H3K27 modifications define segmental regulatory domains in the Drosophila bithorax complex

Author:

Bowman Sarah K12,Deaton Aimee M12,Domingues Heber3,Wang Peggy I12,Sadreyev Ruslan I14,Kingston Robert E12,Bender Welcome3

Affiliation:

1. Department of Molecular Biology, Massachusetts General Hospital, Boston, United States

2. Department of Genetics, Harvard Medical School, Boston, United States

3. Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, United States

4. Department of Pathology, Harvard Medical School, Boston, United States

Abstract

The bithorax complex (BX-C) in Drosophila melanogaster is a cluster of homeotic genes that determine body segment identity. Expression of these genes is governed by cis-regulatory domains, one for each parasegment. Stable repression of these domains depends on Polycomb Group (PcG) functions, which include trimethylation of lysine 27 of histone H3 (H3K27me3). To search for parasegment-specific signatures that reflect PcG function, chromatin from single parasegments was isolated and profiled. The H3K27me3 profiles across the BX-C in successive parasegments showed a ‘stairstep’ pattern that revealed sharp boundaries of the BX-C regulatory domains. Acetylated H3K27 was broadly enriched across active domains, in a pattern complementary to H3K27me3. The CCCTC-binding protein (CTCF) bound the borders between H3K27 modification domains; it was retained even in parasegments where adjacent domains lack H3K27me3. These findings provide a molecular definition of the homeotic domains, and implicate precisely positioned H3K27 modifications as a central determinant of segment identity.

Funder

National Institutes of Health

National Institute of General Medical Sciences

Damon Runyon Cancer Research Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference50 articles.

1. Characterization of the intergenic RNA profile at abdominal-A and Abdominal-B in the Drosophila bithorax complex;Bae;Proceedings of the National Academy of Sciences of USA,2002

2. P element homing to the Drosophila bithorax complex;Bender;Development,2000

3. The border between the Ultrabithorax and abdominal-A regulatory domains in the Drosophila bithorax complex;Bender;Genetics,2013

4. Variant PRC1 complex-dependent H2A ubiquitylation drives PRC2 recruitment and polycomb domain formation;Blackledge;Cell,2014

5. Molecular definition of the morphogenetic and regulatory functions and the cis-regulatory elements of the Drosophila Abd-B homeotic gene;Boulet;Development,1991

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