Gene conversion: point-mutation heterozygosities lower heteroduplex formation.

The effects of heterozygosity on meiotic gene conversion characteristics have been studied in the fungus Ascobolus immersus. The non-Mendelian segregation patterns of seven white ascospore mutants of the b2 gene were established in the presence or the absence of additional neighbouring allelic mutations. These correspond to nine different double mutants with wild-type or pseudo-wild-type phenotypes, constituted by two +1, -1 frameshift mutations of complementary phases. When heterozygous, these double point mutations decrease, by an average of one third, the gene conversion frequencies of the mutants located on their right, toward the low conversion end of the gene. The decrease corresponds either to a reduction in all classes of non-Mendelian segregation (6:2, 5:3 and aberrant 4:4 asci) or to a reduction restricted to the single class of aberrant 4:4 asci. These modifications are explained by changes in hybrid DNA parameter values: frequencies of formation and modalities of distribution (asymmetric versus symmetric ratio). Besides the nature of the non-homology, point mutation versus deletion, which leads to quantitative differential effects, the region where the non-homology is located within the gene also appears to play an important role.     

Rare occurrence of the tetratype tetrads in Saccharomycodes ludwigii.

Genetic data suggesting the absence of crossover in Saccharomycodes ludwigii have been described. Tetrad data obtained from 888 asci from 60 pairs of genes with 22 genetic markers showed the absence of tetratype asci, except for 5 asci in which a single pair of alleles showed tetratype segregation to the other genetic markers in each ascus. Spore arrays in the linear asci showed that the + - + - and + - - + (or - + + -) asci occurred at almost equal frequencies. The two coherent spores at each end of an ascus were always marked with different alleles of a gene.     

Ophiorosellinia costaricensis gen. et sp. nov., a xylariaceous fungus with scolecosporous ascospores

A pyrenomycete featuring uniperitheciate stromata embedded in a subiculum and asci with iodine-positive apical ascal rings that bear scolecosporous ascospores is described as new. The fungus, Ophiorosellinia costaricensis, is known only from the type location in Costa Rica. It has been cultured, but no anamorph was discovered.     

Aggregative structure is the rule in communities of fleas: null model analysis

We used null models to examine patterns of species co‐occurrences in 59 communities of fleas parasitic on small mammals from 4 biogeographic realms (Afrotropics, Nearctic, Neotropics, and Palaearctic). We compared frequencies of co‐occurrences of flea species across host species with those expected by chance, using a null model approach. We used 4 tests for non‐randomness to identify pairs of species (within a community) that demonstrate significant positive or negative co‐occurrence. The majority of flea communities were non‐randomly assembled. Patterns of flea co‐occurrences on the same host species indicated aggregation but not segregation of flea species (except for the flea community of Madagascar). Although only a small fraction of species pairs were associated significantly (264 of 10, 943 species pairs according to the most liberal criterion), most of these associations were positive (except for 2 negatively associated species pairs). Significantly associated pairs were represented mainly by non‐congeneric species. The degree of non‐randomness of the entire flea community was similar among biogeographic regions, but the strength of pair‐wise association varied geographically, being the highest in the Afrotropics and the lowest in the European region of the Palaearctic.     

Genetic recombination at the buff spore colour locus in Sordaria brevicollis

Summary Asci showing aberrant segregation at the buff spore colour locus in Sordaria brevicollis were selected from crosses between buff mutants and wild type in the presence of closely-linked flanking markers. The frequency of crossing-over associated with aberrant segregations was calculated and corrected to allow for crossovers between the flanking markers incidental to the aberrant segregation. The average frequency of crossing over was found to be related to the class of aberrant ascus studied. 5+:3m and 3+:5m asci showed 16% associated marker recombination while 6+:2m and 2+:6m asci showed 27% recombination. The frequency of tritype and tetratype postmeiotic segregation asci was calculated. Only 3% tetratypes were found and this is thought to indicate a low frequency of symmetric hybrid DNA formation.     

