Fertilisation of polar nuclei and formation of early endosperms in Dendrobium catenatum: evidence for the second fertilisation in Orchidaceae

2018 ◽  
Vol 66 (4) ◽  
pp. 354 ◽  
Author(s):  
Yong Chen ◽  
Chu Zhang ◽  
Xiao-feng Wang ◽  
Cheng-qi Ao

Whether the second fertilisation, i.e. fertilisation of polar nuclei, or fusion of the second sperm with polar nuclei occurs in Orchidaceae has long been controversial because of lack of evidence. In the present study, we observed fusion and fertilisation of polar nuclei and formation of early endosperms in the orchid Dendrobium catenatum Lindl., by using a resin-embedded section technique. As the product of the second fertilisation, the primary endosperm nucleus (fertilised polar nuclei) can last until the global embryo stage, indicating that initiation of endosperm development and that of embryo development were fully asynchronous. The present study demonstrated the occurrence of the second fertilisation in D. catenatum by providing lines of new evidence.

Author(s):  
Yuanyuan Li ◽  
Ning-Hua Mei ◽  
Gui-Ping Cheng ◽  
Jing Yang ◽  
Li-Quan Zhou

Mitochondrion plays an indispensable role during preimplantation embryo development. Dynamic-related protein 1 (DRP1) is critical for mitochondrial fission and controls oocyte maturation. However, its role in preimplantation embryo development is still lacking. In this study, we demonstrate that inhibition of DRP1 activity by mitochondrial division inhibitor-1, a small molecule reported to specifically inhibit DRP1 activity, can cause severe developmental arrest of preimplantation embryos in a dose-dependent manner in mice. Meanwhile, DRP1 inhibition resulted in mitochondrial dysfunction including decreased mitochondrial activity, loss of mitochondrial membrane potential, reduced mitochondrial copy number and inadequate ATP by disrupting both expression and activity of DRP1 and mitochondrial complex assembly, leading to excessive ROS production, severe DNA damage and cell cycle arrest at 2-cell embryo stage. Furthermore, reduced transcriptional and translational activity and altered histone modifications in DRP1-inhibited embryos contributed to impeded zygotic genome activation, which prevented early embryos from efficient development beyond 2-cell embryo stage. These results show that DRP1 inhibition has potential cytotoxic effects on mammalian reproduction, and DRP1 inhibitor should be used with caution when it is applied to treat diseases. Additionally, this study improves our understanding of the crosstalk between mitochondrial metabolism and zygotic genome activation.


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.


1986 ◽  
Vol 64 (10) ◽  
pp. 2227-2238 ◽  
Author(s):  
J. H. N. Schel ◽  
H. Kieft

A culture method is described which allows the continuous supply of fresh liquid medium and which prevents the accumulation of toxic metabolites. Development of maize embryos and endosperm after various periods of in vitro ovary culture was studied by light and electron microscopy. Using this method the ultrastructural features of embryo development in vitro were similar to those of in vivo embryos. In contrast, the formation of endosperm was irregular with the absence of cellularization of the inner endosperm being frequent. In some cases, only the endosperm developed without any indication of embryo formation. In a calcium-depleted medium, embryo development was normal but again, endosperm formation was aberrant. No cells were formed in the central part of the endosperm and near the placental region degeneration took place, resulting in vacuoles with dark inclusions, clumps of rough endoplasmic reticulum membranes, and cellular breakdown. The events occurring after in vitro culture strongly resemble those taking place after intergeneric crosses or crosses between diploid and tetraploid strains. It is concluded that defective endosperm development is probably the main factor for the failure of embryo development.


Genome ◽  
1992 ◽  
Vol 35 (1) ◽  
pp. 68-77 ◽  
Author(s):  
R. V. Kowles ◽  
M. D. McMullen ◽  
G. Yerk ◽  
R. L. Phillips ◽  
S. Kraemer ◽  
...  

A group of 35 defective kernel (dek) mutants in maize has been studied with regard to their effect on endosperm development. Information is reported on kernel weight, kernel viability, mutant transmission, DNA content per endosperm nucleus, endosperm cell numbers during development, and DNA endoreduplication patterns. All of the dek mutations reduced mitotic activity and resulted in greatly reduced cell numbers. All except one mutation decreased DNA endoreduplication. The exception indicates that the processes of mitotic activity and endoreduplication can be uncoupled. Notable differences in DNA endoreduplication patterns were observed among the dek strains. Defective kernels with homozygous defective embryos did not germinate in any of these strains, although some morphologically defective kernels did germinate and were shown to have normal embryos of +/+ or +/dek genotype. Dek mutants that had a defective endosperm and an embryo that developed normally were not identified. The mutations investigated are recessive, but F2 segregation for many of the mutants revealed significant deviations from expected 3:1 ratios.Key words: defective kernels, endosperm, endoreduplication.


