Abstract
The white gene in the A(R)4-24 P[white,rosy] insertion on chromosome 2 has a novel expression pattern, in which it is repressed in the dorsal half of the eye. X-ray mutagenesis led to the isolation of six revertants mapping to chromosome 2, which are wild type in a zeste(+) background, and three extreme derivatives, in which white gene expression is repressed in ventral regions of the eye as well. By Southern blot analyses the breakpoints of five of the revertants and one of the extreme derivatives were mapped in the flanking DNA bordering each side of the A(R)4-24 insertion. The revertants show some dorsal repression of white in the presence of z(1), and by this criterion each is only a partial revertant. The extreme derivatives act not only in cis, but also in trans to repress expression of A(R)4-24 and its various derivatives. We provide evidence that these trans effects are proximity-dependent effects, possibly mediated by pairing of gene copies, as they do not extend to copies of the white gene located elsewhere in the genome. We show that one extreme derivative, E1, is a small deletion spanning the insertion site at the 5' end of the white gene, and propose that the distance between a negative regulatory element in the 5' flanking DNA and the white promoter influences the degree of the repression.
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- Abraham J., Nasmyth K. A., Strathern J. N., Klar A. J., Hicks J. B. Regulation of mating-type information in yeast. Negative control requiring sequences both 5' and 3' to the regulated region. J Mol Biol. 1984 Jul 5;176(3):307–331. doi: 10.1016/0022-2836(84)90492-3. [DOI] [PubMed] [Google Scholar]
- Ashburner M. Gene activity dependent on chromosome synapsis in the polytene chromosomes of Drosophila melanogaster. Nature. 1967 Jun 10;214(5093):1159–1160. doi: 10.1038/2141159b0. [DOI] [PubMed] [Google Scholar]
- Babu P., Selvakumar K. S., Bhosekar S. Studies on transvection at the bithorax complex in Drosophila melanogaster. Mol Gen Genet. 1987 Dec;210(3):557–563. doi: 10.1007/BF00327212. [DOI] [PubMed] [Google Scholar]
- Biggin M. D., Bickel S., Benson M., Pirrotta V., Tjian R. Zeste encodes a sequence-specific transcription factor that activates the Ultrabithorax promoter in vitro. Cell. 1988 Jun 3;53(5):713–722. doi: 10.1016/0092-8674(88)90089-x. [DOI] [PubMed] [Google Scholar]
- Bingham P. M. The Regulation of White Locus Expression: A Dominant Mutant Allele at the White Locus of DROSOPHILA MELANOGASTER. Genetics. 1980 Jun;95(2):341–353. doi: 10.1093/genetics/95.2.341. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Castelli-Gair J. E., Micol J. L., García-Bellido A. Transvection in the Drosophila Ultrabithorax gene: a Cbx1 mutant allele induces ectopic expression of a normal allele in trans. Genetics. 1990 Sep;126(1):177–184. doi: 10.1093/genetics/126.1.177. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dutton F. L., Jr, Chovnick A. Developmental regulation of the rosy locus in Drosophila melanogaster. Dev Biol (N Y 1985) 1988;5:267–316. doi: 10.1007/978-1-4615-6817-9_10. [DOI] [PubMed] [Google Scholar]
- Feldman J. B., Hicks J. B., Broach J. R. Identification of sites required for repression of a silent mating type locus in yeast. J Mol Biol. 1984 Oct 5;178(4):815–834. doi: 10.1016/0022-2836(84)90313-9. [DOI] [PubMed] [Google Scholar]
