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Previous work has shown that recombination between alleles of the ftr cistron is disturbed by two "marker effects", one reduces the recombination frequency and the other increases it. These effects have been studied further. The results show that both enhancement and reduction are controlled by single genes which seem to be independent of one another. The genes are symbolized recE (for recombination enhancement) and recR (recombination reduction). Both genes are fully dominant, non-additive, and segregate readily from one another and from the ftr cistron. Recombination between any pair of ftr alleles is increased when recE is part of the genotype, but recE has no effect on recombination between alleles of the me-5 locus. On the other hand, the reduction of recombination caused by recR in the ftr cistron is polarised and alley-specific, but recR increases the frequency of recombination between me-5 alleles. The data are interpreted on the basis that the rec-gene products may be involved in chromatid pairing and that polymorphic variants of them cause differences in pairing which, by altering the opportunities for recombination, are observed as differences in allelic recombination frequency.
Previous work has shown that recombination between alleles of the ftr cistron is disturbed by two "marker effects", one reduces the recombination frequency and the other increases it. These effects have been studied further. The results show that both enhancement and reduction are controlled by single genes which seem to be independent of one another. The genes are symbolized recE (for recombination enhancement) and recR (recombination reduction). Both genes are fully dominant, non-additive, and segregate readily from one another and from the ftr cistron. Recombination between any pair of ftr alleles is increased when recE is part of the genotype, but recE has no effect on recombination between alleles of the me-5 locus. On the other hand, the reduction of recombination caused by recR in the ftr cistron is polarised and alley-specific, but recR increases the frequency of recombination between me-5 alleles. The data are interpreted on the basis that the rec-gene products may be involved in chromatid pairing and that polymorphic variants of them cause differences in pairing which, by altering the opportunities for recombination, are observed as differences in allelic recombination frequency.
Summary An interpretation of carpophore morphogenesis is presented which is derived both from the literature and from original observations. Cultured material of Coprinus cinereus (also called C. macrorhizus and C. lagopus) has been studied using biochemical assays together with light‐, scanning‐ and transmission electron microscopy to provide details of histology and the levels and distribution of protein, glycogen and NADP‐linked glutamate dehydrogenase during the course of development of stipe and cap. Initially, aggregates of hyphae form primordia which subsequently develop into mature carpophores. During stipe development glycogen deposition is at first restricted to cells forming a cup‐shaped mass in the stipe base, but very early in primordium development this deposit is depleted and glycogen accumulates in the gills, particularly the subhymenium, where it probably serves as a reserve material for the later stages of cap development. The distribution of cytochemically detectable protein differs from that of glycogen in that the former initially accumulates in the upper regions of the primordial stipe and in the gill hymenium. The stipe showed no conspicuous change in its content of protein during development although in the cap the fraction of the dry wt represented by protein increased substantially. Primordial stipes are composed of overlapping cells of hyphal dimensions with dense cytoplasm and small vacuoles. Stipe development depends on cell enlargement, this seeming to be biphasic; an initial increase in volume being attributable to an increase in cell diameter to give an undifferentiated dikaryotic central region and a differentiated multi‐nucleate cortex. Stipe growth depends on reallocation of cellular components, no one reserve material being identifiable as of prime importance although a few simple sugars do appear to be correlated with the osmoregulatory activity connected with the large scale uptake of water involved in stipe elongation. In the primordium cap the subhymenium is an open tissue of interwoven hyphae, the cells containing large accumulations of glycogen. The hymenium is formed from dikaryotic branches of the subhymenial hyphae to become an organised layer of hyphal tips. Subsequently, although the subhymenial hyphae remain as such, the hymenial cells become inflated. The paraphyses come to form a pavement of appressed and interlocked cells each containing a large central vacuole. Basidia are only slightly enlarged and contain dense cytoplasm with few vacuoles; they contrast with the much extended and inflated cystidia. Despite their inflation, all three cell types still show continuity with the subhymenial hyphae. During cap expansion the major inflationary force is paraphyseal enlargement but as the gill lamellae are removed by autodigestion fürther cell inflation in the pileal flesh enables it to assume a supportive role. In the earlier stages there is some correlation between declining glycogen content of the cap and increasing activity of NADP‐linked glutamate dehydrogenase. I...
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