Effects of Glucose Repression on the Transmission and Recombination of Mitochondrial Genes in Yeast (SACCHAROMYCES CEREVISIAE)

Matings of a number of Saccharomyces cerevisiae stocks give different output ratios of mitochondrial genotypes depending on whether the cells are glucose-repressed or derepressed. The effects of glucose repression are independent of cellular mating type and mitochondrial genotype, and take place at least in part after zygotes are formed. An explanation is proposed in terms of changes in the relative numbers of mitochondrial DNA molecules contributed by the a and α parents, modified by selective replication or destruction of molecules inside the zygote.     

Sensitivity of Soil Respiration to Variability in Soil Moisture and Temperature in a Humid Tropical Forest

Precipitation and temperature are important drivers of soil respiration. The role of moisture and temperature are generally explored at seasonal or inter-annual timescales; however, significant variability also occurs on hourly to daily time-scales. We used small (1.54 m²), throughfall exclusion shelters to evaluate the role soil moisture and temperature as temporal controls on soil CO₂ efflux from a humid tropical forest in Puerto Rico. We measured hourly soil CO₂ efflux, temperature and moisture in control and exclusion plots (n = 6) for 6-months. The variance of each time series was analyzed using orthonormal wavelet transformation and Haar-wavelet coherence. We found strong negative coherence between soil moisture and soil respiration in control plots corresponding to a two-day periodicity. Across all plots, there was a significant parabolic relationship between soil moisture and soil CO₂ efflux with peak soil respiration occurring at volumetric soil moisture of approximately 0.375 m³/m³. We additionally found a weak positive coherence between CO₂ and temperature at longer time-scales and a significant positive relationship between soil temperature and CO₂ efflux when the analysis was limited to the control plots. The coherence between CO₂ and both temperature and soil moisture were reduced in exclusion plots. The reduced CO₂ response to temperature in exclusion plots suggests that the positive effect of temperature on CO₂ is constrained by soil moisture availability.     

EVOLUTIONARY CONSEQUENCES OF THE LOSS OF PHOTOSYNTHESIS IN CHLAMYDOMONADACEAE: PHYLOGENETIC ANALYSIS OF Rrn18 (18S rDNA) IN 13 POLYTOMA STRAINS (CHLOROPHYTA)1

Complete sequences of the Rrn 18 genes were obtained from 13 strains of the nonphotosynthetic algal genus Polytoma. Phylogenetic analyses showed that these strains formed two clades. One clade shows only modest sequence diversity but is represented by strains collected at widely dispersed sites in Europe and America. The other clade consists of a single isolate from the Canary Islands. Both clades lie well within the extended clade that includes all species of Chlamydomonas for which sequence data are available. The two Polytoma clades are separated from each other by several green species, suggesting that the extant nonphotosynthetic Chlamydomonadaceae arose from photosynthetic ancestors at least twice. These results suggest that nonphotosynthetic mutants are capable of establishing lineages that can spread widely but have a higher probability of extinction than their photosynthetic congeners.     

Early vegetative segregation of mitochondrial genes in Saccharomyces cerevisiae

The vegetative segregation of seven mitochondrial gene loci was studied in yeast. At various times after mating antibiotic resistant and sensitive strains, samples of the diploid progeny were examined to determine the segregation rates of the alleles at each locus in three- and four-factor crosses. The rate of segregation was approximately the same for the cap1, ery1, oli1, oli2, and par1 loci, which are scattered over about two-thirds of the mitochondrial DNA molecule. Differences in segregation rates were found but showed no consistent relationship to the map positions of the loci. This is in contrast to the segregation of chloroplast genes in Chlamydomonas, where loci segregate at rates proportional to their distance from an “attachment point” which appears to govern the partitioning of chloroplast DNA molecules between daughter chloroplasts when the chloroplast divides. Our data are compatible with a model in which the mitochondrial DNA molecules in a cell occur in a small number of groups corresponding to individual nucleoids or mitochondria. Most or all of the molecules in a group carry the same allele at any given locus. These genetically homogeneous groups of molecules may thus be the units of segregation, and may be partitioned randomly between mother cell and bud at each division.     

Uniparental Inheritance of Mitochondrial Genes in Yeast: Dependence on Input Bias of Mitochondrial DNA and Preliminary Investigations of the Mechanism

In Saccharomyces cerevisiae, previous studies on the inheritance of mitochondrial genes controlling antibiotic resistance have shown that some crosses produce a substantial number of uniparental zygotes, which transmit to their diploid progeny mitochondrial alleles from only one parent. In this paper, we show that uniparental zygotes are formed especially when one parent (majority parent) contributes substantially more mitochondrial DNA molecules to the zygote than does the other (minority) parent. Cellular contents of mitochondrial DNA (mtDNA) are increased in these experiments by treatment with cycloheximide, alpha-factor, or the uvsp5 nuclear mutation. In such a biased cross, some zygotes are uniparental for mitochondrial alleles from the majority parent, and the frequency of such zygotes increases with increasing bias. In two- and three-factor crosses the cap1, ery1, and oli1 loci behave coordinately, rather than independently; minority markers tend to be transmitted or lost as a unit, suggesting that the uniparental mechanism acts on entire mtDNA molecules rather than on individual loci. This rules out the possibility that uniparental inheritance can be explained by the conversion of minority markers to the majority alleles during recombination. Exceptions to the coordinate behavior of different loci can be explained by marker rescue via recombination. Uniparental inheritance is largely independent of the position of buds on the zygote. We conclude that it is due to the failure of minority markers to replicate in some zygotes, possibly involving the rapid enzymatic destruction of such markers. We have considered two general classes of mechanisms: (1) random selection of molecules for replication, as for example by competition for replicating sites on a membrane; and (2) differential marking of mtDNA molecules in the two parents, possibly by modification enzymes, followed by a mechanism that "counts" molecules and replicates only the majority type. These classes of models are distinguished genetically by the fact that the first predicts that the output frequency of a given allele among the progeny of a large number of zygotes will approximately equal the average input frequency of that allele, while the second class predicts that any input bias will be amplified in the output. The data suggest that bias amplification does occur. We hypothesize that maternal inheritance of mitochondrial or chloroplast genes in many organisms may depend upon a biased input of organelle DNA molecules, which usually favors the maternal parent, followed by failure of the minority (paternal) molecules to replicate in many or all zygotes.