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. 1980 Jul;95(3):661–672. doi: 10.1093/genetics/95.3.661

Analysis of the Autosomal Mutation abo and Its Interaction with the Ribosomal DNA of DROSOPHILA MELANOGASTER: The Role of X-Chromosome Heterochromatin

Barry Yedvobnick 1, Hallie M Krider 1, Bryan I Levine 1
PMCID: PMC1214253  PMID: 6777245

Abstract

The autosomal recessive, maternal-effect mutation abnormal oocyte (abo: 2–38) preferentially lowers the viability of XO progeny. The severity of the sex-ratio distortion is reduced by duplications of maternal or zygotic heterochromatin (Sandler 1970, 1977; Parry and Sandler 1974). Utilizing X-chromosome inversions that contain modifications in the quantity and arrangement of the heterochromatic functions, Xhabo and cr+, we have extended our investigations of abo's influence on XO male recovery and rDNA redundancy (Krider, Yedvobnick and Levine 1979).——XO males bearing In(1)scS1Lsc4R or In(1)wm4Lsc4R are recovered twice as frequently as X chromosomes containing a single Xh region, implying that these inversions possess a duplication of Xhabo. abo mutant females heterozygous for In(1)scS1Lsc4R and wild-type X chromosomes generate XO progeny that do not contain elevated rDNA redundancies. XO males containing In(1)wm4 exhibit male recoveries and rDNA elevations similar to those of males bearing a wild-type X chromosome, when both derive from a common abo/abo mother. Reciprocal crosses between In(1)wm4 and Canton-S males to attached-X abo females show significant, though reduced, sex ratios in the absence of an rDNA effect. The observation that abo can elevate the rDNA redundancy of In(1)wm4, a chromosome that does not compensate, suggests that abo and cr+ functions are not directly related.

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Selected References

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

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