Neurospora

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Neurospora
Neurospora crassahyphae.jpg
Neurospora crassa
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Fungi
Division: Ascomycota
Class: Sordariomycetes
Order: Sordariales
Family: Sordariaceae
Genus: Neurospora
Shear & B.O.Dodge (1927)
Type species
Neurospora sitophila
Shear & B.O.Dodge (1927)
Synonyms [1]
  • GelasinosporaDowding (1933)
  • AnixiellaSaito & Minoura (1948)
  • AnixiellaSaito & Minoura ex Cain (1961)
  • ChrysoniliaArx (1981)
Oncom, made using Neurospora intermedia var. oncomensis Oncom tekstur.jpg
Oncom, made using Neurospora intermedia var. oncomensis

Neurospora is a genus of Ascomycete fungi. The genus name, meaning "nerve spore" refers to the characteristic striations on the spores that resemble axons.

Contents

The best known species in this genus is Neurospora crassa , a common model organism in biology. Neurospora intermedia var. oncomensis is believed to be the only mold belonging to Neurospora which is used in food production (to make oncom). [2]

Characteristics

Neurospora species are molds with broadly spreading colonies, with abundant production of ascomata. Ascomata are superficial or immersed, perithecial and ostiolate or cleistothecial and non-ostiolate, hairy or glabrous, dark coloured. Peridium membranaceous, asci cylindrical, clavate or subspherical, with a persistent or evanescent wall, usually with a thickened and non-amyloid annular structure at the apex, usually 8-spored. Ascospores broadly fusiform, ellipsoidal, or nearly spherical, unicellular, hyaline to yellowish brown or olive-brown, becoming dark and opaque at maturity, ascospore wall with longitudinal ribs or pitted, occasionally nearly smooth, 1–2 (but rarely up to 12) germ pores disposed at the ends of the ascospores, gelatinous sheaths or appendages are absent. Anamorphs are known in only a relatively small number of species, which belong to the fungi imperfecti genus Chrysonilia. The type species of the genus is Neurospora sitophila Shear. [3]

Systematics

The former genus Gelasinospora is closely related and not resolved as a distinct monophyletic group, [4] thus the former genus is nowadays included as a synonym of Neurospora. [3]

Species

As model organisms

Neurospora is widely used in genetics as a model organism (especially N. crassa) because it quickly reproduces, is easy to culture, [5] and can survive on minimal media (inorganic salts, glucose, water and biotin in agar).

The first studies of sexual reproduction in Neurospora were made by B. O. Dodge. Neurospora was later used by George Wells Beadle and Edward Lawrie Tatum in X-ray mutation experiments to discover mutants that would differ in nutritional requirements. The results of their experiments led them to the one gene-one enzyme hypothesis, in which they postulated that every enzyme was encoded with its own gene.

Research with Neurospora is reported semi-annually at the Neurospora Meeting at Asilomar, California, coordinated by the Fungal Genetics Stock Center. Mutant and wild-type strains of Neurospora are available from the FGSC. The FGSC also publishes the Fungal Genetics Reports.

Important people in Neurospora research:

Sexual reproduction

In the heterothallic species Neurospora crassa, the interaction of haploid strains of opposite mating type is necessary for the occurrence of sexual reproduction and the production of ascospores by meiosis. Ascospores then restore haploid individuals of either mating type. The life cycle phase is thus predominantly haploid, however, upon mating, the nuclei do not immediately fuse: karyogamy is delayed until the very onset of meiosis. The resulting mycelium is called a heterokaryon and is neither diploid nor haploid. The genus Neurospora also includes homothallic species in which a single haploid individual carries both mating type loci and can undergo self-fertilization leading to meiosis and sexual reproduction. Neurospora africana is an example of such a species. [12] [13] Additionally, some "Neurospora" species are said pseudohomothallic. They carry both mating types, but in separate nuclei in the same individual. Two haploid nuclei originating from the same meiosis are packaged into one ascospore. [14] The individual is thus permanently heterokaryotic. Examples of this mating system include "Neurospora tetrasperma" and "Neurospora tetraspora". Because heterothallic species necessarily undergo some degree of outcrossing they may benefit from a higher efficiency of selection because of higher effective recombination rates. In contrast, pseudohomothallic and homothallic species do not outcross (or rarely) and do not experience these benefits: in homothallics a reduced efficiency of negative selection has been shown. [15] However, both hetero- and pseudohomothallic species benefit from the masking of deleterious recessive alleles in the heterokaryotic phase. In addition, all species derive the benefits of meiosis that include the removal of stress-induced DNA damages by homologous recombinational repair, and the formation of stress-resistant ascospores.

