Gametogenesis of Chlamydomonas in the dark

When cells of each mating type of Chlamydomonas sp. (Toyonakastrain) were transferred to a nitrogen-free medium and culturedat low temperature (10?C) for 10 to 12 hr, they showed matingactivity even in the dark. The highest activity observed inthe dark, at about 10?C, was similar to that in the light at20?C. Induction in the dark was suppressed by oxygen deficiency.It was also inhibited by addition of 1 to lOmin concentrationsof nutritional nitrogen compounds such as ammonium, nitrateor urea, and of cycloheximide (2 to 20 µg/ml), but notby addition of chloramphenicol, dihydrostreptomycin or spectinomycin.On the other hand, it was slightly promoted by addition of theophylline,aminophylline, cAMP, DB-cAMP, kinetin and abscisic acid. ¹Present address: Department of Animal Virology, The ResearchInstitute for Microbial Diseases, Osaka University, Suita, Osaka565, Japan. (Received June 3, 1976; )     

Gametogenesis in Fundulus heteroclitus

Our present understanding of the structure of the gonads andof gametogenesis in Fundulus helerodilus is briefly reviewed. The testes contain spermatogenic tubules which distally arecomposed of linearly arranged germinal cysts with clones ofsynchronously developing germ cells, and proximally of efferentducts with mature sperm. Within the tubules, those cysts containingspermatogonia are found close to the testicular periphery, whereascysts with mature sperm are contiguous with the efferent ducts.Cytological details of the three principal stages of spermatogenesis,namely spermatocytogenesis, meiosis, and spermiogenesis, arepresented along with examples of the various somatic cells ofthe testis. The ovary consists of numerous ovigerous lamellae which containrandomly arranged follicles in various stages of development.Since follicular growth is asynchronous, follicles of all sizesare present in the ovary during the breeding season and eggsare continuously ovulated into the ovarian lumen. Oocyte growthis divided into five distinct stages: Primary growth (substagesA and B), cortical alveolus formation, vitellogenesis, oocytematuration (substages A and B), and the ovulated egg. This seriesof stages is based both on cytological observations and physiologicalevents.     

Gametogenesis in the Monothalamous Agglutinated Foraminifer Cribrothalammina alba

Gametogenesis in the foraminifer Cribrothalammina alba involves changes in both the gamontic test and cytoplasm. As gametes begin to differentiate and gametic flagella emerge, pores form in a regular array over the gamontic test, constituting the only avenue for gamete release. The spherical, biflagellated gametes average 1.5μ in diameter and are released in rapidly moving swarms along with flagellated “spherical masses” that probably result from incomplete gametic differentiation. Gametogenesis occurs entirely within the test and utilizes the entire cytoplast. After gamete release is complete, the agglutinated test collapses and disaggregates within a fairly short time. Similar modifications of the gamontic test occur during gametogenesis in Ovammina opaca Dahlgren, but are otherwise unknown among monothalamous agglutinated foraminifera at present.     

Current Topics in Organogenesis and Gametogenesis

At the 49th Annual Drosophila Research Conference from April 3-8, 2008 in San Diego there were eight talks and over ninety posters in the section on Organogenesis and Gametogenesis. These covered a wide range of topics within the two broad categories of organ-specific stem cells (including germ cells) and organ-specific developmental programs. Here we discuss eleven of these presentations describing current research into the formation of the gonad, intestine, trachea, muscle and leg joint. The new insights presented advance our understanding of the molecular events that underlie interactions between stem cells and their niches as well as mechanisms underlying tissue-specific differentiation programs.     

Gametogenesis of tobaccoin vitro

Excised anthers ofNicotiana tabacum L. were culturedin vitro at the stage of pollen tetrads, which proved in our experiments to be the most suitable initial stage for cultivation, up to the stage of mature pollen grains, using Ito and Stern's nutrient medium, or this medium supplemented with uracil. Germinating capacity of the pollen grains formed and the lengths of pollen tubes were quantitatively evaluated.     

Peptide signaling in Hydra

Peptides play a number of crucial roles as signaling molecules in metazoans. In order to elaborate a more complete picture of the roles played by peptides in a single organism, we launched the "Hydra Peptide Project". For this project, we used Hydra magnipapillata, a species belonging to Cnidaria, one of the most basal metazoan phyla, and using a peptidomic approach, we systematically identified a number of peptide signaling molecules, their encoding genes and their functions. In this article, we report the peptides isolated from Hydra and other cnidarians, as well as their synthesis, processing and release from the cells to the target. Possible peptide signaling pathways are overviewed and finally we discuss the evolution of the peptide signaling system.     

