About: Antheridium is a research topic. Over the lifetime, 190 publications have been published within this topic receiving 2974 citations. The topic is also known as: Antheridium.
TL;DR: The investigations led to the conclusion that APt functions by cancelling a light-dependent block to antheridium formation and suggest that in darkness this block decays without the intervention of APt.
Abstract: Dopp has demonstrated an antheridium-inducing hormone (antheridiogen) in P.aquilinum. This antheridiogen (abbr. Apt.) is active in many, if not all, species of the family Polypodiaceae. Among responsive species, the minimally effective concentration varies widely. Apt was assayed againstOnoclea sensibilis because this species fails to form antheridia spontaneously under the prevailing conditions of culture and because none of the many species tested responds to a lower concentration APt is inactive toward the investigated species of the fern families Osmundaceae, Cyatheaceae and Schizaeaceae. The two schizaeaceous speciesAnema phyllitidis andLygodium japonicum also elaborate antheridiogens (abbr. AAn and ALy). Both these antheridiogens are inactive in 0.sensibilis, the species used to assay for APt. AAn, ALy, APt and AOn (the antheridiogen of O.sensibilis) are distinct entities based both on the criteria of cross-testing and of Chromatographic separation. Cross-testing led to the conclusion that the antheridiogen ofCeratopteris thalictroides differ from APt and AAn. Gibberellins have antheridiogenic properties in schizaeaceous species but, like AAn and ALy, they fail to hasten antheridium formation in the species used to assay for APt. The native antheridiogens of schizaeaceous species are more species-selective in their action than is GA3. AAn has recently been isolated. Its structure is similar to, if not identical with, that of gibberellins. AAn behaves like a weak gibberellin in several higher plant assay systems. The prothalli ofP. aquilinum andO. sensibilis become insensitive to Apt as they attain heart shape or shortly thereafter. Prothalli ofP. aquilinum do not begin to synthesize APt and secrete it into the medium, until after they have become insensitive to it. It is in consequence of this that the most rapidly growing and developing individuals attain the archegonial phase without a prior antheridial phase. Various mechanisms and developmental characteristics are described, which strongly favor cross-fertilization inP. aquilinum without, however, eliminating an opportunity for self-fertilization. The cells of abortive antheridium initials, and of “green antheridia”, exhibit certain characteristics of green vegetative cells. These atypical structures appear to arise when early antheridial stages are overtaken by conditions unfavorable to antheridium differentiation. The observations suggest that APt may be required beyond an initial inductive event. The investigations led to the conclusion that APt functions by cancelling a light-dependent block to antheridium formation and suggest that in darkness this block decays without the intervention of APt. InPolypodium crassifolium, the light-effect on antheridium formation is mediated by phytochrome. Other subject matters discussed include: The cellular location of antheridium initials; the relationship of antheridiogen to antheridiogen structure; the existence of a switching mechanism in the sexual development ofO. sensibilis; the retrieval of genetic information in the induction and differentiation of antheridia; the tempero-spatial pattern of competence to antheridiogen in schizaeaceous species and the inducibility of a physiological state antagonistic to antheridium formation in A.phyllitidis.
TL;DR: Findings suggest the VIIIa bHLH proteins as core regulators for reproductive development, including germ cell differentiation, since an early stage of land plant evolution.
TL;DR: This study provides a transcriptional framework on which to study the molecular mechanism of plant motile sperm development in M. polymorpha as a model and shows that some of them had distinct expression patterns in the spermatogenous tissue of developing antheridia.
Abstract: In land plants, there are two types of male gametes: one is a non-motile sperm cell which is delivered to the egg cell by a pollen tube, and the other is a motile sperm cell with flagella. The molecular mechanism underlying the sexual reproduction with the egg and pollen-delivered sperm cell is well understood from studies using model plants such as Arabidopsis and rice. On the other hand, the sexual reproduction with motile sperm has remained poorly characterized, due to the lack of suitable models. Marchantia polymorpha L. is a model basal land plant with sexual reproduction involving an egg cell and bi-flagellated motile sperm. To understand the differentiation process of plant motile sperm, we analyzed the gene expression profile of developing antheridia of M. polymorpha. We performed RNA-sequencing experiments and compared transcript profiles of the male sexual organ (antheridiophore and antheridium contained therein), female sexual organ (archegoniophore) and a vegetative organ (thallus). Transcriptome analysis showed that the antheridium expresses nearly half of the protein-coding genes predicted in the genome, but it also has unique features. The antheridium transcriptome shares some common features with male gamete transcriptomes of angiosperms and animals, and homologs of genes involved in male gamete formation and function in angiosperms and animals were identified. In addition, we showed that some of them had distinct expression patterns in the spermatogenous tissue of developing antheridia. This study provides a transcriptional framework on which to study the molecular mechanism of plant motile sperm development in M. polymorpha as a model.
TL;DR: The formation of the antheridium from an enlarged nodal cell is described and a characteristic, highly organized grouping of many cytoplasmic microtubules forms a band which appears to wind through the cy toplasm; its significance and functions are obscure.
Abstract: The formation of the antheridium from an enlarged nodal cell is described. After a basal cell has been cut off, precisely oriented mitoses divide the antheridial cell initially into octants; then follow two periclinal divisions in each octant. The outer layer of cells become the shield cells, the middle form the manubria, and the inner capitula cells divide further to produce secondary capitula and ultimately the spermatogenous threads. The shield cells become compartmentalized during enlargement by ingrowths in the wall which finally form a very distinctive pattern. Microtubules are associated with the regions of wall deposition. Plastids in the shields accumulate large numbers of globuli, and this is probably associated with the orange pigmentation they acquire. Large amounts of material seem to be secreted into the antheridia by the manubria; this material is formed within large vesicles which are apparently discharged through the plasmalemma. In the young capitula, a characteristic, highly organized grouping of many cytoplasmic microtubules forms a band which appears to wind through the cytoplasm; its significance and functions are obscure. Presumptive "spherosomes" are present in large numbers in these and spermatogenous cells. The spherosomes and lipid-like inclusions are very frequently coated with membranes of the endoplasmic reticulum.