scholarly journals Analysis of Pyrimidine Catabolism in Drosophila melanogaster Using Epistatic Interactions With Mutations of Pyrimidine Biosynthesis and β-Alanine Metabolism

Genetics ◽  
2005 ◽  
Vol 172 (3) ◽  
pp. 1665-1674 ◽  
Author(s):  
John M. Rawls
Genetics ◽  
2000 ◽  
Vol 156 (1) ◽  
pp. 269-282
Author(s):  
Toshiyuki Takano-Shimizu

Abstract Interspecific cross is a powerful means to uncover hidden within- and between-species variation in populations. One example is a bristle loss phenotype of hybrids between Drosophila melanogaster and D. simulans, although both the pure species have exactly the same pattern of bristle formation on the notum. There exists a large amount of genetic variability in the simulans populations with respect to the number of missing bristles in hybrids, and the variation is largely attributable to simulans X chromosomes. Using nine molecular markers, I screened the simulans X chromosome for genetic factors that were responsible for the differences between a pair of simulans lines with high (H) and low (L) missing bristle numbers. Together with duplication-rescue experiments, a single major quantitative locus was mapped to a 13F–14F region. Importantly, this region accounted for most of the differences between H and L lines in three other independent pairs, suggesting segregation of H and L alleles at the single locus in different populations. Moreover, a deficiency screening uncovered several regions with factors that potentially cause the hybrid bristle loss due to epistatic interactions with the other factors.


Genetics ◽  
1998 ◽  
Vol 148 (4) ◽  
pp. 1885-1891 ◽  
Author(s):  
Grażyna M Fedorowicz ◽  
James D Fry ◽  
Robert R H Anholt ◽  
Trudy F C Mackay

Abstract Odor-guided behavior is a polygenic trait determined by the concerted expression of multiple loci. Previously, P-element mutagenesis was used to identify single P[lArB] insertions, in a common isogenic background, with homozygous effects on olfactory behavior. Here, we have crossed 12 lines with these smell impaired (smi) mutations in a half-diallel design (excluding homozygous parental genotypes and reciprocal crosses) to produce all possible 66 doubly heterozygous hybrids with P[lArB] insertions at two distinct locations. The olfactory behavior of the transheterozygous progeny was measured using an assay that quantified the avoidance response to the repellent odorant benzaldehyde. There was significant variation in general combining abilities of avoidance scores among the smi mutants, indicating variation in heterozygous effects. Further, there was significant variation among specific combining abilities of each cross, indicating dependencies of heterozygous effects on the smi locus genotypes, i.e., epistasis. Significant epistatic interactions were identified for nine transheterozygote genotypes, involving 10 of the 12 smi loci. Eight of these loci form an interacting ensemble of genes that modulate expression of the behavioral phenotype. These observations illustrate the power of quantitative genetic analyses to detect subtle phenotypic effects and point to an extensive network of epistatic interactions among genes in the olfactory subgenome.


1995 ◽  
Vol 70 (2) ◽  
pp. 211-221
Author(s):  
Hiroshi MATSUBAYASHI ◽  
Masatoshi TOMARU ◽  
Masami SAWA ◽  
Maki NONAKA ◽  
Yuzuru OGUMA

2020 ◽  
Vol 287 (1937) ◽  
pp. 20200469
Author(s):  
J. Arvid Ågren ◽  
Manisha Munasinghe ◽  
Andrew G. Clark

The coordination between mitochondrial and nuclear genes is crucial to eukaryotic organisms. Predicting the nature of these epistatic interactions can be difficult because of the transmission asymmetry of the genes involved. While autosomes and X-linked genes are transmitted through both sexes, genes on the Y chromosome and in the mitochondrial genome are uniparentally transmitted through males and females, respectively. Here, we generate 36 otherwise isogenic Drosophila melanogaster strains differing only in the geographical origin of their mitochondrial genome and Y chromosome, to experimentally examine the effects of the uniparentally inherited parts of the genome, as well as their interaction, in males. We assay longevity and gene expression through RNA-sequencing. We detect an important role for both mitochondrial and Y-linked genes, as well as extensive mitochondrial-Y chromosome epistasis. In particular, genes involved in male reproduction appear to be especially sensitive to such interactions, and variation on the Y chromosome is associated with differences in longevity. Despite these interactions, we find no evidence that the mitochondrial genome and Y chromosome are co-adapted within a geographical region. Overall, our study demonstrates a key role for the uniparentally inherited parts of the genome for male biology, but also that mito-nuclear interactions are complex and not easily predicted from simple transmission asymmetries.


