Autosomal factors with correlated effects on the activities of the glucose 6-phosphate and 6-phosphogluconate dehydrogenases in Drosophila melanogaster
| Autor: | F. I. Chasalow, C. C. Laurie-Ahlberg, J. H. Williamson, Bruce J. Cochrane, A. N. Wilton |
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| Rok vydání: | 1981 |
| Předmět: |
chemistry.chemical_classification
Genetics Male Recombination Genetic Phosphogluconate Dehydrogenase Structural gene Genetic Variation Biology Pentose phosphate pathway Glucosephosphate Dehydrogenase Investigations biology.organism_classification Chromosomes chemistry.chemical_compound Enzyme Drosophila melanogaster Glucose 6-phosphate chemistry Biochemistry Chromosome 3 Melanogaster Animals Transaldolase |
| Zdroj: | Scopus-Elsevier |
| ISSN: | 0016-6731 |
| Popis: | Isogenic lines, in which chromosomes sampled from natural populations of D. melanogaster are substituted into a common genetic background, were used to detect and partially characterize autosomal factors that affect the activities of the two pentose phosphate pathway enzymes, glucose 6-phosphate dehydrogenase (G6PD) and 6-phosphogluconate dehydrogenase (6PGD). The chromosome 3 effects on G6PD and 6PGD are clearly correlated; the chromosome 2 effects, which are not so great, also appear to be correlated, but the evidence in this case is not so strong. Examination of activity variation of ten other enzymes revealed that G6PD and 6PGD are not the only pair of enzymes showing a high positive correlation, but it is among the highest in both sets of lines. In addition, there was some evidence that the factor(s) affecting G6PD and 6PGD may also affect two other metabolically related enzymes, transaldolase and phosphoglucose isomerase.—Rocket immunoelectrophoresis was used to estimate specific CRM levels for three of the enzymes studied: G6PD, 6PGD and ME. This experiment shows that a large part of the activity variation is accounted for by variation in CRM level (especially for chromosome 3 lines), but there remains a significant fraction of the genetic component of activity variation that is not explained by CRM level.—These results suggest that the autosomal factors are modifiers involved in regulation of the expression of the X-linked structural genes for G6PD and 6PGD, but a role in determining part of the enzymes′ primary structure cannot be excluded with the present evidence. |
| Databáze: | OpenAIRE |
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