| Literature DB >> 31123040 |
Lena Annika Street1, Ana Karina Morao1, Lara Heermans Winterkorn1, Chen-Yu Jiao1, Sarah Elizabeth Albritton1, Mohammed Sadic1, Maxwell Kramer1, Sevinç Ercan2.
Abstract
Condensins are evolutionarily conserved protein complexes that are required for chromosome segregation during cell division and genome organization during interphase. In Caenorhabditis elegans, a specialized condensin, which forms the core of the dosage compensation complex (DCC), binds to and represses X chromosome transcription. Here, we analyzed DCC localization and the effect of DCC depletion on histone modifications, transcription factor binding, and gene expression using chromatin immunoprecipitation sequencing and mRNA sequencing. Across the X, the DCC accumulates at accessible gene regulatory sites in active chromatin and not heterochromatin. The DCC is required for reducing the levels of activating histone modifications, including H3K4me3 and H3K27ac, but not repressive modification H3K9me3. In X-to-autosome fusion chromosomes, DCC spreading into the autosomal sequences locally reduces gene expression, thus establishing a direct link between DCC binding and repression. Together, our results indicate that DCC-mediated transcription repression is associated with a reduction in the activity of X chromosomal gene regulatory elements.Entities:
Keywords: C. elegans; X chromosome; chromatin; condensin; dosage compensation; gene expression; gene regulation; histone modifications; transcription
Mesh:
Substances:
Year: 2019 PMID: 31123040 PMCID: PMC6614895 DOI: 10.1534/genetics.119.302254
Source DB: PubMed Journal: Genetics ISSN: 0016-6731 Impact factor: 4.562