Oogenesis in the suppressor2of Hairy‐wing mutant of Drosophila melanogaster. II. Nucleolar morphology and in vitro studies of RNA protein synthesis
Abstract
Cytological studies of ovaries from Drosophila melanogaster homozygous for the third chromosomal, female sterile gene, suppressor2 of Hairy‐wing (su2‐Hw), demonstrate that the nurse cell components of the egg chambers are primarily affected. Both chromosomes and nucleoli show qualitative and quantitative differencies from wild type. The in vitro culturing of mutant and wild type ovaries in the presence of labeled RNA and protein precursors were examined using liquid scintillation counting and autoradiography. The results of the scintillation experiments showed the mutant ovary to be nearly equivalent to wild type in the synthesis of RNA, but only half as active in protein synthesis. The autoradiographic analysis revealed that during very short incubation periods, the mutant ovary was more active than wild type in the production of RNA but that the mutant RNA was unstable. The lowered protein synthesis by mutant ovaries was also apparent using autoradiography. Morphometric measurements of mutant and wild type nurse nucleoli indicate a severe reduction in su2‐Hw compared to wild type. These findings suggest that the instability of mutant RNA may be due to some deficiency of the ribosomes produced in the absence of the su2‐Hw+ allele. On the other hand, the autoradiographic studies using H3‐uridine revealed the presence of an extranuclear label in the mutant nucleus not apparent in wild type. The possibility exists, therefore, that the unstable mutant RNA is of extranucleolar or…
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A stage 14 oocyte contains approximately 2 × 10^10 ribosomes, the vast majority of which are produced in the nurse cells during stages 7 through 10.
“It has been calculated that a stage 14 oocyte contains approximately 2 × 1010 ribosomes (66), the vast majority of which are produced in the nurse cells during stages 7 through 10 (67).”
From Impaired function of rDNA transcription initiation machinery leads to derepression of ribosomal genes with insertions of R2 retrotransposon (2022) · cites this paper as [66]
Cites
Ritossa, F. M., Atwood, K. C., & Spiegelman, S. (1966) · Genetics · doi:10.1093/genetics/54.3.819 · Cited by 296 · see citing works
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Fefelova, E. A., Pleshakova, I. M., Mikhaleva, E. A., Pirogov, S. A., Poltorachenko, V. A., Abramov, Y. A., Romashin, D. D., Shatskikh, A. S., Blokh, R. S., Gvozdev, V. A., et al. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkab1276 · Cited by 15 · see citing works
“melanogaster ovarian germ cells that are characterized by an especially intense rRNA synthesis required for the oocyte development (66,67).”
Background
- Authors
- Klug, W. S., King, R. C., & Wattiaux, J. M.
- Affiliations
- Northwestern University (US)
- ORCID
- King, Robert C.
- Venue
- Journal of Experimental Zoology
- Publisher
- Wiley
- Published
- 1970-06
- Volume
- 174
- Issue
- 2
- Pages
- 125-140
- ISSN
- 0022-104X (ISSN-L)
- 1097-010X
- OpenAlex
- W2095049226
- Cited by
- 20
- References
- 1
- Citations by year
- 2021: 2 · 2020: 1 · 2019: 1 · 2015: 1 · 2014: 1 · 2012: 1
- FWCI
- 0.91
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Experimental Zoology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Structure and Function
- Keywords
- Drosophila melanogaster, oogenesis, nucleolar morphology, nurse cells, egg chamber, female sterility, RNA synthesis, protein synthesis, ribosome, translation fidelity
- MeSH terms
- Autoradiography, Cell Nucleolus, Chromosomes, Dactinomycin, Drosophila, Female, Heterozygote, Homozygote, Leucine, Molecular Biology, Mutation, Ovary, Ovum, Radiometry, Ribonucleases, Ribosomes, RNA, Suppression, Genetic, Protein Biosynthesis, Tritium, Trypsin, Uridine, Culture Techniques
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