Related Research Articles

<span class="mw-page-title-main">Basidiomycota</span> Division of fungi

Basidiomycota is one of two large divisions that, together with the Ascomycota, constitute the subkingdom Dikarya within the kingdom Fungi. Members are known as basidiomycetes. More specifically, Basidiomycota includes these groups: agarics, puffballs, stinkhorns, bracket fungi, other polypores, jelly fungi, boletes, chanterelles, earth stars, smuts, bunts, rusts, mirror yeasts, and Cryptococcus, the human pathogenic yeast.

<span class="mw-page-title-main">Ascomycota</span> Division or phylum of fungi

Ascomycota is a phylum of the kingdom Fungi that, together with the Basidiomycota, forms the subkingdom Dikarya. Its members are commonly known as the sac fungi or ascomycetes. It is the largest phylum of Fungi, with over 64,000 species. The defining feature of this fungal group is the "ascus", a microscopic sexual structure in which nonmotile spores, called ascospores, are formed. However, some species of Ascomycota are asexual and thus do not form asci or ascospores. Familiar examples of sac fungi include morels, truffles, brewers' and bakers' yeast, dead man's fingers, and cup fungi. The fungal symbionts in the majority of lichens such as Cladonia belong to the Ascomycota.

<span class="mw-page-title-main">Ascus</span> Spore-bearing cell in ascomycete fungi

An ascus is the sexual spore-bearing cell produced in ascomycete fungi. Each ascus usually contains eight ascospores, produced by meiosis followed, in most species, by a mitotic cell division. However, asci in some genera or species can occur in numbers of one, two, four, or multiples of four. In a few cases, the ascospores can bud off conidia that may fill the asci with hundreds of conidia, or the ascospores may fragment, e.g. some Cordyceps, also filling the asci with smaller cells. Ascospores are nonmotile, usually single celled, but not infrequently may be coenocytic, and in some cases coenocytic in multiple planes. Mitotic divisions within the developing spores populate each resulting cell in septate ascospores with nuclei. The term ocular chamber, or oculus, refers to the epiplasm that is surrounded by the "bourrelet".

<i>Neurospora crassa</i> Species of ascomycete fungus in the family Sordariaceae

Neurospora crassa is a type of red bread mold of the phylum Ascomycota. The genus name, meaning 'nerve spore' in Greek, refers to the characteristic striations on the spores. The first published account of this fungus was from an infestation of French bakeries in 1843.

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<i>Aspergillus nidulans</i> Species of fungus

Aspergillus nidulans is one of many species of filamentous fungi in the phylum Ascomycota. It has been an important research organism for studying eukaryotic cell biology for over 50 years, being used to study a wide range of subjects including recombination, DNA repair, mutation, cell cycle control, tubulin, chromatin, nucleokinesis, pathogenesis, metabolism, and experimental evolution. It is one of the few species in its genus able to form sexual spores through meiosis, allowing crossing of strains in the laboratory. A. nidulans is a homothallic fungus, meaning it is able to self-fertilize and form fruiting bodies in the absence of a mating partner. It has septate hyphae with a woolly colony texture and white mycelia. The green colour of wild-type colonies is due to pigmentation of the spores, while mutations in the pigmentation pathway can produce other spore colours.

<span class="mw-page-title-main">Mating in fungi</span> Combination of genetic material between compatible mating types

Fungi are a diverse group of organisms that employ a huge variety of reproductive strategies, ranging from fully asexual to almost exclusively sexual species. Most species can reproduce both sexually and asexually, alternating between haploid and diploid forms. This contrasts with most multicellular eukaryotes such as mammals, where the adults are usually diploid and produce haploid gametes which combine to form the next generation. In fungi, both haploid and diploid forms can reproduce – haploid individuals can undergo asexual reproduction while diploid forms can produce gametes that combine to give rise to the next generation.