1983 ◽  
Vol 42 (1) ◽  
pp. 59-63 ◽  
Author(s):  
Jaime Moscoso del Prado ◽  
Pedro Ripoll

SUMMARYUsing seven newly induced duplications, three Minute loci have been located cytologically: M(3)hS 37 in 65F10–11; 66A (a new Minute locus), M(3)i in 67C, and M(3)hy in 68F; 69F. M(3)hS 37 and M(3)hy were previously thought to be allelic because they do not complement for lethality. The finding of Minute mutations with additive or synergistic rather than epistatic interactions makes us suspect that some other Minute mutations have been erroneously called allelic. The involvement of Minute loci in more than one biochemical pathway is discussed in view of the existence of synergistic interactions and of Minute loci without known mutant alleles.


1995 ◽  
Vol 70 (2) ◽  
pp. 211-221 ◽  
Author(s):  
Hiroshi MATSUBAYASHI ◽  
Masatoshi TOMARU ◽  
Masami SAWA ◽  
Maki NONAKA ◽  
Yuzuru OGUMA

Genetics ◽  
1991 ◽  
Vol 128 (1) ◽  
pp. 89-102 ◽  
Author(s):  
A Caballero ◽  
M A Toro ◽  
C López-Fanjul

Abstract Twenty generations of divergent selection for abdominal bristle number were carried out starting from a completely homozygous population of Drosophila melanogaster. All lines were selected with the same proportion (20%) but at two different numbers of selected parents of each sex (5 or 25). A significant response to selection was detected in eight lines (out of 40) and, in most cases, it could be wholly attributed to a single mutation of relatively large effect (0.5-2 phenotypic standard deviations). The ratio of new mutational variance to environmental variance was estimated to be (0.33 +/- 0.11) X 10(-3). The distribution of mutant effects was asymmetrical, both with respect to bristle number (85% of it was negative) and to fitness (most detected bristle mutations were lethal or semilethal). Moreover, this distribution was leptokurtic, due to the presence of major genes. Gene action on bristles ranged from additive to completely recessive, no epistatic interactions being found. In agreement with theory, larger responses in each direction were achieved by those lines selected at greater effective population sizes. Furthermore, the observed divergence between lines selected in opposite directions was proportional to their effective size, as predicted for mutations of large effect.


2019 ◽  
Author(s):  
Rebecca C. Vaught ◽  
Susanne Voigt ◽  
Ralph Dobler ◽  
David J. Clancy ◽  
Klaus Reinhardt ◽  
...  

ABSTRACTA large body of studies has demonstrated that genetic variation that resides outside of the cell nucleus can affect the organismal phenotype. The cytoplasm is home to the mitochondrial genome and, at least in arthropods, often hosts intracellular endosymbiotic bacteria such as Wolbachia. While numerous studies have implicated epistatic interactions between cytoplasmic and nuclear genetic variation as key to mediating patterns of phenotypic expression, two outstanding questions remain. Firstly, the relative contribution of mitochondrial genetic variation to other cytoplasmic sources of variation in shaping the phenotypic outcomes of cyto-nuclear interactions remains unknown. Secondly, it remains unclear whether the outcomes of cyto-nuclear interactions will manifest differently across the two sexes, as might be predicted given that cytoplasmic genomes are screened by natural selection only through females as a consequence of their maternal inheritance. Here, we address these questions, creating a fully-crossed set of replicated cyto-nuclear populations derived from three geographically distinct populations of Drosophila melanogaster, and measuring the lifespan of males and females from each population. We report cyto-nuclear interactions for lifespan, with the outcomes of these interactions differing across the sexes, and reconcile these findings with information on the full mitochondrial sequences and Wolbachia infection status of each of the populations.


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