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.


2010 ◽  
Vol 278 (1708) ◽  
pp. 1019-1024 ◽  
Author(s):  
T. R. Birkhead ◽  
N. Hemmings ◽  
C. N. Spottiswoode ◽  
O. Mikulica ◽  
C. Moskát ◽  
...  

The offspring of brood parasitic birds benefit from hatching earlier than host young. A proposed but little-known strategy to achieve this is ‘internal incubation’, by retaining the egg in the oviduct for an additional 24 h. To test this, we quantified the stage of embryo development at laying in four brood parasitic birds (European cuckoo, Cuculus canorus ; African cuckoo, Cuculus gularis ; greater honeyguide, Indicator indicator ; and the cuckoo finch, Anomalospiza imberbis ). For the two cuckoos and the honeyguide, all of which lay at 48 h intervals, embryos were at a relatively advanced stage at laying; but for the cuckoo finch (laying interval: 24 h) embryo stage was similar to all other passerines laying at 24 h intervals. The stage of embryo development in the two cuckoos and honeyguide was similar to that of a non-parasitic species that lay at an interval of 44–46 h, but also to the eggs of the zebra finch Taeniopygia guttata incubated artificially at body temperature immediately after laying, for a further 24 h. Comparison with the zebra finch shows that internal incubation in the two cuckoos and honeyguide advances hatching by 31 h, a figure consistent with the difference between the expected and the observed duration of incubation in the European cuckoo predicted from egg mass. Rather than being a specific adaptation to brood parasitism, internal incubation is a direct consequence of a protracted interval between ovulation (and fertilization) and laying, but because it results in early hatching may have predisposed certain species to become brood parasitic.


2003 ◽  
Vol 358 (1434) ◽  
pp. 1085-1093 ◽  
Author(s):  
A. J. Richards

Apomixis is a common feature of perennial plants, which occurs in ca . 60% of the British flora, but has been largely ignored by reproductive theoreticians. Successful individuals may cover huge areas, and live to great ages, favoured by ‘symmetrical’ selection. Apomixis is favoured by colonizing modes, for instance post–glacially. Despite its theoretical advantages, apomixis usually coexists with sexuality, suggesting ‘hidden’ disadvantages. Agamospermy (apomixis by seed) is relatively uncommon, but gains from the attributes of the seed. It pays agamospermy genes, which discourage recombination, to form co–adapted linkage groups, so that they become targets for disadvantageous recessive mutant accumulation. Consequently, agamospermy genes cannot succeed in diploids and agamosperms are hybrid and highly heterotic. Agamospermous endosperm may suffer from genomic imbalance, so that nutritious ovules, which can support embryos without endosperm, may be preadapted for agamospermy. When primary endosperm nucleus fertilization (‘pseudogamy’) continues as a requirement for many aposporous agamosperms, selfing sex becomes preadaptive and archesporial sex remains an option. Apomictic populations can be quite variable although apomictic families are much less variable than sexuals. Only in some diplosporous species does sex disappear completely, and in those species some release of variability may persist through somatic recombination. The search for an agamospermy gene suitable for genetic modification should target fertile sexuals with a single localized agamospermy ( A ) gene, which therefore lack a genetic load. The A gene should coexist alongside sexuality, so that it would be easy to select seedlings of sexual and asexual origins. Plants with sporophytic agamospermy provide all these attributes.


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.


2007 ◽  
Vol 85 (2) ◽  
pp. 216-223 ◽  
Author(s):  
Paulo Monjardino ◽  
Jorge Machado ◽  
Fabíola S. Gil ◽  
Rui Fernandes ◽  
Roberto Salema

Maize coenocytic and cellularizing endosperm development were characterized at optical and transmission electron microscopy levels. Samples were collected daily in 3 consecutive years under different temperature regimes; therefore, the developmental stages were expressed on a growing degree basis. Soon after the primary endosperm nucleus is formed, it starts dividing without cytokinesis, leading to the formation of the coenocyte. The nuclei divide freely on the periphery of the coenocyte and spread from the micropylar region toward the chalazal region. The first anticlinal walls are formed as the nuclei come closer to each other, followed by periclinal wall formation also starting in the micropylar region. As cellularization proceeds, new anticlinal and periclinal walls assume a less organized pattern until the central vacuole is fully occupied by newly formed cells. Overall, our findings suggest that the developmental pattern of maize coenocytic and cellularizing endosperm has many similarities to other species of the Poaceae family.


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