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<span class="mw-page-title-main">Tetrad (meiosis)</span>

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References

  1. "Synonymy: Neurospora Shear & B.O. Dodge, J. Agric. Res., Washington 34: 1025 (1927)". Species Fungorum . Retrieved 13 February 2022.
  2. Ho, C.C. (April 1986). "Identity and characteristics of Neurospora intermedia responsible for oncom fermentation in Indonesia". Food Microbiology. 3 (2): 115–132. doi:10.1016/S0740-0020(86)80035-1.
  3. 1 2 Garcia, D.; et al. (2004). "A synopsis and re-circumscription of Neurospora (syn. Gelasinospora) based on ultrastructural and 28S rDNA sequence data". Mycological Research. 108 (10): 1119–1142. doi:10.1017/s0953756204000218. PMID   15535064. S2CID   31673455.
  4. Cai, L.; et al. (2006). "Phylogenetic investigations of Sordariaceae based on multiple gene sequences and morphology". Mycological Research. 110 (2): 137–150. doi:10.1016/j.mycres.2005.09.014. PMID   16378718.
  5. 1 2 Dodge, B. O. (1932). "Crossing hermaphroditic races of Neurospora". Mycologia. 24 (1): 7–13. doi:10.2307/3753727. JSTOR   3753727.
  6. Zimmer, E. M., August 1946, "MUTANT STRAINS OF NEUROSPORA DEFICIENT IN PARA-AMINOBENZOIC ACID", MA Thesis, Stanford University
  7. Hollaender, A., Sansome E. R., Zimmer, E., Demerec, M., April 1945, "Quantitative Irradiation Experiments with Neurospora crassa. II. Ultraviolet Irradiation", American Journal of Botany 32(4):226-235 Also: "Quantitative effects of radiation on mutation production in Neurospora crassa", Records of the Genetics Society of America, Number Thirteen, 1944
  8. 1 2 Giles, N. H. Jr., Lederberg, E. Z., March 1948, "Induced reversions of biochemical mutants in Neurospora crassa", American Journal of Botany 35(3):150-157
  9. Mitchell HK, Nyc JF (January 1948). "Hydroxyanthranilic Acid as a Precursor of Nicotinic Acid in Neurospora" (PDF). Proc. Natl. Acad. Sci. U.S.A. 34 (1): 1–5. Bibcode:1948PNAS...34....1M. doi: 10.1073/pnas.34.1.1 . PMC   1062899 . PMID   16588774.
  10. Mitchell MB (April 1955). "Aberrant Recombination Of Pyridoxine Mutants of Neurospora". Proc. Natl. Acad. Sci. U.S.A. 41 (4): 215–20. Bibcode:1955PNAS...41..215M. doi: 10.1073/pnas.41.4.215 . PMC   528059 . PMID   16589648.
  11. Merrow, M, Brunner M, Roenneberg T (June 1999). "Assignment of circadian function for the Neurospora clock gene frequency" (PDF). Nature. 399 (6736): 584–586. Bibcode:1999Natur.399..584M. doi:10.1038/21190. hdl: 11370/f3afd147-0431-46a1-9471-3df73e14d070 . PMID   10376598. S2CID   4422762.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  12. Glass NL, Smith ML (August 1994). "Structure and function of a mating-type gene from the homothallic species Neurospora africana". Mol. Gen. Genet. 244 (4): 401–9. doi:10.1007/bf00286692. PMID   8078466. S2CID   19747733.
  13. Metzenberg RL, Glass NL (February 1990). "Mating type and mating strategies in Neurospora". BioEssays. 12 (2): 53–9. doi:10.1002/bies.950120202. PMID   2140508. S2CID   10818930.
  14. Raju, N. B., Perkins, D. D. (1994). "Diverse programs of ascus development in pseudohomothallic species of Neurospora, Gelasinospora, and Podospora". Developmental Genetics. 15 (1): 104–118. doi:10.1002/dvg.1020150111. PMID   8187347.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  15. Nygren, Kristiina, Wallberg, Andreas, Samils, Nicklas, Stajich, Jason E., Townsend, Jeffrey P., Karlsson, Magnus, Johannesson, Hanna (2012). "Analyses of expressed sequence tags in Neurospora reveal rapid evolution of genes associated with the early stages of sexual reproduction in fungi". BMC Evol. Biol. 12 (3): 649–663. doi:10.1016/j.ympev.2011.03.023. PMID   21439389.{{cite journal}}: CS1 maint: multiple names: authors list (link)