Random segregation inNeurospora

Data from five-point crosses involving linkage group I and three-point crosses involving linkage groups VI and VII ofNeurospora crassa andN. sitophila have been analysed in order to detect the phenomena of polarized segregation and partial spindle overlap.The results clearly show absence of polarized segregation in both species. They further show that partial spindle overlap is a rare event if at all it occurs in the two species. The occurrence of a majority of either symmetrical or asymmetrical classes is a feature common to both species.     

Beryllium toxicity inNeurospora crassa

InNeurospora crassa,0.44 mM Be²⁺ caused half-maximal inhibition of growth and this inhibition could be fully counteracted by the addition of 2.5 mM Ca²⁺ to the medium. Mn²⁺ and Mg²⁺ were less effective in reversing the growth inhibition caused by Be²⁺ and the order of effectiveness was Ca²⁺ > Mn2+ > Mg²⁺. Fe3+ and Zn²⁺ were ineffective in reversing Be²⁺ toxicity. Pyruvate, malate and succinate also reversed the growth inhibition caused by Be²⁺ inN. crassa. Pyruvate restored growth by a mechanism not involving control of Be²⁺ accumulation in the mould. The rate of utilisation of glucose by the mycelia grown in the presence of Be²⁺ was reduced, while that of pyruvate was not affected. The results indicate that the primary metabolic lesion in Be²⁺ toxicity inN. crassa is probably a block at some step(s) in the glycolytic sequence.     

Change of the crossing-over frequency inDrosophila during selection for resistance to temperature fluctuations

Significant differences among cage populations ofDrosophila in the dynamics of linkage disequilibrium for marker locib, cn andvg of chromosome 2 have been found at optimum and extreme temperatures. Fifteen generations of selection under extreme conditions considerably increased recombination frequency in thecn-vg region and over the whole of theb-vg interval. From the data obtained it is inferred that recombination-promoting alleles with intermediate expression in the heterozygous state are responsible for these changes.     

Function of crossing-over

The literature data are considered concerning the significance of genetic recombination and crossing over. An obvious result of recombination is production of the genotypically diverse offspring, but the main role of recombination consists of combining the genes from diverging subspecies and races, thus maintaining a rather wide ecological potential of a species. This effect of recombination substantiates the tendency for increasing complexity of organic forms in progressive evolution. Accordingly, evolution is considered as a chain of recombinational "syntheses". The literature data treating crossing over as a mechanism of DNA repair are discussed. This function of crossing over is interpreted, based on a notion implying, from the composition of genetic code, that a crystalline associate composed of bases as free molecules precedes the appearance of DNA in evolution. The stability of the crystalline associate of bases was due to "balanced" distribution of bases for their electrochemical properties. The degeneracy of genetic code seems to provide possibility of construction of the electrostatically "balanced" base sequences in highly expressed bacterial genes. Crossing over possibly recovers "balanced" distribution of bases for their electrochemical properties and thus "repairs" a high level of heterocatalytic DNA activity.     

Unequal crossing-over in Escherichia coli

Unequal crossing-over between sister chromosomes in the process of DNA replication in Escherichia coli leads to the formation of tandem duplications, thus enhancing the activity of certain genes. In conjugational matings between genetically marked E. coli strains, unequal crossing-over leads to the formation of heterozygous tandem duplications. Studying these duplications as model systems allowed the conclusion that unequal crossing-over between direct DNA repeats of sister chromosomes is the main pathway of the formation of selected recombinants in E. coli strains carrying duplications. This was inferred from the data on the segregation of homozygous diploid recombinants by heterozygous duplications. Unequal crossing-over between sister chromosomes occurs as adaptive exchange providing the survival of the greater part of bacterial cells on a selective medium. The known phenomenon of adaptive mutagenesis may also be a consequence of unequal exchanges at the level of DNA mononucleotide repeats.     

Unequal crossing-over in Escherichia coli

Unequal crossing-over between sister chromosomes in the process of DNA replication in Escherichia coli leads to the formation of tandem duplications, thus enhancing the activity of certain genes. In conjugational matings between genetically marked E. coli strains, unequal crossing-over leads to the formation of heterozygous tandem duplications. Studying these duplications as model systems allowed the conclusion that unequal crossing-over between direct DNA repeats of sister chromosomes is the main pathway of the formation of selected recombinants in E. coli strains carrying duplications. This was inferred from the data on the segregation of homozygous diploid recombinants by heterozygous duplications. Unequal crossing-over between sister chromosomes occurs as adaptive exchange providing the survival of the greater part of bacterial cells on a selective medium. The known phenomenon of adaptive mutagenesis may also be a consequence of unequal exchanges at the level of DNA mononucleotide repeats.     

