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Discomycetes

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Discomycetes is a former taxonomic class of Ascomycete fungi which contains all of the cup, sponge and brain fungi, and some club-like fungi. It includes typical cup fungi like the scarlet elf cup and the orange peel fungus , and fungi with fruiting bodies of more unusual shape, such as morels , truffles and the swamp beacon . New taxonomic and molecular data fail to support the monophyly of the Discomycetes.

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37-564: Discomycetes are usually small and cup shaped, and come in singular form. A common feature of Discomycetes are the asci , which are typically produced on the surface of cup-like fruiting bodies. In most discomycetes, each ascus contains eight sexual spores that are forcibly discharged into the air when mature. In modern classifications, the members of the obsolete class are included in Pezizomycetes , Lecanoromycetes , Leotiomycetes and Sordariomycetes . This fungus -related article

74-455: A haploid cells, have been outlined by Fincham and Day and Wagner and Mitchell. After fusion of the cells, the further fusion of their nuclei is delayed. Instead, a nucleus from the fertilizing cell and a nucleus from the ascogonium become associated and begin to divide synchronously. The products of these nuclear divisions (still in pairs of unlike mating type, i.e. A/a ) migrate into numerous ascogenous hyphae, which then begin to grow out of

111-555: A mitotic division. Two meiotic divisions turn the original diploid zygote nucleus into four haploid ones. That is, the single original diploid cell from which the whole process begins contains two complete sets of chromosomes . In preparation for meiosis, all the DNA of both sets is duplicated, to make a total of four sets. The nucleus that contains the four sets divides twice, separating into four new nuclei – each of which has one complete set of chromosomes. Following this process, each of

148-405: A nucleus in each ascus. Meiosis is an essential part of the life cycle of all sexually reproducing organisms, and in its main features, meiosis in N. crassa seems typical of meiosis generally. As the above events are occurring, the mycelial sheath that had enveloped the ascogonium develops as the wall of the perithecium, becomes impregnated with melanin, and blackens. The mature perithecium has

185-488: A . There is no evident morphological difference between the A and a mating type strains. Both can form abundant protoperithecia, the female reproductive structure (see Figure). Protoperithecia are formed most readily in the laboratory when growth occurs on solid (agar) synthetic medium with a relatively low source of nitrogen. Nitrogen starvation appears to be necessary for expression of genes involved in sexual development. The protoperithecium consists of an ascogonium,

222-479: A coiled multicellular hypha that is enclosed in a knot-like aggregation of hyphae. A branched system of slender hyphae, called the trichogyne, extends from the tip of the ascogonium projecting beyond the sheathing hyphae into the air. The sexual cycle is initiated (i.e. fertilization occurs) when a cell (usually a conidium) of opposite mating type contacts a part of the trichogyne (see Figure). Such contact can be followed by cell fusion leading to one or more nuclei from

259-401: A few cases, the ascospores can bud off conidia that may fill the asci (e.g. Tympanis ) 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 (lacking a septum ), and in some cases coenocytic in multiple planes. Mitotic divisions within

296-432: A flask-shaped structure. A mature perithecium may contain as many as 300 asci, each derived from identical fusion diploid nuclei. Ordinarily, in nature, when the perithecia mature the ascospores are ejected rather violently into the air. These ascospores are heat resistant and, in the lab, require heating at 60 °C for 30 minutes to induce germination. For normal strains, the entire sexual cycle takes 10 to 15 days. In

333-448: A mature ascus containing eight ascospores, pairs of adjacent spores are identical in genetic constitution, since the last division is mitotic, and since the ascospores are contained in the ascus sac that holds them in a definite order determined by the direction of nuclear segregations during meiosis. Since the four primary products are also arranged in sequence, a first division segregation pattern of genetic markers can be distinguished from

370-504: A more variable developmental patterns. The fungi Saccharomyces produces ascospores when grown on V-8 medium, acetate ascospore agar, or Gorodkowa medium. These ascospores are globose and located in asci. Each ascus contains one to four ascospores. The asci do not rupture at maturity. Ascospores are stained with Kinyoun stain and ascospore stain. When stained with Gram stain, ascospores are gram-negative while vegetative cells are gram-positive. The fission yeast Schizosaccharomyces pombe

407-420: A second division segregation pattern. Because of the above features N. crassa was found to be very useful for the study of genetic events occurring in individual meioses. Mature asci from a perithecium can be separated on a microscope slide and the spores experimentally manipulated. These studies usually involved the separate culture of individual ascospores resulting from a single meiotic event and determining

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444-536: Is a stub . You can help Misplaced Pages by expanding it . Ascus An ascus (from Ancient Greek ἀσκός ( askós )  'skin bag, wineskin'; pl. : asci ) is the sexual spore -bearing cell produced in ascomycete fungi . Each ascus usually contains eight ascospores (or octad), 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 (e.g. Monosporascus cannonballus ), two, four, or multiples of four. In