GENETICS OF SORDARIA FIMICOLA. V. ABERRANT SEGREGATION AT THE G LOCUS

Kitani , Y., L. S. Olive , and Arif S. El -Ani . (Columbia U., New York City.) Genetics of Sordaria fimicola. V. Aberrant segregation at the g locus. Amer. Jour. Bot. 49(7): 697–706. Illus. 1962.—Aberrant segregation of the gray-spore color locus in Sordaria fimicola was studied with the aid of closely linked markers. It was found that 6:2 and 5:3 asci occur with about the same frequency, but asci with an excess of wild-type spores occur with a frequency 5.5 times that of asci with an excess of gray spores. Also, the frequency of related crossing over (occurring close to the miscopied loeus and involving the miscopying strand) was much higher than the expected value, and in 5:3 asci it appears to be at least twice that found in 6:2 asci. Nine aberrant 4:4 asci, each with 2 spore pairs heterogeneous for color, were found. These are believed to have resulted from reciprocal double transreplication. The rarest aberrant type was represented by a single 7:1 ascus, which is difficult to explain on the basis of a single meiotic process. Miscopying is discussed with relation to an 8-strand model of paired homologues and the occurrence of localized chromosome pairing during prezygotene DNA synthesis. Several possible explanations for the occurrence of aberrant tetrads are considered. Miscopying has also been found to involve several spore-color loci not previously studied; whereas, several other such mutant loci fail to show evidence of it. One locus (m) shows abnormal segregation of the 6:2 but not the 5:3 type.     

Ascus development in two temperature-sensitive four-spore mutants of Neurospora crassa

Two nonallelic Four-spore mutants are known in which ascospore walls enclose the four immediate products of meiosis rather than the normal eight products of a postmeiotic mitosis. Expression depends on temperature. The Four-spore phenotype is expressed when the developing asci are subjected either to high temperatures (25-30 degrees C) for Fsp-1 or to low temperatures (15-20 degrees C) for Fsp-2. Heterozygous Fsp-1 X Fsp-1+ crosses make eight-spored asci at 15-20 degrees C but produce many four-spored asci at 25 degrees C and mostly four-spored asci at 30 degrees C. Homozygous Fsp-1 X Fsp-1 crosses respond similarly to increasing temperature but make 40-50% four-spored asci even at 20 degrees C. Heterozygous Fsp-2 X Fsp-2+ crosses produce almost exclusively four-spored asci at 15 degrees C but a mixture of four- and eight-spored asci at 20, 25, and 30 degrees C. Homozygous Fsp-2 X Fsp-2 crosses make all four-spored asci at 15 and 20 degrees C and a mixture of four- and eight-spored asci at 25 and 30 degrees C. When both Fsp-1 and Fsp-2 are present in a cross, either homozygous or heterozygous, no asci contain more than four ascospores at any temperature. Limited temperature-shift experiments with Fsp-1 and Fsp-2 show that the sensitive period for Four-spore expression is sometime after meiotic prophase, possibly at interphase II.     

A system for the study of meiotic non-disjunction using Sordaria bervicolis

A system is described for the study of abnormal chromosome segregation in Sordaria brevicolis. The system utilizes two complementing alleles of the b₁ locus on linkage group II. Abnormal asci containing black disomic ascospores were detected which fall into two main categories. (a) Non disjunctional asci in which the disomic spores were present together with an equal number of abortive (nullosomic) spores and (b) asci in which an extra replication of the chromosomes had occurred resulting in pseudo-wild types being formed without accompanying spore abortion. Calculations indicate that the non-disjunction frequencies at the first and second divisions of meiosis are 4.25×10⁻⁴ and 4.35×10⁻⁴ respectively. It is suggested that the system is potentially a valuable one both for the study of meiotic non-disjunction and other causes of aneuploidy.     

