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A variably occupied CTCF binding site in the ultrabithorax gene in the Drosophila bithorax complex.


Type

Article

Change log

Authors

Magbanua, Jose Paolo 
Runneburger, Estelle 
Russell, Steven 

Abstract

Although the majority of genomic binding sites for the insulator protein CCCTC-binding factor (CTCF) are constitutively occupied, a subset show variable occupancy. Such variable sites provide an opportunity to assess context-specific CTCF functions in gene regulation. Here, we have identified a variably occupied CTCF site in the Drosophila Ultrabithorax (Ubx) gene. This site is occupied in tissues where Ubx is active (third thoracic leg imaginal disc) but is not bound in tissues where the Ubx gene is repressed (first thoracic leg imaginal disc). Using chromatin conformation capture, we show that this site preferentially interacts with the Ubx promoter region in the active state. The site lies close to Ubx enhancer elements and is also close to the locations of several gypsy transposon insertions that disrupt Ubx expression, leading to the bx mutant phenotype. gypsy insertions carry the Su(Hw)-dependent gypsy insulator and were found to affect both CTCF binding at the variable site and the chromatin topology. This suggests that insertion of the gypsy insulator in this region interferes with CTCF function and supports a model for the normal function of the variable CTCF site as a chromatin loop facilitator, promoting interaction between Ubx enhancers and the Ubx transcription start site.

Description

Keywords

Animals, Binding Sites, CCCTC-Binding Factor, Chromatin, Chromatin Immunoprecipitation, Crosses, Genetic, Drosophila Proteins, Drosophila melanogaster, Enhancer Elements, Genetic, Homeodomain Proteins, Larva, Oligonucleotide Array Sequence Analysis, Promoter Regions, Genetic, Protein Binding, Repressor Proteins, Transcription Factors

Journal Title

Mol Cell Biol

Conference Name

Journal ISSN

0270-7306
1098-5549

Volume Title

35

Publisher

Informa UK Limited
Sponsorship
Wellcome Trust (089834/Z/09/Z)
The work was supported by the Wellcome Trust [089834/Z/09/Z] and ER was supported by the Erasmus Programme.