481-477: Is a single-celled haploid organism that reproduces asexually by mitosis and fission. However, exposure to the DNA damaging agent hydrogen peroxide induces pair-wise mating of haploid cells of opposite mating type to form transient diploid cells that then undergo meiosis to form asci, each with four ascospores. The production of viable ascospores depends on successful recombinational repair during meiosis. When this repair

518-509: Is actively used in research around the world. It is important in the elucidation of molecular events involved in circadian rhythms, epigenetics and gene silencing , cell polarity , cell fusion , development, as well as many aspects of cell biology and biochemistry. Sexual fruiting bodies (perithecia) can only be formed when two mycelia of different mating type come together (see Figure). Like other Ascomycetes, N. crassa has two mating types that, in this case, are symbolized by A and

555-652: Is an example of positive feedback . A faint hissing sound can also be heard for species of Peziza and other cup fungi . Asci, notably those of Neurospora crassa , have been used in laboratories for studying the process of meiosis, because the four cells produced by meiosis line up in regular order. By modifying genes coding for spore color and nutritional requirements, the biologist can study crossing over and other phenomena. The formation of asci and their use in genetic analysis are described in detail in Neurospora crassa . Asci of most Pezizomycotina develop after

592-491: Is defective a quality control mechanism prevents germination of damaged ascospores. These findings suggest that mating followed by meiosis is an adaptation for repairing DNA damage in the parental haploid cells in order to allow production of viable progeny ascospores. Neurospora crassa Neurospora crassa is a type of red bread mold of the phylum Ascomycota . The genus name, meaning 'nerve spore' in Greek, refers to

629-400: Is favored by natural selection. In haploid multicellular fungi, such as N. crassa , meiosis occurring in the brief diploid stage is one of their most complex processes. Although physically much larger than the diploid stage, the haploid multicellular vegetative stage characteristically has a simple modular construction with little differentiation. In N. crassa , recessive mutations affecting

666-436: Is the only diploid nucleus in the entire life cycle of N. crassa . The diploid nucleus has 14 chromosomes formed from the two fused haploid nuclei that had 7 chromosomes each. Formation of the diploid nucleus is immediately followed by meiosis . The two sequential divisions of meiosis lead to four haploid nuclei, two of the A mating type and two of the a mating type. One further mitotic division leads to four A and four

703-477: The "one gene, one enzyme" hypothesis that specific genes code for specific proteins . Their hypothesis was later elaborated to enzyme pathways by Norman Horowitz , also working on Neurospora . As Norman Horowitz reminisced in 2004, "These experiments founded the science of what Beadle and Tatum called 'biochemical genetics'. In actuality, they proved to be the opening gun in what became molecular genetics and all developments that have followed from that." In

740-474: The Ascomycota . There are four basic types of ascus. An ascospore is a spore contained in an ascus, or that was produced inside an ascus. This kind of spore is specific to fungi classified as ascomycetes ( Ascomycota ). The ascospores of Blumeria graminis are formed and released under the humid conditions. After landing onto a suitable surface, unlike conidia , ascospores of Blumeria graminis showed

777-411: The pan-2 gene, so that a cross of B5 ´ B3 yields wild-type recombinants at low frequency. An analysis of 939 asci in which the genotypes of all meiotic products (ascospores) could be determined found 11 asci with an exceptional segregation pattern. These included six asci in which there was one wild-type meiotic product but no expected reciprocal double-mutant (B5B3) product. Furthermore, in three asci

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814-456: The 24 April 2003 issue of Nature , the genome of N. crassa was reported as completely sequenced . The genome is about 43 megabases long and includes approximately 10,000 genes. There is a project underway to produce strains containing knockout mutants of every N. crassa gene. In its natural environment, N. crassa lives mainly in tropical and sub-tropical regions. It can be found growing on dead plant matter after fires. Neurospora

851-414: The above example). Thus studies of gene conversion allowed insight into the details of the molecular mechanism of recombination. Over the decades since the original observations of Mary Mitchell in 1955, a sequence of molecular models of recombination have been proposed based on both emerging genetic data from gene conversion studies and studies of the reaction capabilities of DNA. Current understanding of

888-420: The ascogonium. Each of these ascogenous hypha bends to form a hook (or crozier) at its tip and the A and a pair of haploid nuclei within the crozier divide synchronously. Next, septa form to divide the crozier into three cells. The central cell in the curve of the hook contains one A and one a nucleus (see Figure). This binuclear cell initiates ascus formation and is called an "ascus-initial" cell. Next

925-423: The characteristic striations on the spores . The first published account of this fungus was from an infestation of French bakeries in 1843. Neurospora crassa is used as a model organism because it is easy to grow and has a haploid life cycle that makes genetic analysis simple since recessive traits will show up in the offspring. Analysis of genetic recombination is facilitated by the ordered arrangement of