PHENOTYPE DISTRIBUTIONS IN ASCI OF NEUROSPORA CRASSA

Fourteen crosses are described from which 3103 asci were dissected and scored with respect to phenotype distribution patterns of 1, 2 or 3 markers. The results illustrate the following points. There may regularly occur preferred ratios, including 8:1, 4:1, 2:1 and 1:2, of first to second division segregation patterns. Variations in this ratio (designated here as S/C, meaning simple to complex phenotype distribution patterns), shown by the same marker in different crosses, may regularly be discontinuous in that the ratio may shift from one preferred value to another. Values of linkage-correction factors applicable to certain crosses suggest that these factors also may constitute a discontinuous series. Control of phenotype distributions in asci by a systematic, but unknown, mechanism is thought to be suggested. Characteristics of the order of isolation of asci, from 2 crosses treated in a special way, are consistent with the possibility that members of adjacently formed, twin asci are frequently, or even regularly, alike with respect to phenotype distribution class.     

The Genetic Analysis of Distributive Segregation in Drosophila Melanogaster. I. Isolation and Characterization of Aberrant X Segregation (Axs), a Mutation Defective in Chromosome Partner Choice

We describe the isolation and characterization of Aberrant X segregation (Axs), a dominant female-specific meiotic mutation. Although Axs has little or no effect on the frequency or distribution of exchange, or on the disjunction of exchange bivalents, nonexchange X chromosomes undergo nondisjunction at high frequencies in Axs/+ and Axs/Axs females. This increased X chromosome nondisjunction is shown to be a consequence of an Axs-induced defect in distributive segregation. In Axs-bearing females, fourth chromosome nondisjunction is observed only in the presence of nonexchange X chromosomes and is argued to be the result of improper X and fourth chromosome associations within the distributive system. In XX females bearing a compound fourth chromosome, the frequency of nonhomologous disjunction of the X chromosomes from the compound fourth chromosome is shown to account for at least 80% of the total X nondisjunction observed. In addition, Axs diminishes or ablates the capacity of nonexchange X chromosomes to form trivalents in females bearing either a Y chromosome or a small free duplication for the X. Axs also impairs compound X from Y segregation. The effect of Axs on these segregations parallels the defects observed for homologous nonexchange X chromosome disjunction in Axs females. In addition to its dramatic effects on the X chromosome, Axs exerts a similar effect on the segregation of a major autosome. We conclude that Axs defines a locus required for proper homolog disjunction within the distributive system.     

Pulsed-field gel electrophoresis indicates genotypic heterogeneity among Campylobacter upsaliensis strains

Abstract A non-flocculent strain of Saccharomyces cerevisiae was selected after EMS mutation of a flocculent and heterozygous FLO1 locus diploid. The analysis of 25 asci from this diploid showed in all cases segregation 0F:4NF, thus confirming that it was probably affected in the desired gene. After sporulation and dissection of asci, three haploid strains were chosen, which were altered in the locus FLO1 . Crossing these three strains with two other ones having markers for ADE1 and pho11::LEU2 , we could map the mutation at ca. 4.3 cM and ca. 37.7 cM from the PHO11 and ADE1 loci respectively.     

Ascospore Dimorphism and Mating Type in Chromocrea spinulosa (Fuckel) Petch n. comb

The asci contain four large and four small ascospores, eachtwo-celled, arranged in the six patterns expected if spore sizewere controlled by a pair of allelic genes, the locus showing65 per cent, second-division segregation. The small ascosporesproduce sterile colonies, the large ones moderately fertilecolonies whose asci again show segregation for spore size. Fertilityis stimulated where colonies from large and small spores meet.In crosses of various mutants with the wild type, all asci inperithecia developed along the line of junction show segregationfor the mutant as well as for spore size. Evidently Chromocreais heterothallic, the spore-size difference being a pleiotropicexpression of mating type. One allele, that governing largespores, occasionally mutates to the other allele, resultingin fertility of colonies from large spores.     

