Reference Report
| Reference | |||
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| Citation | Ronsseray, S., Lehmann, M., Nouaud, D., Anxolabehere, D. (1996). The regulatory properties of autonomous subtelomeric P elements are sensitive to a Suppressor of variegation in Drosophila melanogaster. Genetics 143(4): 1663--1674. (Export to RIS) | ||
| FlyBase ID | FBrf0089801 | ||
| Publication Type | Research paper | ||
| PubMed ID | 8844154 | ||
| PubMed Abstract | Genetic recombination was used in Drosophila melanogaster to isolate P elements, inserted at the telomeres of X chromosomes (cytological site IA) from natural populations, in a genetic background devoid of other P elements. We show that complete maternally inherited P repression in the germline (P cytotype) can be elicited by only two autonomous P elements at 1A and that a single element at this site has partial regulatory properties. The analysis of the surrounding chromosomal regions of the P elements at 1A shows that in all cases these elements are flanked by Telomeric Associated Sequences, tandemly repetitive noncoding sequences that have properties of heterochromatin. In addition, we show that the regulatory properties of P elements at 1A can be inhibited by some of the mutant alleles of the Su(var)205 gene and by a deficiency of this gene. However, the regulatory properties of reference P strains (Harwich and Texas 007) are not impaired by Su(var)205 mutations. Su(var)205 encodes Heterochromatin Protein 1 (HP1). These results suggest that the HP1 dosage effect on the P element properties is site-dependent and could involve the structure of the chromatin. | ||
| DOI | |||
| Related Publication(s) | |||
| Erratum | The regulatory properties of autonomous subtelomeric P elements are sensitive to a Suppressor of variegation in Drosophila
melanogaster. Ronsseray et al., 1996, Genetics 144(3): 1329 [FBrf0091286] |
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| Language of Publication | English | ||
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Parent Publication
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| Publication Type | Journal | ||
| Abbreviation | Genetics | ||
| Title | Genetics | ||
| Publication Year | 1916- | ||
| ISBN/ISSN | 0016-6731 | ||
Data from Reference
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Aberrations (1)
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Alleles (10)
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Genes (11)
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Insertions (3)
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Natural transposons (1)
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