- Gelbart W. M. Synapsis-dependent allelic complementation at the decapentaplegic gene complex in Drosophila melanogaster. Proc Natl Acad Sci U S A. 1982 Apr;79(8):2636–2640. doi: 10.1073/pnas.79.8.2636. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gelbart W. M., Wu C. T. Interactions of zeste mutations with loci exhibiting transvection effects in Drosophila melanogaster. Genetics. 1982 Oct;102(2):179–189. doi: 10.1093/genetics/102.2.179. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hazelrigg T., Levis R., Rubin G. M. Transformation of white locus DNA in drosophila: dosage compensation, zeste interaction, and position effects. Cell. 1984 Feb;36(2):469–481. doi: 10.1016/0092-8674(84)90240-x. [DOI] [PubMed] [Google Scholar]
- Jack J. W., Judd B. H. Allelic pairing and gene regulation: A model for the zeste-white interaction in Drosophila melanogaster. Proc Natl Acad Sci U S A. 1979 Mar;76(3):1368–1372. doi: 10.1073/pnas.76.3.1368. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Judd B. H. Transvection: allelic cross talk. Cell. 1988 Jun 17;53(6):841–843. doi: 10.1016/s0092-8674(88)90209-7. [DOI] [PubMed] [Google Scholar]
- Kornher J. S., Brutlag D. Proximity-dependent enhancement of Sgs-4 gene expression in D. melanogaster. Cell. 1986 Mar 28;44(6):879–883. doi: 10.1016/0092-8674(86)90010-3. [DOI] [PubMed] [Google Scholar]
- Levis R., Hazelrigg T., Rubin G. M. Effects of genomic position on the expression of transduced copies of the white gene of Drosophila. Science. 1985 Aug 9;229(4713):558–561. doi: 10.1126/science.2992080. [DOI] [PubMed] [Google Scholar]
- Lindsley D. L., Sandler L., Baker B. S., Carpenter A. T., Denell R. E., Hall J. C., Jacobs P. A., Miklos G. L., Davis B. K., Gethmann R. C. Segmental aneuploidy and the genetic gross structure of the Drosophila genome. Genetics. 1972 May;71(1):157–184. doi: 10.1093/genetics/71.1.157. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mansukhani A., Crickmore A., Sherwood P. W., Goldberg M. L. DNA-binding properties of the Drosophila melanogaster zeste gene product. Mol Cell Biol. 1988 Feb;8(2):615–623. doi: 10.1128/mcb.8.2.615. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mansukhani A., Gunaratne P. H., Sherwood P. W., Sneath B. J., Goldberg M. L. Nucleotide sequence and structural analysis of the zeste locus of Drosophila melanogaster. Mol Gen Genet. 1988 Jan;211(1):121–128. doi: 10.1007/BF00338402. [DOI] [PubMed] [Google Scholar]
- Micol J. L., García-Bellido A. Genetic analysis of "transvection" effects involving contrabithorax mutations in Drosophila melanogaster. Proc Natl Acad Sci U S A. 1988 Feb;85(4):1146–1150. doi: 10.1073/pnas.85.4.1146. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pirrotta V., Manet E., Hardon E., Bickel S. E., Benson M. Structure and sequence of the Drosophila zeste gene. EMBO J. 1987 Mar;6(3):791–799. doi: 10.1002/j.1460-2075.1987.tb04821.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Robertson H. M., Preston C. R., Phillis R. W., Johnson-Schlitz D. M., Benz W. K., Engels W. R. A stable genomic source of P element transposase in Drosophila melanogaster. Genetics. 1988 Mar;118(3):461–470. doi: 10.1093/genetics/118.3.461. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schnell R., Rine J. A position effect on the expression of a tRNA gene mediated by the SIR genes in Saccharomyces cerevisiae. Mol Cell Biol. 1986 Feb;6(2):494–501. doi: 10.1128/mcb.6.2.494. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smolik-Utlaut S. M., Gelbart W. M. The effects of chromosomal rearrangements on the zeste-white interaction in Drosophila melanogaster. Genetics. 1987 Jun;116(2):285–298. doi: 10.1093/genetics/116.2.285. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wu C. T., Goldberg M. L. The Drosophila zeste gene and transvection. Trends Genet. 1989 Jun;5(6):189–194. doi: 10.1016/0168-9525(89)90074-7. [DOI] [PubMed] [Google Scholar]