Subcellular differentiation in sporulating yeast cells

We have previously described the induction of two sets of sporulation-specific mRNAs in Saccharomyces cerevisiae. Herein we correlate the appearance of these RNAs with the major morphogenic events of sporulation, and we analyze the spatial distribution of the RNAs within the ascus. Several observations suggest that the first set of messages is involved in spore wall synthesis. In fractionation experiments, these mRNAs are detected in the ascal cytoplasm but not in developing spores, indicating that the proteinaceous component of the spore wall is synthesized from the external compartment. The second set of messages is induced later in the course of spore maturation. These mRNAs accumulate within the spores and, unlike the first set of mRNAs, are retained in mature asci until the early stages of germination. We conclude that the development of ascospores proceeds through the differentiation of functionally distinct subcellular compartments.     

Male meiotic segregation of gonosomes analysed by two colour FISH in human interphase spermatozoa

Human meiotic segregation of X and Y chromosomes was simultaneously analysed by dual fluorescence in situ hybridization (FISH) on 10638 interphase spermatozoa from the same donor. A modified method for sperm decondensation ensured access of both X and Y probes to the sperm chromatin and a 99% hybridization efficiency. Expected sex ratios were obtained (49.30% haploidy X and 49.22% haploidy Y). The frequencies of meiotic II non-disjunctions for X and Y chromosomes (0.05%) were similar to those observed in sperm karyotypes after heterospecific fertilization of hamster eggs. In contrast, the frequency of XY bearing cells was significantly higher (0.42%). However, XY cells detected by FISH could either be diploid somatic cells, diploid germinal cells or hyperhaploid XY spermatozoa, the latter resulting from meiotic I non-disjunctions.     

Two new species of Erysiphe sect. Uncinula (Erysiphales): Erysiphe fernandoae and E. michikoae

Two new species of Erysiphe section Uncinula are described and illustrated based on the molecular and morphological analyses: (1) Erysiphe fernandoae sp. nov. on Fernandoa adenophylla is distinct from other Erysiphe species on the plant family Bignoniaceae by having smaller asci, ca 12 appendages per chasmothecium and being found only in Asia; (2) Erysiphe michikoae sp. nov. on Celtis jessoensis differs from Erysiphe kusanoi on other Celtis species in having smaller chasmothecial, ascal and ascospore dimensions, and fewer number of chasmothecium appendages. The phylogenetic relationships of the two new species with other closely related species are discussed based on 28S and ITS rDNA sequences.     

Two-spored asci produced by interrupted sporulation: a novel approach to linkage analysis in yeast

Genetical analysis of two-spored asci formed by interrupted sporulation offers a novel procedure for mapping of centromere-linked genes in Saccharomyces cerevisiae. Unlike the two-spored asci encountered under normal sporulation conditions, these asci are produced by a nonrandom mechanism. They fall into three categories (+ +), (+ -) and (- -) with respect to any marker. The percentage of (+ -) asci varies directly as a function of centromere-linkage of a gene. It is observed that almost 100% asci are of the (+ -) type in case of very tightly linked genes like trp-1 and cdc-10, while in case of markers unlinked to the centromere, e.g, trp-5 and met-8, the (+ -) asci constitute 50% of the total number of asci. Other markers with varying degrees of linkage, e.g. ura-3 and lys-1 show corresponding numbers of (+ -) asci between 50% and 100% of the total asci. These findings are in contrast to the results expected from a random abortion of two spores, in which case the (+ -) asci would constitute 67% of the total number of asci irrespective of the degree of centromere linkage of a marker. The linkage-dependent segregation of markers in these new kind of two-spored asci permits a rapid and accurate estimate of centromere linkage of a gene.     

