration. At the boundary of the ESR, the endosperm cells are partially degenerated with a large accumulation of lipids. The bulk of the endosperm cells next to the seed coat persist and they are responsible for the production and accumulation of storage lipids and proteins.


Author(s):  
P.V. Rattray ◽  
K.T. Jagusch ◽  
K.S. Maclean

In a trial conducted at Ruakura over 5 years, mixed-age flocks of Coopworth, Perendale, High Fertility Romney and Control Romney ewes were run on separate farmlets stocked at 26, 21 or 16 ewes/ha. At any given pasture allowance the Coopworth ate more pasture than the other breeds. Lambing performance, weight of lamb weaned and fleece weight were curvilinearly related to allowance. Lamb production per ewe tended to level out at a DM allowance of 4 kg/ewe/day for the Perendale and about 5 kg/ewe/day for the other breeds. Pasture allowance accounted for an appreciable amount of variation in animal production between years and stocking rates; litter size, 38 to 90%; lambs weaned/ewes mated. 29 to 71'%; weight of lamb weaned/ewe mated, 26 to 62%; and fleece weight, 25 to 49%. Pasture allowance accounted for the least variation in all variables in the Perendale compared with the other breeds.


1976 ◽  
Vol 18 (4) ◽  
pp. 687-700 ◽  
Author(s):  
J. B. Thomas ◽  
P. J. Kaltsikes

Differential staining of telomeric rye heterochromatin and telocentric chromosomes were used to identify chromosomes which were unpaired at first meiotic metaphase of hexaploid triticale (× Triticosecale Wittmack). Both approaches showed that it was the rye chromosomes which were seen as univalents. Differences in the rate of pairing from triticale to triticale were mostly explained by variation in the pairing of the rye genome. Within the rye genome, chromosome arms with telomeric heterochromatin showed pairing rates much lower than chromosome arms lacking heterochromatin. Wheat telocentrics and heterochromatin-free rye telocentrics which showed intermediate levels of pairing failure (65-90%), had mostly terminal chiasmata. On the other hand rye telocentrics with large heterochromatin bands on the telomeres had mostly nonterminal chiasmata and very low pairing (5-35%). It is concluded that the presence of heterochromatin on certain telomeres of rye chromosomes blocks the formation of terminal chiasmata and this results in desynapsis and univalents at MI.


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