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. 1983 Apr;103(4):649–658. doi: 10.1093/genetics/103.4.649

Dosage Compensation in Drosophila: Nadp-Enzyme Activities and Cross-Reacting Material

John H Williamson 1,2, Michael M Bentley 1,2
PMCID: PMC1202046  PMID: 6406296

Abstract

The relationships between gene dosage, enzyme activities and CRM levels have been determined for G6PD and 6PGD. Enzyme activities and CRM levels were directly proportional and increased in genotypes carrying duplications of the respective structural genes. When a duplication consisting of the distal 45% of the X chromosome was used to duplicate Pgd+, 6PGD activity and CRM increased and G6PD activity decreased. When the proximal 55% of the X chromosome was duplicated, G6PD activity and CRM increased whereas 6PGD activity and CRM levels decreased. These observations support the model of dosage compensation of X-linked genes that invokes an autosomal activator in limited concentrations for which X-linked loci compete. The distal 45% of the X chromosome, when duplicated, caused a significant increase in NADP-malic enzyme activity and CRM levels, as if a structural gene for NADP-ME is sex-linked.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1006/abio.1976.9999. [DOI] [PubMed] [Google Scholar]
  2. Geer B. W., Krochko D., Williamson J. H. Ontogeny, cell distribution, and the physiological role of NADP-malic enxyme in Drosophila melanogaster. Biochem Genet. 1979 Oct;17(9-10):867–879. doi: 10.1007/BF00504309. [DOI] [PubMed] [Google Scholar]
  3. Kazazian H. H., Jr, Young W. J., Childs B. X-linked 6-phosphogluconate dehydrogenase in drosophila: subunit associations. Science. 1965 Dec 17;150(3703):1601–1602. doi: 10.1126/science.150.3703.1601. [DOI] [PubMed] [Google Scholar]
  4. Lucchesi J. C. Dosage compensation in Drosophila. Annu Rev Genet. 1973;7:225–237. doi: 10.1146/annurev.ge.07.120173.001301. [DOI] [PubMed] [Google Scholar]
  5. Maroni G., Kaplan R., Plaut W. RNA synthesis in Drosophila melanogaster polytene chromosomes. Indications of simultaneous dosage compensation and dosage effect in X chromosomes. Chromosoma. 1974;47(2):203–212. doi: 10.1007/BF00331807. [DOI] [PubMed] [Google Scholar]
  6. Maroni G., Lucchesi J. C. X-chromosome transcription in Drosophila. Chromosoma. 1980;77(3):253–261. doi: 10.1007/BF00286051. [DOI] [PubMed] [Google Scholar]
  7. Maroni G., Plaut W. Dosage compensation in Drosophila melanogaster triploids. I. Autoradiographic study. Chromosoma. 1973;40(4):361–377. doi: 10.1007/BF00399428. [DOI] [PubMed] [Google Scholar]
  8. Meidinger E. M., Williamson J. H. Genetic control of aldehyde oxidase activity and cross-reacting-material in Drosophila melanogaster. Can J Genet Cytol. 1978 Dec;20(4):489–497. doi: 10.1139/g78-057. [DOI] [PubMed] [Google Scholar]
  9. Mukherjee A. S., Beermann W. Synthesis of ribonucleic acid by the X-chromosomes of Drosophila melanogaster and the problem of dosage compensation. Nature. 1965 Aug 14;207(998):785–786. doi: 10.1038/207785a0. [DOI] [PubMed] [Google Scholar]
  10. Stewart B. R., Merriam J. R. Regulation of gene activity by dosage compensation at the chromosomal level in drosophila. Genetics. 1975 Apr;79(4):635–647. doi: 10.1093/genetics/79.4.635. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Stewart B. R., Merriam J. R. Segmental aneuploidy and enzyme activity as a method for cytogenetic localization in drosophila melanogaster. Genetics. 1974 Feb;76(2):301–309. doi: 10.1093/genetics/76.2.301. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Voelker R. A., Ohnishi S., Langley C. H., Gausz J., Gyurkovics H. Genetic and cytogenetic studies of malic enzyme in Drosophila melanogaster. Biochem Genet. 1981 Jun;19(5-6):525–534. doi: 10.1007/BF00484624. [DOI] [PubMed] [Google Scholar]

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