Frequencies of Twelve Ascus-Types and Arrangement of Three Genes from Tetrad Data

Equations expressing the theoretical frequencies of twelve ascus-types in the tetrad analysis of a triply heterozygous diploid are described. Using these equations, a mapping procedure for a gene X, is proposed. The procedure requires that two genes, X and Y, of the same phenotype be heterozygous and that the map position of Y be known, and that another standard gene, Z, show an independent phenotype from X and Y. This procedure does not require the laborious allelism test of the segregants to determine the allelic 2:2 segregation in tetrads for the X and Y genes, which is indispensable for mapping by the conventional procedure. The exact placement of the X gene on a chromosome is possible by the chi2 minimization procedure in comparison with the expected frequencies of the six ascus-types or four spore-types deduced from the twelve expected ascus-types to give the optimal fit with the observed data.     

Enhanced Gene Conversion and Postmeiotic Segregation in Pachytene-Arrested SACCHAROMYCES CEREVISIAE

Previous study has demonstrated that incubation of yeast cells of strain AP-1 in sporulation medium at 36° permits them to begin meiosis but that they become arrested at pachytene and undergo enhanced intragenic recombination between ade2 heteroalleles. Tetrad analysis was undertaken to characterize the altered program of meiotic recombination more widely. In one set of experiments, pachytene-arrested cells were permitted to resume sporulation upon transfer to the permissive temperature. In the resulting asci, both postmeiotic segregation and gene conversion were increased several-fold at a number of loci relative to unarrested controls, whereas reciprocal recombination increased two- to threefold. Another set of experiments analyzed the genetic consequences of inducing the pachytene-arrested cells to revert directly to mitotic growth without completion of meiosis. The appearance of homozygous sectors from heterozygous markers revealed that these cells had become committed to appreciable recombination but that reciprocal exchange was less frequent than in normal asci. Taken together, the data indicate that pachytene arrest rendered the cells committed to enhanced recombination upon resumption of sporulation but that most of the crossing over did not occur until release from the arrest. —The genetic basis of pachytene arrest by AP-1 was investigated by mating each of its parents with progeny of strain Y55, which is able to sporulate at 36°. Both of these diploids sporulated at 36°, and asci from the one studied further exhibited 2:2 segregation of the sporulation defect, indicating that pachytene arrest is dependent on a recessive, temperature-sensitive allele at a chromosomal locus.     

Characterization of the genetic system of the xylose-fermenting yeast Pichia stipitis

High mutant frequencies indicated that the wild-type strains of Pichia stipitis are haploid. Sporulation ability of these clones pointed to a homothallic life cycle. Mating was induced by cultivation under nutritionally poor conditions on malt extract medium. Conjugation was followed immediately by sporulation. However, hybrids could be rescued by transferring the nascent zygotes to complete medium before meiosis had started. Under rich nutritional conditions, hybrids were mitotically stable and did not sporulate. The segregation pattern of auxotrophic markers of diploid zygotes indicated regular meiosis, although asci contained preferentially spore dyads. Received: 29 February 1996 / Accepted: 29 March 1996     

ASCI OF THE PEZIZALES III: THE APICAL APPARATUS OF EUGYMNOHYMENIAL REPRESENTATIVES

Morphological, developmental and cytochemical examinations were made with light and electron microscopy on the apical apparatuses of four eugymnohymenial species, Pyronema domesticum, Ascodesmis sphaerospora, Coprotus winteri and C. lacteus. Ascal tips in all four species were notably thinner walled than the rest of the ascus. Ultrastructurally, demarcation of the opercula was enhanced after staining with silver methenamine. Wide zones of dehiscence are formed in the outer layer of A. sphaerospora and C. winteri. In P. domesticum the outer layer of the operculum is differentially stained from the rest of the ascal wall. Wall dimensions in the multispored asci of C. winteri are approximately three times greater than those in the eight-spored asci of C. lacteus. The shape of the apical apparatus of C. lateus is almost identical to that of C. winteri. Morphological and cytochemical similarities of the apical apparatuses in Ascodesmis, Pyronema and Coprotus help demonstrate greater relationship between these taxa and support the belief that these taxa are most closely related to members of the Otideaceae and Aleuriaceae.