scholarly journals Deletion of an Insulator Element by the Mutation facet-strawberry in Drosophila melanogaster

Genetics ◽  
2000 ◽  
Vol 155 (3) ◽  
pp. 1297-1311
Author(s):  
Julio Vazquez ◽  
Paul Schedl

Abstract Eukaryotic chromosomes are thought to be subdivided into a series of structurally and functionally independent units. Critical to this hypothesis is the identification of insulator or boundary elements that delimit chromosomal domains. The properties of a Notch mutation, facet-strawberry (faswb), suggest that this small deletion disrupts such a boundary element. faswb is located in the interband separating polytene band 3C7, which contains Notch, from the distal band 3C6. The faswb mutation alters the structural organization of the chromosome by deleting the interband and fusing 3C7 with 3C6. Genetic studies also suggest that faswb compromises the functional autonomy of Notch by allowing the locus to become sensitive to chromosomal position effects emanating from distal sequences. In the studies reported here, we show that a DNA fragment spanning the faswb region can insulate reporter transgenes against chromosomal position effects and can block enhancer-promoter interactions. Moreover, we find that insulating activity is dependent on sequences deleted in faswb. These results provide evidence that the element defined by the faswb mutation corresponds to an insulator.

Genetics ◽  
2000 ◽  
Vol 155 (3) ◽  
pp. 1195-1211 ◽  
Author(s):  
Albert Briscoe ◽  
John E Tomkiel

Abstract In Drosophila melanogaster, the rDNA loci function in ribosome biogenesis and nucleolar formation and also as sex chromosome pairing sites in male meiosis. These activities are not dependent on the heterochromatic location of the rDNA, because euchromatic transgenes are competent to form nucleoli and restore pairing to rDNA-deficient X chromosomes. These transgene studies, however, do not address requirements for the function of the endogenous rDNA loci within the heterochromatin. Here we describe two chromosome rearrangements that disrupt rDNA functions. Both rearrangements are translocations that cause an extreme bobbed visible phenotype and XY nondisjunction and meiotic drive in males. However, neither rearrangement interacts with a specific Y chromosome, Ymal+, that induces male sterility in combination with rDNA deletions. Molecular studies show that the translocations are not associated with gross rearrangements of the rDNA repeat arrays. Rather, suppression of the bobbed phenotypes by Y heterochromatin suggests that decreased rDNA function is caused by a chromosomal position effect. While both translocations affect rDNA transcription, only one disrupts meiotic XY pairing, indicating that there are different cis-acting requirements for rDNA transcription and rDNA-mediated meiotic pairing.


Author(s):  
I. I. Deak ◽  
A. Rähmi ◽  
P. R. Bellamy ◽  
M. Bienz ◽  
A. Blumer ◽  
...  

1995 ◽  
Vol 42 (2) ◽  
pp. 161-170
Author(s):  
R Miassod ◽  
N Jullien

We have investigated the loop organization of a 835 kilobases DNA fragment from the Drosophila genome. This analysis has focused on the periodicity of the distribution of anchoring sequences (SARs) and its relationship to the distribution of A,T-rich regions, transcription units, repeated elements, putative replication origins and topoisomerase II cleavage sites. Altogether, the data support the idea of an active participation of SARs to the structural organization and functioning of this eukaryotic genome.


Genetics ◽  
2013 ◽  
Vol 195 (3) ◽  
pp. 871-881 ◽  
Author(s):  
Bianca Diaconeasa ◽  
G. Harper Mazock ◽  
Anthony P. Mahowald ◽  
Ronald R. Dubreuil

Genetics ◽  
1990 ◽  
Vol 125 (1) ◽  
pp. 141-154 ◽  
Author(s):  
B T Wakimoto ◽  
M G Hearn

Abstract The light (lt) gene of Drosophila melanogaster is located at the base of the left arm of chromosome 2, within or very near centromeric heterochromatin (2Lh). Chromosome rearrangements that move the lt+ gene from its normal proximal position and place the gene in distal euchromatin result in mosaic or variegated expression of the gene. The cytogenetic and genetic properties of 17 lt-variegated rearrangements are described in this report. We show that five of the heterochromatic genes adjacent to lt are subject to inactivation by these rearrangements and that the euchromatic loci in proximal 2L are not detectably affected. The properties of the rearrangements suggest that proximity to heterochromatin is an important regulatory requirement for at least six 2Lh genes. We discuss how the properties of the position effects on heterochromatic genes relate to other proximity-dependent phenomena such as transvection.


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