Gametangiogamy

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The steps of life cycle of fungus Taphrina, with karyogamy (4) and gametangiogamy (A) Taphrina life cycle.svg
The steps of life cycle of fungus Taphrina, with karyogamy (4) and gametangiogamy (A)

Gametangiogamy is the fusion or copulation of whole gametangia in certain Zygomycetes and Ascomycetes. The copulated union of multinuclear cells is followed after a more or less long period dikaryophase, by a pairwise fusion (karyogamy) of sexually different nuclei.

In this case, karyogamy takes place simultaneously between the nuclei of many pairs of nuclei, not as in gametogamy between two gametic nuclei (polyfertilization). [1] [2]

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Karyogamy

Karyogamy is the final step in the process of fusing together two haploid eukaryotic cells, and refers specifically to the fusion of the two nuclei. Before karyogamy, each haploid cell has one complete copy of the organism's genome. In order for karyogamy to occur, the cell membrane and cytoplasm of each cell must fuse with the other in a process known as plasmogamy. Once within the joined cell membrane, the nuclei are referred to as pronuclei. Once the cell membranes, cytoplasm, and pronuclei fuse together, the resulting single cell is diploid, containing two copies of the genome. This diploid cell, called a zygote or zygospore can then enter meiosis, or continue to divide by mitosis. Mammalian fertilization uses a comparable process to combine haploid sperm and egg cells (gametes) to create a diploid fertilized egg.

Plasmogamy is a stage in the sexual reproduction of fungi, in which the protoplasm of two parent cells fuses together without the fusion of nuclei, effectively bringing two haploid nuclei close together in the same cell. This state is followed by karyogamy, where the two nuclei fuse together and then undergo meiosis to produce spores. The dikaryotic state that comes after plasmogamy will often persist for many generations before the fungi undergoes karyogamy. In lower fungi however, plasmogamy is usually immediately followed by karyogamy. A comparative genomic study indicated the presence of the machinery for plasmogamy, karyogamy and meiosis in the Amoebozoa.

Heterokaryon

A heterokaryon is a multinucleate cell that contains genetically different nuclei. Heterokaryotic and heterokaryosis are derived terms. This is a special type of syncytium. This can occur naturally, such as in the mycelium of fungi during sexual reproduction, or artificially as formed by the experimental fusion of two genetically different cells, as e.g., in hybridoma technology.

Dikaryon

The dikaryon is a nuclear feature which is unique to certain fungi. Compatible cell-types can fuse cytoplasms (plasmogamy). When this occurs, the two nuclei of two cells pair off and cohabit without fusing (karyogamy). This can be maintained for all the cells of the hyphae by synchronously dividing so that pairs are passed to newer cells. In the Ascomycota this attribute is most often found in the ascogenous hyphae and ascocarp while the bulk of the mycelium remains monokaryotic. In the Basidiomycota this is the dominant phase, with most Basidiomycota monokaryons weakly growing and short-lived.

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Teliospore

Teliospore is the thick-walled resting spore of some fungi, from which the basidium arises.

Sporogenesis is the production of spores in biology. The term is also used to refer to the process of reproduction via spores. Reproductive spores were found to be formed in eukaryotic organisms, such as plants, algae and fungi, during their normal reproductive life cycle. Dormant spores are formed, for example by certain fungi and algae, primarily in response to unfavorable growing conditions. Most eukaryotic spores are haploid and form through cell division, though some types are diploid or dikaryons and form through cell fusion.

Dikarya Subkingdom of fungi

Dikarya is a subkingdom of Fungi that includes the divisions Ascomycota and Basidiomycota, both of which in general produce dikaryons, may be filamentous or unicellular, but are always without flagella. The Dikarya are most of the so-called "higher fungi", but also include many anamorphic species that would have been classified as molds in historical literature. Phylogenetically the two divisions regularly group together. In a 1998 publication, Thomas Cavalier-Smith referred to this group as the Neomycota.

The parasexual cycle, a process restricted to fungi and single-celled organisms, is a nonsexual mechanism of parasexuality for transferring genetic material without meiosis or the development of sexual structures. It was first described by Italian geneticist Guido Pontecorvo in 1956 during studies on Aspergillus nidulans. A parasexual cycle is initiated by the fusion of hyphae (anastomosis) during which nuclei and other cytoplasmic components occupy the same cell. Fusion of the unlike nuclei in the cell of the heterokaryon results in formation of a diploid nucleus (karyogamy), which is believed to be unstable and can produce segregants by recombination involving mitotic crossing-over and haploidization. Mitotic crossing-over can lead to the exchange of genes on chromosomes; while haploidization probably involves mitotic nondisjunctions which randomly reassort the chromosomes and result in the production of aneuploid and haploid cells. Like a sexual cycle, parasexuality gives the species the opportunity to recombine the genome and produce new genotypes in their offspring. Unlike a sexual cycle, the process lacks coordination and is exclusively mitotic.

Brachymeiosis

Brachymeiosis was a hypothesized irregularity in the sexual reproduction of ascomycete fungi, a variant of meiosis following an "extra" karyogamy step. The hypothesized process would have transformed four diploid nuclei into eight haploid ones. The current scientific consensus is that brachymeiosis does not occur in any fungi.

References

  1. Hartmann M. (1904): Sexuele Differenzirung und relative Sexualität. Studia Mendeliana, Brünn: 203.
  2. Kniep H. (1928): Die Sexualität der niederen Pflanzen. Fischer, Jena.