Intra-chromosomal position interference inNeurospora crassa

Multiple-point crosses where 20 pairs of regions (ten loosely linked markers) for the study of contiguous exchanges involving two linkage groups, capable of being investigated at a time, were utilized. In order to find out the effect of a chelating agent on interference, crosses were treated with different molar concentrations of ethylene-diamine tetraacetic acid (EDTA). All marker strains were standardized before use by inbreeding with a wild-type of known parentage.Since tests based on Coefficient of Coincidence and on Poisson distribution for finding out the position interference are rather unsatisfactory, a method based onContingency Chi-square test for detecting the intensity and nature of interference is described.Data obtained from 1813 analyzable ordered tetrads show that positive interference is absent in the control crosses. It is present among certain regions in crosses when treated with 4×10^–5M and 10×10^–5M EDTA but it vanishes again in crosses when treated with 20×10^–5M EDTA. Negative interference is present in the control crosses but it varies among pairs of regions on the two linkage groups. The localization and intensity of interference are alterable with EDTA treatment. The data are discussed in the light of certain concepts invoking to explain the mechanism that involves a genetic exchange.     

Somatic crossing-over in the housefly

Summary X-rays were found to produce genetically marked cells and cell clones in heterozygous larvae of Musca domestica. The results favor the conclusion that these marked clones originated by somatic crossing-over. The technique should prove useful in developmental analyses of the housefly.     

Features of crossing-over in virus-infected tomato

The evidence of increased crossing over rate in tomato hybrids infected with TAV (Tomato aspermy virus), PVX (Potato virus X), TMV (Tobacco mosaic virus), TMV+PVX indicates the recombinogenic effect of viral infection. Cytological studies of the early diakinesis in healthy and virus-infected tomato revealed significant changes in chiasma number and position. The most significant changes were established for bivalents with two interstitial chiasmata and with one terminal and one interstitial. The data obtained indicate redistribution of the chiasmata position and induction of additional exchanges. The virus-induced recombination is segment-specific and depends on the host plant genotype, virus infection and the interaction between them.     

Calcium and tip growth inNeurospora crassa

Summary We examined the ionic regulation of tip growth inNeurospora crassa by a combination of electrophysiology and confocal microscopy. To determine if transmembrane ionic fluxes are required for tip growth, we voltage clamped the membrane from –200 to +50 mV. In this voltage range, transmembrane ionic fluxes would either reverse (e.g., K⁺) or change dramatically (e.g., Ca²⁺ influx) but had no effect on hyphal growth rates. Therefore, ionic fluxes (including Ca²⁺ influx) may not be required for tip growth. However, intracellular Ca²⁺ may still play an obligatory role in tip growth. To assess this possibility, we first increased cytosolic Ca²⁺ directly by ionophoresis. Elevated Ca²⁺ induced subapical branch initiation, often multiple tips. At hyphal tips, fluorescence ratio imaging using fluo-3 and fura-red revealed a pronounced tip-high Ca²⁺ gradient within 10 m of the tip in growing hyphae which was not observed in nongrowing hyphae. Injection of the Ca²⁺ chelator 1,2-bis(ortho-aminophenoxy)ethane-N,N,N,N-tetrapotassium acetate consistently inhibited growth concomitantly with a depletion of intracellular Ca²⁺ and dissipation of the tip-high gradient. We conclude that Ca²⁺ plays a regulatory role in tip initiation and the maintenance of tip growth. Because plasma membrane ionic fluxes do not play a role in tip growth, we suggest that the tip-high Ca²⁺ gradient is generated from intracellular Ca²⁺ stores in the ascomyceteN. crassa.Abbreviations BAPTA 1,2-bis(ortho-aminophenoxy)ethane-N,N,N,N-tetrapotassium acetate - [Ca²⁺]_i intracellular Ca²⁺ concentration - fluo-3 2,7-dichloro-6-hydroxy-3-oxo-9-xanthenyl-4-methyl-2,2-(ethylenedioxy)dianiline-N,N,N,N-tetraacetic acid