植物雌配子体发育研究进展

高等植物雌配子体的形成涉及孢原细胞和大孢子母细胞的确立与分化、大孢子发生、功能大孢子以及胚囊的形成和发育等多种复杂调控过程。随着当代生物技术及功能基因组学的发展,近年对雌配子体发育的研究已从细胞学描述逐渐过渡到对基因和发育调控分子机理的探索。以拟南芥、水稻和玉米等模式植物为材料进行的相关研究,丰富了人们对于植物雌配子体和其它有性生殖过程遗传调控机理的认识。本文着重阐述了植物雌配子体发生和发育过程,并综述了这一领域最新研究进展。     

水螅的有性生殖

介绍了水螅的有性生殖,包括精卵发生,受精和胚胎发育,并讨论了杂交受精在水螅分类问题上的意义。     

Axial Patterning in Hydra

Morphogen gradients play an important role in pattern formation during early stages of embryonic development in many bilaterians. In an adult hydra, axial patterning processes are constantly active because of the tissue dynamics in the adult. These processes include an organizer region in the head, which continuously produces and transmits two signals that are distributed in gradients down the body column. One signal sets up and maintains the head activation gradient, which is a morphogenetic gradient. This gradient confers the capacity of head formation on tissue of the body column, which takes place during bud formation, hydra''s mode of asexual reproduction, as well as during head regeneration following bisection of the animal anywhere along the body column. The other signal sets up the head inhibition gradient, which prevents head formation, thereby restricting bud formation to the lower part of the body column in an adult hydra. Little is known about the molecular basis of the two gradients. In contrast, the canonical Wnt pathway plays a central role in setting up and maintaining the head organizer.Morphogen gradients play a critical role in the early stages of embryogenesis in a number of metazoans in that they initiate and are involved in axial patterning processes. Such a gradient also plays a role in axial patterning in hydra, a primitive metazoan. However, unlike in most metazoans, this gradient is continuously active in an adult hydra as part of the tissue dynamics of the adult animal.The structure of a hydra is fairly simple (Fig. ​(Fig.1).1). It consists of a single axis with radial symmetry, which contains a head, body column, and foot along the axis. The head consist of two parts: the hypostome in the apex, and the tentacle zone from which the tentacles emerge in the basal part of the head. The body column has three parts: the gastric region and peduncle in the apical, and basal parts with a budding zone between the gastric region and peduncle. Buds, hydra''s mode of asexual reproduction, emerge from the budding zone between the gastric region and peduncle.Open in a separate windowFigure 1.Longitudinal cross section of an adult hydra. The multiple regions are labeled. The two protrusions from the body column are early and late stages of bud development. The arrows indicate the direction of tissue displacement. (Reprinted from Bode 2001.)Three cell lineages are involved. The axis consists of a cylindrical shell that is made up of two concentric epithelial layers, the ectoderm and endoderm, which are separated by a basement membrane. Interspersed among the epithelial cells of both layers are the cells of the third lineage, the interstitial cell lineage. It consists of interstitial cells, which are multipotent stem cells (David and Murphy 1977), located primarily in the ectoderm throughout the body column. They give rise to neurons, secretory cells, and nematocytes, which are the stinging cells that are typical of cnidarians, as well as gametes when a hydra undergoes sexual reproduction (David and Murphy 1977).In an adult hydra, the epithelial cells of both layers are constantly in the mitotic cycle (David and Campbell 1972; Campbell and David 1974). The expanding tissue in the upper part of the body column is continuously displaced apically into the head (Fig. 1). Once there, it is displaced onto and along the tentacles or into the hypostome, and eventually sloughed when reaching the extremities (Campbell 1967; Otto and Campbell 1977). Tissue in the remainder of the body column is displaced basally either onto developing buds, or further down onto the foot, where it is sloughed at the bottom of the foot. Thus, the tissues of an adult hydra are continuously in a steady state of production and loss. As a hydra has no defined lifetime (Martinez 1998), this activity goes on indefinitely.