| Literature DB >> 30082280 |
Anna Fedotova1, Tsutomu Aoki2, Mikaël Rossier3, Rakesh Kumar Mishra4, Chaevia Clendinen2, Olga Kyrchanova1, Daniel Wolle2, Artem Bonchuk1, Robert K Maeda3, Annick Mutero4, Fabienne Cleard3, Vladic Mogila1, François Karch3, Pavel Georgiev1, Paul Schedl5.
Abstract
Boundaries (insulators) in the Drosophila bithorax complex (BX-C) delimit autonomous regulatory domains that orchestrate the parasegment (PS)-specific expression of the BX-C homeotic genes. The Fab-7 boundary separates the iab-6 and iab-7 regulatory domains, which control Abd-B expression in PS11 and PS12, respectively. This boundary is composed of multiple functionally redundant elements and has two key functions: it blocks cross talk between iab-6 and iab-7 and facilitates boundary bypass. Here, we show that two BEN domain protein complexes, Insensitive and Elba, bind to multiple sequences located in the Fab-7 nuclease hypersensitive regions. Two of these sequences are recognized by both Insv and Elba and correspond to a CCAATTGG palindrome. Elba also binds to a related CCAATAAG sequence, while Insv does not. However, the third Insv recognition sequences is ∼100 bp in length and contains the CCAATAAG sequence at one end. Both Insv and Elba are assembled into large complexes (∼420 and ∼265-290 kDa, respectively) in nuclear extracts. Using a sensitized genetic background, we show that the Insv protein is required for Fab-7 boundary function and that PS11 identity is not properly established in insv mutants. This is the first demonstration that a BEN domain protein is important for the functioning of an endogenous fly boundary.Entities:
Keywords: Abdominal B; BEN DNA-binding domain; Elba; Fab-7; Insensitive; bithorax; boundary; chromatin; insulator; parasegment identity
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Year: 2018 PMID: 30082280 PMCID: PMC6216583 DOI: 10.1534/genetics.118.301259
Source DB: PubMed Journal: Genetics ISSN: 0016-6731 Impact factor: 4.562