962-424: The developing spores populate each resulting cell in septate ascospores with nuclei. The term ocular chamber , or oculus , refers to the epiplasm (the portion of cytoplasm not used in ascospore formation) that is surrounded by the "bourrelet" (the thickened tissue near the top of the ascus). Typically, a single ascus will contain eight ascospores (or octad). The eight spores are produced by meiosis followed by

999-410: The diploid stage of the life cycle are quite frequent in natural populations. These mutations, when homozygous in the diploid stage, often cause spores to have maturation defects or to produce barren fruiting bodies with few ascospores (sexual spores). Most of these homozygous mutations cause abnormal meiosis (e.g., disturbed chromosome pairing or pachytene or diplotene). The number of genes affecting

1036-450: The diploid stage was estimated to be at least 435 (about 4% of the total number of 9,730 genes). Thus, outcrossing, promoted by the necessity for the union of opposite mating types, likely provides the benefit of masking recessive mutations that would otherwise be harmful to sexual spore formation (see Complementation (genetics) ). Neurospora crassa is not only a model organism for the study of phenotypic types in knock-out variants, but

1073-443: The fertilizing cell migrating down the trichogyne into the ascogonium. Since both A and a strains have the same sexual structures, neither strain can be regarded as exclusively male or female. However, as a recipient, the protoperithecium of both the A and a strains can be thought of as the female structure, and the fertilizing conidium can be thought of as the male participant. The subsequent steps following fusion of A and

1110-479: The formation of croziers at their base. The croziers help maintain a brief dikaryon . The compatible nuclei of the dikaryon merge forming a diploid nucleus that then undergoes meiosis and ultimately internal ascospore formation. Members of the Taphrinomycotina and Saccharomycotina do not form croziers. The form of the ascus, the capsule which contains the sexual spores, is important for classification of

1147-607: The four new nuclei duplicates its DNA and undergoes a division by mitosis. As a result, the ascus will contain four pairs of spores. Then the ascospores are released from the ascus. In many cases the asci are formed in a regular layer, the hymenium , in a fruiting body which is visible to the naked eye, here called an ascocarp or ascoma . In other cases, such as single-celled yeasts , no such structures are found. In rare cases asci of some genera can regularly develop inside older discharged asci one after another, e.g. Dipodascus . Asci normally release their spores by bursting at

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1184-633: The genotype of each spore. Studies of this type, carried out in several different laboratories, established the phenomenon of "gene conversion" (e.g. see references ). As an example of the gene conversion phenomenon, consider genetic crosses of two N. crassa mutant strains defective in gene pan-2 . This gene is necessary for the synthesis of pantothenic acid (vitamin B5), and mutants defective in this gene can be experimentally identified by their requirement for pantothenic acid in their growth medium. The two pan-2 mutations B5 and B3 are located at different sites in

1221-530: The molecular mechanism of recombination is discussed in the Misplaced Pages articles Gene conversion and Genetic recombination . An understanding of recombination is relevant to several fundamental biologic problems, such the role of recombination and recombinational repair in cancer (see BRCA1 ) and the adaptive function of meiosis (see Meiosis ). That mating in N. crassa can only occur between strains of different mating types suggests that some degree of outcrossing

1258-568: The products of meiosis in Neurospora ascospores . Its entire genome of seven chromosomes has been sequenced. Neurospora was used by Edward Tatum and George Wells Beadle in their experiments for which they won the Nobel Prize in Physiology or Medicine in 1958. Beadle and Tatum exposed N. crassa to x-rays, causing mutations . They then observed failures in metabolic pathways caused by errors in specific enzymes . This led them to propose

1295-432: The ratio of meiotic products was 1B5:3B3, rather than in the expected 2:2 ratio. This study, as well as numerous additional studies in N. crassa and other fungi (reviewed by Whitehouse ), led to an extensive characterization of gene conversion. It became clear from this work that gene conversion events arise when a molecular recombination event happens to occur near the genetic markers under study (e.g. pan-2 mutations in

1332-435: The tip, but they may also digest themselves, passively releasing the ascospores either in a liquid or as a dry powder. Discharging asci usually have a specially differentiated tip, either a pore or an operculum. In some hymenium forming genera, when one ascus bursts, it can trigger the bursting of many other asci in the ascocarp resulting in a massive discharge visible as a cloud of spores – the phenomenon called "puffing". This

1369-404: The two uninucleate cells on either side of the first ascus-forming cell fuse with each other to form a binucleate cell that can grow to form a further crozier that can then form its own ascus-initial cell. This process can then be repeated multiple times. After formation of the ascus-initial cell, the A and a nucleus fuse with each other to form a diploid nucleus (see Figure). This nucleus

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